NOVEL GLP-1 COMPOUNDS. FIELD OF THE INVENTION The present invention relates to novel GLP-1 compounds, to pharmaceutical compositions comprising these compounds and to the use of the compounds for the treatment of diseases related to diabetes. BACKGROUND OF THE INVENTION Diabetes mellitus is a metabolic disorder in which the ability to utilize glucose is partly or completely lost. About 5% of all people suffer from diabetes and the disorder ap­proaches epidemic proportions. Since the introduction of insulin in the 1920's, continuous efforts have been made to improve the treatment of diabetes mellitus.One peptidej expected to become very important in the treatment of diabetes is gluca-gon-like peptide-1 (GLP-1). Human GLP-1 is a 37 amino acid residue peptide originating from preproglucagon which is synthesized i.a. in the L-cells in the distal ileum, in the pancreas and in the brain. GLP-1 is an important gut hormone with regulatory function in glucose metabo­lism and gastrointestinal secretion and metabolism. GLP-1 stimulates insulin secretion in a glucose-dependant manner, stimulates insulin biosynthesis, promotes beta cell rescue, de­creases glucagon secretion, gastric emptying and food intake. Human GLP-1 is hydrolysed to GLP-1 (7-37) and GLP-1 (7-36)-amide which are both insulinotropic peptides.. A simple sys­tem is used to describe fragments and analogues of this peplide. Thus, for example. [GIY8]GLP-1(7-37) designates an analogue of GLP-1(7-37) formally derived from GLP-1(7-37) by substituting the naturally occurring amino acid residue in position 8 (Ala) by Gly. Simi­larly, (NE34-tetradecanoyl)[Lys34]GLP-1(7-37) designates GLP-1 (7-37) wherein the e-amino group of the Lys residue in position 34 has been tetradecanoylated. PCT publications WO 98/08871 and WO 99/43706 disclose stable derivatives of GLP-1 analogues, which have a lipophilic substituent. These stable derivatives of GLP-1 analogues have a protracted profile of action compared to the corresponding GLP-1 analogues.In the last decade a number of peptides have been isolated from the venom of the Gila monster lizards (Heloderma suspectum and Heloderma horridum). Exendin-4 is a 39 amino acid residue peptide isolated from the venom of Heloderma suspectum, and this peptide shares 52% homology with GLP-1(7-37) in the overlapping region. Exendin-4 is a potent GLP-1 recep­tor agonist which has been shown to stimulate insulin release and ensuing lowering of the blood glucose level when injected into dogs. The group of exendin-4(1-39), certain fragments thereof, analogs thereof and derivatives thereof, are potent insulinotropic agents. Most importantly the group of exendin-4(1-39), insulinotropic fragments thereof, insulinotropic analogs thereof and insulinotropic derivatives thereof.Common to GLP-1 and exendins are that an extensive amount of variants have been synthesized and studied in particular in relation the plasma half-life. Low plasma half-lifes may be due to chemical stability towards peptidases (mainly dipeptidyl aminopeptidase IV) and to renal clearance. However, these analogues and derivatives of insulionotropic pep-tides lack a satisfactory bioavailability when administered by the pulmonary route, i.e. when administered to the lower respira'ry tract such as through the bronchioles or alveoli.WO 00/66629 discloses modified exendin agonists which have been coupled to olyethyleneglycol via a lysine residue to decrease renal clearance.WO 03/40309 discloses peptide acting as both GLP-1 receptor agonists and gluca-gon receptor antagonists. Among the disclosed peptides are two peptides which have been coupled to polyethyleneglycol via a C-temninal cycteine residue.WO 2004/093823 discloses polyethylene glycolated GLOP-1 peptides. Pulmonary administration of GLP-1 peptides have been disclosed in WO 01/51071 and WO 00/12116.The insulinotropic peptides derived from GLP-1 and Exendin-4 stimulatesd insulin release only when plasma glucose levels are high, the risk of hypoglycaemic events is re­duced. Thus, the peptides are particularly useful for patients with diabetes who no longer re­spond to OHA's (oral hyperglycaemic agents) and who should from a strict medical point of view be administered insulin. Patients and to some extent also doctors are often not keen on initiating insulin treatment before this is absolutely necessary, presumably because of the fear of hypoglycaemic events or the fear of injections/needles. Thus, there is a need for insu­linotropic peptides which are sufficiently potent and which can be administered by the pul­monary route.Thus, it is an object of the present invention to provide insulinotropic peptides which have sufficient pulmonary bioavailability to serve as an alternative to peptides for paranteral ad­ministration. Insulinotropic peptides having pulmonary bioavailability is a balance between potency and bioavailability. It is also an object of the present invention to provide insulino­tropic peptides which are less prone to aggregation, a well known problem associated with the glucagon-like peptides. Being less prone to aggregation facilitates economical manufac­turing processes as well as enabling the compounds to be administered by medical infusion pumps. DEFINITIONS •In the present specification", the following terms have the indicated meaning : The term "polypeptide" and "peptide" as used herein means a compound composed of at least five constituent amino acids connected by peptide bonds. The constituent amino acids may be from the group of the amino acids encoded by the genetic code and they may natural amino acids which are not encoded by the genetic code, as well as synthetic amino acids. Natural amino acids which are not encoded by the genetic code are e.g. hy-droxyproline, y-carboxyglutamate, omithine, phosphoserine, D-alanine and D-glutamine.Synthetic amino acids comprise amino acids manufactured by chemical synthesis, i.e. D-isomers of the amino acids encoded by the genetic code such as D-alanine and D-leucine, Aib (o-aminoisobutyric acid), Abu (α -aminobutyric acid), Tle (tert-butylglycine), -βalanine, 3-aminomethyl benzoic acid, anthranilic acid.The term "analogue" as used herein referring to a polypeptide means a modified peptide wherein one or more amino acid residues of the peptide have been substituted by other amino acid residues and/or wherein one or more amino acid residues have been de­leted from the peptide and/or wherein one or more amino acid residues have been deleted from the peptide and or wherein one or more amino acid residues have been added to the peptide. Such addition or deletion of amino acid residues can take place at the N-terminal of the peptide and/or at the C-terminal of the peptide. A simple system is often used to describe analogues : For example [Arg34lGLP-l(7-37)Lys designates a GLP-1(7-37) analogue wherein the naturally occuring lysine at position 34 has been substituted with arginine and wherein a lysine has been added to the terminal amino acid residue, i.e. to the Gly37. All amino acids for which the optical isomer is not stated is to be understood to mean the L-isomer. The term "derivative" as used herein in relation to a peptide means a chemically modified peptide or an analogue thereof, wherein at least one substituent is not present in the unmodi-fied peptide or an analogue thereof, i.e. a peptide which has been covalently modified. Typi­cal modifications are amides, carbohydrates, alkyl groups, acyl groups, esters and the tike. An example of a derivative of GLP-1 (7-37) is Ne26-((4S)-4-(hexadecanoylamino)-butanoyOfArg34, Lys26]GLP-l-(7-37).The term "insulinotropic agent" as used herein means a compound which is an ago­nist of the human GLP-1 receptor, i.e. a compound which stimulates the formation of cAMP in a suitable medium containing the human GLP-1 receptor (one such medium disclosed be­low). The potency of an insulinotropic agent is determined by calculating the EC50 value from the dose-response curve as described below.Baby hamster kidney (BHK) cells expressing the cloned human GLP-1 receptor (BHK- 467-12A) were grown in DMEM media with the addition of 100 IU/mL penicillin, 100 ug/mL streptomycin, 5% fetal calf serum and 0.5 mg/mL Geneticin G-418 (Life Technolo­gies). The cells were washed twice in phosphate buffered saline and harvested with Versene. Plasma membranes were prepared from the cells by homogenisation with an Ultra-turrax in buffer 1 (20 mM HEPES-Na, 10 mM EDTA, pH 7.4). The homogenate was centri-fuged at 48,000 x g for 15 min at 40C. The pellet was suspended by homogenization in buffer 2 (20 mM HEPES-Na, 0.1 mM EDTA, pH 7.4), then centrifuged at 48,000 x g for 15 min at 4°C. The washing procedure was repeated one more time. The final pellet was suspended in buffer 2 and used immediately for assays or stored at -80°C.The functional receptor assay was carried out by measuring cyclic AMP (cAMP) as a response to stimulation by the insulinotropic agent. cAMP formed was quantified by the Al-phaScreen™ cAMP Kit (Perkin Elmer Life Sciences). Incubations were carried out in half-area 96-well microtiter plates in a total volume of 50 μL buffer 3 (50 mM Tris-HCI, 5 mM HEPES. 10 mM MgCI2, pH 7.4) and with the following addiditions: 1 mM ATP, 1 μM GTP, 0.5 mM 3-isobutyl-1-methy!xanthine (IBMX), 0.01 % Tween-20, 0.1% BSA, 6 μg membrane preparation, 15 ug/mL acceptor beads, 20μg/mL donor beads preincubated with 6 nM bioti-nyl-cAMP. Compounds to be tested for agonist activity were dissolved and diluted in buffer 3. GTP was freshly prepared for each experiment. The plate was incubated in the dark with slow agitation for three hours at room temperature followed by counting in the Fusion™ in­strument (Perkin Elmer Life Sciences). Concentration-response curves were plotted for the individual compounds and EC50 values estimated using a four-parameter logistic model withPrism v. 4.0 (GraphPad, Carlsbad, CA).The term "GLP-1 peptide" as used herein means GLP-1 (7-37) (SEQ ID No 1), aGLP-1 (7-37) analogue, a GLP-1 (7-37) derivative or a derivative of a GLP-1 (7-37) analogue. In one embodiment the GLP-1 peptide is an insulinotropic agent.The term "exendin-4 peptide" as used herein means exendin-4(1-39) (SEQ ID No 2). an exendin-4(1-39) analogue, an exendin-4 (1-39) derivative or a derivative of an exendin-4(1-39) analogue. In one embodiment the exendin-4 peptide is an insulinotropic agent.The term "DPP-IV protected" as used herein referring to a polypeptide means a poly-peptide which has been chemically modified in order to render said compound resistant to the plasma peptidase dipeptidyl aminopeptidase-4 (DPP-IV). The DPP-IV enzyme in plasma is known to be involved in the degradation of several peptide hormones, e.g. GLP-1, GLP-2, Ex­endin-4 etc. Thus, a considerable effort is being made to develop analogues and derivatives of the polypeptides susceptible to DPP-IV mediated hydrolysis in order to reduce the rate of deg­radation by DPP-IV. In one embodiment a DPP-IV protected peptide is more resistant to DPP-IV than GLP-1 (7-37) or Exendin-4(1-39).Resistance of a peptide to degradation by dipeptidyl aminopeptidase IV is determined by the following degradation assay :Aliquots of the peptide (5 nmol) are incubated at 37 °C with 1 μL of purified dipeptidyl amin­opeptidase IV corresponding to an enzymatic activity of 5 mU for 10-180 minutes in 100 μL of 0.1 M triethylamine-HCI buffer, pH 7.4. Enzymatic reactions are terminated by the addition of 5 μL of 10% trifluoroacetic acid, and the peptide degradation products are separated and quantified using HPLC analysis. One method for performing this analysis is : The mixtures are applied onto a Vydac C18 widepore (30 nm pores. 5 μm particles) 250 x 4.6 mm column and eluted at a flow rate of 1 ml/min with linear stepwise gradients of acetonitrile in 0.1% trifluoroacetic acid (0% acetonitrile for 3 min, 0-24% acetonitrile for 17 min, 24-48% acetoni­trile for 1 min) according to Siegel et a!., Regul. Pept. 1999:79:93-102 and Mentlein et al. Eur. J. Biochern. 1993:214:829-35. Peptides and their degradation products may be moni­tored by their absorbance at 220 nm (peptide bonds) or 280 nrn (aromatic amino acids), and are quantified by integration of their peak areas related to those of standards. The rate of hy­drolysis of a peptide by dipeptidyl aminopeptidase IV is estimated at incubation times which result in less than 10% of the peptide being hydrolysed.The term "mPEGyl" means a polydisperse or monodisperse radical of the structurewherein m is an integer larger than 1 . Thus, a mPEGyl wherein m is 90 has a molecular weight of 3991 Da, i.e. approx 4kDa. Likewise, a mPEGyl with an average molecular weigt of 20 kDa has an average m of 454. Due to the process for producing mPEGyl these molecues often have a distribution of molecular weights. This distribution is described by the polydis-persity index.The term "polydispersity index" as used herein means the ratio between the weight average molecular weight and the number average molecular weight, as known in the art of polymer chemistry (see e.g. "Polymer Synthesis and Characterization", J.a: Nairn, diversity of Utah. 2003). The polydispersity index is a number which is greater than or qual to one, and it may be estimated from Gel Permeation Chromatographic data. When the polydisper­sity index is one the product is monodisperse. and is thus made up of a single moleculer weight. When the polydispersity index is greater than one it is a measure of the polydisper­sity of that polymer, i.e. how broad the distribution of polymers with different molecular weights is.The term "C^-alkyl" as used herein means a saturated, branched, straight or cyclic hydrocarbon group having from 1 to 6 carbon atoms. Representative examples include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, butyl, isobutyl, sec-butyl, terf-butyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, n-hexyl, isohexyl, cyclohexane and the like. The term "pharmaceutically acceptable" as used herein means suited for normal pharmaceu­tical applications, i.e. giving rise to no adverse events in patients etc.The term "heavy atom" as used herein means an atom having a molar weight equal to or larger than carbon, e.g. C, N, O and S.The term "excipient" as used herein means the chemical compounds which are normally added to pharmaceutical compositions, e.g. buffers, tonicity agents, preservatives and the like.The term "effective amount" as used herein means a dosage which is sufficient to be effec­tive for the treatment of the patient compared with no treatment.The term "pharmaceutical composition" as used herein means a product comprising an ac­tive compound or a salt thereof together with pharmaceutical excipients such as buffer, pre­servative, and optionally a tonicity modifier and/or a stabilizer. Thus a pharmaceutical com­position is also known in the art as a pharmaceutical formulation.The term "treatment of a disease" as used herein means the management and care of a pa­tient having developed the disease, condition or disorder. The purpose of treatment is to combat the disease, condition or disorder. Treatment includes the administration of the active compounds to eliminate or control the disease, condition er disorder as well as to alleviate the symptoms or complications associated with the disease, condition or disorder. DESCRIPTION OF THE INVENTION In one aspect the present invention relates to a compound having the structure of the formula (I):Insulinotropic agent(-Y-C')rQ (I)whereinInsulinotropic agent is a radical derived from an insulinotropic peptide which binds to the hu­man GLP-1 receptor, or a redical derived from a peptide in which 22 positions out of the first 30 are identical to those found in corresponding positions in GLP-1 or found in corresponding positions in Exendin-4, andY is a bivalent connecting chemical group connecting C' with the Insuljnotropic agent, and C' is a bivalent polar separating chemical group where 50 - 20% of the heavy atoms are ei-therO or N, and f is 0 or 1 and Q is selected from (Figure Removed) whereinA is a polar chemical group of a single molecular size (monodisperse) or of several molecular sizes (polydisperse) where50 - 20% of the heavy atoms are independently oxygen or nitrogen, andW is a bivalent chemical group whereby A is connected, andX is a bivalent connecting chemical group whereby B is connected, and B is a connecting or branching chemical group.In another aspect the present invention relates to a compound having the structure of the formula (I) : Insulinotropic agent(-Y-')Q0)whereinInsulinotropic agent is a redical derived from an insulinotropic peptide which binds to the hu­man GLP-1 receptor, or a radical derived from a peptide in which 22 positions out of the first 30 are identical to those found in corresponding positions in GLP-1 or found in corresponding positions in Exendin-4. with the proviso that the C-terminal amino acid residue of said insuli­notropic agent is not cysteine, andY is a bivalent connecting chemical group connecting C' with the Insulinotropic agent, and«C" is a bivalent polar separating chemical group where 50 - 20% of the heavy atoms are ei­ther O or N, andf is 0 or 1 and Q is selected from (Figure Removed) A is a polar chemical group of a single molecular size (monodisperse) or of several molecular sizes (polydisperse) where 50 - 20% of the heavy atoms are independently oxygen or nitrogen, andW is a bivalent chemical group whereby A is connected, andX is a bivalent connecting chemical group whereby B is connected, and B is a connecting or branching chemical group.The general formula (I) and the encompassed peptide radical is to be understood as follows. The following compound is encompassed by formula (I): Ne37-(mPEGyl)propionyWAib'-^.Lys^lGLP-l^-S?) amide wherein mPEGyl is polydis-perse and has a molecular weight of approximately 2 kDa (Figure Removed) The insulinotropic agent is the radical comprising the peptide including the four methylene groups in the lysine residue in position 37. The group A is the mPEGyl-CH2CH2- wherein mPEGyl has a molecular weight of approximately 2 kDa. The bivalent chemical group W whereby mPEGyl-CH2CH2- is connected to the radical derived from the insulinotropic peptide is the amide -C(O)-NH-.In one embodiment of the invention A is a monodisperse or polydisperse chemical group having the structure -(CH2)1O[(CH2)nO]m(CH2)p-H, where I. n and p independently are an in­teger in the range from 1 to 10, m is an integer in the range from 1 to 5000, and where m multiplied by n+1 is less than 10000.In another embodiment of the invention A is a monodisperse or polydisperse chemical group having the structure -{CH2)1C(=O)O[(CH2)nO] m(CH2)p-H, where I, n and p independently are an integer in the range from 1 to 10, m is an integer in the range from 1 to 5000, and where m multiplied by n+1 is less than 10000. In another embodiment of the invention n is 2 or 3. In another embodiment of the invention m is in the range from 10-1000, or in the range from 20-250.In another embodiment of the invention A is a monodisperse or polydisperse chemical group having the structure-(Z1(CH2)lO[(CH2)2O]m(CH2)0-NR1)q-Z2,where Z1 is -CO- or -CO-(CH2)n-CO-NH-. and Z2 is -R1. -CO-(CH2)n-R1. -(CH2),O[(CH2)2O] m(CH2)p-R1 wherein I and n and p independently are integers in the range from 1 to 10. and R' is -OH, -NH2, -NH-R2, -NH(-R2)-R2 ,-COOH, C^-alkyl. or -NH-CH(R2)-COOH, and where m and q are independently integers in the range from 1 to 20, and where I, n and p are inde­pendently integers in the range from 1 to 6, and R2 is hydrogen or d^-alkyl. In another embodiment of the invention A is mPEGyl.In another embodiment of the invention A is mPEGyl-C(=O)-(CH2),-, wherein r is an integer in the range from 1-10.In another embodiment of the invention A is monodisperse, i.e. it is made up of only onecomponent.In another embodiment of the invention A has a polydispersity index from 1.00 to 1.10.In another embodiment of the invention A is polydisperse and preferably having a polydis-persity index which is less than 1 .2, less than 1.1, less than 1 .05, less than 1 .03, less than1.02, less than 1.010, less than 1.008, less than 1.005 or less than 1.0025.In another embodiment of the invention the branching chemical group B is selected from (Figure Removed) wherein a, b, c, d ,e ,f ,g, h, i are integers independently selected from the range from 0 to24.•In another embodiment of the invention the branching group B is (Figure Removed) In another embodiment of the invention the branching chemical group B is selected from(CHA_ (Figure Removed) wherein a. b, c, d ,e ,f ,g, h, i are integers independently selected from the range from 0 to 24. In another embodiment of the invention the insulinotropic agent is attached to B via the left hand terminal of B.In another embodiment of the invention a+b is less than 6 or a+b+c is less than 14 or a+b+c+d+e+f+g+h+l is less than 16. In another embodiment of the invention a is 0 or 1 and b, c. d, e, f, h and i are all in the range from 0 to 5.In another embodiment of the invention a, c, d, e, g and i are all 0 and b, f and h are all in the range from 1 to 4.In another embodiment of the invention a, c, d, e, g and I are all 0 and b, f and h are all in the range from 1 to 4.In another embodiment of the invention, W and X are independently selected from the bi­valent connecting chemical groups comprising amides: -C(O)-NR-, where R is hydrogen or C^-alkyl, amines: -NR-, where R is hydrogen or C^-alkyl,thioethers: -S-, -S-(CH2)r-SOr- orethers: -O-,urethanes: -^(RVCO-NfR2}-. where R1 and R2 independently is hydrogen or C^-alkyl.carbamates: -O-CO-N(R)-, where R is hydrogen or C,_&-alkyt,R_ I hydrazines: H ~ where R is hydrogen or C1-6-alkyl, oximes: -O-N=C(-R)-, where R is hydrogen or C1-6-alkyl, (Figure Removed) The hydrazine derivatives of the formula, where R is hydrogen or d-e-alkyl may be formed by reaction of an aldehyde derivative (-CO-H) or a ketone derivative (-CO-R) with hydrazine derivatives (-NH-NH2) or hydVazine carboxylate derivatives (-0-C(O)-NH-NH2) or semicarbazide derivatives (-NH-C(O)-NH-NH2) or thiosemicarbazide derivatives (-NH-C(S)-NH-NH2) or carbonic acid dihydrazide derivatives (-NHC(0)-NH-NH-C(0)-NH-NH2) or carbazide derivatives (-NH-NH-C(O)-NH-NH2) or thiocarbazide derivatives (-NH-NH-C(S)-NH-NH2) or aryl hydrazide derivatives (-NH-C(O)-C6H4NH-NHz) or hydrazide derivatives (-C(O)-NH-NH2). The oximes of the formula -O-N=C(-R)-, where R is hydrogen or C1-6-alkyl and may be formed by reaction of an aldehyde (-CO-H) or a ketone (-CO-R) with oxylamine (-O-NH2) or -C(O)-O-NH2 or -NH-C(O)-O-NH2 or -NH-C(S)-O-NH2. In another embodiment of the invention W is -C(O)-NR-, where R is hydrogen or C^-alkyl. In another embodiment of the invention the insulinotropic agent is attached to W via the left hand terminal (the carbon) of W. In another embodiment of the invention the insuiinotropic agent is attached to W via the right hand terminal (the nitrogen) of W. In another embodiment of the invention, f is 0. In another embodiment of the invention C' is -{CH2)n,O[(CH2)n2O] n3(CH2)M-, where n1 , n2 and n4 independently is an integer in the range from 1 to 10, n3 is an integer in the range from 1 to 5000, and where n3 multiplied by n2+1 is less than 10000. In another embodiment of the invention n2 is 2 or 3. In another embodiment of the invention n3 is in the range from 1-20. In another embodiment of the invention C' is -(CH2)n5-, where n5 is an integer in the range from 1 to 10. In another embodiment of the invention Y is selected from the bi-valent connecting chemical groups comprising amides: -C(O}-NR-, where R is hydrogen or C1-6-alkyl, amines: -NR-, where R is hydrogen or C1-6-alkyl, thioethers: -S-, -S-(CH2)2-SO2- or ethers: -O-, urethanes: -N(R1)-CO-N(R2)-. where R' and R2 independently is hydrogen or C^-alkyl, carbamates: -O-CO-N(R)-. where R is hydrogen or C1-6-alkyl, hydrazines: H - where R is hydrogen or C,1-6-alkyl, oximes: -O-N=C(-R)-, where R is hydrogen or C1-6-alkyl, oxazolidines or thiazolidines: (Figure Removed) In another embodiment of the invention the insulinotropic agent is a DPPIV protected pep-tide.In another embodiment of the invention the insulinotropic agent has an ECso of less than 1 nM as determined by the functional receptor assay disclosed herein. In another embodiment of the invention the insulinotropic agent has an EC50 of less than 300 pM, less than 200 pM or less than 100 pM as determined by the functional receptor assay disclosed herein.I In another embodiment of the invention the insulinotropic agent is derived from a peptide having a length between 27 and 45 amino acid residues in which 22 out of the first 28 amino acid residues are identical to those found in corresponding positions in GLP-1(7-37) (SEQ ID No. 1) or in corresponding positions in Exendin-4(1-39) (SEQ ID No. 2). In another embodiment of the invention the insulinotropic agent is derived from a peptide having a length between 28 and 45 amino acid residues in which 22 out of the first 28 amino acid residues are identical to those found in corresponding positions in GLP-1(7-37) or in cor­responding positions in Exendin-4(1-39).In another embodiment of the invention the insulinotropic agent is selected from a peptide comprising the amino acid sequence of the formula (II): Xaa7-Xaa8-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Xaa,8-Ser-Xaa18-Xaa19-Xaa20-Glu-Xaa22-Xaa23-Ala-Formula (II) (SEQ ID No: 3) wherein Xaa7 is L-histidine, D-histidine. desamino-histidine. 2-amino-histidine, -βhydroxy-histidine, homohistidine. N'-aqetyl-histidine, cr-fluoromethyl-histidine, a-methyl-histidine, 3-pyridylalanine, 2-pyridylalanine or 4-pyridylalanine;Xaa8 is Ala, D-Ala. Gly, Val, Leu, lie, Lys, Aib, (1-aminocyclopropyl) carboxylic acid, (1-aminocyclobutyl) carboxylic acid. (1-aminocyclopentyl) carboxylic acid, (1-aminocyclohexyl) carboxylic acid, (1-aminocycloheptyl) carboxylic acid, or (1-aminocyclooctyl) carboxylic acid; Xaat8 is Val or Leu; Xaa,8 is Ser, Lys or Arg; Xaat9 is Tyr or Gin; Xaa20 is Leu or Met; Xaa22 is Gly, Glu or Aib; Xaa23 is Gin, Glu, Lys or Arg; Xaa25 is Ala or Val; Xaaja is Lys, Glu or Arg; Xaa2y is Glu or Leu; Xaa30 is Ala, Glu or Arg; Xaa33 is Val or Lys; Xaa34 is Lys, Glu, Asn or Arg; Xaa3S is Gly or Aib;XaaM is Arg, Gly or Lys; Xaa3r is Gly, Ala. Glu. Pro, Lys. amide or is absent; XaaM is Lys, Ser, amide or is absent. XaaM is Ser, Lys, amide or is absent; Xaa<0 is Gly, amide or is absent; Xaa4i is Ala, amide or is absent; Xaa42 is Pro, amide or is absent; Xaa« is Pro, amide or is absent; Xaa44 is Pro, amide or is absent; Xaa4S is Ser, amide or is absent; Xaa46 is amide or is absent; provided that if XaaM, Xaa39, Xaa40. Xaa41, Xaa42, Xaa43, Xaa44, Xaa45 or Xaa46 is absent then each amino acid residue downstream is also absent.In another embodiment of the invention the insulinotropic agent is a peptide comprising the amino acid sequence of formula (III): Xaa7-Xaaa-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Xaa16-Tyr-Leu-Glu-Xaa22-Xaa23-AJa-Ala-Xaa29-Glu-Phe-!le-Xaa3o-Trp-Leu-Val-Xaa:34-Xaa3s-Xaa36-Xaa37-Xaa38Formula (II!) (SEQ ID No: 4) whereinXaa7 is L-histidine, D-histidine, desamino-histidine, 2-amino-histidine, /9-hydroxy-histidine, homohistidine, NT-acetyl-histidine, o-fluoromethyl-histidine, cr-methyl-histidine, 3-pyridylalanine, 2-pyridylalanine or 4-pyridylalanine;Xaa8 is Ala, D-Ala, Gly, Val. Leu, lie, Lys, Aib, (1-aminocyclopropyl) carboxylic acid, (1-aminocyclobutyl) carboxylic acid, (1-aminocyclopentyl) carboxylic acid, (1-aminocyclohexyl) carboxylic acid, (1-aminocycloheptyl) carboxylic acid, or (1-aminocyclooctyl) carboxylic acid; Xaais is Ser, Lys or Arg; Xaa22 is Gly, Glu or Aib; Xaa23 is Gin, Glu. Lys or Arg; Xaa26 is Lys, Glu or Arg; Xaa30 is Ala, Glu or Arg; Xaa34is Lys, Glu or Arg; Xaa35 is Gly or Aib; Xaa38 is Arg or Lys; Xaa37 is Gly, Ala, Glu or Lys; XaaM is Lys, NH2 or is absent.In another embodiment of the invention the insulinolropic agent is selected from GLP-1{7-35), GLP-1(7-36), GLP-1(7-36)-amide, GLP-1(7-37). GLP-1(7-38), GLP-1(7-39), GLP-1(7-40), GLP-1(7-41) or an analogue thereof.In another embodiment of the invention the insulinotropic agent comprises no more than fif­teen amino acid residues which have been exchanged, added or deleted as compared to GLP-1(7-37) (SEQ ID No. 1), or no more than ten amino acid residues which have been ex­changed, added or deleted as compared to GLP-1(7-37) (SEQ ID No. 1). In another embodiment of the invention the insulinotropic agent comprises no more than six amino acid residues which have been exchanged, added or deleted as compared to GLP-1(7-37) (SEQ ID No.*1). In another embodiment of the invention the insulinotropic agent comprises no more than 4 amino acid residues which are not encoded by the genetic code. In another embodiment of the invention the insulinotropic agent comprises an Aib residue as the second amino acid residue from the N-te?minal.In another embodiment of the invention the N-terminal amino acid residue (position 7 in for­mulae II and III) of said insulinotropic agent is selected from the group consisting of D-histidine, desamino-histidine, 2-amino-histidine. /?-hydroxy-histidine, homohistidine, N°-acetyl-histidine , o-fluoromethyl-histidine, a-methyl-histidine, 3-pyridylalanine, 2-pyridylalanine and 4-pyridylalanine. In another embodiment of the invention the insulinotropic agent is selected from the group consisting of [ArgM]GLP-1 (7-37), [Arg*iJ4]GLP-1(7-37)Lys. (Lys38Arg2e':M]GLP-1(7-36). [Aib"-22-35]GLP-1(7-37),[Aib8 35]GLP-1 (7-37), (Aib8-22]GLP-1(7-37), [Aib8-2235Arg26.34]GLP-1(7-37)Lys, [Aiba'35Arg28-34]GLP-1(7-37)Lys, [Aibs'22Arg2(!-34]GLP-1(7-37)Lys, [Aiba'22-35Arg26'J4]GLP-1(7-37)Lys, [Aib8'35Arg?9-34]GLP-1(7-37)Lys.[Aib822-35Arg26]GLP-1(7-37)Lys, [AibM5Arg2e]GLP-1(7-37)Lys, [AibB'22Arg26]GLP-1(7-37)Lys. [Aib8-22-35 Arg^JGLP-l(7-37)Lys. [Aib^Arg^GLP-l(7-37)Lys. [Aib8'22Arg34]GLP-1 (7-37)Lys, [Aibs-22-35Ala37]GLP-1(7-37)Lys, [Aib8'35Ala37]GLP-1(7-37)Lys, [Aib8'22Ala37]GLP-1(7-37)Lys. [Aib8 22-35Lys37]GLP-1 (7-37). [Aib8'35Lys37]GLP-1(7-37), [Aib8 ^Lys^jGLP-l (7-37) or deriva­tives thereof which has been amidated on the C-terminal. In another embodiment of the invention the insulinolropic agent comprises at least one Aib residue. In another embodiment of the invention the insulinotropic agent contains two Aib residues.In another embodiment of the invention the insulinotropic agent comprises a serine residue at position 18 relative to GLP-1(7-37) (SEQ ID. No. 1), corresponding to position 12 relative toExendin-4(1-39).In another embodiment of the invention the insulinotropic agent comprises a tyrosine residue at position 19 relative to GLP-1(7-37) (SEQ ID. No. 1), corresponding to position 13 relative toExendin-4(1-39).In another embodiment of the invention the insulinotropic agent comprises a glycine residue at position 22 relative to GLP-1{7-37) {SEQ ID. No. 1), corresponding to position 16 relative toExendin-4(1-39). In another embodiment of the invention the insulinotropic agent comprises a glutamine resi­due at position 23 relative to GLP-1(7-37) (SEQ ID. No. 1). corresponding to position 17 rela­tive to Exendin-4(1-39).In another embodiment of the invention the insulinotropic agent comprises a lysine residue at position 26 relative to GLP-1(7-37) (SEQ ID. No. 1), corresponding to position 20 relative to Exendin-4(1-39).In another embodiment of the invention the insulinotropic agent comprises a glutamate resi­due at position 27 relative to GLP-1(7-37) (SEQ ID. No. 1), corresponding to position 21 rela­tive to Exendin-4( 1-39). In another embodiment of the invention the insulinotropic agent is exendin-4(1-39). In another embodiment of the invention the insulinotropic agent is ZP-10, i.e. [Ser3aLys39]Exendin-4(1-39)LysLysLysLysLys-amide (SEQ ID No. 5). In another embodiment of the invention the insulinotropic agent is attached to Y-C'-Q or Q via the amino acid residue in position 25 to 45 relative to the amino acid sequence SEQ ID No 1.In another embodiment of the invention the insulinotropic agent is attached to Y-C'-Q or Q via an amino acid residue selected from one of the 10 C-terminal amino acid residues. In another embodiment of the invention the insulinotropic agent is attached to Y-C'-Q or Q via the amino acid residue in position 23, 26, 34, 36 or 38 relative to the amino acid sequence SEQ ID No: 1. In another embodiment of the invention the insulinotropic agent is attached to Y-C'-Q or Q via the amino acid residue in position 17, 20, 28, 30 or 32 relative to the amino acid se­quence SEQ ID No:2.In another embodiment of the invention the insulinotropic agent is attached to Y-C'-Q or Q via the C-terminal amino acid residue.!n another embodiment of the invention the insulinotropic agent is attached to Y-C'-Q or Q via a carboxyl group, an amino group, a keto group, a hydroxyl group, a thiol group or a hy-drazide group.in another embodiment of the invention the insulinotropic agent is attached to Y-C"-Q or Q via a the epsilon-amino group on a lysine residue.In another embodiment of the invention the insulinotropic agent comprises only one lysine residue.In another embodiment of the invention the insulinotropic agent comprises only one lysine residue which is the C-terminal amino acid residue of said insulinotropic agent. In another embodiment the compound according to the present invention has an ECX of less than 1000 pM, less than 500 pM, less than 300 pM, less than 200 pM, less than 100 pM, less than 50 pM or less than 10 pM as determined by the functional receptor assay disclosed herein.In another embodiment the compound according to the present invention is selected from the group consisting ofA/E37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl)[Aib822-:!S,Lys37]GLP-1 (7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, /Ve37-(3-(mPEGyl)propionyl)[Aib8-22'35,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, Ne37-(3-(mPEGyl)propionyl)[A.\b8-22-3S.Lys31]GL.P-'\(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa, A/e37-(3-{mPEGyl)propionyl)[AibB'22i35,Lys37]GLP-1(7-37) amide wherein mPEGyl is polydis­perse and has a molecular weight of approximately 2 kDa, We26-{3-(mPEGyl)propionyl)[Aib8,Glu22-M,Lys33,Asn:MlGly35-36,Pro37lGLP-1(7-37)ylSerSerGly AlaProProProSer amide wherein mPEGyl is polydisperse and has a molecularweight of ap­proximately 2 kDa,Na-[Aib822-35]GLP-1-(7-37)yl(A/-(3-(mPEGyl)propionyl)Lysinamide) wherein mPEGyl is polydisperse and has a molecularweight of approximately 750 Da, Ne-(Aib822.-35]GLP-1(7-37)yl(S'-(1-mPEGylpropyl-2,5-dioxo-pyrrolidin-3-yl)Cysteinamide wherein mPEGyl is polydisperse and has a molecular weight of approximately 5000 Da, A/Q-(3-(3H-imidazol-4-yl)-propionyl[Aib22-3S,Arg26'34]GLP-1-(8-37))yl(/VE-(3-(mPEGyl)propionyl)Lysinamide) wherein mPEGyl is polydisperse and has a molecularweight of approximately 2000 Da,wherein mPGyl is polydisperse and has amolecular weight of approximately 2 kDa, and (S)-W-{(S)-5-(W-((S)-5-carbamoyl-5-{mPEGylpropionylamino)pentyl)carbamoyl)-5-(mPEGylpropionylamino)pentyl)-5-(/^7-(3-(4-imidazolyl)propionyl)[Aib22'35.Arg28'34]GLP-1-(8-37)yl)-2-(mPEGylpropionylamino)hexanoic amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 750 Da,In another embodiment the compound according to the present invention is selected from thegroup consisting of Wt37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl){Aib8-22-3S,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, Wc37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'2i'ls,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa, M37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aibe'22-l5.Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, W37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22-35,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, /VE37-({2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22-:i5,Lys:s7]GLP-1(7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, Wt37-((2S)-2l6-di-(mPEGylcarbonylamino)hexanoyl)[Aibv22-J5.Lys37]GLP-1(7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa. rVc37-((2S)-2,6-dHmPEGylcarbonylamino)hexanoyl)[Aib822-35,Lys37]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, r/37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib82235,Lys37]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, Wc37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22-35,Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, /VE37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22-3S.Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa, /Vc37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8•22-35,Lys37lGLP-1 (7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, Wt37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8•"•M.Lys37]GLP-1 (7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, ATJ7-((2S)-2,6-dKmPEGylcarbonylamino)hexanoyl)[Aib8-22^.Lys^JGLP-l (7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, Wc37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib5-22-35.Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa. AT37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22'35.Lys3']GLP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, A/c37-{(2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22 35,Lys37]GLP-1 (7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, /Vc37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[AibB-22,Lys37lGLP-1 (7-37) wherein mPE-Gyl is polydisperse and has a molecular weight of approximately 2 kDa, A/e37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22,Lys37]GLP-1 (7-37) wherein mPE: Gyl is polydisperse and has a molecular weight of approximately 5 kDa, Wt37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'22,Lys37]GLP-1 (7-37) where in mPE-Gyl is polydisperse and has a molecular weight of approximately 20 kDa, Nc37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl)[AibB-22,Lys37]GLP-1 (7-37) wherein mPE-Gyl is polydisperse and has a molecular weight of approximately 40 kDa, Ne37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'22,Lys37]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, Nc37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'22,Lys37]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa, //37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'22.Lys37]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, Ne7-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'22,Lys37]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, A/c37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22,Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, A/e37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'22.Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa, /Ve37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22,Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, /vr537-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)(Aibe-22,Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, /Ve37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22.Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa.N37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl)[AJb8l22,Lys37]6LP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa. N37-((2S)-2,6-dHmPEGy1carbonylamino)hexanoyl)[Aib8-22,LysJ7]GLP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, N37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-22,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, /Vt37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-35.Lys37]GLP-1 (7-37) wherein mPE-Gyl is polydisperse and has a molecular weight of approximately 2 kDa, Ne37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'35.Lys37]GLP-1 (7-37) wherein mPE-Gyl is polydisperse and has a molecular weight of approximately 5 kDa, Ne37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl){Aib8-35,Lys37]GLP-1(7-37) wherein mPE-Gyl is polydisperse and has a molecular weight of approximately 20 kDa, Ne37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'35.Lys37]GLP-1 (7-37) wherein mPE-Gyl is polydisperse and has a molecular weight of approximately 40 kDa, Ne37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-35.Lys37]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, /Ve37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-35.Lys37]GLP-1 (7-37) amide wherein * mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa. /Vc37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'35.Lys37]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, Nt37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-35,Lys37]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, Wt37-((2S>2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib6'35,Lys:j7]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, AA3r-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8 35,Lys37)GLP-1 (7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa, /Vc37-((2S)-2.6-dKmPEGylcarbonylamino)hexanoyl)[Aib8'35,Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, Arj37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8'35.Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, /Vt37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl)tAib8-3S,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, A/t37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8.35,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa.We37-((2S)-2l6-di.(mPEGylcarbonylamino)hexanoyl)[AibM5,Lys37]GLP-1{7.37)Lys amide wherein mPEGyl is poiydisperse and has a molecular weight of approximately 20 kDa, Wc37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-35,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is poiydisperse and has a molecular weight of approximately 40 kDa, ArS7-(3-(mPEGyl)propionyl)[Aibe-2*-s5,Lys3T]GLP-1 (7-37) wherein mPEGyl is poiydisperse and has a molecular weight of approximately 2 kDa, /Vt37-(3-(mPEGyl)propionyl)[Aib8-2235.Lys37]GLP-1 (7-37) wherein mPEGyl is poiydisperse and has a molecular weight of approximately 5 kDa, Wc37-(3-(mPEGyl)propionyl)[Aib8'22'35,Lys37]GLP-1(7-37) wherein mPEGyl is poiydisperse and has a molecular weight of approximately 10 kDa, /7:37-(3-(mPEGyl)Propionyl)[Aib8'22'3S,Lys37]GLP-1(7-37) wherein mPEGyl is poiydisperse and has a molecular weight of approximately 20 kDa, A/37-(3-(mPEGyl)propionyl)[Aib8'22'35,Lys37]GLP-1(7-37) wherein mPEGyl is poiydisperse andhas a molecular weight of approximately 40 kDa, //37-(3-(mPEGyl)propionyl)[Aibe^35,Lys37]GLP-1(7-37) amide wherein mPEGyl is poiydis­perse and has a molecular weight of approximately 2 kDa, ^7-(3-(mPEGyl)propionyl)[Aib8-2j-3S,Lys37]GLP-1(7-37) amide wherein mPEGyl is polydis-* perse and has a molecular weight of approximately 5 kDa,WE37-(3-(mPEGyl)propionyl)[Aib8-22'35,Lys37]GLP-1(7-37) amide wherein mPEGyl is poiydis­perse and has a molecular weight of approximately 10 kDa,N^7-(3-(mPEGyl)propionyi)lAib872'35,Lys37]GLP-1(7-37) amide wherein mPEGyl is poiydis­perse and has a molecular weight of approximately 20 kDa. ^37-(3-(mPEGyl)propionyl)[Aib8'2'-35,Lys37]GLP-1(7-37) amide wherein mPEGyl is poiydis­perse and has a molecular weight of approximately 40 kDa, Ar37-(3-(mPEGyl)propionyl)[Aibe-2i-35,Lys37]GLP-1(7-37)Lys wherein mPEGyl is poiydisperse and has a molecular weight of approximately 2 kDa, ^37-(3-(mPEGyl)Propionyl)[Aib8'2i-35,Lys37]GLP-1(7-37)Lys wherein mPEGyl is poiydisperse and has a molecular weight of approximately 5 kDa, Wc37-(3-(mFrEGyl)propionyl)[Aib8-22'35,Lys37]GLP-1(7-37)Lys wherein mPEGyl is poiydisperse and has a molecular weight of approximately 10 kDa, W37-(3-(mPEGyl)propionyl)[Aib8'2235,Lys37]GLP-1(7-37)Lys wherein mPEGyl is poiydisperse and has a molecular weight of approximately 20 kDa, We37-(3-(mPEGyl)propionyl)[Aib8'2235.Lys37lGLP-1(7-37)Lys wherein mPEGyl is poiydisperse and has a molecular weight of approximately 40 kDa,amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, -O-PEGyOpropionyOIAib.Lys^JGLP-ICT-a/JLys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kOa, Nt37-(3-(mPEGyl)propionyl)[Aib8-22'35,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 10 kDa, A/;3r-(3-(mPEGyl)propionyl)[Aibe-22-3S,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kOa, Wc37-(3-(mPEGyl)propionyl)[Aib8'22-35,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, A/37-(3-(mPEGyl)propionyl){Aib8-22,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa. /Vc37-(3-(mPEGyl)propionyl)[Aib8'22,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDaAf37-(3-(mPEGyl)propionyl)[Aib8l22,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 10 kDa, A/c37-(3-(mPEGyl)propionyl)(Aib8-22.Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa,A/c37-(3-(mPEGyl)propionyl)[Aib8'22,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, Nt37-{3-(mPEGyl)propionyl)[Aib8'22,Lys37]GLP-1(7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kOa,A/eJ7-(3-(mPEGyl)propionyl)[Aib8-22,Lys37]GLP-1(7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa,A/37-(3-(mPEGyl)propionyl)[Aib8'22,Lys37JGLP-1(7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 10 kDa, Af37-(3-(mPEGyl)propionyl)[Aib8-22,Lys37]GLP-1(7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, A/t37-(3-(mPEGyl)propionyl)[Aib8l22,Lys37]GLP-1(7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, //37-{3-(mPEGyl)propionyl)[Aib8-22.Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, A^37-(3-(mPEGyl)propionyl)[Aib8-22,Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa,'/Vc37-(3-(mPEGyl)propionyl)[Aib8'22,Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 10 kDa,Nc37-(3-(mPEGyl)propionyl)[Aib8-22,Lys37lGLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa,A/^7-(3-(mPEGyl)propionyl)[Aib8-22,Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa,Ne37-(3-(mPEGyl)propionyl)[Aib8'22,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydis­perse and has a molecular weight of approximately 2 kDa,Wc37-(3-(mPEGyl)propionyl)[Aib8'22,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydis­perse and has a molecular weight of approximately 5 kDa,Nc37-(3-(mPEGyl)propionyl)[Aib8'22,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydis­perse and has a molecular weight of approximately 10 kDa,//37-(3-(mPEGyl)propionyl)[Aib8'22,Lys37]GlP-1(7-37)Lys amide wherein mPEGyl is polydis­perse and has a molecular weight of approximately 20 kDa, We37-(3-(mPEGyl)propionyl)[Aib8'22,Lys37]GLP-1{7-37)Lys amide wherein mPEGyl is polydis­perse and has a molecular weight of approximately 40 kDa, W37-(3-(mPEGyl)propionyl)(Aib8-35,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, A^37-{3-(mPEGyl)propionyl)[Aib8'3S,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa, /Vt37-(3-(mPEGyl)propionyl)[Aib8'3S,Lys37]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 10 kDa, A/t37-(3-(mPEGyl)propionyl)(Aiba>35.Lys37]GLP-1 (7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, /Ve37-(3-(mPEGyl)propionyl)[Aib8-3S,Lys37]GLP-1 (7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, A/E37-(3-(mPEGyl)propionyl)[Aib8'35,Lys37]GLP-1(7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, /^"-(^(mPEGyOpropionyOfAib^.Lys^lGLP-l(7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa, Nc37-(3-(mPEGyl)propionyl)[Aib8'35,Lys:i7]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 10 kDa, /Vc37-(3-(mPEGyl)propionyl)[Aib8-35,Lys37]GLP-1(7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, '' W37-(3-(mPEGyl)propionyl)[Aib8 35,l_ys37]GLP-1 (7-37) amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, A/=37-(3-(mPEGyl)propionyl)[Aib8'35,Lys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa, N37-(3-(mPEGyi)propionyl)[Aib8-M.Lys37]GLP-1-(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa, /Ve37-(3-(mPEGyl)propionyl)[Aib*'35,Lys37]GLP-1{7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 10 kDa, /Vc37-(3-(mPEGyl)propionyl)[Aib8-35lLys37]GLP-1(7-37)Lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa, AA37-(3-(mPEGyl)propionyl)[Aib8'3S,Lys37]GLP-1(7-37)lys wherein mPEGyl is polydisperse and has a molecular weight of approximately 40 kDa, /^37-(3-(mPEGyl)propionyl)[Aib8'35.Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydis­perse and has a molecular weight of approximately 2 kDa, A/e37-(3-(mPEGyl)propionyl)[Aib8'35,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydis­perse and has a molecular weight of approximately 5 kDa, /VE37-(3-(mPEGyl)propionyl)[Aib8'35.Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydis- « perse and has a molecular weight of approximately 10 kDa, A/E37-(3-(mPEGyl)propionyl)[Aib8'35,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydis­perse and has a molecular weight of approximately 20 kDa, and Nc37-(3-(mPEGyl)propionyl)[Aib8-35,Lys37]GLP-1(7-37)Lys amide wherein mPEGyl is polydis­perse and has a molecular weight of approximately 40 kDa. In another embodiment the compound according to the present invention is selected from the group consisting ofW37-(3-(mPEGyl)propionyl) [Lys3?]GLP-1-(7-37) where mPEGyl is polydisperse and is polydisperse and has a Mw of approx 750 Da, AA37-(3-(mPEGyl)propionyl) [Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 750 Da, GLP-1-{7-37)yl(A/E-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 750 Da, GLP-1-(7-37)yl(Nei-(3-{mPEGyl)propionyl))Lysinamide where mPEGy! is polydisperse and has a Mw of approx 750 Da.26 lb35. Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da. /^-(S-fmPEGyOpropionyl) [Aib35. Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 750 Da, N>-[Aib35]GLP-1-(7-37)yl(Nc-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 750 Da, A/J-[Aib35]GLP-1-(7-37)yl(A/!-(3-(mPEGyl)prapionyl)}Lysinamide where mPEGyl is polydis- perse and has a Mw of approx 750 Da, Af37-(3-(mPEGyl)propionyl) [Aib22. Lys37]GLP-1 -{7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da, /^-(S-fmPEGyOpropionyl) [Aib22. Lys37]GLP-1-{7-37) amide where mPEGyl is polydisperse and has a Mw of approx 750 Da, A/°-[AibZ2]GLP-1-(7-37)yl(/Vc-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 750 Da, A/°-[Aib22]GLP-1-(7-37)yl(/V;-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis- perse and has a Mw of approx 750 Da, A/37-{3-(mPEGyl)propionyl) [Aib8, Lys37]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 750 ba, Wt37-(3-(mPEGyl)propionyl) [Aib8, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 750 Da, N°-[Aib8]GLP-1-(7-37)yl(A/t-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 750 Da, A/°-[Aib8]GLP-1-(7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 750 Da, /^-(XmPEGyOpropionyl) [Aib8-35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da, //37-{3-(mPEGyl)propionyl) [Aib8-35, Lys37]GLP-1-{7-37) amide where mPEGyl is polydisperse and has a Mw of approx 750 Da, Wt7-[Aib8'35]GLP-1-(7-37)yl(Nt-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 750 Da, /V°-[Aib8'35]GLP-1-(7-37)yl(Wt-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis- perse and has a Mw of approx 750 Da, ^-^-(mPEGyOpropiony!) [Aib22'35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da,//"-(S-fmPEGylJpropionyl) [Aib22-35, Lys37]GLP-1-{7-37) amide where mPEGyl is polydis-perse and has a Mw of approx 750 Da, W-[Aibin-35]GLP-1-(7-37)yl(r/-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 750 Da, A/7-[Aib22'35]GLP-1-(7-37}yl(A/c-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 750 Da, //"-(S-fmPEGyOpropionyl) [Aib8'35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da. /V37-(3-(mPEGyl)propionyl) [Aib8'35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 750 Da, A/'-[Aib8-35]GLP-1-(7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 750 Da, /V0-[Aib8'35]GLP-1-(7-37)yl(A/:-(3-{mPEGyl)propionyl))Lysinamide where mPEGyl is poiydis-perse and has a Mw of approx 750 Da, Af37-(3-(mPEGyl)propionyl) [Aib8-22, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da, AA37-(3-(mPEGyl)propionyl) [Aib8'22, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse t and has a Mw of approx 750 Da, /V°-[Aib8'22]GLP-1-(7-37)yl(AJt-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 750 Da, W-[Aib8-22]GLP-1-(7-37)yl(A^-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 750 Da, /^"-^-(mPEGyOpropionyl) [Aib8'22-35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da, /^"-(S-CmPEGyOpropionyl) [Aib8'22'35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 750 Da, A/"-[Aib8'22-35]GLP-1-{7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 750 Da, A/°-[Aib8'22'35]GLP-1-(7-37)yl(/Vc-(3-(mPEGyl)prapionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 750 Da, A/°-[Aib8, Arg26':M]GLP-1-(7-37)yl(A/E-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydis­perse and has a Mw of approx 750 Da, A/°-[Aib8, Arg26'3*]GLP-1-{7-37)yl(/Ve-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 750 Da-(a-CmPEGyOpropionyl) [Aib8, Arg^.Lys^JGLP-l-(7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da, Ar^-WmPEGyOpropionyl) [Aib8, Arg^.Lys^GLP-l-^^) amide where mPEGyl is polydisperse and has a Mw of approx 750 Da. r/^-O-tmPEGyOpropionyl) [Aib', Lys26,Lys34]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da, A/^-WmPEGyOpropionyl) [Aib8, Lys26,Lys34]GLP-1-{7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 750 Da, yV°-[Arg29-34]GLP-1-(7-37)yl{Ne-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 750 Da, Ar*-[ Arg26'34]GLP-1-(7-37)yK/V-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 750 Da, /^-(S-CmPEGyOpropionyl) [ Arg26.34.Lys36GLP-l-(7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da, //^-(S-CmPEGyOpropionyl) [ Arg26-34.Lys36]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 750 Da, /^-^-(mPEGyOpropionyl) [ Lys26,Lys34]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of apprbx 750 Da, ^-^-(mPEGyOpropionyl) [ Lys26,Lys34]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 750 Da, //'-[Ala8, Arg28'34,]GLP-1-(7-37)yl(N0:-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydis­perse and has a Mw of approx 750 Da, /V-[Ala8. Arg28'34]GLP-1-(7-37)yl(NE-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 750 Da, /^-(S-fmPEGyOpropionyl) [Ala8, Arg28-w,Lys38]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da, /^-(S-OnPEGylJpropionyl) [Ala8, Arg2fl'34.Lys36]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 750 Da, //"-(S-fmPEGyOpropionyl) [Ala8, Lys2a,Lys34]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 750 Da, /^-(S-fmPEGyOpropionyl) [Ala8, Lys26,Lys34]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 750 Da, A/^S-fmPEGylJpropionyl) [Lys^Exendin-A-O-SQ) amide where mPEGyl is poiydisperse and has a Mw of approx 750 Da, -(S-fmPEGyOpropionyl) [Lys32]Exendin-4-(1-39) amide where mPEGyl is polydisperse and has a Mw of approx 750 Da, -(S-tmPEGyOpropionyl) lLysao,Argl"7]Exendin-^-{1-39) amide where mPEGyl is polydis-perse and has a Mw of approx 750 Da, and •(S-fmPEGyOpropionyl) [Lys32,Argl2'27]Exendin-4-(1-39) amide where mPEGyl is polydis­perse and has a Mw of approx 750 Da. In another embodiment the compound according to the present invention is selected from the group consisting of ^37-(3-(mPEGyl)propionyl) [Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, //"-(S-fmPEGylJpropionyl) [Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, GLP-1-(7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 2000 Da, GLP-1-(7-37)yl(A/c-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, A/t37-(3-(mPEGyl)pi'opionyt) [Aib35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, //"-(S-CmPEGyOpropiony!) [Aib35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx. 2000 Da, A/'-[Aib35]GLP-1-(7-37)yl(/S/t-(3-(mPEGyl)propionyl})Lysine where mPEGyl is polydisperse and has a Mw of approx 2000 Da, AT'-[Aib35]GLP-1-(7-37)yl(A/-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, /^-(S-CmPEGyOpropionyl) [Aib22, Lys37lGLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, //37-(3-(mPEQyl)propionyl) [Aib22, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, /Va-[Aib22]GLP-1-(7-37)yl(yVc-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 2000 Da, A/'-[Aib22]GLP-1-{7-37)yl(/Vt-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da. ib8, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and hasa Mw of approx 2000 Da. N37-{3-(mPEGyl)propionyl) [Aib8, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, W-[Aib8]GLP-1-(7-37)yi(A/E-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 2000 Da, A/'-[Aib8]GLP-1-(7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, N37-(S^mPEGyOpropionyl) [Aib8'35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, N37-(3-(mPEGyl)propionyl) [Aib8'35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, A/MAib8'35]GLP-1-{7-37)yl(/SM3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 2000 Da, A/°-[Aib8-35]GLP-1-(7-37)yl(A^(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis- perse and has a Mw of approx 2000 Da, N37-(3-(mPEGyl)propionyl) [Aib2235. Lys37]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, N37-(3-{mPEGyl)propionyl) [Aib22-35. Lys37]GLP-1-(7-37) amide where mPEGyl is polydis- perse and has a Mw of approx 2000 Da, N37-[Aib22-35]GLP-1-(7-37)yl(Ne-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 2000 Da, N°-[Aib2Z35]GLP-1-(7-37)yl(Ne;-(3-{mPEGyl)propionyl))Lysinamide where mPEGyl is polydis- perse and has a Mw of approx 2000 Da, N37-(3-(mPEGyl)propionyl) [Aib8-35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, Nc37-(3-{mPEGyl)propionyl) [Aib8-35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, N37-[Aib8'35]GLP-1-(7-37)yl(Ne-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 2000 Da, N37-[Aib8-35]GLP-1-(7-37)y!(Ne-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, /Vc37-(3-(mPEGyl)propionyl) [Aib822, Lys37]GLP-1 -(7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, /V37-(3-(mPEGyl)propionyl) [Aib*'22, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 2000 Da. N°-[Aib8-2Z]GLP-1-(7-37)yl(r/-(3-(mPEGyl)propionyl))Lysine where mPEGyi is polydisperse and has a Mw of approx 2000 Da, N37-[Aib8'22]GLP-1-(7-37)yl(//-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, N37-(3-(mPEGyl)propionyl) [Aib8'22'35. Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, -(S-CmPEGyOpropionyl) [Aib8'22-35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, -[Aib8'22-35]GLP-1-(7-37)yl(N0:-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 2000 Da, N7-{Aib8-22-35]GLP-1-(7-37)yl(N0:-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, N°-[Aib8, Argaa'34]GLP-1-(7-37)yl(N0;-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydis­perse and has a Mw of approx 2000 Da. N°-(Aib8, Arg2834]GLP-1-(7-37)yl(A/t-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and ha"s a Mw of approx 2000 Da (S-OnPEGyOpropionyl) [Aib8, Arg26'34,Lys36]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, -fXmPEGyOpropionyl) [Aib8. Arg28-34,Lys36]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, -(mPEGyOpropionyl) [Aib8, Lys^.Lys^JGLP-l-^-S?) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, (S-OnPEGyOpropionyl) [Aib8, Lys26,Lys34]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, MN°-[Arg28'34]GLP-1-{7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 2000 Da, W-[ Arg2a-34]GlP-1-(7-37)yl(f/-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, /^-(S-fmPEGyOpropionyl) [ Arg28-34,Lys36]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da. A/38-(3-(mPEGyl)propionyl) [ Arg26-3*,Lys36]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, -(mPEGyOpropionyl) [ Lys28.Lys34]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, S-fmPEGyOpropionyl) [ Lysz6.Lys34]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, [Ala8, Arg29-M,]GLP-1-(7-37)yl(NE-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, -[Ala8, Arg26-34]GLP-1-(7-37)yl(Ne-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, -(S-fmPEGyOpropionyl) [Ala6, Arg26-34.Lys36]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 2000 Da, -O-fmPEGyOpropionyl) [Ala8, Arg28'34.Lys38lGLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, -^-(mPEGyOpropionyl) [Ala8, Lys2fl,Lys34]GLP-1-(7-37) where mPEGy! is polydisperse and has a Mw of approx 2000 Da, /^-(S^mPEGyOpropionyl) [Ala8, Lys26,Lys34]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, /^-(S-fmPEGyOpropionyl) [Lys^Exendin^-CI-SG) amide where mPEGyl is polydisperse and has a Mw of a'pprox 2000 Da. //"-(S-OnPEGyOpropionyl) [Lys32]Exendin~4-(1-39) amide where mPEGyl is polydisperse and has a Mw of approx 2000 Da, /^-(S-fmPEGyOpropionyl) [Lys^Arg'^JExendin-^CI-SS) amide where mPEGyl is polydis­perse and has a Mw of approx 2000 Da, and Af"-(3-(mPEGyl)propionyl) [L.ys3Z,ArgA"7]Exendin-4-{1-39) amide where mPEGy! is polydis­perse and has a Mw of approx 2000 Da. In another embodiment the compound according to the present invention is selected from the group consisting of Af37-(3-(mPEGyl)propionyl) [Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A/^-CS-CmPEGyOpropionyl) [Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, GLP-1-(7-37)yl(/\f-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 5000 Da,GLP-1'(7-37)yK^-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse andhas a Mw of approx 5000 Da, /^•^-(mPEGylJpropionyl) (Aib35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da,//37-{3-{mPEGyl)propionyl) [Aib35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A/°-[Aib35]GLP-1-(7-37)yl(A/t-(3-{mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A/'-[Aibl5]GLP-1-(7-37)yl(A/i:-{3-(rnPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da,W^-fS-trnPEGyOpropiony!) [Aib22, Lys3r]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A/^SKmPEGyOpropionyl) [Aib22, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A/°-[Aib22]GLP-1-(7-37)yl(We-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 5000 Da,AA'-[Aib22]GLP-1-{7-37)yl(/Vt-(3-{mPEGyl)propionyl)}Lysinamide where mPEGyl is polycis-perse and has a Mw'of approx 5000 Da, //^-^-(mPEGyOpropionyl) [Aib8. Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da,/^"-(S-OnPEGyOpropiony!) [Aib8, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, ^-[Aib*]GLP-1-(7-37)yl(N0t-{3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A/°-[Aiba]GLP-1-(7-37)yl(Ne-{3-{mPEGyl)propionyl})Lysinamide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, Nt37-(3-(mPEGyl}propionyl) [Aib8-35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da,A/^-CS^mPEGyOpropionyl) [Aib8'35, Lys37jGLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, /V°-[Aibe-35]GLP-1-(7-37)yl(A/:-(3-(mPEGyl)propionyl})Lysine where mPEGyl is polydisperse and has a Mw of approx 5000 Da,A/ff-[Aibs35]GLP-1-(7-37)yl(Wc-{3-{mPEGyl)propionyl)}Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, /^-(S-lmPEGyOpropionyl) [Aib22-35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, /^-(a-fmPEGyOpropionyl) [Aib22-35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, /V-[Aib22'35]GLP-1-(7-37)yl(/Vt-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A/°-[Aib22-35]GLP-1-(7-37)yl(A/E-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, /Ve37-(3-(mPEGyl)propionyl) [Aib8'35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, Af37-(3-(mPEGyl)propionyl) [Aib8'35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, N0'-[Aib8-35]GLP-1-(7-37)yl(A/t-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 5000 Da, N°-[Aib8i35]GLP-1-(7-37)yl(A/E-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, N+-(S-fmPEGyOpropionyl) [Aib822, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, N0-(S-CmPEGyOpropionyl) [Aib8-22, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da. N0-[Aib8-22]GLP-1-(7-37)yl{/Vt-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 5000 Da. N °-[Aib8-22]GLP-1-(7-37)yf(A/X3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, N37-(3-(mPEGyl)propionyl) {Aib8'22-35, Lys37]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, N-(S-OnPEGylJpropionyl) [Aib8-22-35. Lys37]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, Ay°-[Aib8'2235]GLP-1-(7-37)yl(Nc-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A/°-[Aib8'22-35]GLP-1-(7-37)yl(Nc-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, A/°-[Aib8, Arg28-34]GLP-1-{7-37)yl(Nc-{3-(mPEGyl)propionyl))Lysine where mPEGyl is polydis­perse and has a Mw of approx 5000 Da,N°-[Aib8. Arg*-w]GLP-1-(7-37)yl(//-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 5000 Da A^-O-fmPEGyOpropiony!) [Aib8. Arg^.Lys^GLP-l-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, //"-(a-fmPEGyfJpropiony!) [Aib8, Arg2834,Lys36]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, /^-(S-fmPEGyOpropionyl) [Aib8, Lys28,Lys34]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, N^-O-fmPEGyOpropionyi) [Aib8, Lys29,Lys34]GLP-1-{7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, W"-[Arg26<34]GLP-1-(7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 5000 Da, N°.[ Arg2e'34]GLP-1-(7-37)yl(We-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, WE38-(3-(mPEGyl)propionyl) [ Arg26-34.Lys36]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, AT38-(3-(mPEGyl)propionyl) [ Arg26-34,Lys38]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, ^-(S-OnPEGylJpropionyl) [ Lys26,Lys34]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, /^-(S-fmPEGyOpropionyl) [ Lys26,Lys34]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, W-[Ala8, Arg2fl-M,]GLP-1-(7-37)yl(A/-(3-{mPEGyl)propionyl))Lysine where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, N°-[Ala8. Arg2fl':M]GLP-1-(7-37)yl(WE-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, Ar^-O-fmPEGyOpropionyl) [Ala8. Arg^.Lys^GLP-l -(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A^38-(3-(mPEGyl)propionyl) [Ala8, Arg26'34,Lys35]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, ^-(S-CmPEGyOpropionyl) [Ala8, Lys26.Lys34]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 5000 Da, /^-(S-fmPEGyOpropionyl) [Ala8, Lys28.LysM]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da,/V*°-(3-{mPEGyl)propionyl) [Lys^Exendin^-O-SS) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A/32-{3-(mPEGyl)propionyl) [Lys32]Exendin-4-(1-39) amide where mPEGyl is polydisperse and has a Mw of approx 5000 Da, A^-Ca-fmPEGyOpropionyl) [Lys^.Arg^lExendin^-CI-aS) amide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da, and /^-(S-fmPEGyOpropionyl) [Lys32,Arg'2>27]Exendin-4-{1-39) amide where mPEGyl is polydis­perse and has a Mw of approx 5000 Da. In another embodiment the compound according to the present invention is selected from the group consisting of //"-(a-OnPEGyOpropionyl) (Lys37]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, ^-(S-OnPEGyOpropionyl) [|_ys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, GLP-1-(7-37)yl(^-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 10 kDa, 4 GLP-1-{7-37)yl(^-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, r/37-(3-{mPEGyl)propionyl) [Aib35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, A/E37-(3-(mPEGyl)propionyl) [Aib35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /V-[Aib35]GLP-1-(7-37)yl(r/-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 10 kDa, A/'-[Aib35]GLP-1-(7-37)yl(rV:-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is pclydis- perse and has a Mw of approx 10 kDa, A/37-(3-(mPEGyl)propionyl) [Aib22, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, N37-(3-{mPEGyl)propionyl) [Aib22, LysJ7]GLP-1-(7-37) amide where mPEGyl is polycisperse and has a Mw of approx 10 kDa, N0-[Aib22]GLP-1-(7-37)yl(Wc-{3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 10 kDa, [Aib^GLP-1-(7-37)yl(Af-(3HmPEGyl)propionyl))Lysinamide where mPEGyl is potydis- perse and has a Mw of approx 10 kDa, -(S-tmPEGyOpropionyl) (Aib8, LysJ7]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /V37-(3-{mPEGyl)propionyl) [Aib8, Lys37]GLP-1-{7-37) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, s-[Aib8]GLP-1-(7-37)yl(yS/t-{3-{mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 10 kDa, N°-[Aib8]GLP-1-(7-37)yl(/VX3-(mPEGyl)propionyl)}Lysinamide where mPEGy! is polydisperse and has a Mw of approx 10 kDa, N0-tS-fmPEGyOpropionyl) [Aib8-35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, ^MS-CmPEGyllpropicnyl) [Aib8-35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, -[Aib8-35]GLP-1-(7-37)yl(Wc-(3-(mPEGy!)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /V-[Aib8>35]GLP-1-(7-37)yl{Wc-(3-(mPEGyl)propionyl)}Lysinamide where mPEGyl is polydis- * perse and has a Mw of approx 10 kDa, Nc37-(3-(mPEGyl)propionyl) [Aib22-35, Lys37]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, -O-fmPEGylJpropionyl) [Aib22-55, Lys37]GLP-1-(7-37) amide where mPEGyt is polydis­perse and has a Mw of approx 10 kDa, °-[Aib22-35]GLP-1-(7-37)yl(/V-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /V-[Aib22-35]GLP-1-(7-37)yl(A/E-{3-{mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa, //^-(S^mPEGylJpropionyl) [Aib6-35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /Vt37-(3-(mPEGyl)propionyl) [Aib8JS, Lys37jGLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, rVD-[Aib835]GLP-1-(7-37)yl(NE-(3-(mPEGy))propionyl})Lysine where mPEGyl is polydisperse and has a Mw of approx 10 kDa, yV-[Aib835]GLP-1-(7-37)yl{A/c-(3-(mPEGyl)propionyl)}Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa,/V37-(3-(mPEGyl)propionyl) [Aib8-22, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, //"-(S-fmPEGyOpropionyl) [Aib8-22, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /^'-[Aib8'22]GLP-1-(7-37)yl(/V-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /Vff-[Aib8'22]GLP-1-(7-37)yl(Wt-(3-(mPEGyl)propionyl})Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa, //37-(3-(mPEGyl)propionyl) [Aib8-22-35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, r/37-(3-(mPEGyl)propionyl) [Aib8'22'35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa, /V°-[Aiba'22-35]GLP-1-(7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /V-{Aib8-22-3S]GLP-1-(7-37)yl(Ne-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa, /V-[Aib8. Arg2fl-34]GLP-1-(7-37)yl(W-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydis­perse and has a Mv) of approx 10 kDa, W-[Aib8, Arg28-34]GLP-1-(7-37)yl(/l/-(3-(mPEGyl)propionyl})Lysinamide where mPEGyl is polydisperse and has a Mw of approx 10 kDa //^-(S-fmPEGylJpropionyl) [Aib8, Arg28'34.Lys36]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, A/E38-(3-(mPEGyl)propionyl) [Aib8, Arg26-34.Lys38]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, ^-(S-fmPEGyOpropionyl) [Aib8, Lys^.Lys^GLP-l -(7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /^-(S-CmPEGylJpropionyl) [Aib8, Lys^.Lys^JGLP-l-^-S?) amide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa, A/'-[Arg26-34]GLP-1-(7-37)yl(A/e-{3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 10 kDa, Af-[ Arg28'34]GLP-1-(7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa, Af38-(3-{mPEGyl)propionyl) [ ArgZ8'34,Lys:J6]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, 3-(mPEGyl)propionyl) {Arg2eM,LysM]GLP-1-{7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa, /^-(S-tmPEGylJpropionyl) [ Lys2fl.Lys34]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa. /^•"-(S^mPEGylJpropionyl) {Lys26,Lys34]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, A/°-[Ala8. Arg26'34.]GLP-1-(7-37)yl(/Vc-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydis­perse and has a Mw of approx 10 kDa, /V-[Ala8. Arg26'34]GLP-1-(7-37)yl(/Vc-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /^-(S-fmPEGyOpropionyl) [Ala8, Arg^.Lys^GLP-l-^-a?) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /^-^-(mPEGyOpropionyl) [Ala8. Arg26l34,Lys36]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /^-(S^mPEGyOpropionyl) [Ala8. Lys26,Lys34]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 10 kDa, r/^-Q^mPEGyOpropionyl) [Ala8, LysZ9,Lysl4]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa, A/c20-(3-(mPEGyl)propionyl) (Lys20]Exendin-4-{1-39) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, A/e32-(3-(mPEGyl)propionyl) (Lys32]Exendin-4-{1-39) amide where mPEGyl is polydisperse and has a Mw of approx 10 kDa, /^-(S-fmPEGyOpropionyl) (Lys^Arg^lExendin-MI-Sg) amide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa, and /Vc32-(3-(mPEGyl)propionyl) [Lys32.Arg'2'27]Exendin-4-(1-39) amide where mPEGyl is polydis­perse and has a Mw of approx 10 kDa.In another embodiment the compound according to the present invention is selected from the group consisting of A/c37-(3-(mPEGyl)propionyf) (Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, //37-(3-(mPEGyl)propionyl) [Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa.GLP-1-(7-37)yl(fVc-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a - Mw of approx 20 kDa, GLP-1-(7-37)yl{A/-{3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /^-(3-{mPEGyl)propionyl) [Aib35. Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa. /V^-O-CmPEGyOpropionyl) [Aib35, Lys37JGLP-1-(7-37) amide where mPEGyl is pofydisperse and has a Mw of approx 20 kDa. AA'-[Aib35]GLP-1-(7-37)yl{A^.(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, ^-[Aib3S]GLP-1-(7-37)yl(rVt-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, M37-(3-(mPEGyl)propionyl) [Aib22, Lys37]GLP-1-(7-37) where mPEGyi is polydisperse and has a Mw of approx 20 kDa, ^37-(3-{mPEGyl)propionyl) [Aib22, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A^-[Aib22]GLP-1-(7-37)yl{A/-{3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A^-[Aib22]GLP-1-(7-37)yi(/Vc-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis-perse and has a Mw of approx 20 kDa, Wc37-(3-(mPEGyi)propionyl) [Aib8. Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, ^37-(3-(mPEGyl}propionyl) [Aib8. Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W-{Aib8]GLP-1-(7-37)yl(Nc-(3-(mPEGyl)propionyi))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W-[Aib8]GLP-1-(7-37)yi(/Ve-(3-(mPEGyl)ProPionyi))Lysinamide where mPEGyi is Polydisperse and has a Mw of approx 20 kDa, /V37-(3-(mPEGyl)propionyl) [Alb"'35, Lys37]GLP-1-(7-37) where mPEGyi is polydisperse and has a Mw of approx 20 kDa, /^"•(S-dnPEGyOpropionyl) [Aib8'35, Lys37]GLP-1-{7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W-[Aib8-3S]GLP-1-(7-37)yl(Wc-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDaAib8|l^GLP-1-(7-37)yl(/SfX3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis-perse and has a Mw of approx 20 kDa. /V37-(3-(mPEGyl)propionyl) [Aib22-35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa,-(a^mPEGylJpropionyl) [Aib22-35, Lys"]GLP-1-(7-37) amide where mPEGy! is polydis­perse and has a Mw of approx 20 kDa, A/9-[Aib22>3S]GLP-1-(7-37)yl(A/-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa,-[Aib22-35]GLP-1-(7-37)yl(Ayc-{3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, N37-(3-(mPEGyl)propionyl) [Aib8'35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa,/V37-(3-(mPEGyl)propionyl) [Aib8'35. Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V°-[Aib8'35]GLP-1-(7-37)yl(W;-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V-[Aib8'35]GLP-1-(7-37)yl(A/r--{3-(mPEGyl)propionyl)}Lysinamide where mPEGyl is polydis- 4 perse and has a Mw of approx 20 kDa, A/^-p-fmPEGyOpropionyl) [Aib8'22. Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Af37-(3-(mPEGyl)propionyl) [Aib8'22, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/T-[Aib*'22]GLP-1-(7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/'-[Aib8'22]GLP-1-(7-37)yl(A/c-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, //"-(S-tmPEGyOpropionyl) [Aib8-22'35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /^"-(S-CmPEGyOpropionyl) [Aib8'22'35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, /N/0-[Aib8'22'35]GLP-1-(7-37)yl(Nc-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/'-[Aib822'3S]GLP-1-(7-37)yl(A/-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, [Aib8. ArgZ8'M]GLP-1-(7-37)yl(A/t-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydis-perse and has a Mw of approx 20 kDa, /V-lAib8. Arg26':"]GLP-1-{7-37)yl(A/c-(3-(mPEGyl)propionyl)}Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa ^-O-fmPEGyOpropionyl) [Aib8, Arg^.Lys^GLP-l-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, N^-O-fmPEGylJpropionyl) [Aib8, Arg^.Lys^GLP-l-a-S?) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, -(S-fmPEGyOpropionyl) [Aib8, Lys^.Lys^JGLP-l-^-S?) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, -(S-fmPEGyOpropionyl) [Aib8. Lys26,Lys3*]GLP-1-{7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, -[Arg2e'34]GLP-1-(7-37)yl(A/e-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V-[ Arg2B-34]GLP-1-(7-37)yl(A/;-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, N37-(S-fmPEGyOpropionyl) [ Arg^.Lys^GLP-l-^-S?) where mPEGyl is polydisperse and has a Mw of approx'20 kDa, /V38-(3-(mPEGyl)propionyl) (Arg2BJ4,LysM]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, -(S-fmPEGyOpropionyl) [ Lys^.Lys^GLP-l-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, ^-(mPEGyOpropionyl) [ Lys26,Lys34]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V°-[Ala8, Arg26-34,]GLP-1-(7-37)yl(A'E-(3-(mPEGyl)propionyl))Lysine where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, /V-[A!a8. Arg2fl':M]GLP-1-(7-37)yl(A/:-(3-(mPEGyl)propionyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Af3e-(3-(mPEGyl)propionyl) [Ala8, Arg28-34,Lys36]GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /^-^-(mPEGyOpropionyl) [Ala8, Arg29'34,Lys36]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W^-WmPEGyOproptonyl) [Ala8, Lys26,Lys34]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, ^-(S-fmPEGyOpropionyl) [Ala8, Lys26.Lys34]GLP-1-{7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, r/^-p-CmPEGyOpropionyl) [Lys^Exendin-MI-Sg) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/^S-fmPEGyOpropionyl) [Lys32]Exendin-4-(1-39) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /^-(S-fmPEGyOpropionyl) [Lys^.Arg^Exendin^-d-sg) amide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa, and Ars32-(3-(mPEGyl)propionyl) [Lys32,Arg12'27]Exendin-4-(1-39) amide where mPEGyl is polydis­perse and has a Mw of approx 20 kDa. In another embodiment the compound according to the present invention is selected from the group consisting of A/^MS^mPEGyObutanoyl) [Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, //^-(S-fmPEGyObutanoyl) [Lys37]GLP-1-{7-37) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, GLP-1-(7-37)yl(r/-(3-(mPEGyl)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 30 kDa, GLP-1-(7-37)yl(rVc-(3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, Af37-(3-(mPEGyl)butanoyl) [Aib35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa. r/37-(3-(mPEGyl)butanoyl) [Aib35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, A/'-[Aib35]GLP-1-(7-37)yl(A/e-(3-(mPEGyl)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 30 kDa, r7J-[Aib35]GLP-1-(7-37)yl(/Ve-(3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, Af37-(3-(mPEGyl)butanoyl) [Aib22, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, ^"-^-(mPEGyObutanoyl) [Aib22. Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa.A/°-[Aib^GLP-1-(7-37)yl{//-{3-(mPEGyl)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 30 kOa./V0-[Aib22]GLP-1-(7-37)yf(A/e-(3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa. A/^-CS-fmPEGyObutanoyl) [Aib8, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, /^-(S-fmPEGylJbutanoyl) [Aib6. Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, A/a-[Aib8]GLP-1-(7-37)yl(Af-(3-(mPEGyl)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 30 kDa, Ar'-[Aib8]GLP-1-(7-37)yl(A/t-(3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, Af37-(3-(mPEGyl)butanoyl) [Aib8'35. Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, //^-{S^mPEGyObutanoyl) [Aib8'35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, /V°-[Aib8i3S]GLP-1-(7-37)yl(/l/-(3-{mPEGyl)butanoyl)}Lysine where mPEGyl is polydisperse and has a Mw of approx 30 kDa, A/°-[Aib8'35]GLP-1-(7-37)yl(A/:-{3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, A/37-(3-(mPEGyl)butanoyl) (Aib22-35. Lys37)GLP-1-{7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, /^"-(S-fmPEGyObutanoyl) [Aib22-*5. Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, Ar7-[Aib22-35]GLP-1-(7-37)yl(A/e-(3-(mPEGyl)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 30 kDa, N°-[Aib22'35]GLP-1-(7-37)yl(A/e-(3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, A/37-(3-(mPEGyl)butanoyl) [Aib8'3*, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, /Vt37-(3-(mPEGyl)butanoyl) [Aib835, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, A/°-[Aib8'35]GLP-1-(7-37)yl(/Vc-(3-(mPEGyl)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 30 kDa,'-[Aib8i35]GLP-1-(7-37)yl(Wt-(3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydis-N perse and has a Mw of approx 30 kDa, Ar37-(3-(mPEGyl)butanoyl) [Aib822, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, A/*7-(3-(mPEGyl)butanoyl) [Aib822. Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, /V-[Aib8l22]GLP-1-(7-37)yt(Wc-(3-{mPEGyl)bu(anoyl))Lysine where .mPEGyl is polydisperse and has a Mw of approx 30 kDa. /V°-[Aib8-22]GLP-1-(7-37)yl(/VM3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, //^-(S-fmPEGyObutanoyl) [Aib8'22'35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, Af37-(3-(mPEGyl)butanoyl) [Aib8-22-35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, /V°-{Aib8-22-35]GLP-1-(7-37)yl(A/;-(3-{mPEGyl)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 30 kDa, W-[Aib8'22'3S]GLP-1-(7-37)yl(Wc-(3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydis­perse and has a MW of approx 30 kDa, N°-[Mb6. Arg26'34]GLP-1-(7-37)yl(^-(3-(mPEGyl)butanoyl))Lysine where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, Af-rAib8, Arg29'34]GLP-1-(7-37)yl(/^-(3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, /^-(S-OnPEGyObutanoyl) [Aib8, Arg2834,Lys36]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, /^-(S-fmPEGyObutanoyl) [Aib8, Arg2634,Lys36]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, A/E34-{3-(mPEGyl)butanoyO [Aib8, Lys^.Lys^GLP-l-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, A/:34-(3-(mPEGyl)butanoyl) [Aib8, Lys29,Lys34]GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, A/3-[Arg2fl'34]GLP-1-(7-37)yl(/V:-(3-(mPEGyl)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 30 kDa, /V-[ Arg26'34]GLP-1-(7-37)yl(A/-(3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa,M-3M-ys38JGLP-1-(7-37) where mPEGyl Is polydisperse andhas a Mw of approx 30 kDa,f/M-{3-(mPEGyl)butanoy1) [ Arg28'34.Lys36]GLP-l-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, ^-(MmPEGyObutanoyl){Lys'M.ys^jGLP-l-^-S?) wheremPEGyl is polydisperse and has a Mw of approx 30 kDa, /^-(S-tmPEGyl^utanoyt) {Lys*,Lys:MJGLP-1-(7-37) amide where mPEGyl is poiydisperse and has a Mw of approx 30 kDa, /V-[Ala8, Arg26'34,]GLP-l-(7-37)yl(r/-(3-(mPEGyl)butanoyl))Lysine where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, rV-{Ala6, Arg^]GLP-H7-37)y)(//-{3-(mPEGyl)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, rV3a-(3-(mPEGyl)butanoyl) [Ala8, Arg2M4,Lys3elGLP-H7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kDa, /V3a-(3-(mPEGyl)butanoyl) [Ala8, ArgaW4lLys38]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, Ar^-fXmPEGyObutanoyl) [Ala8, Lys26,Lys34]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 30 kOa, Ne:M-{3-{mPEGyl)butanoyl) [Ala8, Lys2S,LysJ4)GLP-1-(7-37) amide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, /^-(S-fmPEGyObutanoyl) [Lys20]Exendin-4-0-39) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, fV^S-fmPEGyObutanoylHLys^lExendin-Ml-Sg) amide where mPEGyl is polydisperse and has a Mw of approx 30 kDa, (S-CmPEGyObutanoyl) (Lysw.Argl2'27lExendin-4-(1-39) amide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa, and (mPEGyObutanoyl) [Lys32,Arg'z'2i>]Exendin-4-{1-39} amide where mPEGyl is polydis­perse and has a Mw of approx 30 kDa.In another embodiment the compound according to the present invention is selectedfrom the group consisting of-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Lys37]GLP-l-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/tJ7-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Lys3r]GLP-1-(7-37) amide where mPE-vGyl is polydisperse and has a Mw of approx 20 kDa, GLP-1-(7-37)yl(Wc-((2S)-2.6-di-{mPEGylcarbonylamino)hexanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, GLP-1-(7-37)yl(A/c-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa. /Vt37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib35, Lys37]GLP-1-(7-37) where mPE-Gyl is polydisperse and has a Mw of approx 20 kDa, /V37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib35. Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/0-[Aib3S]GLP-1-(7-37)yl(r/-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/7-[Aib35]GLP-1-(7-37)yl(A/e-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/t37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib22. Lys37]GLP-1-(7-37) where mPE-Gyl is polydisperse and has a Mw of approx 20 kDa, AA37-((2S)-2,6-di-(mPEGylcarbony!amino)hexanoyl) [Aib22. Lys37]GLP-1-(7-37) amide where mPEGyl is polydispetse and has a Mw of approx 20 kDa, /V-[AibZ2]GLP-1-(7-37)yl(/Vc-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/'-[Aib22]GLP-1-(7-37)yl(rVc-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /Vc37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib8, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V=37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib8, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V-[Aib8]GLP-1-(7-37)yl(Ari-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V°-[Aib8]GLP-1-(7-37)yl(/\r-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Af37-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl) [Aib8-35. Lys37]GLP-1-(7-37) where mPE-Gyl is polydisperse and has a Mw of approx 20 kDa, /V37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib8'35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa.A/8-[Aib*JS]GLP-1-(7-37)yl(A/e-((2S)-2,6-di-(mPEGylcarbonylamino}hexanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa. W7-[Aibe-35]GLP-1-{7-37)yl(/^-((2S}-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Wc3!'-{(2S)-2,6-di-(mPEGylcafbonylamino)hexanoyl) [Aib22-35, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /Y*7-({2S)-2.6-dKmPEGylcarbonylamino)hexanoyl) [Aib22-35, Lys37]GI_P-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa. Ar>-[Aib22-35]GLP-1-(7-37}yl(/l/-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl))Lysine where mPEGyl is pofydisperse and has a Mw of approx 20 kDa. /V-(Aib22'35]GLP-1-(7-37)yl{/^-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A^37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib8-35, Lys37]GLP-1 -(7-37) where mPE-Gyl is polydisperse and has a Mw of approx 20 kDa, Af37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib835, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W-[Aib8-35)GLP-1-(7-37)yl(Nt-((2S)-2,6-di-{mPEGylcarbonylamino)hexanoyl))Lysine where mPEGyl is poiydispense and has a Mw of approx 20 kDa, Wff-[Aibe-a&jGLP-1-(7-37)yl(/Vc-({2S)-2,6-di-(mPEGyicarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/c37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib8-22, Lys37)GLP-1-(7-37) where mPE-Gyl is polydisperse and has a Mw of approx 20 kDa, A/t37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib8-22, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V"-[Aib822]GLP-1-(7-37)yl(AA-{{2S)-2.6-di-(mPEGylcarbanylamino)hexanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, //'-[Aib8-22]GLP-1-(7-37)yl(A/c-{(2S}-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/e37-((2S)-2,6-di-{mPEGylcarbonylamino)hexanoyl) [Aib82235, Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/E37-((2S)-2.6-di-(mPEGyicarbonylamino)hexanoyl) [Aib8-22-35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W-[Aib8-22-35]GLP-1-{7-37)yl(A/c-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysine where mPEGy! is polydisperse and has a Mw of approx 20 kDa,/V-[Aib8-22-35JGLP-1-{7-37)yl(/Vc-((2S)-2,6-di-(mPEGyJcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/'-[Aib8lArg2<>-:j4]GLP-1-(7-37)yl(Ne-((2S)-2t6-di-(mPEGylcarbonylamino)hexanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V-[Aib8.Arg26-:MlGLP-1.(7-37)yl(Wc-((2S)-2l6-di- (mPEGylcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa. AA*-{(2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib8, Arg26>34,Lys3a]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/38-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aiba, Arg28-34,Lys36]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /Vc34-((2S)-2.6-di-(mPEGylcarbonylamino)hexanoyl) [Aib8. Lys26,Lys:M]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A^34-{(2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Aib8, Lys26,Lys34]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/J-{Arg28-54]GLP-1-(7-37)yl(Ar:-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyi)}Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/9-[Arg26-34]GLP-'1-(7-37)yl(A/l-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/c38-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [ Arg28-34,Lys36]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/cM-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [ Arg28-34,Lys36]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /VE34-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [ Lys26,Lys34]GLP-1-(7-37) where mPE-Gyl is polydisperse and has a Mw of approx 20 kDa, /Vc34-((2S)-2,6-di-(mPEGylcarbonylamino}hexanoyl) [ Lys26,Lys34]GLP-1-(7-37) amide where mPEGyi is polydisperse and has a Mw of approx 20 kDa, AT-fAla8, Arg2e'M,]GLP-1-(7-37)yl(/VE-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyt))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A^-[Alaa, Arg26-l4]GLP-1-(7-37)yl(/VE-((2S)-2,6-di- (mPEGylcarbonylamino)hexanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/t36-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Ala8, Arg^.Lys^GLP-l-fJ-S?) where mPEGyl is polydisperse and has a Mw of approx 20 kDa,/VcM-{(2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Ala8. Arg^.Lys^GLP-l-^-S?) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /\fM-{(2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Ala8, Lys^.Lys^jGLP-l-^-S?) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, rVtW-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Ala8. Lys^.Lys^jGLP-HT-S?) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, AA20-((2S)-2.6-di-{mPEGylcarbonylamino)hexanoyl) [Lys20]Exendin-4-(1-39) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa. r\f32-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl) [Lys32]Exendin-4-(1-39) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A^20-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Lys20,Arg12-27lExendin-4-(l-39) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, and /^2-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Lys32,Argl2'27]Exendin-4-(1-39) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa. In another embodiment the compound according to the present invention is selected from the group consisting of Wc37-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl)[Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, GLP-1-(7-37)yl(A/E-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, GLP-1-(7-37)yl(/Ve-(4-(1,3-bts(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, AA:37-(4-(1l3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl)[Aib35, Lys37]GI_P-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/*7-(4-(1 ,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa. A/°-[Aib35]GLP-1-(7-37)yl(A/t-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa. A/7-[Aib35]GLP-1-(7-37)yl(/VE-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Af37-(4-(1,3-bis(mPEGylethylaminocarbony!oxy)prop-2-yloxy)butanoyl) [Aib22. Lys3r]GLP-1 - (7-37) where mPEGyt is polydisperse and has a Mw of approx 20 kDa, W37-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)bulanoyl) [Aib22, Lys37]GLP-1- (7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa. Ar*-tAib22]GLP-1-(7-37)yl(A/e-(4-(1.3-bis(mPEGylethylaminocarbonyloxy)prop-2- yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Ar-{Aib22]GLP-1-(7-37)yl(/Vt-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2- yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa. AA37-(4-(1,3-bis(mPEGylethy!aminocarbonyloxy)prop-2-yloxy)butanoyl) (Aib8, Lys37]GLP-1-(7- 37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Nc37-{4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib8, Lys37]GLP-1-(7- 37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V°-(Aib8]GLP-1-(7-37)yl(//-(4-(1,3-bis(mPEGylethylaminocarbony!oxy)prop-2- yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V°-[Aib8]GLP-1-(7-37)yl(A/c-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2- yloxy)butanoyl))Lysinamide where mPEGyl is'poly disperse and has a Mw of approx 20 kDa, A/c37-{4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib8'35. Lys37]GLP-1 - (7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa. /V37-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib8'35, Lys37]GLP-1- (7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W°-[AibB'353GLP-1-(7-37)yl(A/c-(4-(1.3-bis(mPEGylethylaminocarbonyloxy)prop-2- yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, AAJ-[Aib8-35]GLP-1-(7-37)yl(Wc-(4-(1.3-bis(mPEGylethylaminocarbonyloxy)prop-2- yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W37-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib22'35. Lys37]GLP-1 - (7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa. /^37-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) (Aib2235. Lys37]GLP-l- (7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/'-[Aib22-35]GLP-1-(7-37)yl(Wc-(4-(1,3-bis(mPEGylethy]aminocarbonyloxy)prop-2- yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa. /V°-[Aib22'35]GLP-1-(7-37)yl(/Vt-{4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2- yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W"37-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib8'35, Lys37lGLP-1- (7-37) where mPEGyi is polydisperse and has a Mw of approx 20 kDa, (4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib8'35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa. A/°-[Aib8'35]GLP-1-{7-37)yt(A/c-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/°-[Aib8-35]GLP-l-(7-37)yl(/Vc-(4-(1,3-bis{mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa. A/"37-(4-(1 ,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib8'22, Lys37)GLP-1 -(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Wt37-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib8'22. Lys37]GLP-1 -(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W-[Aib8'22]GLP-1-(7-37)yl(/S/e-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W°-[Aib8'22]GLP-1-(7-37)yl(A^-(4-(1,3-bis(mPEGy!ethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/c37-(4-(1,3-bis(mPEGy!ethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib8'2"5. Lys37]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, //37-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib8-22-35, Lys37]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /V-[Aib8'2Z35lGLP-1-(7-37)yKf/-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, N0-[Aib8>22-35]GLP-1-(7-37)yl(A/:-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/'-tAib8, Arg^GLP-l-(7-37)yl(r/-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W-[Aib8, Arg2fU4]GLP-1 -(7-37)yl(A/c-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /Vt38-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl)[Aib8, Arg28'34,Lys3a]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /VE36-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl)[Aib8. Arg26-34,Lys36]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, AfM-(4-(1.3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Aib8, Lys26,Lys34]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, ^^-(l.a-bistmPEGylethylaminocarbonyloxyJprop^-yloxyJbutanoyOIAib8. Lys^.Lys^lGLP-l-^-a?) amide where mPEGyl is polydisperse and has a Mw of approx 20 kOa, /V-[Arg28-:M]GLP-1-(7-37)yl(A/l-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2- yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/'-[Arg28-:M]GLP-H7-37)yl(Ne-(4-(1l3-bis(rnPEGylethylarninocarbonyloxy)prop-2- yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Af*-{4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [ Arg (7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /Vc38-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) (7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, a/^-^-ci ,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) (7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Wc3<-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [ Lys28,Lys*]GLP-1 - (7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W-[Ala8, Arg^JGLP-1 -(7-37)yl(Af-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2- yloxy)butanoyl))Lysine where mPEGyl is polydisperse and has a Mw of approx 20 kDa, Af-[Alae. Arg26 ^GLP-1 -(7-37)yl(A/c-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2- yloxy)butanoyl))Lysinamide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /7:36-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) (Ala8, Arg28'34.Lys38]GLP-1-(7-37) where mPEGyl is polydisperse and has a Mw of approx 20 kDa, /Vc38-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Ala8, ArgM'34,Lys38]GLP-1-(7-37) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/:34-(4-(l,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl)[Ala8, Lys^.Lys^jGLP-l-^-S?) where mPEGyl is polydisperse and has a Mw of approx 20 kOa, //34-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Ala8, Lys^.Lys^GLP-l-^-S/) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, W^-^-CI ,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Lys20]Exendin-4-(1 -39) amide where mPEGyl is polydisperse and has a Mw of approx 20 kDa, A/c32-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Lys32]Exendin-4-(1-39) arnide where mPEGyl is polydisperse and has a Mw of approx 20 kDa,ArJO-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [LysM.Arg12-27]Exendin-4-(1-39) amide where mPEGyl is polydisperse and has a Mwof approx 20 kOa, ^32-(4-(1,3-bis(mPEGylethylaminocarbonyloxy)prop-2-yloxy)butanoyl) [Lys32,Arg1227jExendin-4-(1-39) amide where mPEGyl is polydisperse and has a Mw of approx 20 KDa, The compounds of the present invention can be produced by classical peptide synthe­sis, e.g. solid phase peptide synthesis using t-Boc or Fmoc chemistry or other well established techniques., see e.g. Green and Wuts, "Protecting Groups in Organic Synthesis", John Wiley & Sons, 1999. These methods are preferred when the insulinotropic agent is a peptide comprising non-natural amino acid residues. When the insulinotropic agent is a polypeptide comprising only amino acid residues encoded by the genetic code, the polypeptides can also be produced by a method which com­prises culturing a host cell containing a DNA sequence encoding the polypeptide and capable of expressing the polypeptide in a suitable nutrient medium under conditions permitting the ex­pression of the peptide, after which the resulting peptide is recovered from the culture and then derivatized to the cpmpound of formula (I). The medium used to culture the cells may be any conventional medium suitable for growing the host cells, such as minimal or complex media containing appropriate supplements. Suitable media are available from commercial suppliers or may be prepared according to pub­lished recipes (e.g. in catalogues of the American Type Culture Collection). The peptide pro­duced by the cells may then be recovered from the culture medium by conventional procedures including separating the host cells from the medium by centrifugation or filtration. For extracellu­lar products the proteinaceous components of the supernatant are isolated by filtration, column chromatography or precipitation, e.g. microfiltation, ultrafiltration, isoelectric precipitation, purifi­cation by a variety of chromatographic procedures, e.g. ion exchange chromatography. hydro-phobic interaction chromatography, gel filtration chromatography, affinity chromatography, or the like, dependent on the type of pofypeptide in question. For intracellular or periplasmic prod­ucts the cells isolated from the culture medium are disintegrated or permeabilised and extracted to recover the product polypeptide or precursor thereof.The DNA sequence encoding the therapeutic polypeptide may suitably be of genomic or cDNA origin, for instance obtained by preparing a genomic or cDNA library and screening for DNA sequences coding for all or part of the peptide by hybridisation using synthetic oligonucleo-tide probes in accordance with standard techniques (see, for example, Sambrook, J, Fritsch, EFand Maniatis. T. Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press. New York, 1989). The DNA sequence encoding the polypeptide may also be prepared synthetically by established standard methods, e.g. the phosphoamidite method described by Beaucage and Caruthers. Tetrahedron Letters 22 (1981). 1859 -1869. or the method described by Matthes et al., EMBO Journal 3 (1984). 801 - 805. The DNA sequence may also be prepared by polymerase chain reaction using specific primers, for instance as described in US 4,683,202 or Saiki et al.. Science 239 (1988), 487 - 491. The DNA sequence may be inserted into any vector which may conveniently be sub­jected to recombinant DNA procedures, and the choice of vector will often depend on the host cell into which it is to be introduced. Thus, the vector may be an autonomously replicating vec­tor, i.e. a vector which exists as an extrachromosomal entity, the replication of which is inde­pendent of chromosomal replication, e.g. a plasmid. Alternatively, the vector may be one which, when introduced into a host cell, is integrated into the host cell genome and replicated together with the chromosome(s) into which it has been integrated. The vector is preferably an expression vector in which the DNA sequence encoding the polypeptide is operably linked to additional segments required for transcription of the DNA, such as a promoter. The promoter may be any DNA sequence which shows transcriptional ac­tivity in the host cell of choice and may be derived from genes encoding proteins either homolo­gous or heterologous to the host cell. Examples of suitable promoters for directing the transcrip­tion of the DNA encoding the peptide of the invention in a variety of host cells are well known in the art, cf. for instance Sambrook era/., supra.The DNA sequence encoding the polypeptide may also, if necessary, be operably connected to a suitable terminator, polyadenylation signals, transcriptional enhancer se­quences, and translational enhancer sequences. The recombinant vector of the invention may further comprise a DNA sequence enabling the vector to replicate in the host celLin question. The vector may also comprise a selectable marker, e.g. a gene the product of which complements a defect in the host cell or one which confers resistance to a drug, e.g. ampicillin, kanamycin, tetracyclin, chloramphenicol, neomycin. hygromycin or methotrexate. For large scale manufacture the selectable marker preferably is not antibiotic resistance, e.g. antibiotic resistance genes in the vector are preferably excised when the vector is used for large scale manufacture. Methods for eliminating antibiotic resistance genes from vectors are known in the art, see e.g. US 6,358.705 which is incorporated herein by reference.To direct a parent peptide of the present invention into the secretory pathway of the host cells, a secretory signal sequence (also known as a leader sequence, prepro sequence or pre sequence) may be provided in the recombinant vector. The secretory signal sequence isjoined to the DNA sequence encoding the peptide in the correct reading frame. Secretory signal sequences are commonly positioned 5* to the DNA sequence encoding the peptide. The secre­tory signal sequence may be that normally associated with the peptide or may be from a gene encoding another secreted protein. The procedures used to ligate the DNA sequences coding for the present peptide. the promoter and optionally the terminator and/or secretory signal sequence, respectively, and to insert them into suitable vectors containing the information necessary for replication, are well known to persons skilled in the art (cf.. for instance, Sambrook et a/.., supra). The host cell into which the DNA sequence or the recombinant vector is introduced may be any cell which is capable of producing the present peptide and includes bacteria, yeast, fungi and higher eukaryotic cells. Examples of suitable host cells well known and used in the art are, without limitation, E. coll, Saccharomyces cerevisiae, or mammalian BHK or CHO cell lines. Pharmaceutical compositions containing a compound according to the present inven­tion may be prepared by conventional techniques, e.g. as described in Remington's Pharma­ceutical Sciences, 1985 or in Remington: The Science and Practice of Pharmacy, 19th edition, 1995. One object of the present invention is to provide a pharmaceutical formulation com­prising a compound according to the present invention which is present in a concentration from about 0.1 mg/ml to about 25 mg/ml. and wherein said formulation has a pH from 2.0 to 10.0. The formulation may further comprise a buffer system, preservative(s), isotonicity agent(s), chelating agent(s), stabilizers and surfactants. In one embodiment of the invention the pharmaceutical formulation is an aqueous formulation, i.e. formulation comprising water. Such formulation is typically a solution or a suspension. In a further embodiment of the inven­tion the pharmaceutical formulation is an aqueous solution. The term "aqueous formulation" is defined as a formulation comprising at least 50 %w/w water. Likewise, the term "aqueous solution" is defined as a solution comprising at least 50 %w/w water, and the term "aoueous suspension" is defined as a suspension comprising at least 50 %w/w water. In another embodiment the pharmaceutical formulation is a freeze-dried formulation, whereto the physician or the patient adds solvents and/or diluents prior to use. In another embodiment the pharmaceutical formulation is a dried formulation (e.g. freeze-dried or spray-dried) ready for use without any prior dissolution.In a further aspect the invention relates to a pharmaceutical formulation comprising an aqueous solution of a compound according to the present invention, and a buffer, wherein said compound is present in a concentration from 0.1 mg/ml or above, and wherein said formulation has a pH from about 2.0 to about 10.0.In another embodiment of the invention the pH of the formulation is from about 7.0 to about 9.5. In another embodiment of the invention the pH of the formulation is from about 3.0 to about 7.0. In another embodiment of the invention the pH of the formulation is from about 5.0 to about 7.5. In another embodiment of the invention the pH of the formulation is from about 7.5 to about 9.0. In another embodiment of the invention the pH of the formulation is from about 7.5 to about 8.5. In another embodiment of the invention the pH of the formula­tion is from about 6.0 to about 7.5. In another embodiment of the invention the pH of the for­mulation is from about 6.0 to about 7.0. In another embodiment of the invention the pH of the formulation is from about 3.0 to about 9.0, and said pH is at least 2.0 pH units from the isoelectric pH of compound of the present invention.In a further embodiment of the invention the buffer is selected from the group consisting of sodium acetate, sodium carbonate, citrate, glycylglycine, histidine. glycine, lysine, arginin, sodium dihydrogen phosphate, disodium hydrogen phosphate, sodium phosphate, and tris(hydroxymethyl\-aminomethan, bicine, tricine, malic acid, succinate, maleic acid, fumaric acid, tartaric acid, aspartic acid or mixtures thereof. Each one of these specific buffers consti­tutes an alternative embodiment of the invention. In a further embodiment of the invention the formulation further comprises a pharmaceutically acceptable preservative. In a further embodiment of the invention the preservative is selected from the group consisting of phenol, o-cresol, m-cresol. p-cresol, methyl p-hydroxybenzoate. propyl p-hydroxybenzoate, 2-phenoxyethanol, butyl p-hydroxybenzoate, 2-phenylethanol, benzyl alcohol, chlorobutanol, and thiomerosal, bronopol, benzole acid, imidurea, chlorohexidine, sodium dehydroacetate. chlorocresol, ethyl p-hydroxybenzoate, benzethonium chloride, chlorphenesine (3p-chlorphenoxypropane-1,2-diol) or mixtures thereof. In a further embodiment of the invention the preservative is present in a concentration from 0.1 mg/ml to 20 mg/ml. -In a further embodiment of the invention the preservative is present in a concentration from 0.1 mg/ml to 5 mg/ml. In a further embodiment of the invention the preservative is present in a concentration from 5 mg/ml to 10 mg/ml. In a further embodiment of the invention the preservative is present in a concentration from 10 mg/ml to 20 mg/ml. Each one of these specific preservatives constitutes an alternative embodiment of the invention. The use of a preservative in pharmaceutical^compositions is well-known to the skilled person. For convenience reference is made to Remington: The Science and Practice of Pharmacy. 19th edition, 1995.In a further embodiment of the invention the formulation further comprises an isotonic agent. In a further embodiment of the invention the isotonic agent is selected from the group consisting of a salt (e.g. sodium chloride), a sugar or sugar alcohol, an amino acid (e.g. L-glycine, L-histidine, arginine, lysine, isoleucine, aspartic acid, tryptophan. threonine), an alditol (e.g. glycerol (glycerine). 1,2-propanediol (propyleneglycol), 1,3-propanediol, 1.3-butanediol) polyethyleneglycol (e.g. PEG400), or mixtures thereof. Any sugar such as mono-, di-, or polysaccharides, or water-soluble glucans, including for example fructose, glucose, mannose, sorbose, xylose, maltose, lactose, sucrose, trehalose. dextran, pullulan, dextrin, cyclodextrin, soluble starch, hydroxyethyl starch and carboxymethylcellulose-Na may be used. In one embodiment the sugar additive is sucrose. Sugar alcohol is defined as a C4-C8 hydrocarbon having at least one -OH group and includes, for example, mannitol, sorbitol, inositol, galacititol, dulcitol, xylitol, and arabitol. In one embodiment the sugar alcohol additive is mannitol. The sugars or sugar alcohols mentioned above may be used individually or in combination. There is no fixed limit to the amount used, as long as the sugar or sugar alcohol is soluble in the liquid preparation and does not adversely effect the stabilizing effects achieved using the methods of the invention. In one embodiment, the sugar or sugar alcohol concentration is between about 1 mg/ml and about 150 mg/ml. In a further embodiment of the invention the isotonic agent is present in a concentration from 1 mg/ml to 50 mg/ml. In a further embodiment of the invention the isotonic agent is present in a concentration from 1 mg/ml to 7 mg/ml. In a further embodiment of the invention the isotonic agent is present in a concentration from 8 mg/ml to 24 mg/ml. In a further embodiment of the invention the isotonic agent is present in a concentration from 25 mg/ml to 50 mg/ml. Each one of these specific isotonic agents constitutes an alternative embodiment of the invention. The use of an isotonic agent in pharmaceutical compositions is well-known to the skilled person. For convenience reference is made to Remington: The Science and Practice of Pharmacy, 19th edition, 1995.In a further embodiment of the invention the formulation further comprises a chelating agent. In a further embodiment of the invention the chelating agent is selected from salts of ethylenediaminetetraacetic acid (EDTA), citric acid, and aspartic acid, and mixtures thereof. In a further embodiment of the invention the chelating agent is present in a concentration from 0.1 mg/ml to 5mg/ml. In a further embodiment of the invention the chelating agent is present in a concentration from 0.1 mg/ml to 2mg/ml. In a furthersmbodiment of the invention the chelating agent is present in a concentration from 2mg/ml to 5mg/ml. Each one of these specific chelating agents constitutes an alternative embodiment of the invention. The use of a chelating agent in pharmaceutical compositions is well-known to the skilled person. For convenience reference is made to Remington: The Science and Practice of Pharmacy, 19th edition. 1995. In a further embodiment of the invention the formulation further comprises a stabi­liser. The use of a stabilizer in pharmaceutical compositions is well-known to the skilled per­son. For convenience reference is made to Remington: The Science and Practice of Phar­macy, 19th edition, 1995. More particularly, compositions of the invention are stabilized liquid pharmaceutical compositions whose therapeuticaliy active components include a polypeptide that possibly exhibits aggregate formation during storage in liquid pharmaceutical formulations. By "aggre­gate formation" is intended a physical interaction between the polypeptide molecules that re­sults in formation of oligomers, which may remain soluble, or large visible aggregates that precipitate from the solution. By "during storage" is intended a liquid pharmaceutical compo­sition or formulation once prepared, is not immediately administered to a subject. Rather, fol­lowing preparation, \\ is packaged for storage, either in a liquid form, in a frozen state, or in a dried form for later reconstitution into a liquid form or other form suitable for administration to a subject. By "dried form" is intended the liquid pharmaceutical composition or formulation is dried either by freeze drying (i.e., lyophilization; see, for example, Williams and Polli (1984) J. Parenteral Sci. Technol. 38:48-59), spray drying (see Masters (1991) in Spray-Drying Hand­book (5th ed; Longman Scientific and Technical, Essez, U.K.), pp. 491-676; Broadhead et al. (1992) Drug DeveJ. Ind. Pharm. 18:1169-1206; and Mumenthaler et al. (1994) Pharm. Res. 11:12-20), or air drying (Carpenter and Crowe (1988) Cryobiology 25:459-470;and Roser (1991) Biopharm. 4:47-53). Aggregate formation by a polypeptide during storage of a liquid pharmaceutical composition can adversely affect biological activity of that polypeptide, result­ing in loss of therapeutic efficacy of the pharmaceutical composition. Furthermore, aggregate formation may cause other problems such as blockage of tubing, membranes, or pumps when the polypeptide-containing pharmaceutical composition is administered using an infu­sion system.The pharmaceutical compositions of the invention may further comprise an amount of an amino acid base sufficient to decrease aggregate formation by the polypeptide during storage of the composition. By "amino acid base" is intended an amino acid or a combination of amino acids, where any given amino acid is present either in its free base form or in its saltform. Where a combination of amino acids is used, all of the amino acids may be present in their free base forms, all may be present in their salt forms, or some may be present in their free base forms while others are present in their salt forms. In one embodiment, amino acids to use in preparing the compositions of the invention are those carrying a charged side chain, such as arginine, lysine. aspartic acid, and glutamic acid. Any stereoisomer (i.e., L, D. or DL isomer) of a particular amino acid (e.g. glycine, methionine. histidine, imidazole, arginine. ly­sine, isoleucine, aspartic acid, tryptophan, threonine and mixtures thereof) or combinations of these stereoisomers, may be present in the pharmaceutical compositions of the invention so long as the particular amino acid is present either in its free base form or its salt form. In one embodiment the L-stereoisomer is used. Compositions of the invention may also be formu­lated with analogues of these amino acids. By "amino acid analogue" is intended a derivative of the naturally occurring amino acid that brings about the desired effect of decreasing ag­gregate formation by the polypeptide during storage of the liquid pharmaceutical composi­tions of the invention. Suitable arginine analogues include, for example, aminoguanidine, or-nithine and N-monoethyl L-arginine, suitable methionine analogues include S-ethyl homocys-teine and S-butyl homocysteine and suitable cystein analogues include S-methyl-L cystein. As with the other amino acids, the amino acid analogues are incorporated into the composi­tions in either their free base form or their salt form. In a further embodiment of the invention the amino acids or amino acid analogues are used in a concentration, which is sufficient to prevent or delay aggregation of the protein.In a further embodiment of the invention methionine (or other sulphur containing amino acids or amino acid analogous) may be added to inhibit oxidation of methionine resi­dues to methionine sulfoxide when the polypeptide acting as the therapeutic agent is a poly­peptide comprising at least one methionine residue susceptible to such oxidation. By "inhibit" is intended minimal accumulation of methionine oxidized species over time. Inhibiting me­thionine oxidation results in greater retention of the polypeptide in its proper molecular form. Any stereoisomer of methionine (L, D, or DL isomer) or combinations thereof can be used. The amount to be added should be an amount sufficient to inhibit oxidation of the methionine residues such that the amount of methionine sulfoxide is acceptable to regulatory agencies. Typically, this means that the composition contains no more than about 10% to about 30% methionine sulfoxide. Generally, this can be achieved by adding methionine such that the ratio of methionine added to methionine residues ranges from about 1:1 to about 1000:1, such as 10:1 to about 100:1.In a further embodiment of the invention the formulation further comprises a stabiliser selected from the group of high molecular weight polymers or low molecularcompounds. In a further embodiment of the invention the stabilizer is selected from polyethylene glycol (e.g. PEG 3350). polyvinylalcohol (PVA). polyvinylpyrrolidone, carboxy-/hydroxycellulose or derivates thereof (e.g. HPC, HPC-SL. HPC-L and HPMC), cyclodextrins, sulphur-containing substances as monothioglycerol, thioglycolic acid and 2-methylthioethanol. and different salts (e.g. sodium chloride). Each one of these specific stabilizers constitutes an alternative embodiment of the invention. The pharmaceutical compositions may also comprise additional stabilizing agents, which further enhance stability of a therapeutically active polypeptide therein. Stabilizing agents of particular interest to the present invention include, but are not limited to, methionine and EDTA, which protect the polypeptide against methionine oxidation, and a nonionic surfactant, which protects the polypeptide against aggregation associated with freeze-thawing or mechanical shearing. In a further embodiment of the invention the formulation further comprises a surfactant. In a further embodiment of the invention the surfactant is selected from a detergent, ethoxylated castor oil, polyglycolyzed glycerides. acetylated monoglycerides, sorbitan fatty acid esters, polyoxypropylene-polyoxyethylene block polymers (eg. poloxamers such a.s Pluronic® F68. poloxamer 188 and 407, Triton X-100 ), polyoxyethylene sorbitan fatty acid esters, polyoxyethylene and polyethylene derivatives such as alkylated and alkoxylated derivatives (tweens, e.g. Tween-20, Tween-40. Tween-80 and Brij-35), monoglycerides or ethoxylated derivatives thereof, diglycerides or polyoxyethylene derivatives thereof, alcohols, glycerol, lecitins and phospholipids (eg. phosphatidyl serine, phosphatidyl choline, phosphatidyl ethanolamine. phosphatidyl inositol, diphosphatidyl glycerol and sphingomyelin), derivates of phospholipids (eg. dipalmitoyl phosphatidic acid) and lysophospholipids (eg. palmitoyl lysophosphatidyl-L-serine and 1-acyl-sn-glycero-3-phosphate esters of ethanolamine, choline, serine or threonine) and alkyl, alkoxyl (alkyl ester), alkoxy (alkyl ether)- derivatives of lysophosphatidyl and phosphatidylcholines, e.g. lauroyl and myristoyl derivatives of lysophosphatidylcholine, dipalmitoylphosphatidylcholine, and modifications of the polar head group, that is cholines, ethanolamines, phosphatidic acid, serines, threonines, glycerol, inositol, and the positively charged DODAC, DOTMA, DCP, BISHOP, lysophosphatidylserine and lysophosphatidylthreonine, and glycerophospholipids (eg. cephalins), glyceroglycolipids (eg. galactopyransoide), sphingoglycolipids (eg. ceramides, gangliosides), dodecylphosphocholine, hen egg lysolecithin, fusidic acid derivatives- (e.g. sodium tauro-dihydrofusidate etc.), long-chain fatty acids and salts thereof C6-C12 (eg. oleic acid and caprylic acid), acylcarnitines and derivatives, Na-acylated' derivatives of lysine. arginine or histidine. or side-chain acylated derivatives of lysine or arginine. N°-acylated derivatives of dipeptides comprising any combination of lysine, arginine or histidine and a neutral or acidic amino acid, N°-acylated derivative of a tripeptide comprising any combination of a neutral amino acid and two charged amino acids, DSS {docusate sodium, CAS registry no [577-11-7]), docusate calcium, CAS registry no [128-49-4]), docusate potassium, CAS registry no [7491-09-0]), SDS (sodium dodecyl sulfate or sodium lauryl sutfate), sodium caprylate. cholic acid or derivatives thereof, bile acids and salts thereof and glycine or taurine conjugates, ursodeoxycholic acid, sodium cholate, sodium deoxycholate, sodium taurocholate, sodium glycocholate, N-hexadecyl-N,N-dimethyl-3-ammonio-1 -propanesulfonate. anionic (alkyl-aryl-sulphonates) monovalent surfactants, zwitterionic surfactants (e.g. N-alkyl-N,N-dimethylammonio-1-propanesulfonates, 3-cholamido-1-propyldimethylammonio-1 -propanesulfonate, cationic surfactants (quartemary ammonium bases) (e.g. cetyl-trimethylammonium bromide, cetylpyridinium chloride), non-ionic surfactants (eg. dodecyl p-D-glucopyranoside), poloxamines (eg. Tetronic's), which are tetrafunctional block copolymers derived from sequential addition of propylene oxide and ethylene oxide to ethylenediamine, or the surfactant may be selected from the group of imidazoline derivatives, or mixtures thereof. Each one of these specific surfactants constitutes an alternative embodiment of the invention. The use of a surfactant in pharmaceutical compositions is well-known to the skilled person. For convenience reference is made to Remington: The Science and Practice of Pharmacy, 19th edition, 1995.It is possible that other ingredients may be present in the peptide pharmaceutical formulation of the present invention. Such additional ingredients may include wetting agents, emulstfiers, antioxidants, bulking agents, tonicity modifiers, chelating agents, metal ions, ole­aginous vehicles, proteins (e.g., human serum albumin, gelatin or proteins) and a zwitterion (e.g., an amino acid such as betaine, taurine, arginine, glycine, lysine and histidine). Such additional ingredients, of course, should not adversely affect the overall stability of the phar­maceutical formulation of the present invention.Pharmaceutical compositions containing a compound according to the present in­vention may be administered to a patient in need of such treatment at several sites, for ex­ample, at topical sites, for example, skin and mucosal sites, at sites which bypass absorp­tion, for example, administration in an artery, in a vein, in the heart, and at sites which involve absorption, for example, administration in the skin, under the skin, in a musde or in the ab­domen. Administration of pharmaceutical compositions according to the invention may be through several routes of administration, for example, lingual, sublingual, buccal, in the mouth, oral, in the stomach and intestine, nasal, pulmonary, for example, through the bron­chioles and alveoli or a combination thereof, epidermal, dermal, transdermal, vaginal, rectal, ocular, for examples through the conjunctiva, uretal, and parenteral to patients in need of such a treatment. In one aspect the present invention relates to a pharmaceutical composition com­prising a compound according to Formula (I), and a pharmaceuticaliy acceptable excipient. In one embodiment the pharmaceutical composition is suited for pulmonary admini­stration. In another aspect the present invention relates to the use of a compound of formula (I) for the preparation of a pulmonary medicament. Compositions of the current invention may be administered in several dosage forms, for example, as solutions, suspensions, emulsions, microemulsions, multiple emulsion, foams, salves, pastes, plasters, ointments, tablets, coated tablets, rinses, capsules, for ex­ample, hard gelatine capsules and soft gelatine capsules, suppositories, rectal capsules, drops, gels, sprays, powder, aerosols, inhalants, eye drops, ophthalmic ointments, ophthal­mic rinses, vaginal pessaries, vaginal rings, vaginal ointments, injection solution, in situ transforming solutions, for example in situ gelling, in situ setting, in situ precipitating, in situ crystallization, infusion solution, and implants. Compositions of the invention may further be compounded in, or attached to, for ex­ample through covalent, hydrophobic and electrostatic interactions, a drug carrier, drug de­livery system and advanced drug delivery system in order to further enhance stability of the compound, increase bioavailability, increase solubility, decrease adverse effects, achieve chronotherapy well known to those skilled in the art, and increase patient compliance or any combination thereof. Examples of carriers, drug delivery systems and advanced drug deliv­ery systems include, but are not limited to. polymers, for example cellulose and derivatives, polysaccharides, for example dextran and derivatives, starch and derivatives, poly(vinyl al­cohol), acrylate and methacrylate polymers, polylactic and polyglycolic acid and block co-polymers thereof, polyethylene glycols, carrier proteins, for example albumin, gels, for exam­ple, thermogelling systems, for example block co-polymeric systems well known to those skilled in the art, micelles, liposomes, microspheres, nanoparticulates, liquid crystals anddispersions thereof. L2 phase and dispersions there of. well known to those skilled in the art of phase behaviour in lipid-water systems, polymeric micelles, multiple emulsions, self-emulsifying, self-microemulsifying, cyclodextrins and derivatives thereof, and dendrimers. Compositions of the current invention are useful in the formulation of solids, semisol-ids, powder and solutions for pulmonary administration of the compound, using, for example a rnetered dose inhaler, dry powder inhaler and a nebulizer, all being devices well known to those skilled in the art.Compositions of the current invention are specifically useful in the formulation of controlled, sustained, protracting, retarded, and slow release drug delivery systems. More specifically, but not limited to, compositions are useful in formulation of parenteral controlled release and sustained release systems (both systems leading to a many-fold reduction in number of administrations), well known to those skilled in the art. Even more preferably, are controlled release and sustained release systems administered subcutaneous. Without limit­ing the scope of the invention, examples of useful controlled release system and comoosi-tions are hydrogels, oleaginous gels, liquid crystals, polymeric micelles, microspheres, nanoparticles, Methods to produce controlled release systems useful for compositions of the cur­rent invention include, but are not limited to, crystallization, condensation, co-cystallization. precipitation, co-precipitation, emulsification, dispersion, high pressure homogenizaticn, en­capsulation, spray drying, microencapsulation. coacervation, phase separation, solvent evaporation to produce microspheres, extrusion and supercritical fluid processes. General reference is made to Handbook of Pharmaceutical Controlled Release (Wise, D.L., ed. Mar­cel Dekker, New York, 2000) and Drug and the Pharmaceutical Sciences vol. 99: Protein Formulation and Delivery (MacNally. E.J.. ed. Marcel Dekker, New York, 2000). Parenteral administration may be performed by subcutaneous, intramuscular, in-traperitoneal or intravenous injection by means of a syringe, optionally a pen-like syringe. Alternatively, parenteral administration can be performed by means of an infusion pump. A further option is a composition which may be a solution or suspension for the administration of the compound according to the present invention in the form of a nasal or pulmonai spray. As a still further option, the pharmaceutical compositions containing the compound of the in­vention can also be adapted to transdermal administration, e.g. by needle-free injection or from a patch, optionally an iontophoretic patch, or transmucosal, e.g. buccal, administration. The term "stabilized formulation" refers to a formulation with increased physical stability, increased chemical stability or increased physical and chemical stability. The term "physical stability" of the protein formulation as used herein refers to the tendency of the protein to form biologically inactive and/or insoluble aggregates of the protein as a result of exposure of the protein to thermo-mechanical stresses and/or interac­tion with interfaces and surfaces that are destabilizing, such as hydrophobia surfaces and interfaces. Physical stability of the aqueous protein formulations is evaluated by means of visual inspection and/or turbidity measurements after exposing the formulation filled in suit­able containers (e.g. cartridges or vials) to mechanical/physical stress (e.g. agitation) at dif­ferent temperatures for various time periods. Visual inspection of the formulations is per­formed in a sharp focused light with a dark background. The turbidity of the formulation is characterized by a visual score ranking the degree of turbidity for instance on a scale from 0 to 3 (a formulation showing no turbidity corresponds to a visual score 0, and a formulation showing visual turbidity in daylight corresponds to visual score 3). A formulation is classified physical unstable with respect to protein aggregation, when it shows visual turbidity in day­light. Alternatively, the turbidity of the formulation can be evaluated by simple turbidity meas­urements well-known to the skilled person. Physical stability of the aqueous protein formula­tions can also be evaluated by using a spectroscopic agent or probe of the conformational status of the protein. The probe is preferably a small molecule that preferentially binds to a non-native conforrqer of the protein. One example of a small molecular spectroscopic probe of protein structure is Thioflavin T. Thioflavin T is a fluorescent dye that has been widely used for the detection of amyloid fibrils. In the presence of fibrils, and perhaps other protein configurations as well, Thioflavin T gives rise to a new excitation maximum at about 450 nm and enhanced emission at about 482 nm when bound to a fibril protein form. Unbound Thioflavin T is essentially non-fluorescent at the wavelengths. Other small molecules can be used as probes of the changes in protein structure from native to non-native states. For instance the "hydrophobic patch" probes-that bind pref­erentially to exposed hydrophobic patches of a protein. The hydrophobic patches are gener­ally buried within the tertiary structure of a protein in its native state, but become exposed as a protein begins to unfold or denature. Examples of these small molecular, spectroscopic probes are aromatic, hydrophobic dyes, such as antrhacene, acridine, phenanthroline or the like. Other spectroscopic probes are metal-ammo acid complexes, such as cobalt metal complexes of hydrophobic amino acids, such as phenylalanine, leucine, isoleucine, methion-ine, and valine, or the like.The term "chemical stability" of the protein formulation as used herein refers to chemical covalent changes in the protein structure leading to formation of chemical degrada- \ lion products with potential less biological potency and/or potential increased immunogenic properties compared to the native protein structure. Various chemical degradation products can be formed depending on the type and nature of the native protein and the environment to which the protein is exposed. Elimination of chemical degradation can most probably not be completely avoided and increasing amounts of chemical degradation products is often seen during storage and use of the protein formulation as well-known by the person skilled in the art. Most proteins are prone to deamidatJon, a process in which the side chain amide group in glutaminyl or asparaginyl residues is hydrolysed to form a free carboxylic acid. Other de­gradations pathways involves formation of high molecular weight transformation products where two or more protein molecules are covalently bound to each other through transami-dation and/or disulfide interactions leading to formation of covalently bound dimer, oligomer and polymer degradation products (Stability of Protein Pharmaceuticals, Ahem. T.J. & Man­ning M.C., Plenum Press, New York 1992). Oxidation (of for instance methionine residues) can be mentioned as another variant of chemical degradation. The chemical stability of the protein formulation can be evaluated by measuring the amount of the chemical degradation products at various time-points after exposure to different environmental conditions (the for­mation of degradation products can often be accelerated by for instance increasing tempera­ture). The amount of each individual degradation product is often determined by separation of the degradation products depending on molecule size and/or charge using various chro-matography techniques (e.g. SEC-HPLC and/or RP-HPLC). Hence, as outlined above, a "stabilized formulation" refers to a formulation with in­creased physical stability, increased chemical stability or increased physical and chemical stability. In general, a formulation must be stable during use and storage (in compliance with recommended use and storage conditions) until the expiration date is reached. In one embodiment of the invention the pharmaceutical formulation comprising the compound according to the present invention is stable for more than 6 weeks of usage and for more than 3 years of storage. In another-embodiment of the invention the pharmaceutical formulation comprising the compound according to the present invention is stable for more than 4 weeks of usage and for more than 3 years of storage. In a further embodiment of the invention the pharmaceutical formulation comprising the compound according to the present invention is stable for more than 4 weeks of usage and for more than two years of storage.In an even further embodiment of the invention the pharmaceutical formulation com­prising the compound is stable for more than 2 weeks of usage and for more than two years of storage.In another aspect the present invention relates to the use of a compound according to the invention for the preparation of a medicament. In one embodiment a compound according to the invention is used for the preparation of a medicament for the treatment or prevention of hyperglycemia, type 2 diabetes, impaired glucose tolerance, type 1 diabetes, obesity, hypertension, syndrome X, dysiipidemia, cognitive disorders, atheroschlerosis, myocardial infarction, coronary heart disease and other cardiovas­cular disorders, stroke, inflammatory bowel syndrome, dyspepsia and gastric ulcers. In another embodiment a compound according to the invention is used for the prepara­tion of a medicament for delaying or preventing disease progression in type 2 diabetes. In another embodiment a compound according to the invention is used for the prepara­tion of a medicament for decreasing food intake, decreasing £-cell apoptosis, increasing £-cell function and /9-cell mass, and/or for restoring glucose sensitivity to /?-cells. The treatment with a compound according to the present invention may also be com­bined with combined with a second or more pharmacologically active substances, e.g. se­lected from antidiabetic agents, antiobesity agents, appetite regulating agents, antihyperten-sive agents, agents for the treatment and/or prevention of complications resulting from or as­sociated with diabetes and agents for the treatment and/or prevention of complications and disorders resulting from or associated with obesity. Examples of these pharmacologically ac­tive substances are : Insulin, sulphonylureas, biguanides, meglitinides, glucosidase inhibi­tors, glucagon antagonists, DPP-IV (dipeptidyl peptidase-IV) inhibitors, inhibitors of hepatic enzymes involved in stimulation of gluconeogenesis and/or glycogenolysis, glucose uptake modulators, compounds modifying the lipid metabolism such as antihyperlipidemic agents as HMG CoA inhibitors (statins), compounds lowering food intake, RXR agonists and agents acting on the ATP-dependent potassium channel of the p-cells; Cholestyramine, cotestipol, clofibrate, gemfibrozil, lovastatin, pravastatin, simvastatin, probucol, dextrothyroxine, neteglinide, repaglinide; (3-biockers such as alprenolol, atenolol, timolol, pindolol, prcpranolol and metoprolol, ACE (angiotensin converting enzyme) inhibitors such as benazepril, capto-pril, enalapril, fosinopril, lisinopril, alatriopril, quinapril and ramipril, calcium channel blockers such as nifedipine, felodipine, nicardipine, isradipine, nimodipine, diltiazem and verapamil, and a-blockers such as doxazosin, urapidil, prazosin and terazosin; CART (cocaine am- phetamine regulated transcript) agonists, NPY (neuropeptide Y) antagonists, MC4 (melano-cortin 4) agonists, orexin antagonists, TNF (tumor necrosis factor) agonists, CRF (corticotro-pin releasing factor) agonists, CRF BP (corticotropin releasing factor binding protein) an­tagonists, urocortin agonists, 03 agonists, MSH (melanocyte-stimulating hormone) agonists, MCH (melanocyte-concentrating hormone) antagonists. CCK (cholecystokinin) agonists, se­rotonin re-uptake inhibitors, serotonin and noradrenaline re-uptake inhibitors, mixed sero­tonin and noradrenergic compounds, 5HT (serotonin) agonists, bombesin agonists, galanin antagonists, growth hormone, growth hormone releasing compounds, TRH (thyreotropin re­leasing hormone) agonists, UCP 2 or 3 (uncoupling protein 2 or 3) modulators, leptin ago­nists, DA agonists (bromocriptin, doprexin), lipase/amylase inhibitors, RXR (retinoid X recep­tor) modulators, TR P agonists; histamine H3 antagonists.It should be understood that any suitable combination of the compounds according to the invention with one or more of the above-mentioned compounds and optionally one or more further pharmacologically active substances are considered to be within the scope of the present invention.The present invention is further illustrated by the following examples which, however, are not to be construed as limiting the scope of protection. The features disclosed in the forego­ing description and in the following examples may, both separately and in any combination thereof, be material for realising the invention in diverse forms thereof. EXAMPLES Abbreviations used: r.t retention time TFE trifluoroethanol DIEA diisopropylethylamine H2O water CH3CN acetonitrile DMF NN dimethylformamide HBTU 2-(1H-Benzotriazol-1-yl-)-1,1,3,3 tetramethyluronium hexafluorophosphate HATU O-(7-Azaben20triazol-1-yl)-N,N,N',N'-Tetramethyluronium Hexafluorophosphate ImPr 3-(1 -lmidazol-4-yl)-propionyl Adoc 1 -Adamantyloxycarbonyl Fmoc ' 9 H-fluoren-9-ylmethoxycarbonyl Boc tert butyloxycarbonyl OtBu tert butyl ester tBu tert butyl Trt triphenylmethyl Pmc 2,2,5,7,8-Pentamethyl-chroman-6-sulfonyl Ode 1 -(4,4-Dimethyl-2,6-dioxocyclohexylidene)ethyl ivDde 1 -(4.4-Dimethyl-2,6-dioxocyclohexylidene)-3-Methylbutyl DCM dichloromethane TIS triisopropylsilane) TFA: trifluoroacetic acid Et2O: diethylether NMP 1 -Methyl-pyrrolidin-2-one Aib o-aminoisobutyric acid Analysis HPLC analysis by the methods A1. B1 and B6 was performed on a Waters 2690 Separation Module equipped with a Waters 996 diode array detector. A Vydac 218TP54 4.6mm x 250mm 5\j.m C-18 silica column (The Separations Group, Hesperia) was used and detection was by UV at 214 nm. 254 nm, 280 nm and 301 nm.HPLC analysis by the method 01_B4_2 was performed on a Waters 600S system fitted with a Waters 996 diode array detector. A Symmetry300 C18 ,5 urn, 3.9 mm x 150 mm column (Waters) was used and detection was by UV at 214 nm and 254 nm.In method A1 the column was equilibrated with 0.05 M NH4SO4 pH 3.5 and eluted by a gra­dient of 0 to 60% CH3CN in 0.05 M (NH4)2SO4 pH 3.5 over 50 min at 42 °C, with a flow of 0.5ml/min.In method B1 the column was equilibrated with 0.1% TFA / H2O and eluted by a gradient of 0 to 60% CH3CN against 0.1%TFA/H2O over 50 min at 42 °C, with a flow of 0.5ml/min.In method B6 the column was equilibrated with 0.1% TFA / H2O and eluted by a gradient of 0 to 90% CH3CN against 0.1%TFA/H2O over 50 min at 42 °C, with a flow of 0.5ml/min.In method 01_B4_2 the column was equilibrated with 5% acetonitrile in water with 0.05% TFA and eluted by a gradient of 5 to 65% CH3CN against 0.05 %TFA/H2O over 15 min at 42 °C, with a flow of 1ml/min.Protein amount was calculated by comparing the UV detector response of the sample with the detector response from at of from a hGH standard for which the amount has been deter­mined by amino acid analysis.LC-MS analysis was performed on a PE-Sciex API 100 mass spectrometer equipped with two Perkin Elmer Series 200 Micropumps. a Perkin Elmer Series 200 autosampler, a Applied Biosystems 785A UV detector and a Sedex 75 Evaporative Light scattering detector. A Wa­ters Xterra 3.0 mm x 50 mm 5n C-18 silica column was eluted at 1.5 ml/min at room tem­perature. It was equilibrated with 5 % CH3CN / 0.1% TFA / H2O and eluted for 1.0 min with 5% CH3CN/0.1% TFA/H2Oand then with a linear gradient to 90% CH3CN / 0.1% TFA/ H2O over 7 min. Detection was by UV detection at 214nm and Evaporative light Scattering. A fraction of the column eluate was introduced into the ionspray interface of a PE-Sciex API 100 mass spectrometer. The mass range 300 - 2000 amu was scanned every 2 seconds during the run.Maldi TOF MS analysis was performed on a Bruker Autoflex instrument in linear mode. Sam­ples a prepared by the thin layer dried droplet method using er-cyano-4-hydroxycinnamic acid as the matrix.Example 1Preparation of A/t37-(3-(mPEGyl)propionyl)[Aib'-22l",Lys37]GLP-1(7-37) amide whereinmPEGyl is polydisperse and has a molecular weight of approximately 2 kDa(Figure Removed)1.a Synthesis of the protected peptidyl resin.Boc-His(Boc)-Aib-Glu(OtBu)-Gly-Thr(tBu)-Phe-Thr(tBu)-Ser(tBu)-Asp(OtBu)-Val-Ser(tBu)-Ser(tBu)-Tyr(tBu)-Leu-Glu(OtBu)-Aib-Gln(Trt)-Ala-Ala-Lys(Boc)-Glu(OtBu)-Phe-lle-Ala-Trp(Boc)-Leu-Val-Lys(Bcx:)-Aib-Arg(Pmc)-Lys(Dde)-Rink amide resin was prepared accord­ing to the Fmoc strategy on an Applied Biosystems 433A peptide synthesizer in 0.25 mmol scale using the manufacturer supplied FastMoc UV protocols which employ HBTU mediated couplings in NMP,' and UV monitoring of the deprotection of the Fmoc protection group. To improve the coupling efficiency, Aib residues and residues following Aib, these residues were coupled using HATU instead of HBTU as the coupling reagent. The starting resin (438 mg) used for the synthesis was 4-(2',4'-Dimethoxyphenyl-Fmoc-aminomethyl)-phenoxy resin (Rink amide resin) (Merck Biosciences GmbH, Germany, cat. #: 01-12-0013) with a substitu­tion capacity of 0.57 mmol / g. The protected amino acid derivatives used were (2S)-6-[l-(4,4-Dimethyl-2,6-dioxo-cyclohexylidene)-ethylamino]-2-(9 H-fluoren-9-ylmethoxycarbony!amino)-hexanoicacid (Fmoc-Lys(Dde)-OH). Fmoc-Arg(Pmc)-OH. Fmoc-Aib-OH, Fmoc-l_ys(Boc)-OH, Fmoc-Val-OH, Fmoc-Leu-OH, Fmoc-Trp(Boc)-OH, Fmoc-Ala-OH. Fmoc-lle-OH , Fmoc-Phe-OH, Fmoc-Glu(OtBu)-OH, Fmoc-Gln(Trt)-OH. Fmoc-Tyr(tBu)-OH, Fmoc-Ser(tBu)-OH, Fmoc-Asp(OtBu)-OH1 Fmoc-Thr(tBu)-OH, Fmoc-Gly-OH and Boc-His(Boc)-OH The yield was 1.37 g of dry peptidyl resin.1.b Characterisation of the peptidyl resinThe resin was characterized by cleaving off the crude peptide from 50 mg of this resin by treating it for 2 hours with a mixture of 14 til TIS, 14 |il H2O and 0.5 ml TFA. The resin was 72 removed by filtration and the crude peptide was isolated by precipitation and wash with Et2O. HPLC and LC-MS analysis was performed on the dry precipitate. Analytical results:(Table Removed)1 .c Deprotection of DdeThe protected peptidyl resin resulting from (1.a) (1.35 g. 250 ^imol) was washed in NMPrDCM 1:1 (15 ml) twice. A freshly prepared solution of hydrazine hydrate 2% in NMP (20ml) was added. The reaction mixture was shaken for 12 min at room temperature,-and then filtered. The hydrazine treatment was repeated twice. After this the resin was washed extensively with NMP, DCM and NMP.1.d Pegylation The Dde deprotected resin was suspended in NMP ( 20ml). 3-(mPEGyl)propionic acid 2,5-dioxo-pyrrolidin-1-yl ester (2.0 g. 1 mmol, 4 eq.) and DIEA (344 ^l, 2 mmol, 8 eq.) was added and the suspension was shaken overnight. Then the resin was isolated by filtration and washed extensively with NMP, DCM, 2-propanol, methanol and Et2O and dried in vacuo. 1 .e Cleavage of the product The resin from 1 .d was stirred for 3 h at room temperature with a mixture of 350 fil TIS, 350 ^il H2O and 14 ml TFA. The resin was removed by filtration and washed with 3 ml TFA. The collected filtrates were concentrated in vacuo. to 5 ml and the crude product was precipitated by addition of 40 ml EtzO followed by centrifugation. The pellet was washed with 40 ml Et20 two times and then air dried. Results from HPLC of the dry precipitate: (TableRemoved) Purification of product.The crude peptide was dissolved in H2O7AcOH (40:4) (40ml) and purified by semipreparative HPLC in 2 runs on a 25 mm x 250 mm column packed with 7p C-18 silica. The column was eluted with a gradient of CH3CN from 40 to 62% against 0.1% TFA / H2O at 10 ml/min at a temperature of 40°C for 47min. The peptide containing fractions are collected, diluted with 3 volumes of H2O and lyophilized. The final product obtained was characterized by HPLC. (Table Removed) Example 2 /Ve37-(3-(mPEGyl)propionyl)[Aib'-22'ls,Lys37]GLP-1(7.37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 5 kDa (Figure Removed) 2.a Synthesis of the protected peptidyl resin The protected peptidyl resin Boc-His(Boc)-Aib-Glu(OtBu)-Gly-Thr(tBu)-Phe-Thr(tBu)-Ser(tBu)-Asp(OtBu)-Val-Ser(tBu)-Ser(tBu)-Tyr(tBu)-Leu-Glu(OtBu)-Aib-Gln(Trt)-A!a-Ala-Lys(Boc)-Glu(OtBu)-Phe-lle-Ala-Trp(Boc)-Leu-Val-Lys(Boc)-Aib-Arg(Pmc)-Lys(Dde)-2-Chlorotrityl resin was synthesized using the procedures in example 1.a. with the exception that the starting resin was 337 mg of (2S)-6-[1-(4,4-Dimethyl-2.6- dioxocyclohexylidene)ethylamino]-2-(((9H-fluoren-9-yl)methoxycarbonyl)amino)hexanoyl 2-Chlorotrityl resin (Fmoc-Lys(Dde)-2-CITrt resin). This Fmoc-Lys(Dde)-2-CITrt resin was pre­pared by suspending 1g of 2-Chlorotrityl chloride resin (Bachem, Switzerland, cat. #: D-1965), having a substitution capacity of 1.15 mmol / g in a mixture of 10 ml DCM and 100 li! DMF. To this was added 533 mg Fmoc-Lys(Dde)-OH (Merck Biosciences, Germany cat. # 04-12-1121) and 684 jj.1 DIEA and the mixture was stirred for 2 hours. The resin was isolated by filtration and then washed three times with 10 ml of DCM/ MeOH / DIEA 17:2:1. three limes with 10 ml DCM, two times with 10 ml NMP, two times with 10 ml DCM and then finally dried in vacuo. The synthesis resulted in approximately 1.2 g of protected peptidyl resin (air dried). 2.b Deprotection of Dde and cleavage of protected peptide. 1.0 g of the protected peptidyl resin from 2.a was treated with 25 ml 2% hydrazine hydrate in DMF for 25 min and the resin was isolated by filtration. This was repeated further two times and after this the resin was thoroughly washed sequentially with DMF, DCM, 2-propanol. methanol Et2O ether and then dried in vacuo. This resin which was characterized as in example 1 .b. Analytical results: (Table Removed) The dry resin was stirred with 25 ml of a mixture of Acetic acid / TFE / DCM 1:1:3 for 2 h and then filtered and washed thoroughly with further 25 ml of this mixture. The pooled fil­trates were concentrated to an oil in vacuo. and the oil was stripped 5 times with heptane to remove residual acetic acid. 2.c Pegylation and final deprotection. To 100 mg of crude protected peptide from 2.b was dissolved in 1 ml TFE at 45 °C and 8.5 ^ DIEA was added. A solution of 100 mg mPEG-5000-SPA (mPEG-SPA m.w. 5.000 Lot. PT-09B-12, Shearwater, Alabama, USA) in 100^1 H2O and 900 jal NMP was added and the mix­ture was stirred overnight at r.t. After this 48 ml Et2O was added and the precipitate was col­lected and washed two times 50 ml Et2O and dried in vacuo. The dried material was then stirred for 1 h. with a mixture of 2 ml TFA, 50 jil TIS and 50 jil H2O and the crude pegylated peptide was isolated by precipitation with 50 ml Et2O and washed three times with 50 ml Et20 and then dried in vacuo. The crude peptide was dissolved in 20 ml H2O and characterized as follows: (Table Removed) 2.d Purification The crude peptide in solution from 2.c was purified by semipreparative HPLC in one run on a 25 mm x 250 mm column packed with 7/jm C-18 silica. The column was eluted with a gradi­ent of 30 to 65% CH3CN in 0.1% TFA / H2O at 10 ml/min at a temperature of 40 CC for 47min. The peptide containing fractions corresponding to the major peak was collected, diluted to 30 ml with approximately 3 volumes of H2O and lyophilized. The final product obtained was characterized as follows: (Table Removed) Example 3 //37-{3-(mPEGyl)propionyl)[Aib'-22'3S,LysJ7]GLP-1(7-37) wherein mPEGyl is polydisperse and has a molecular weight of approximately 20 kDa. (Figure Removed) This compound was prepared from 100 mg of crude protected peptide from 2.b using proce­dures similar to those in example 2.c and 2.b with the major exception that 400 mg 100 mg mPEG-20000-SPA (mPEG-SPA m.w. 20.000 Lot PT-05C-11, Shearwater, Alabama, USA) was used for the pegylation.The final product obtained was characterized as follows: (Table Removed) Example 4Ne37-((2S)-2,6-di-(mPEGylcarbonylamino)hexanoyl)[Aib8-2"5,LysJ7]GLP-1(7-37) wherein mPEGyl Is polydisperse and has a molecular weight of approximately 20 kDa.(Figure Removed) This compound was prepared from 100 mg of crude protected peptide from 2.b using proce­dures similar to those in example 2.c and 2.b with the major exception that 800 mg mPEG2-40000-NHS ester (mPEG2-NHS ester m.w. 40.000 Lot. PT-11C-06, Shearwater. Alabama. USA) was used for the pegylation. The final product obtained was characterized as follows: (Table Removed) Example 5 Ne263-(mPEGyl)propionyl)[Aibl,Glu22.30Lys3l,Asn34,Gly35'36lPro37]GLP-1(7. 37)ylSerSerGly AlaProProProSer amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 KDa, (Figure Removed) The fully protected peptidyl resin Boc-His(Boc>-Aib-Glu(OtBu)-Gly-Thr(tBu)-Phe-Thr(tBu)-Ser(tBu)-Asp(OtBu)-Val-Ser(tBu)-Ser(tBu)-Tyr(tBu)-Leu-Glu(OtBu)-G!u(OtBu)-Gln-Ala-Ala-Lys(Dde)-Glu(OtBu)-Phe-lle-Glu(OtBu)-Trp(Boc)-Leu-Lys(Boc)-Asn(Trt)-Gly-Gly-Pro-Ser(tBu)-Ser(tBu)-Gly-Ala-Pro-Pro-Pro-Ser(tBu)-Rink amide resin was prepared using proce­dures similar to those used in example 1a. from 0,25 mmol Rink amide resin having a substi­tution capacity of 0,61 mmol / g. The yield was 1.4 g. Analytical results from characterization of the resin as in Example 1.5 were: (Table Removed) The Ode protection was then removed from 350 mg of this fully protected peptidyl resin using the procedures of example I.e. and the resulting resin was then pegylated using the proce­dure of example 1 .d using (mPEGyl)propionic acid 2,5-dioxo-pyrrolidin-1-yl ester (Shear­water cat. no.2M4MOD01, mPEG-SPA , MW 2,000 ) (0.5 g. 0.25 mmol, 4 eq.) and DIEA (43 |il, 0.25 mmol, 4 eq.)The pegylated peptide was then cleaved from the resin using procedures similar to those of example I.e. and purified using a procedures similar to those of example 1.f The yield was 0.125 mg and the results from HPLC and LC-MS analysis:(Table Removed) Example 6Na-[Aib8.22,35]GLP-1-(7-36)yl(Ne-(3-(mPEGyl)propionyl)Lysinamide) wherein mPEGyl ispolydlsperse and has a molecular weight of approximately 750 Da. (Figure Removed) The fully protected peptidyl resin Boc-His(Boc)-Aib-Glu(OtBu)-Gly-Thr(tBu)-Phe-Thr(tBu)-Ser(tBu)-Asp(OtBu)-Val-Ser(tBu)-Ser{tBu)-Tyr(tBu)-Leu-Glu(OtBu)-Aib-Gln(Trt)-Ala-Ala-Lys(Boc)-Glu(OtBu)-Phe-lle-Ala-Trp(Boc)-Leu-Val-Lys(Boc)-Aib-Arg(Pmc)-Lys(ivDde)-PAL-PEG-PS resin was prepared using procedures similar to those used in example 1a. from 0,25 mmol PAL-PEG-PS resin (Applied [3iosystem Cat. no. GEN 913398) having a substitu­tion capacity of 0,38 mmol / g. The yield was 1.935 g. The ivDde protection was removed from the protected peptidyl resin as follows. The resin (382 mg, 90 μmol) was washed in NMP. A freshly prepared solution of hydrazine hydrate 2% in NMP (20ml) was added and the reaction mixture was shaken for 12 min at room tempera­ture, and then filtered. The hydrazine treatment was repeated twice. After this the resin was washed extensively with NMP and coupled with (A/-(2-mPEGyl-ethyl)-4-(2,5-dioxo-pyrrolidin-1-yl)-4-oxo-butyramide (a-Methoxy-co-NHS ester PEG, Rapp Polymere GmbH, Tubingen, FRG. cat no. 12 750-35) (0.27 g, 0.36 mmol, 4 eq.) using the procedures of example 1.d. The pegylated peptide was then cleaved and characterized from the resin using procedures similar to those of example I.e. Results from HPLC anc LC-MS analysis of the dry precipitate: (Table Removed) Example 7 Ne-[Aib8.22.35GLP-1(7-37)yl(S-(l-mPEGylpropyl-2.5-dioxo-pyrrolidin-a-ylJCysteinamide wherein mPEGyl is polydisperse and has a molecular weight of approximately 5000 Da. (Figure Removed) The crude peptide His-Aib-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Aib-Gln-Ala-Ala-Lys-Glu-Phe-lle-Ala-Trp-Leu-Val-Lys-Aib-Arg-Gly-Cys(H) amide was prepared using procedures similar to those used in example 1a., and 1.e from 0,25 mmol Rink amide resin having a substitution capacity of 0,61 mmol / g. The yield was 121 mg Results from HPLC and LC-MS analysis of the dry precipitate of crude peptide: (Table Removed) A fraction of the crude peptide (10 mg, 3 ^imol) was dissolved in phosphate buffer (15 ml) and pH was adjusted to 6.5 and mPEG-Mal 5000 (Shearwater cat. no. 2D2MOH01. mPEG-MAL, MW 5,000) (28 mg, 6 ymol ) was added and the mixture was stirred for 30 min. The final product was isolated from this mixture using procedures similar to those of example 1.f. The yield was 2.2 mg and the results from HPLC and LC-MS analysis: (Table Removed) Example 8 /YM3-<3 H-imidazol-4-yl)-propionyl [Alba*,ArgIM4]GI-P-1-(8.37))yl(Ar.<3-(mPEGyl)proplonyl)Lysinamide) wherein mPEGyl is polydisperse and has a molecular weight of approximately 2000 Da. (Figure Removed) The fully protected peptidyl resin lmPr(Adoc)-Ala-Glu(OtBu)-Gly-Thr(tBu)-Phe-Thr(tBu)-Ser(tBu)-As'p(OtBu)-Val-Ser(tBu)-Ser{tBu)-Tyr(tBu)-Leu-Glu(OtBu)-Aib-Gln-Ala-Ala-Arg(Pmc)-Glu(OtBu)-Phe-lle-Ala-Trp(Boc)-Leu-Val-Arg(Pmc)-Aib-Arg(Pmc)-Gly-Lys(Boc)-Rink amide resin usi/ig procedures similar to those used in example 1a in 1mmol scale, with the exception that HATU was used as the coupling agent throughout the synthesis. The resin used was a hydrophilic Rink amide resin (HypoGel® 200 RAM) (Rapp Polymere cat. # SP200 110150 230) resin having a substitution capacity of 0,61 mmol / g. Cleavage and purification was carried out as in the examples 1e and 1f. The yield was 210 mg and the results from HPLC and LC-MS analysis: Analytical method. Result: HPLC A1 r.t.: 36.51 min., LC-MS r.t. 3.69 min., mass for (M-+3H*) / 3 : 1194.4 Da . (calc.: 1193.4 Da)The pegylation was performed as follows. 20 mg of the unprotected peptide was dissolved in 600 |il water and 100 mg of the pegylation reagent (mPEGyl)propionic acid 2,5-dioxo-pyrrolidin-1-yl ester) (Shearwater cat. no.2M4MOD01? mPEG-SPA , MW 2,000) was added together with 9nl DIEA and stirred for 24 h. The final product was isolated from this mixture -using procedures similar to those of example 1.f. The yield was 3.7 mg of the title compound and results from HPLC and MALDI analysis were:Analytical method. Result: HPLC 01_B4_2 r.t.: 10.96 min.. MALDI-TOF Average mass for (M*): 5724 Da Example 9 Preparation of /^'-^-(rnPEGyOpropionylHArg^JGLP-l-fZ-ay) wherein mPEGyl is polydisperse and has a molecular weight of approximately 2 kDa (Figure Removed) This compound was prepared by acylation in solution of unprotected which was obtained by expression in yeast. [Arg34]GLP-1-(7-37) peptide (0.3 g, 30% peptide content) was dissolved in water containing DIEA (101 nl. 20 e.g.) and acylated with mPEG SPA 2000 (Shearwater Cat. no. 2M4MOD01, mPEG-SPA, MW 2,000) (89 mg. 1.5 e.q.) for 1 h at room temperature. The final product was isolated from this mixture using procedures similar to those of example 1.f. The yield of the title compound was 61 mg and the results from HPLC and Maidi TOP MS analysis analysis were: (Table Removed) Example 10 (S)-A/-{(S).5-(/V-{(S)-5-carbamoyl-5-(mPEGylpropionylamino)pentyl)carbamoyl)-5-(mPEGylpropionylamino)pentyl)-5-(No7-<3-{4-imidazolyOpropionyl)[Aib22>35,ArgM-:M]GLP-1-{8-37)yl)-2-(mPEGylpropionylamino)hexanoic amide wherein mPEGyl is polydisperse and has a molecular weight of approximately 750 Da (Figure Removed) The fully protected peptidyl resin Boc-Lys(Boc-Lys(Boc-Lys(lmPr(Adoc)-Ala-Glu(OtBu)-Gly- Thr(tBu)-Phe-Thr(tBu)-Ser(tBu)-Asp(OtBu)-Val-Ser(tBu)-Ser(tBu)-Tyr(tBu)-Leu-Glu(OtBu)- Aib-Gln(Trt)-Ala-A!a-Arg(Pmc)-Glu(OtBu)-Phe-lle-Ala-Trp(Boc)-Leu-Val-Arg(Pmc)-Aib- Arg(Pmc))))-Rink amide resin was synthesized using the procedures in example 1.a. lmPr(Adoc)-OH was used for the introduction of the N-terminal 3-(4-lmidazolyl)propinoyl group and Boc-Lys(Fmoc)-OH was used for introducing three side chain linked Lys residues in the C-terminal of the sequence. The corresponding unprotected peptide, H-Lys(H-Lys(H-Lys(lmPr-Ala-Glu-Gly-Thr-Phe-Thr- Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Aib-Gln-Ala-Ala-Arg-Glu-Phe-lle-Ala-Trp-Leu-Val-Arg-Aib- Arg)}) amide, was cleaved from the resin using procedures similar to those of example"! .e. and purified using procedures similar to those in example 1 .f.The results from the characterization of this intermediate peptide were: (Table Removed) 3,84 mg this purified peptide dissolved it in 0.4 ml NMP and pegylated by stirring at room temperature for 4h with 8 mg with (A/-(2-mPEGyl-ethyl)-4-{2,5-dioxo-pyrrolidin-1-yl)-4-oxo-butyramide (a-Methoxy-