CA2264243C - Glp-1 derivatives - Google Patents

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CA2264243C
CA2264243C CA002264243A CA2264243A CA2264243C CA 2264243 C CA2264243 C CA 2264243C CA 002264243 A CA002264243 A CA 002264243A CA 2264243 A CA2264243 A CA 2264243A CA 2264243 C CA2264243 C CA 2264243C
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Liselotte Bjerre Knudsen
Per Olaf Huusfeldt
Per Franklin Nielsen
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Novo Nordisk AS
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/575—Hormones
    • C07K14/605—Glucagons
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22—Hormones
    • A61K38/26—Glucagons
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22—Hormones
    • A61K38/28—Insulins
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A61K47/542—Carboxylic acids, e.g. a fatty acid or an amino acid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
    • A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin

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Abstract

Derivatives of GLP-1 and analogues thereof having a lipophilic substituent have interesting pharmacological properties, in particular they have a more protracted profile of action than GLP-1(7-37).

Description

101520253035CA 02264243 1999-02-25W0 93/08871 PCT/DK97/00340GLP-1 DERIVATIVESFIELD OF THE INVENTIONThe present invention relates to novel derivatives of human glucagon-like peptide-1 (GLP-1)and fragments thereof and analogues of such fragments which have a protracted profile ofaction and to methods of making and using them.BACKGROUND OF THE INVENTIONPeptides are widely used in medical practice, and since they can be produced byrecombinant DNA technology it can be expected that their importance will increase also inthe years to come. When native peptides or analogues thereof are used in therapy it isgenerally found that they have a high clearance. A high clearance of a therapeutic agent isinconvenient in cases where it is desired to maintain a high blood level thereof over aprolonged period of time since repeated administrations will then be necessary. Examples ofpeptides which have a high clearance are: ACTH, corticotropin-releasing factor, angiotensin,calcitonin, insulin, glucagon, glucagon-like peptide-1, glucagon-like peptide-2, insulin-likegrowth factor-1, insulin-like growth factor—2, gastric inhibitory peptide, growth hormone-releasing factor, pituitary adenylate cyclase activating peptide, secretin, enterogastrin,somatostatin. somatotropin, somatomedin, parathyroid hormone, thrombopoietin,erythropoietin, hypothalarnic releasing factors. prolactin, thyroid stimulating hormones,endorphins, enkephalins. vasopressin, oxytocin. opiods and analogues thereof, superoxidedismutase, interferon, asparaginase, arginase, arginine deaminase, adenosine deaminaseand ribonuclease. in some cases it is possible to influence the release profile of peptides byapplying suitable pharmaceutical compositions, but this approach has various shortcomingsand is not generally applicable.The hormones regulating insulin secretion belong to the so-called enteroinsular axis,designating a group of hormones, released from the gastrointestinal mucosa in responseto the presence and absorption of nutrients in the gut, which promote an early andpotentiated release of insulin. The enhancing effect on insulin secretion, the so—calledincretin effect, is probably essential for a normal glucose tolerance. Many of thegastrointestinal hormones, includino oastrin and secretin (cholecystokinin is not101520253035CA 02264243 1999-02-25W0 98/08871 PCT/DK97/00340insulinotropic in man), are insulinotropic, but the only physiologically important ones, thosethat are responsible for the incretin effect, are the glucose—dependent insulinotropicpolypeptide, GIP, and glucagon-like peptide-1 (GLP-1). Because of its insulinotropic effect,GIP, isolated in 1973 (1) immediately attracted considerable interest among diabetologists.However, numerous investigations carried out during the following years clearly indicatedthat a defective secretion of GlP was not involved in the pathogenesis of insulin dependentdiabetes mellitus (IDDM) or non insulin-dependent diabetes mellitus (NIDDM) (2).Furthermore, as an insulinotropic hormone, GIP was found to be almost ineffective inNIDDM (2). The other incretin hormone, GLP-1 is the most potent insulinotropic substanceknown (3). Unlike GIP, it is surprisingly effective in stimulating insulin secretion in NIDDMpatients. In addition, and in contrast to the other insulinotropic hormones (perhaps with theexception of secretin) it also potently inhibits glucagon secretion. Because of these actionsit has pronounced blood glucose lowering effects particularly in patients with NIDDM.GLP-1, a product of the proglucagon (4), is one of the youngest members of the secretin-VlP family of peptides, but is already established as an important gut hormone withregulatory function in glucose metabolism and gastrointestinal secretion and metabolism(5). The glucagon gene is processed differently in the pancreas and in the intestine. In thepancreas (9), the processing leads to the formation and parallel secretion of 1) glucagonitself, occupying positions 33-61 of proglucagon (PG); 2) an N-terminal peptide of 30amino acids (PG (1-30)) often called glicentin-related pancreatic peptide, GRPP (10, 11);3) a hexapeptide corresponding to PG (64-69); 4) and, finally, the so-called majorproglucagon fragment (PG (72-158)), in which the two glucagon-like sequences are buried(9). Glucagon seems to be the only biologically active product. In contrast, in the intestinalmucosa, it is glucagon that is buried in a larger molecule, while the two glucagon-likepeptides are formed separately (8). The following products are formed and secreted inparallel: 1) glicentin, corresponding to PG (1-69), with the glucagon sequence occupyingresidues Nos. 33-61 (12); 2) GLP-1(7-36)amide (PG (78-107))amide (13), not as originallybelieved PG (72-107)amide or 108, which is inactive). Small amounts of C-terminallyglycine-extended but equally bioactive GLP-1(7-37), (PG (78-108)) are also formed (14);3) intervening peptide-2 (PG (111-122)amide) (15); and 4) GLP-2 (PG (126-158)) (15, 16).A fraction of glicentin is cleaved further into GRPP (PG (1-30)) and oxyntomodulin (PG(33-69)) (17, 18). Of these peptides, GLP-1, has the most conspicuous biological activities.Being secreted in parallel with glicentin/enteroglucagon, it follows that the many studies ofenteroglucagon secretion (6, 7) to some extent also apply to GLP-1 secretion, but GLP-1is metabolised more quickly with a plasma half-life in humans of 2 min (19). Carbohydrate101520253035CA 02264243 1999-02-25W0 93/03371 PCT/DK97/00340or fat-rich meals stimulate secretion (20), presumably as a result of direct interaction of yetunabsorbed nutrients with the microvilli of the open-type L-cells of the gut mucosa.Endocrine or neural mechanisms promoting GLP-1 secretion may exist but have not yetbeen demonstrated in humans.The incretin function of GLP-1(29-31) has been clearly illustrated in experiments with theGLP-1 receptor antagonist, exendin 9-39, which dramatically reduces the incretin effectelicited by oral glucose in rats (21, 22). The hormone interacts directly with the B-cells viathe GLP-1 receptor (23) which belongs to the glucagonNlP/calcitonin family of G-protein-coupled 7-transmembrane spanning receptors. The importance of the GLP-1 receptor inregulating insulin secretion was illustrated in recent experiments in which a targeteddisruption of the GLP-1 receptor gene was carried out in mice. Animals homozygous forthe disruption had greatly deteriorated glucose tolerance and fasting hyperglycaemia, andeven heterozygous animals were glucose intolerant (24). The signal transductionmechanism (25) primarily involves activation of adenylate cyclase, but elevations ofintracellular Ca2+ are also essential (25, 26). The action of the hormone is best describedas a potentiation of glucose stimulated insulin release (25), but the mechanism thatcouples giucose and GLP-1 stimulation is not known. it may involve a calcium-inducedcalcium release (26, 27). As already mentioned, the insulinotropic action of GLP-1 ispreserved in diabetic B-cells. The relation of the latter to its ability to convey "glucosecompetence" to isolated insulin-secreting cells (26. 28), which respond poorly to glucose orGLP-1 alone, but fully to a combination of the two, is also not known. Equally importantly.however, the hormone also potently inhibits glucagon secretion (29). The mechanism isnot known, but seems to be paracrine, via neighbouring insulin or somatostatin cells (25).Also the glucagonostatic action is glucose-dependent, so that the inhibitory effectdecreases as blood glucose decreases. Because of this dual effect, if the plasma GLP-1concentrations increase either by increased secretion or by exogenous infusion the molarratio of insulin to glucagon in the blood that reaches the liver via the portal circulation isgreatly increased, whereby hepatic glucose production decreases (30). As a result bloodglucose concentrations decrease. Because of the glucose dependency of the insulinotropicand glucagonostatic actions, the glucose lowering effect is self-limiting, and the hormone,therefore, does not cause hypoglycaemia regardless of dose (31). The effects arepreserved in patients with diabetes mellitus (32), in whom infusions of slightlysupraphysiological doses of GLP-1 may completely normalise blood glucose values inspite of poor metabolic control and secondary failure to sulphonylurea (33). Theimportance of the glucagonostatic effect is illustrated by the finding that GLP-1 also lowersblood glucose in type-1 diabetic patients without residual (3—cell secretory capacity (34).101520253035CA 02264243 1999-02-25W0 98/08871 PCT/DK97/00340In addition to its effects on the pancreatic islets, GLP-1 has powerful actions on thegastrointestinal tract. amounts, GLP-1 potently inhibitspentagastrin-induced as well as meal-induced gastric acid secretion (35, 36). it alsoInfused in physiologicalinhibits gastric emptying rate and pancreatic enzyme secretion (36). Similar inhibitoryeffects on gastric and pancreatic secretion and motility may be elicited in humans uponperfusion of the ileum with carbohydrate- or lipid-containing solutions (37, 38).Concomitantly, GLP-1 secretion is greatly stimulated, and it has been speculated thatGLP-1 may be at least partly responsible for this so-called "ileal-brake" effect (38). In fact,recent studies suggest that, physiologically, the ileal-brake effects of GLP-1 may be moreimportant than its effects on the pancreatic islets. Thus, in dose response studies GLP-1influences gastric emptying rate at infusion rates at least as low as those required toinfluence islet secretion (39).GLP-1 seems to have an effect on food intake. lntraventricular administration of GLP-1profoundly inhibits food intake in rats (40, 42). This effect seems to be highly specific.Thus, N-terminally extended GLP-1 (PG 72-107)amide is inactive and appropriate dosesof the GLP-1 antagonist, exendin 9-39, abolish the effects of GLP-1 (41). Acute, peripheraladministration of GLP-1 does not inhibit food intake acutely in rats (41, 42). However, itremains possible that GLP-1 secreted from the intestinal L-cells may also act as a satietysignal.Not only the insulinotropic effects but also the effects of GLP-1 on the gastrointestinal tractare preserved in diabetic patients (43), and may help curtailing meal-induced glucoseexcursions, but, more importantly, may also influence food intake. Administeredintravenously, continuously for one week, GLP-1 at 4 ng/kg/min has been demonstrated todramatically improve glycaemic control in NIDDM patients without significant side effects(44). The peptide is fully active after subcutaneous administration (45), but is rapidlydegraded mainly due to degradation by dipeptidyl peptidase lV-like enzymes (46, 47).The amino acid sequence of GLP-1 is given i.a. by Schmidt et al. (Diabetologia 28 704-707(1985). Although the interesting pharmacological properties of GLP-1(7-37) and analoguesthereof have attracted much attention in recent years only little is known about thestructure of these molecules. The secondary structure of GLP-1 in micelles has beendescribed by Thorton et al. (Biochemistry 33 3532-3539 (1994)), but in normalsolution,GLP-1 is considered a very flexible molecule. Surprisingly, we found thatderivatisation of this relatively small and very flexible molecule resulted in compounds101520253035CA 02264243 1999-02-25wo 93/03371 PCT/DK97l00340whose plasma profile were highly protracted and still had retained activity.GLP-1 and analogues of GLP-1 and fragments thereof are potentially useful i.a. in thetreatment of type 1 and type 2 diabetes. However, the high clearance limits the usefulness ofthese compounds, and thus there still is a need for improvements in this field. Accordingly, itis one object of the present invention to provide derivatives of GLP-1 and analogues thereofwhich have a protracted profile of action relative to GLP-1(7-37). It is a further object of theinvention to provide derivatives of GLP-1 and analogues thereof which have a lowerclearance than GLP-1(7-37). it is a further object of the invention to provide a pharmaceuticalcomposition comprising a compound according to the invention and to use a compound ofthe invention to provide such a composition. Also, it is an object of the present invention toprovide a method of treating insulin dependent and non-insulin dependent diabetes mellitus.References.1. Pederson RA. Gastric inhibitory Polypeptide. in Walsh JH, Dockray GJ (eds) Gutpeptides: Biochemistry and Physiology. Raven Press, New York 1994, pp. 217259.2. Krarup T. lmmunoreactive gastric inhibitory polypeptide. Endocr Rev 1988;93:122-134.3. Grskov C. Glucagon-like peptide-1. a new hormone of the enteroinsular axis.Diabetologia 1992; 35:701-711.4. Bell Gl, Sanchez-Pescador R, Laybourn PJ, Najarian RC. Exon duplication anddivergence in the human preproglucagon gene. Nature 1983; 304: 368-371.5. Holst JJ. Glucagon-like peptide-1 (GLP-1) - a newly discovered GI hormone.Gastroenterology 1994; 107: 1848-1855.6. Holst JJ. Gut glucagon, enteroglucagon, gut GLl,Gastroenterology 1983;84:1602-1613.glicentin - current status.7. Holst JJ, Qrskov C. Glucagon and other proglucagon-derived peptides. in Welsh JH,Dockray GJ, eds. Gut peptides: Biochemistry and Physiology. Raven Press, New York,.. .~.._,...........i................A...:....-........a......_.... ........ . ,.,.. .............s . ,.‘IO15202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/00340pp. 305-340, 1993.8. flrskov C, Holst JJ, Knuhtsen S, Baldissera FGA, Poulsen SS, Nielsen OV.Glucagon-like peptides GLP-1 and GLP-2, predicted products of the glucagon gene, aresecreted separately from the pig small intestine, but not pancreas. Endocrinology1986;119:1467-1475.9. Holst JJ. Bersani M, Johnsen AH, Kofod H, Hartmann B, Grskov C. Proglucagonprocessing in porcine and human pancreas. J Biol Chem, 1994; 269: 18827-1883.10. Moody AJ, Holst JJ, Thim L, Jensen SL. Relationship of glicentin to proglucagon andglucagon in the porcine pancreas. Nature 1981; 289: 514-516.11. Thim L, Moody AJ, Purification and chemical characterisation of a glicentin-relatedpancreatic peptide (proglucagon fragment) from porcine pancreas. Biochim BiophysActa 1982;703:134-141.12. Thim L, Moody AJ. The primary structure of glicentin (proglucagon). Regul Pept1981;2:139-151.13. Qrskov C, Bersani M, Johnsen AH, Hzjrup P, Holst JJ. Complete sequences ofglucagon-like peptide-1 (GLP-1) from human and pig small intestine. J. Biol. Chem.1989;264:12826-12829.14. Qrskov C, Rabenhrzij L, Kofod H, Wettergren A, Holst JJ. Production and secretion ofamidated and glycine-extended glucagon-like peptide-1 (GLP-1) in man. Diabetes 1991;43: 535-539.15. Buhl T, Thim L, Kofod H, Qrskov C, Harling H, & Holst JJ: Naturally occurring productsof proglucagon 111-160 in the porcine and human small intestine. J. Biol. Chem.1988;263:8621-8624.16. Qrskov C, Buhl T, Rabenhoj L, Kofod H, Holst JJ: Carboxypeptidase-B-like processingof the C-terminus of glucagon-like peptide-2 in pig and human small intestine. FEBS1015202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/00340letters, 1989;247:193-106.17. Holst JJ. Evidence that enteroglucagon (ll) is identical with the C-terminal sequence(residues 33-69) of glicentin. Biochem J. 1980;187:337—343.18. Bataille D, Tatemoto K, Gespach C, Jornvall H, Rosselin G, Mutt V. Isolation ofglucagon-37 (bioactive enteroglucagon/oxyntomodulin) from porcine jejuno-ileum.Characterisation of the peptide. FEBS Lett 1982;146:79-86.19. Qrskov C, Wettergren A, Hoist JJ. The metabolic rate and the biological effects ofGLP-1 7—36amide and GLP-1 7-37 in healthy volunteers are identical. Diabetes1993;42:658-661.20. Elliott RM, Morgan LM, Tredger JA, Deacon S, Wright J, Marks V. Glucagon-likepeptide-1 (7-36)amide and glucose-dependent insuiinotropic polypeptide secretion inresponse to nutrient ingestion in man: acute post-prandial and 24-h secretion patterns.J Endocrinol 1993; 138: 159-166.21. Kolligs F, Fehmann HC, Goke R, Goke B. Reduction of the incretin effect in rats by theglucagon-like peptide-1 receptor antagonist exendin (9-39)amide. Diabetes 1995; 44:16-19.22. Wang Z, Wang RM, Owji AA, Smith DM, Ghatei M, Bloom SR. Glucagon-like peptide-1is a physiological incretin in rat. J. Clin. Invest. 1995; 95: 417-421.23. Thorens B. Expression cloning of the pancreatic b cell receptor for the gluco-incretinhormone glucagon-like peptide 1. Proc Natl Acad Sci 1992;89:8641-4645.24. Scrocchi L, Auerbach AB, Joyner AL, Drucker DJ. Diabetes in mice with targeteddisruption of the GLP-1 receptor gene. Diabetes 1996; 45: 21A.25. Fehmann HC, Goke R, Goke B. Cell and molecular biology of the incretin hormonesglucagon-like peptide-I (GLP-1) and glucose-dependent insulin releasing polypeptide(GIP). Endocrine Reviews. 1995; 16: 390-410..,...d.....J.........._................................... .1015202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/0034026. Gromada J, Dissing S, Bokvist K, Renstrbm E, Frokjaer-Jensen J, Wulff BS, RorsmanP. Glucagon-like peptide I increases cytoplasmic calcium in insulin-secreting bTC3-cellsby enhancement of intracellular calcium mobilisation. Diabetes 1995; 44: 767-774.27. Holz GG, Leech CA, Habener JF. Activation of a cAMP-regulated Ca“-signalingpathway in pancreatic B-cells by the insulinotropic hormone glucagon-like peptide-1. JBiol Chem, 1996; 270: 17749-17759.28. Holz GG, Ktihltreiber WM, Habener JF. Pancreatic beta-cells are rendered glucosecompetent by the insulinotropic hormone glucagon-like peptide-1(7-37). Nature1993;361:362-365.29. Qrskov C, Holst JJ, Nielsen OV: Effect of truncated giucagon—iike peptide-1(proglucagon 78-107 amide) on endocrine secretion from pig pancreas, antrum andstomach. Endocrinology 1988;123:2009-2013.30. Hvidberg A, Toft Nielsen M, Hilsted J, Qrskov C, Holst JJ. Effect of giucagon—iikepeptide-1 (proglucagon 78-107amide) on hepatic glucose production in healthy man.Metabolism 1994;43:104-108.31. Qualmann C, Nauck M, Holst JJ, Zrskov C, Creutzfeldt W. lnsulinotropic actions ofintravenous glucagon-like peptide-1 [7-36 amide] in the fasting state in healthy subjects.Acta Diabetologica, 1995; 32: 13-16.32. Nauck MA, Heimesaat MM, Qrskov C, Holst JJ, Ebert R, Creutzfeldt W. Preservedincretin activity of GLP-1(7-36amide) but not of synthetic human GlP in patients withtype 2-diabetes mellitus. J Clin Invest 1993;91:301-307.33. Nauck MA, Kleine N, Qrskov C, Holst JJ, Willms B, Creutzfeldt W. Normalisation offasting hyperglycaemia by exogenous GLP-1(7-36amide) in type 2-diabetic patients.Diabetologia 1993;36:741-744.34. Creutzfeldt W, Kleine N, Willms B, Erskov C, Holst JJ, Nauck MA. GlucagonostaticCA 02264243 1999-02-25WO 98/08871 PCTIDK97/00340actions and reduction of fasting hyperglycaemia by exogenous glucagon-liem,peptide-1(7-36amide) in type I diabetic patients. Diabetes Care 1996; 19: 580-586.35. Schjoldager BTG, Mortensen PE, Christiansen J, Qirskov C, Holst JJ. GLP-15 (glucagon-like peptide-1) and truncated GLP-1, fragments of human proglucagon,inhibit gastric acid secretion in man. Dig. Dis. Sci. 1989; 35:703-708.36. Wettergren A, Schjoldager B, Mortensen PE, Myhre J, Christiansen J, Holst JJ.Truncated GLP-1 (proglucagon 72-107amide) inhibits gastric and pancreatic functions10 in man. Dig Dis Sci 1993;38:665-673.37. Layer P, Holst JJ, Grandt D, Goebell H: lleal release of glucagon-like peptide-1(GLP-1): association with inhibition of gastric acid in humans. Dig Dis Sci 1995; 40:1074-1082.1538. Layer P, Holst JJ. GLP-1: A humoral mediator of the lleal brake in humans? Digestion1993; 54: 385-386.39. Nauck M, Ettler R, Niedereichholz U, Zrskov C, Holst JJ. Schmiegel W. Inhibition of20 gastric emptying by GLP-1(7-36 amide) or (7-37): effects on postprandial glycaemiaand insulin secretion. Abstract. Gut 1995; 37 (suppl. 2): A124.40. Schick RR, vorm Walde T, Zimmermann JP, Schusdziarra V, Classen M.Glucagon-like peptide 1 - a novel brain peptide involved in feeding regulation. in25 Ditschuneit H, Gries FA, Hauner H, Schusdziarra V, Wechsler JG (eds.) Obesity inEurope. John Libbey & Company ltd, 1994; pp. 363-367.41. Tang-Christensen M, Larsen PJ, Goke R, Fink-Jensen A, Jessop DS, Mialler M, SheikhS. Brain GLP-1(7-36) amide receptors play a major role in regulation of food and water30 intake. Am. J. Physiol., 1996, in press.42. Turton MD, O'Shea D, Gunn l, Beak SA, Edwards CMB, Meeran K, et al. A role forglucagon-like peptide-1 in the regulation of feeding. Nature 1996; 379: 6972.1015202530CA 02264243 1999-02-25W0 98/08871 PCT/DK97/003401043. Willms B, Werner J, Creutzfeldt W, Qrskov C, Holst JJ, Nauck M. Inhibition of gastricemptying by glucagon-like peptide-1 (7-36 amide) in patients with type-2-diabetesmellitus. Diabetologia 1994; 37, suppl.1: A118.44. Larsen J, Jallad N, Damsbo P. One-week continuous infusion of GLP-1(7-37) improvesglycaemic control in NIDDM. Diabetes 1996; 45, suppl. 2: 233A.45. Ritzel R, Qrskov C, Holst JJ, Nauck MA. Pharmacokinetic, insulinotropic, andglucagonostatic properties of GLP-1 [7-36 amide] after subcutaneous injection inhealthy volunteers. Dose-response relationships. Diabetologia 1995; 38: 720-725.46. Deacon CF, Johnsen AH, Holst JJ. Degradation of giucagon-like peptide-1 by humanplasma in vitro yields an N-terminally truncated peptide that is a major endogenousmetabolite in vivo. J Clin Endocrinol Metab 1995; 80: 952-957.47. Deacon CF, Nauck MA, Toft-Nielsen M, Pridal L, Willms B, Holst JJ. 1995. Bothsubcutaneous and intravenously administered glucagon~like peptide-1 are rapidlydegraded from the amino terminus in type ll diabetic patients and in healthy subjects.Diabetes 44: 1126-1131.SUMMARY OF THE INVENTIONHuman GLP-1 is a 37 amino acid residue peptide originating from preproglucagon which issynthesised i.a. in the L-cells in the distal ileum, in the pancreas and in the brain. Processingof preproglucagon to give GLP-1(7—36)amide, GLP-1(7-37) and GLP-2 occurs mainly in theL—cells. A simple system is used to describe fragments and analogues of this peptide. Thus,for example, Gly°-GLP-1(7-37) designates a fragment of GLP-1 formally derived from GLP-1by deleting the amino acid residues Nos. 1 to 6 and substituting the naturally occurring aminoacid residue in position 8 (Ala) by Gly. Similarly, l_ys3“(N‘-tetradecanoyl)-GLP-1(7-37)designates GLP-1(7-37) wherein the e-amino group of the Lys residue in position 34 hasbeen tetradecanoylated. Where reference in this text is made to C-terminally extended GLP-1 analogues, the amino acid residue in position 38 is Arg unless otherwise indicated, theoptional amino acid residue in position 39 is also Arg unless otherwise indicated and the1015202530CA 02264243 1999-02-25wo 98/08871 PCT/DK97/0034011optional amino acid residue in position 40 is Asp unless otherwise indicated. Also, if a C-terminally extended analogue extends to position 41, 42, 43, 44 or '45, the amino acidsequence of this extension is as in the corresponding sequence in human preproglucagonunless othen/vise indicated.in its broadest aspect, the present invention relates to derivatives of GLP-1 and analoguesthereof. The derivatives according to the invention have interesting pharmacologicalproperties, in particular they have a more protracted profile of action than the parentpeptides.In the present text, the designation “an analogue" is used to designate a peptide wherein oneor more amino acid residues of the parent peptide have been substituted by another aminoacid residue and/or wherein one or more amino acid residues of the parent peptide havebeen deleted and/or wherein one or more amino acid residues have been added to theparent peptide. Such addition can take place either at the N-terminal end or at the C-terminalend of the parent peptide or both.The term "derivative" is used in the present text to designate a peptide in which one or moreof the amino acid residues of the parent peptide have been chemically modified, e.g. byalkylation, acylation, ester formation or amide formation.The term “a GLP-1 derivative” is used in the present text to designate a derivative of GLP-1or an analogue thereof. in the present text, the parent peptide from which such a derivative isformally derived is in some places referred to as the "GLP-1 moiety” of the derivative.in a preferred embodiment, as described in Claim 1, the present invention relates to a GLP-1derivative wherein at least one amino acid residue of the parent peptide has a lipophilicsubstituent attached with the proviso that if only one lipophilic substituent is present and thissubstituent is attached to the N-terminal or to the C-terminal amino acid residue of the parentpeptide then this substituent is an alkyl group or a group which has an co-carboxylic acidgroup.In another preferred embodiment, as described in Claim 2, the present invention relates to aGLP-1 derivative having only one lipophilic substituent.1015202530CA 02264243 1999-02-25W0 98/08871 PCT/DK97l0034012in another preferred embodiment, as described in Claim 3, the present invention relates to aGLP-1 derivative having only one lipophilic substituent which substituent is an alkyl group ora group which has an co-carboxylic acid group and is attached to the N-terminal amino acidresidue of the parent peptide.in another preferred embodiment, as described in Claim 4, the present invention relates to aGLP-1 derivative having only one lipophilic substituent which substituent is an alkyl group ora group which has an co-carboxylic acid group and is attached to the C-terminal amino acidresidue of the parent peptide.in another preferred embodiment, as described in Claim 5, the present invention relates to aGLP-1 derivative having only one llpophilic substituent which substituent can be attached toany one amino acid residue which is not the N-terminal or C-terminal amino acid residue ofthe parent peptide.In another preferred embodiment, as described in Claim 6, the present invention relates to aGLP-1 derivative wherein two lipophilic substituents are present.In another preferred embodiment, as described in Claim 7. the present invention relates to aGLP-1 derivative wherein two lipophilic substituents are present, one being attached to theN-terminal amino acid residue while the other is attached to the C-terminal amino acidresidue.In another preferred embodiment, as described in Claim 8, the present invention relates to aGLP-1 derivative wherein two lipophilic substituents are present, one being attached to theN-terminal amino acid residue while the other is attached to an amino acid residue which isnot N-terminal or the C-terminal amino acid residue.in another preferred embodiment, as described in Claim 9, the present invention relates to aGLP-1 derivative wherein two lipophilic substituents are present, one being attached to theC-terminal amino acid residue while the other is attached to an amino acid residue which isnot the N-terminal or the C-terminal amino acid residue. 1015202530CA 02264243 1999-02-25wo 93/03371 PCT/DK97/0034013lnfurther preferred embodiment, as described in Claim 10, the present invention relates to aderivative of GLP-1(7-C), wherein C is selected from the group comprising 38, 39, 40, 41, 42,43, 44 and 45 which derivative has just one Iipophilic substituent which is attached to the C-terminal amino acid residue of the parent peptide.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein the Iipophilic substituent comprises from 4 to 40 carbon atoms, more preferred from8 to 25 carbon atoms.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein a lipophilic substituent is attached to an amino acid residue in such a way that acarboxyl group of the lipophilic substituent forms an amide bond with an amino group of theamino acid residue.in a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein a lipophilic substituent is attached to an amino acid residue in such a way that anamino group of the lipophilic substituent forms an amide bond with a carboxyl group of theamino acid residue.in a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein a lipophilic substituent is attached to the parent peptide by means of a spacer.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein a lipophilic substituent - optionally via a spacer - is attached to the e-amino group ofa Lys residue contained in the parent peptide.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein a lipophilic substituent is attached to the parent peptide by means of a spacer whichis an unbranched alkane on,m-dicarboxylic acid group having from 1 to 7 methylene groups,preferably two methylene groups which spacer forms a bridge between an amino group ofthe parent peptide and an amino group of the lipophilic substituent.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein a lipophilic substituent is attached to the parent peptide by means of a spacer which1015202530CA 02264243 1999-02-25W0 98/08871 PCT/DK97/00340‘I4is an amino acid residue except Cys, or a dipeptide such as Gly-Lys. In the present text, theexpression “a dipeptide such as Gly-Lys" is used to designate a dipeptide wherein the C-terminal amino acid residue is Lys, His or Trp, preferably Lys, and wherein the N-terminalamino acid residue is selected from the group comprising Ala, Arg, Asp, Asn, Gly, Glu, Gin,lie, Leu, Val, Phe and Pro.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein a lipophilic substituent is attached to the parent peptide by means of a spacer whichis an amino acid residue except Cys, or is a dipeptide such as Gly-Lys and wherein acarboxyl group of the parent peptide forms an amide bond with an amino group of a Lysresidue or a dipeptide containing a Lys residue, and the other amino group of the Lys residueor a dipeptide containing a Lys residue forms an amide bond with a carboxyl group of thelipophilic substituent.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein a lipophilic substituent is attached to the parent peptide by means of a spacer whichis an amino acid residue except Cys, or is a dipeptide such as G|y—l_ys and wherein an aminogroup of the parent peptide forms an amide bond with a carboxylic group of the amino acidresidue or dipeptide spacer, and an amino group of the amino acid residue or dipeptidespacer forms an amide bond with a carboxyl group of the lipophilic substituent.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein a lipophilic substituent is attached to the parent peptide by means of a spacer whichis an amino acid residue except Cys, or is a dipeptide such as Gly-Lys and wherein acarboxyl group of the parent peptide forms an amide bond with an amino group of the aminoacid residue spacer or dipeptide spacer, and the carboxyl group of the amino acid residuespacer or dipeptide spacer forms an amide bond with an amino group of the lipophilicsubstituent.in a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein a lipophilic substituent is attached to the parent peptide by means of a spacer whichis an amino acid residue except Cys, or is a dipeptide such as Gly-Lys, and wherein acarboxyl group of the parent peptide forms an amide bond with an amino group of a spacerwhich is Asp or Glu, or a dipeptide spacer containing an Asp or Glu residue, and a carboxyl1015202530CA 02264243 1999-02-25W0 98/0887] PCT/DK97/0034015group of the spacer forms an amide bond with an amino group of the lipophilic substituent.In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which comprises a partially or completely hydrogenatedcyclopentanophenathrene skeleton.ln a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which is a straight-chain or branched alkyl group.In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which is the acyl group of a straight-chain or branched fatty acid.In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which is an acyl group selected from the group comprisingCH3(CH2),,CO-, wherein n is an integer from 4 to 38, preferably an integer from 4 to 24, morepreferred selected from the group comprising CH3(CH2),.,CO-, CH3(CH2)8CO—, CH3(CH2),,,CO-,CH3(CH2),2CO-. CH3(CH2),.,CO-, CH3(CH2),6CO-, CH3(CH2),,,CO-, CH3(CH2)2oCO-CH3(CH2)22CO-.andIn a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which is an acyl group of a straight-chain or branched alkane (1.0)-dicarboxylic acid.In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which is an acyl group selected from the group comprisingHOOC(CH2),,,CO-, wherein m is an integer from 4 to 38, preferably an integer from 4 to 24.more preferred selected from the group comprising HOOC(CH2),4CO—, HOOC(CH2),6CO-,HOOC(CH2),,,CO-, HOOC(CH2)2oCO— and HOOC(CH2)22CO-.In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which is a group of the formula CH3(CH2),,((CH2)qCOOH)CHNH-CO(CH2)2CO-, wherein p and q are integers and p+q is an integer of from 8 to 33, preferablyfrom 12 to 28. V‘IO15A202530CA 02264243 1999-02-25WO 98/08871 PCTIDK97/0034016In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinggroup of the CH3(CH2),CO-NHCH(COOH)(CH2)2CO-, wherein r is an integer of from 10 to 24.a lipophilic substituent which is a formulaIn a further preferred embodiment, the present invention relates to a GLP-1 derivative havinggroup of the formula CH3(CH2)sCO-NHCH((CH2)2COOH)CO-, wherein s is an integer of from 8 to 24.a lipophilic substituent which is aIn a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which is a group of the formula COOH(CH2),CO- wherein t is aninteger of from 8 to 24.In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which is a group of the formula -NHCH(COOH)(CH2),,NH-CO(CH2),,CH3, wherein u is an integer of from 8 to 18.In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which is a group of the formula -NHCH(COOH)(CH2)4NH-COCH((CH2)2COOH)NH-CO(CH2)wCH3, wherein w is an integer of from 10 to 16.In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophiiic substituent which is a group of the formula —NHCH(COOH)(Cl-l2)4NH-CO(CH2)2CH(COOH)NH-CO(CH2),CH3, wherein x is an integer of from 10 to 16.In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which is a group of the formula -NHCH(COOl~l)(CH2)4NH-CO(CH2)2CH(COOH)NHCO(CH2)yCH3, wherein y is zero or an integer of from 1 to 22.In a further preferred embodiment, the present invention relates to a GLP-1 derivative havinga lipophilic substituent which can be negatively charged. Such a lipophilic substituent can forexample be a substituent which has a carboxyl group.In a further preferred embodiment, the present invention relates to a GLP-1 derivative theparent peptide of which is selected from the group comprising GLP-1(1—45) or an analogue51O1U12O2530CA 02264243 1999-02-25wo 93/03371 PCT/DK97/0034017thereof.In a further preferred embodiment, the present invention relates to a GLP-1 derivativederived from a GLP-1 fragment selected from the group comprising GLP-1(7-35), GLP-1(7-36), GLP—1(7-36)amide, GLP-1(7-37), GLP-t(7-38), GLP-1(7-39), GLP-1(7-40) and GLP-1(7-41) or an analogue thereof.In a further preferred embodiment, the present invention relates to a GLP-1 analogue derivedfrom a GLP-1 analogue selected from the group comprising GLP-1(1-35), GLP-1(1—36),GLP-1(1-36)amide, GLP-1(1-37), GLP-1(1-38), GLP-1(1—39), GLP-1(1-40) and GLP-1(‘l-41)or an analogue thereof.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein the designation analogue comprises derivatives wherein a total of up to fifteen,preferably up to ten amino acid residues have been exchanged with any or-amino acidresidue.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein the designation analogue comprises derivatives wherein a total of up to fifteen,preferably up to ten amino acid residues have been exchanged with any on-amino acidresidue which can be coded for by the genetic code.In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein the designation analogue comprises derivatives wherein a total of up to six aminoacid residues have been exchanged with another on-amino acid residue which can be codedfor by the genetic code.in a further preferred embodiment, the present invention relates to a GLP—‘l(A-B) derivativewherein A is an integer from 1 to 7 and B is an integer from 38 to 45 or an analogue thereofcomprising one lipophilic substituent attached to the C-terminal amino acid residue and,optionally, a second lipophilic substituent attached to one of the other amino acid residues.In a further preferred embodiment, a parent peptide for a derivative according to theinvention is selected from the group comprising Argzs-GLP-1(7-37); Arg°“—GLP-1 (7-37); Lys°5- 1015202530CA 02264243 1999-02-25wo 98/08871 PCT/DK97/0034018GLP-1(7-37); Arg2“"“‘Lys3“’-GLP-1(7-37); Arg”-"““Lys3"GLP-1(7-38); Argzs-3‘Lys39-GLP-1(7-39);Arg2°'3‘Lys‘°-GLP-1(7-40); Arg25Lys35-GLP-1(7-37); Arg3“Lys35-GLP-1(7-37); Arg"’Lys39-GLP-1(7-39); Arg"“Lys“°-GLP-1(7-40); Arg25'3‘Lys3°'39-GLP-1(7-39); Arg2"'3"Lys3‘5"‘°-GLP-1(7-40);Giy”Arg26-GLP-1(7-37); G|y"Arg3“-GLP-1(7-37); G1y‘Lys“5-GLP-1(7-37); G|y“Arg2°"“Lys36-GLP-1(7-37); Gly“Arg26'3‘Lys39-GLP-1(7-39); Gly"Arg25-"“Lys“°-GLP-1(7-40); GIy°Arg25Lys3“-GLP-1(7-37); G1y“Arg3“Lys““-GLP-‘I(7-37); GIy*’Arg25Lys39-GLP-1(7-39); G1y“Arg““Lys“°-GLP-1(7-40); Gly“Arg2“'3‘Lys3"'“9-GLP-1 (7-39) and G|y"Arg2“"3“Lys“‘5~“°-GLP-1 (7-40).In a further preferred embodiment, a parent peptide for a derivative according to theinvention is selected from the group comprising Arg2“'3“Lys3"GLP-1(7-38); Arg2°-3‘Lys“9GLP-1(7-39); Arg2‘""3“Lys“°GLP-1(7-40); Arg2““Lys“‘GLP-1 (7-41); Arg25'3‘Lys‘2GLP-1 (7-42);Arg2“'°“‘Lys“°GLP-1 (7-43);Argzs-3‘Lys“°GLP-1 (1-38);Argze-3‘Lys“GLP-1 (1-41);Arg25~3‘Lys“GLP-1 (1-44);Argze-3‘Lys39G LP-1 (2-39);Arg2°'3‘Lys“2GLP—1 (2-42);Argze-3“Lys“5GLP-1 (2-45);Arg”-3“Lys“°GLP-1 (3-40);Arg25'3“Lys‘3GLP—1 (3-43);Arg2"”'3“Lys3"GLP-1 (4-38);Arg2'""3‘Lys“GLP-1(4-41);Arg25'3‘Lys“GLP-1 (4-44);Arg’5'3‘Lys39GLP-1 (5-39);Arg2'5""Lys“GLP-1 (5-42);Arg2°'3‘Lys‘5GLP-1 (5-45);Argzs-°“Lys“°GLP-1 (6-40);Arg2"3'3“Lys““GLF’-1 (7-44);Arg2°'3‘Lys39GLP-1(1-39);Arg2‘"’-3“Lys‘2GLP-1(1—42);Arg’5'3‘Lys‘5GLP-1 (1-45);Arg2‘5'3“Lys“°GLP-1 (2-40);Arg2°'3‘Lys‘°GLP-1 (2-43);Arg25'3‘Lys3°GLP-1 (3-38);Arg26'3“Lys‘“GLP-1 (3-41 );Arg26'“Lys‘“G LP-1 (3-44);Arg2°'3“Lys3°GLP-1 (4-39);Arg2°°“Lys‘2G LP-1 (4-42);Arg2“‘3‘Lys‘5GLP-1 (4-45);Arg2°'3‘Lys“°GLP-1 (5-40);Arg25""‘Lys“‘*GLP-1 (5-43);Argzs-3‘Lys3"GLP-1 (6-38);Arg2”‘Lys“GLP-1 (6-41 );Arg25'3‘Lys‘5GLP-1 (7-45);Arg2°-3‘Lys‘°GLP-1 (1-40);Arg2“'3‘Lys“GLP-1 (1-43);Arg2“'3“Lys3“GLP-1 (2-38);Arg2°'3‘Lys" GLP-1 (2-41 );Arg2‘"’-"“Lys““GLP-1 (2-44);Arg2°-3‘Lys39GLP-1 (3-39);Arg2°‘“Lys‘2GLP-1 (342);Arg26'“Lys‘5GLP-1 (3-45);Arg25'3“Lys‘°GLP-1 (4-40);Arg25""‘Lys‘”GLP-1 (4-43);Arg”-3‘Lys3"GLP-1 (5-38);Argzs-““Lys‘“GLP-1 (5-41);Arg2“'“Lys“G LP-1 (5-44);Arg"’°-3‘Lys‘“’GLP-1 (6-39);Arg"""3“Lys“2GLP-1 (6-42);Arg25"“Lys““GLP-1(6-43); Argzs-3“Lys““GLP-1(6-44); Arg2°'3‘Lys‘5GLP-1(6-45); Arg2°Lys“GLP-1(1-38);Arg“ Lys3"GLP-1 (1-38);Arg2”“Lys3°'3“GLP-1 (1-38);Arg2“Lys‘°“GLP-1 (7-38);Arg3“Lys3“GLP-1(7-38); Arg2°-3“Lys3°'3°GLP-1(7-38); Arg2°'“Lys33GLP-1(7-38); Arg25Lys39GLP-1(1-39);Arg3“Lys39GLP-1(1-39);Arg3“Lys39GLP-1 (7-39) and Arg26'“Lys35-3°GLP-1(7-39).Arg"-5'3‘Lys3*“’-3"GLP-1 (1-39);Arg25Lys39GLP-1 (7-39);in a further preferred embodiment. the present invention relates to a GLP-1 derivative1015202530CA 02264243 1999-02-25wo 93/03371 PCT/DK97/0034019wherein the parent peptide is selected from the group comprising Argzs-GLP-1(7-37), Arg“-GLP-1(7-37), Lys”-GLP-1(7-37), Arg2““Lys““-GLP-1(7-37), Arg'25Lys”“-GLP-1(7-37),Arg°‘Lys35-GLP-1(7-37), Gly°Arg25-GLP-1(7-37). Giy“Arg3“-GLP-1(7-37), Gly“Lys“°-GLP-1(7-37), G|y“Arg2°'3‘Lys3‘5-GLP-1(7-37), Gly"Arg25Lys3“-GLP-1(7-37) and G|y“Arg3“Lys"“-GLP-1(7-37).in a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein the parent peptide is selected from the group comprising Arg2°Lys3”-GLP—1(7-38),Arg2"'3“Lys3°-GLP-1 (7-38), Arg"""3‘Lys3”"-GLP-1(7-38), G|y°Arg25Lys‘“’-GLP-1 (7-38)Gly“Arg2”‘Lys35'3°-GLP-1 (7-38).andIn a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein the parent peptide is selected from the group comprising Arg26Lys39-GLP-1(7-39),Arg2°‘3“Lys35'39-GLP-1 (7-39), Gly“Arg"*"’Lys3"-GLP-1 (7-39) and G|y“Arg26-3‘Lys35-39-GLP-1 (7-39).In a further preferred embodiment, the present invention relates to a GLP-1 derivativewherein the parent peptide is selected from the group comprising Arg3“Lys“°—GLP-1(7-40),Arg25'3‘Lys36"°-GLP-1 (7-40), G|y“Arg3“Lys“°-GLP-1 (7-40) and Gly°Arg25-3‘Lys35-‘°-GLP-1(7-40).In a further preferred embodiment, the present invention relates to a GLP-1 derivative whichis selected from the group comprising:Lys’5(N‘-tetradecanoyl)-GLP-1(7-37);Lys°“(N‘-tetradecanoyl)-GLP-1 (7-37);Lys2°-3‘-bis(N‘-tetradecanoyl)-GLP-1 (7-37);Gly°Lys2‘5(N‘-tetradecanoyl)-G LP-1 (7-37);Gly“Lys3‘(N‘-tetradecanoyl)-GLP-1(7-37);Gly”Lys2”‘-bis(N‘-tetradecanoyl)-G LP-1 (7-37);Arg26Lys3“(N‘-tetradecanoy|)-GLP-1 (7-37);Lys’°(N‘-tetradecanoyl)-GLP-1 (7-38);Lys“(N‘-tetradecanoyl)-G LP-1 (7-38);Lys“-3‘-bis(N‘-tetradecanoyl)-GLP-1(7-38);Gly“Lys25(N‘-tetradecanoyl)-GLP-1 (7-38);Gly"Lys3“(N‘-tetradecanoyl)-GLP-1(7-38);1015202530CA 02264243 1999-02-25WO 98/0887120Gly“Lysze-3‘-bis(N‘-tetradecanoyl)-G LP-1 (7-38);Arg25Lys“(Nfitetradecanoyl)-GLP-1(7-38);Lys25(N‘-tetradecanoyl)-GLP-1(7-39);Lys3“(N‘-tetradecanoyl)-GLP-1(7-39);Lysm‘-bis(N‘-tetradecanoyl)-G LP-1 (7-39);Gly°Lys26(Nfitetradecanoyl)-GLP-1(7-39);Gly5Lys3“(N‘-tetradecanoyl)—GLP—1 (7-39);Gly"Lysm‘-bis(N‘-tetradecanoyi)-GLP—1(7-39);Arg25Lys3‘(N‘-tetradecanoyl)-GLP-1(7-39);Lys26(N‘-tetradecanoyl)-GLP-1(7-40);Lys““(N‘-tetradecanoyl)-GLP-1(7-40);Lysm“-bis(N‘-tetradecanoyl)-GLP-1 (7-40);Gly°Lys25(N‘-tetradecanoyl)—GLP-1(7-40);Gly“Lys3“(N‘-tetradecanoyl)-GLP-1(7-40);Gly“Lys2“"“‘-bis(N‘-tetradecanoyl)-G LP-1 (7-40);Arg26Lys3‘(N‘-tetradecanoyl)—GLP-1(7-40);Lys2"(N‘-tetradecanoy|)-GLP-1(7-36);Lys3“(N‘-tetradecanoy!)-GLP-1(7-36);Lys26'3“-bis(N‘-tetradecanoyl)-GLP-1(7-36);Gly“Lys25(N‘-tetradecanoyl)-GLP—1 (7-36);GIy"Lys3“(N‘-tetradecanoyl)-GLP—1(7-36);Gly“Lyszs“-bis(N°-tetradecanoyl)-GLP-1(7-36);Arg“Lys“(N‘-tetradecanoy|)-GLP-1(7-36);Lys25(N‘-tetradecanoyl)-GLP-1 (7-35);Lys3“(N‘-tetradecanoyl)-GLP-1 (7-35);Lys25'3‘—bis(N‘-tetradecanoy!)-GLP-1(7-35);GlyeLys25(N‘-tetradecanoyl)—GLP—1(7-35);G|y°Lys3“(N‘-tetradecanoy|)—G LP-1 (7-35);Gly‘*Lys2°"°“-bis(N‘-tetradecanoyl)-GLP-1 (7-35);Arg2“Lys3‘(N‘-tetradecanoyI)—GLP-1 (7-35);Lys2°(N‘-tetradecanoy|)-GLP-1(7-36)amide;Lys3“(N‘-tetradecanoyl)-GLP-1(7-36)amide;Lys"'""3“-bis(N‘—tetradecanoyl)—GLP-1(7-36)amide;PCT/DK97/003401015202530CAW0 98/0887121Gly°Lys25(N°-tetradecanoyl)-GLP-1(7-36)amide;Gly3Lys3"(N‘-tetradecanoyl)-GLP-1(7-36)amide;Gly“Lys2‘5'3‘-bis(N‘-tetradecanoyl)-GLP-1(7-36)amide;Arg25Lys““(N‘-tetradecanoyl)-GLP-1(7-36)amide;G|y“Arg26Lys3“(N‘-tetradecanoyl)-G LP-1 (7-37);Lys2°(N‘-tetradecanoyl)Arg3“-GLP-1 (7-37);Gly°Lys2‘°‘(N‘-tetradecanoyl)Arg3“-GLP-1 (7-37);Arg2°'°“Lys36(N‘-tetradecanoyl)-GLP-1(7-37);Gly°Arg25'°‘Lys35(N‘-tetradecanoyl)-GLP-1 (7-37);Gly“Arg2°Lys3“(N"-tetradecanoyl)-G LP-1 (7-38);Lys25(N‘-tetradecanoyl)Arg3“-G LP-1 (7-38);GlyeLys25(N‘-tetradecanoy|)Arg3“-GLP-1(7-38);Argzw Lys°“(N‘-tetradecanoyl)-G LP-1 (7-38);Arg26'3‘Lys3°(N‘-tetradecanoyl)-GLP—1(7-38);Gly°Arg2°~3‘Lys°“(N‘-tetradecanoy|)-GLP-1 (7-38);Gly5Arg26Lys3“(N‘-tetradecanoyl)-GLP-1 (7-39);Lys25(N‘-tetradecanoy|)Arg3‘-GLP-1(7-39);G|y“Lys25(N‘-tetradecanoy|)Arg3“-G LP-1 (7-39);Arg25'3"Lys35(N‘-tetradecanoyl)-GLP-1 (7-39);GIy"Arg2°'3‘Lys3“(N‘-tetradecanoyl)-GLP-1(7-39);Gly°Arg25Lys”(N‘-tetradecanoyl)-GLP-1 (7-40);Lys2“(N‘-tetradecanoy|)Arg°“-GLP-1 (7-40);Gly°Lys25(N‘-tetradecanoyl)Arg““-GLP-1 (7-40);Arg2°-3‘Lys3“(N‘-tetradecanoyl)-GLP-1 (7-40);GIy“Arg2"““Lys3"(N‘-tetradecanoyl)-GLP-1 (7-40);Lys2°(N‘-(ca-carboxynonadecanoyI))-GLP—1(7-37);Lys“(N‘-(an-carboxynonadecanoyl))-GLP-1(7-37);Lys25'3‘—bis(N‘-(co-carboxynonadecanoyl))—GLP-1 (7-37);Gly“Lys26(N‘-(co-carboxynonadecanoy|))-GLP-1 (7-37);Gly°Lys°‘(N‘-(co-carboxynonadecanoy|))-GLP-1(7-37);G|y*’Lys25'3‘-bis(N‘-(m—carboxynonadecanoyl))-GLP-1 (7-37);Lys2“(N‘-(m-carboxynonadecanoyl))-GLP-1(7-38);Lys3‘(N‘-(co-carboxynonadecanoyl))-GLP-1(7-38);02264243 1999-02-25PCTIDK97/003401015202530CA 02264243 1999-02-25WO 98/0887122Lys2°'“-bis(N‘-(cu-carboxynonadecanoyI))-GLP-1 (7-38);GIy“Lys26(N‘-(m-carboxynonadecanoyl))-GLP-1(7-38);Gly8Lys3“(N‘-(tn-carboxynonadecanoyl))-GLP-1(7-38);Gly"Lys2°'3‘-bis(N‘-(m-carboxynonadecanoyl))-GLP—1(7-38);Lys‘°-‘"’(N‘-(co-carboxynonadecanoyl))-G LP-1 (7-39);Lys3“(N‘-(co-carboxynonadecanoy|))-GLP-1 (7-39);Lyszs-3‘-bis(N‘-(cu-carboxynonadecanoyl))-GLP-1(7-39);Gly“Lys25(N‘-(co-carboxynonadecanoyl))-GLP-1(7-39);G|y“Lys3“(N‘-(co-carboxynonadecanoy|))-GLP-1(7-39);Gly"Lys25'3“-bis(N‘-(co-carboxynonadecanoy|))-GLP-1(7-39);Lys2“(N‘-(co-carboxynonadecanoyl))-GLP-1(7-40);Lys°“(N‘-(m-carboxynonadecanoyl))-GLP-1(7-40);Lys2““-bis(N‘-(co-carboxynonadecanoyI))-GLP-1 (7-40);Gly”Lys25(N‘-(a)-carboxynonadecanoyl))-GLP-1 (7-40);Gly“Lys3“(N‘-(co-carboxynonadecanoyl))-GLP-1(7-40);Gly“Lys2‘5'3“—bis(N‘-(m-carboxynonadecanoyl))-GLP-1 (7-40);Lys2°(N‘-(on-carboxynonadecanoyl))-GLP-1(7-36);Lys3“(N‘-(co-carboxynonadecanoyl))-G LP-1 (7-36);Lys2°'3“-bis(N‘-(ca-carboxynonadecanoyI))-GLP-1 (7-36);Gly“Lys2‘5(N‘-(co-carboxynonadecanoyl))-GLP-1(7-36);Gly3Lys““(N‘-(on-carboxynonadecanoy|))-GLP-1(7-36);Gly°Lys2°‘3‘-bis(N‘-(co-carboxynonadecanoyl))-G LP-1 (7-36);Lys2“(N°-(ca-carboxynonadecanoyl))-GLP-1(7-36)amide;Lys“(N‘-(cu-carboxynonadecanoyl))-GLP-1(7-36)amide;Lysm“-bis(N‘-(m-carboxynonadecanoyl))-GLP-1(7-36)amide;Gly“Lys25(N‘-(co-carboxynonadecanoyl))-GLP-1(7-36)amide;GIy“Lys3“(N‘-(co-carboxynonadecanoy|))-GLP-1(7-36)amide;Gly“Lys2°'3“-bis(N‘-(oo-carboxynonadecanoyl))-GLP-1(7-36)amide;Lys25(N‘-(co-carboxynonadecanoy|))-GLP-1 (7-35);Lys3“(N‘-(w—carboxynonadecanoyl))-GLP-‘I (7-35);Lysm‘-bis(N‘-(u>—carboxynonadecanoyl))-G LP-1 (7-35);GlyeLys26(N‘-(co—carboxynonadecanoyl))-GLP-1(7-35);Gly"Lys3“(N‘-(m—c:arboxynonadecanoyl))-GLP-1(7-35);PCT/DK97/003401015202530CA 02264243 1999-02-25WO 98/0887]23Gly°Lys2“'3‘-bis(N‘-(cn—carboxynonadecanoy|))-G LP-1 (7-35);ArgzeLys“(N‘-(awcarboxynonadecanoyl))-G LP-1 (7-37);GIy“Arg25Lys3“(N‘-(as-carboxynonadecanoyl))-GLP-1 (7-37);Lys2°(N‘-(a>—carboxynonadecanoy|))Arg3“-GLP-1 (7-37);Gly”Lys2"(N‘—(o)—carboxynonadecanoyl))Arg3“-GLP-1 (7-37);Arg2“'3‘Lys3‘"’(N‘-(co—carboxynonadecanoy|))-GLP-1 (7-37);G|y“Arg2°'3“Lys3"(N‘—(u)—carboxynonadecanoy|))-GLP-1 (7-37);Arg"-5Lys3‘(N‘-(m—carboxynonadecanoy|))-G LP-1 (7-38);Gly°Arg2“Lys3“(N‘-(o)—carboxynonadecanoyI))-GLP-1 (7-38);Lys2“(N‘-(co-carboxynonadecanoy|))Arg3“-GLP-1(7-38);Gly”Lys25(N‘-(m-carboxynonadecanoyl))Arg3“-GLP-1(7-38);Arg25'3‘Lys35(N‘-(w—carboxynonadecanoy|))-GLP-1(7-38);Argzs“Lys°‘(N‘-(cn—carboxynonadecanoy|))-G LP-1 (7-38);G|y‘Arg25-3‘Lys3“(N‘-(<n—carboxynonadecanoyl))-GLP-1 (7-38);ArgzeLys3“(N‘-(m—carboxynonadecanoy|))-GLP-1 (7-39);Gly"Arg2°Lys3“(N‘-(urcarboxynonadecanoyl))-GLP-1 (7-39);Lys2°(N‘-(co—carboxynonadecanoyl))Arg3“-GLP—1 (7-39);Gly"Lys"'°(N‘-(co—carboxynonadecanoy|))Arg3“-G LP-1 (7-39);Arg2°'°“Lys3“(N‘-(oa—carboxynonadecanoyl))-GLP-1 (7-39);G|y"Arg2”“Lys"5(N‘-(orcarboxynonadecanoyl))-GLP-1(7-39);Arg2"Lys3‘(N‘-(m—carboxynonadecanoy|))-GLP-1 (7-40);Gly"Arg2°Lys3“(N‘-(co—carboxynonadecanoy|))-GLP-1(7-40);Lys26(N‘-(m—carboxynonadecanoyl))Arg3“-GLP-1(7-40);G|y"Lys25(N‘-(oo—carboxynonadecanoyl))Arg““-G LP-1 (7-40);Argza-3‘Lys35(N°-(w—carboxynonadecanoyl))-GLP-1 (7-40);GIy°Arg25-3‘Lys35(N‘-(oa—carboxynonadecanoyl))-GLP-1(7-40);Lys2“(N‘-(7-deoxycho|oy|))-G LP-1 (7-37);Lys3“(N‘-(7-deoxychoIoyl))-G LP-1 (7-37);Lys2°'3‘-bis(N‘-(7-deoxycholoyl))-GLP-1(7-37);Gly‘Lys25(N‘-(7-deoxycholoyl))-GLP-1(7-37);G|y°Lys“(N‘-(7-deoxycho|oyl))-GLP-1 (7-37);Gly”Lysm“-bis(N‘-(7-deoxycholoyl))-GLP-1 (7-37);Arg26Lys°‘(N‘-(7-deoxycholoyl))-GLP-1 (7-37);PCT/DK97l003401015202530CA 02264243 1999-02-25WO 98/0887]24Lys"'5(N‘-(7-deoxycho|oy|))-GLP-1(7-38);Lys3“(N‘-(7-deoxycholoyl))-GLP-1(7-38);Lys2°-'°"‘-bis(N‘-(7-deoxychoIoyl))-GLP-1 (7-38);Gly°Lys26(N‘-(7-deoxychoIoyl))-GLP-1(7-38);G)y“Lys3“(N‘-(7-deoxycholoy|))-GLP-1(7-38);G|y“Lys2°'3“-bis(N“-(7-deoxycholoyl))-G LP-1 (7-38);ArgzfiLys°"(N‘-(7-deoxychoIoyl))-GLP-1(7-38);Lys25(N‘-(7-deoxycholoyl))-GLP-1(7-39);Lys3"(N‘-(7-deoxycho|oyl))-GLP-1 (7-39);Lys2““-bis(N‘-(7-deoxycholoyl))-GLP-1 (7-39);GIy°Lys25(N‘-(7-deoxycholoyl))-GLP-1 (7-39);G|y"Lys3“(N‘-(7-deoxychoIoyI))-GLP-1 (7-39);GIy°Lys2°~3‘-bis(N‘-(7-deoxycho1oy|))-G LP-1 (7-39);ArgzsLys3"(N‘-(7-deoxycholoyl))-G LP-1 (7-39);Lys2°(N‘-(7-deoxycho|oyl))-G LP-1 (7-40);Lys3“(N‘-(7-deoxycholoyl))-GLP-1(7-40);Lyszw-bis(N‘-(7-deoxycholoyl))-GLP-1(7-40);G|y°Lys2‘5(N‘-(7-deoxycholoyl))-GLP-1(7-40);Gly“Lys3“(N‘-(7-deoxycholoyl))-GLP-1(7-40);G!y"Lys2“"‘-bis(N‘-(7-deoxycholoyl))-GLP—1 (7-40);Arg25Lys3“(N‘-(7—deoxycholoy|))-GLP-1(7-40);Lys"’5(N‘-(7-deoxycho|oy|))-GLP—1 (7-36);Lys3“(N‘-(7-deoxycholoyl))-GLP-1 (7-36);Lys25'3‘-bis(N‘—(7-deoxycholoyl))-GLP-1(7-36);Gly“Lys2“(N‘-(7-deoxycholoyl))-GLP-1 (7-36);Gly"Lys3“(N‘-(7-deoxycholoyl))-GLP-1 (7-36);Gly”Lys2“‘—bis(N‘-(7-deoxycholoyl))-GLP—1 (7-36);ArgzsLys3“(N‘-(7-deoxycholoyl))-GLP-1(7-36);Lys2"(N‘-(7-deoxycholoyl))-GLP~1 (7-35);Lys3“(N‘-(7-deoxycholoyl))-GLP-1 (7-35);Lys2°-3‘-bis(N‘-(7-deoxycholoyl))-GLP-1(7-35);Gly”Lys25(N‘-(7-deoxycholoyl))-GLP-1(7-35);Gly“Lys3“(N‘-(7-deoxycholoyl))-GLP-1 (7-35);PCT/DK97/003401015202530CA 02264243 1999-02-25W0 98/0887125GlyaLyszw-bis(N‘-(7-deoxycholoyl))-G LP-1 (7-35);Arg26Lys°“(N‘-(7-deoxycholoy|))—GLP-1 (7-35);Lys2°(N‘-(7-deoxycholoyl))-GLP-1(7-36)amide;Lys“(N‘-(7-deoxycho!oy|))-GLP-1(7-36)amide;Lysm‘-bis(N‘-(7-deoxycholoy|))-G LP-1 (7-36)amide;Gly“Lys2°(N‘-(7-deoxycholoyl))-GLP-1(7-36)amide;Gly"Lys3“(N‘-(7-deoxycholoyl))-GLP-1(7—36)amide;Gly“Lyszw-bis(N‘-(7-deoxycholoyl))-GLP—1(7-36)amide;Arg25Lys3‘(N‘-(7-deoxycholoyl))-GLP-1(7-36)amide;Gly"Arg25Lys3“(N‘-(7-deoxycholoyI))-GLP-1(7-37);Lys25(N‘-(7-deoxycho|oyl))Arg3“-G LP-1 (7-37);GlyaLys25(N‘-(7—deoxycho|oy|))Arg3“-GLP-1(7-37);Argzs“ Lys35(N‘-(7-deoxycholoyl))—G LP-1 (7-37);Gly“Arg2‘5-3‘Lys35(N‘-(7-deoxycholoy|))—G LP-1 (7-37);Lys26(N°-(choloyl))-GLP-1(7-37);Lys3“(N‘-(choloy|))-GLP-1(7-37);Lys25'3“-bis(N‘—(choloy|))-GLP—1 (7-37);G|y°Lys2"(N‘-(choloyl))—GLP-1(7-37);GlyeLys3"(N°-(choloyl))—GLP-1(7-37);Gly°Lys2°'3“-bis(N°—(cho|oy|))-GLP-1(7-37);Arg25Lys3“(N‘-(choloyl))—G LP-1 (7-37);Gly"Arg26Lys3“(N‘-(7—deoxychoIoyl))-GLP-1(7-38);Lys25(N‘—(7-deoxycho|oyl))Arg3“-G LP-1 (7-38);Gly“Lys2°(N‘-(7-deoxycholoyl))Arg3“-G LP-1 (7-38);Arg26‘3‘Lys3°(N‘-(7-deoxycho|oyl))-GLP-1(7-38);Argzs-3“Lys°‘(N°-(7-deoxycholoy|))-GLP-1 (7-38);Gly°Arg’6'3‘Lys°“(N‘—(7—deoxycholoyl))-G LP-1 (7-38);Lys2°(N‘-(cho|oy|))—GLP-1(7-38);Lys“(N‘-(choloyI))-GLP-1(7-38);Lys26'°‘-bis(N‘-(choloyl))-GLP-1(7-38);Gly"Lys26(N‘-(choloyI))-GLP—1(7-38);G|y"Lys"“(N‘-(choloy|))—GLP~1(7-38);Gly°Lys26'“—bis(N‘—(choIoyl))-GLP-1 (7-38);PCT/DK97/003401015202530CA 02264243 1999-02-25WO 98/0887126Arg25Lys3“(N‘-(choloyl))-GLP-1 (7-38);Gly“Arg‘°'6Lys3‘(N‘-(7-deoxycholoyl))-GLP—1 (7-39);Lys25(N‘-(7-deoxycholoyl))Arg3“-GLP-1(7-39);GIy”Lys25(N‘-(7-deoxycholoyI))Arg3“—GLP-‘I (7-39);Arg2“'3‘Lys°5( N‘-(7—deoxychoIoy|))-G LP-1 (7-39);GIy"Arg26'°‘Lys35(N‘-(7-deoxycholoy|))-G LP-1 (7-39);Lys2“(N‘-(choloyl))—GLP-1(7-39);Lys3“(N‘—(choloyl))-GLP-1(7-39);Lys25'3“-bis(N‘-(choioyl))—GLP-1 (7-39);Gly"Lys26(N‘—(cho|oyl))-GLP-1(7-39);Gly5Lys3“(N‘—(choloyl))-GLP-1(7-39);Gly“Lysm‘-bis(N‘-(choloyl))-GLP-1 (7-39);Arg2"Lys"“(N‘-(choloyl))-GLP-1(7-39);Gly“Arg25Lys3"(N‘-(7-deoxycholoyl))-GLP-1(740);Lys2‘5(N‘-(7-deoxycholoyl))Arg3“—GLP-1 (7-40);Gly°Lys”6(N‘-(7-deoxycholoyl))Arg3“—GLP-1 (7-40);Arg25'3‘Lys36(N‘-(7-deoxycholoyl))—GLP—1 (7-40);GIy“Arg25'3“Lys3"(N‘-(7-deoxycholoyl))-GLP-1(7-40);Lys2"(N‘-(choloyl))-GLP-1(7-40);Lys3“(N‘-(choloy|))-GLP-1(7-40);Lyszs“-bis(N‘—(cho|oyl))—GLP-1 (7-40);GIy“Lys2°(N‘-(choloy|))-GLP-1(7-40);Gly“Lys"“(N‘-(c:holoyl))-GLP-1(7-40);Gly“Lys25'3‘-bis(N‘-(choloyI))-GLP-1(7-40);Arg26Lys3“(N‘-(choloyl))-GLP-1(7-40);Lys2‘"’(N‘-(choloyl))-GLP-1 (7-36);Lys°“(N‘-(choloyl))-G LP-1 (7-36);Lys2°'3‘-bis(N‘-(cho|oyI))-GLP-1 (7-36);Gly°Lys2°(N‘-(choloy|))-GLP-1 (7-36);G|y“Lys3“(N‘-(choloyl))-GLP—1 (7-36);G|y"Lys2‘5'3“—bis(N‘-(choloyl))-GLP-1 (7-36);Arg25Lys3“(N‘-(choloyl))—GLP-1 (7-36);Lys25(N‘-(choloyi))-GLP-1 (7-35);PCT/DK97/003401015202530CA 02264243 1999-02-25W0 98/0887127Lys3“(N‘-(choloy|))-GLP-1 (7-35);Lys25'3“-bis(N‘-(choloy|))-GLP-1 (7-35);G|y“Lys’°(N‘-(choloyl))-G LP-1 (7-35);Gly”Lys‘“(N‘-(choloy|))-GLP-1 (7-35);Gly"Lys2'5'3‘—bis(N‘—(choIoyl))-GLP-1 (7-35);Arg25Lys3“(N‘-(cho|oyl))-GLP-1 (7-35);Lys25(N‘-(choloyl))—GLP-1(7-36)amide;Lys3“(N‘-(choloyl))-GLP—1(7-36)amide;Lys25-3‘-bis(N‘-(cho|oy|))-GLP-1(7—36)amide;G|y°Lys2"(N‘-(choIoy|))-GLP-1(7-36)amide:Gly"Lys3“(N‘-(choloy|))-GLP-1(7-36)amide;Gly°Lys25'°“-bis(N‘-(cho|oyl))—GLP-1(7-36)amide;Arg2‘5Lys°“(N‘-(choloyl))-GLP-1(7-36)amide;G|y"Arg2“Lys3“(N‘-(choloy|))-G LP-1 (7-37);Lys25(N‘—(ChOlOy|))Arg34-GLF’—1 (7-37);G|y"Lys2‘5(N‘-(choloyl))Arg3“-GLP-1(7-37);Arg25'3‘Lys35(N‘-(choloyl))—GLP-1(7-37);Gly“Arg2°'3‘Lys3“(N‘—(choloyl))-GLP—1 (7-37);Lys2°(N‘-(|ithocho|oyl))-GLP-1(7-37);Lys3“(N‘-(lithocholoyI))-GLP-1(7-37);Lys2°-3‘-bis(N‘-(lithocholoyl))-GLP-1(7-37);Gly"Lys25(N‘-(lithocho|oy|))-GLP—1(7-37);Gly3Lys3‘(N“-(Iithocholoyl))-GLP-1(7-37);Gly"Lys2"~3‘-bis(N°—(lithocholoyl))—GLP-1(7-37);Arg26Lys3“(N‘-(|ithocho|oy|))-GLP-1(7-37);G|y"Arg’°Lys°“(N‘-(cho|oy|))-GLP-1 (7-38);Lys26(N°-(choloyl))Arg3“-GLP-1(7-38);Gly°Lysze(N‘-(choloy|))Arg3‘-G LP-1 (7-38);Arg25'3‘Lys35(N‘-(choloyl))-GLP—1(7-38);Arg”-3“Lys3°(N‘-(choloyl))-GLP-1(7-38);G|y"Arg2“~3“Lys3‘5(N‘-(choloyl))-GLP-1 (7-38);Lys26(N‘-(lithocholoyl))-GLP-1(7-38);Lys3‘(N‘-(|ithochoIoyl))-GLP-1(7-38);PCT/DK97/003401015202530CA 02264243 1999-02-25W0 98/0887128Lys25'3“-bis(N‘-(|ithocho|oy|))-GLP-1(7-38);G|y"Lys2°(N‘—(lithocholoy|))-GLP-1 (7-38);Gly°Lys3“(N°-(lithocholoyl))-GLP-1(7-38);G|y°Lys"""°‘-bis(N‘-(lithocho|oyl))-GLP-1 (7-38);Arg25Lys“(N‘-(Iithocholoyl))-GLP-1(7-38);Gly“Arg25Lys°“(N‘-(choloyl))-GLP-1(7-39);Lys25(N‘-(ChO|0y|))Arg3‘-G LP-1 (7-39);Gly“Lys25(N‘-(choloy|))Arg3“-GLP-1(7-39);Arg25'3“Lys35(N‘-(cho|oy|))-GLP-1(7-39);Gly“Arg25'“Lys35(N‘-(cho|oyl))-GLP-1(7-39);Lys26(N‘-(lithocholoyl))-GLP—1(7-39);Lys3“(N‘-(lithocholoyl))-GLP-1 (7-39);Lysze“-bis(N‘-(lithocho|oy|))-GLP-1(7-39);GlyaLys2“(N”-(lithocholoy|))-GLP-1(7-39);GIyaLys“(N‘-(|ithocho|oyI))-GLP-1(7-39);G|y°Lys25'3‘—bis(N‘-(lithocholoyl))-GLP-1(7-39);Arg2"Lys3‘(N‘-(lithocholoyl))-GLP-1(7-39);Gly"Arg26Lys3“(N‘-(choloyl))-GLP-1 (7-40);Lys25(N‘-(choloyl))Arg3“-GLP-1 (7-40);G|y"Lys26(N‘-(choloyi))Arg3“-GLP-1(7-40);Arg25'3‘Lys35(N‘-(choloyl))—GLP-‘I (7-40);Gly"Arg2°'3“Lys35(N‘-(choIoy|))-GLP—1(7-40);Lys2'"’(N‘-(lithocholoyl))-GLP-1(7-40);Lys°"(N‘-(IithocholoyI))—GLP-1(7-40);Lys26'3‘-bis(N‘-(|ithoCh0loyI))-GLP-1(7-40);G|y"Lys26(N‘-(|ithochoIoyl))-GLP-1(7-40);Gly‘Lys3“(N‘-(Iithocholoy|))-GLP-1(7-40);Gly“Lys2"-3“—bis(N‘-(Iithocholoyl))—GLP-1 (7-40);Arg2°Lys3“(N‘-(lithocholoyl))-GLP-1 (7-37);Lys25(N‘-(lithocho|oyI))-GLP-1 (7-36);Lys3“'(N‘-(lithocholoy|))-GLP-1 (7-36);Lyszs-3‘-bis(N‘-(lithocho|oyl))-GLP—1 (7-36);Gly”Lys2‘5(N‘-(|ithochoIoy|))-GLP-1 (7-36);PCT/DK97/00340 1015202530CA 02264243 1999-02-25W0 98/0887129Gly"Lys°“(N‘-(lithochoIoyl))-GLP-1 (7-36);GlyaLys2“'3“-bis(N‘-(Iithocho|oy|))-GLP-1 (7-36);Arg25Lys““(N‘-(lithochoIoy|))-GLP-1 (7-36);Lys25(N‘-(lithocholoyl))-GLP-1 (7-35);Lys3“(N‘-(lithocho1oy|))-GLP-1(7-35);Lysm‘-bis(N‘-(lithocho!oy|))-GLP—1(7-35);Gly"Lys25(N‘-(lithocholoy|))—GLP-1(7-35);Gly"Lys3“(N°-(|ithocho|oy|))—GLP-1(7-35);GIy“Lys2°"“-bis(N‘-(lithocholoyl))-GLP-1(7-35);Arg25Lys3“(N‘-(lithochoIoy|))-GLP-1(7-35);Lys2“(N‘-(lithochoIoy|))-GLP-1(7-36)amide;Lys°“(N‘-(lithocho|oyl))-GLP-1(7-36)amide;Lys"""“-bis(N"—(lithocho|oy|))-GLP-1(7-36)amide;Gly°Lys25(N‘-(|ithochoioy|))-GLP-1(7-36)amide;Gly“Lys3“(N‘-(iithochoIoyl))-GLP-1(7-36)amide;G|y”Lys2“'3“-bis(N‘-(lithocholoyl))-GLP-1(7—36)amide;Arg25Lys3“(N‘-(|ithocholoy|))—GLP—1(7-36)amide;G|y°Arg26Lys3“(N‘-(lithocholoy|))—GLP-1 (7-37);Lys2“(N‘-(lithocholoyl))Arg3“-GLP-1(7-37);Gly"Lys25(N‘—(lithocho|oy|))Arg”“—GLP-1 (7-37);Arg26'3‘Lys3°(N‘—(Iithocho|oy|))-GLP-1 (7-37);ArgzwLys3“(N‘-(lithocholoy|))-GLP-1(7-37);G|y°Arg26'3“Lys3°(N‘-(|ithocho|oyl))-GLP-1 (7-37);GIy°Arg26Lys3“(N‘-(lithocho|oyl))-G LP-1 (7-38);Lys25(N‘-(lithocholoyl))Arg3‘-GLP-1(7-38);Gly“Lys2“(N°-(Iithocholoyl))Arg°“-GLP-1 (7-38);Arg25'3“Lys3“(N‘-(|ithocholoyl))-GLP-1(7-38);Arg2““Lys3”(N‘-(lithocholoy|))-G LP-1 (7-38);G|y“Arg2““Lys35(N‘-(IithocholoyI))-GLP—1 (7-38);GIy"Arg2°Lys3“(N‘-(lithocholoyl))-GLP-1 (7-39);Lys25(N‘-(lithocholoyl))Arg3“-GLP-1 (7-39);G|y"Lys2“(N‘-(Iithocho|oy|))Arg°“-GLP-1 (7-39);Arg26'3‘Lys3°(N‘-(Iithocholoyl))-GLP-1 (7-39);PCT/DK97/003401015202530CA 02264243 1999-02-25WO 98/08871 PCTIDK97/0034030G|y’3Arg25'3“Lys3°(N‘-(|ithocholoy|))—GLP-1 (7-39);Gly"Arg25Lys3“(N‘-(Iithocholoy|))-GLP-1(7-40);Lys25(N‘-(lithocholoyl))Arg3‘-GLP-1 (7-40);Gly“Lys2‘5(N‘-(Iithocholoy|))Arg3“-GLP-1 (7-40);Arg25'3“Lys36(N‘-(lithocholoyl))-GLP-1 (7-40) andGly“Arg25'“Lys3°(N‘-(lithocholoyI))-G LP-1 (7-40).In a further preferred embodiment, the present invention relates to a pharmaceuticalcomposition comprising a GLP—1 derivative and a pharmaceutically acceptable vehicle orcarrier.In a further preferred embodiment, the present invention relates to the use of a GLP-1derivative according to the invention for the preparation of a medicament which has aprotracted profile of action relative to GLP-1 (7-37).In a further preferred embodiment, the present invention relates to the use of a GLP-1derivative according to the invention for the preparation of a medicament with protractedeffect for the treatment of non-insulin dependent diabetes mellitus.in a further preferred embodiment, the present invention relates to the use of a GLP-1derivative according to the invention for the preparation of a medicament with protractedeffect for the treatment of insulin dependent diabetes mellitus.in a further preferred embodiment, the present invention relates to the use of a GLP-1derivative according to the invention for the preparation of a medicament with protractedeffect for the treatment of obesity.In a further preferred embodiment, the present invention relates to a method of treatinginsulin dependent or non-insulin dependent diabetes mellitus in a patient in need of such atreatment, comprising administering to the patient a therapeutically effective amount of aGLP-1 derivative according to claim 1 together with a pharmaceutically acceptable carrier.DETAILED DESCRIPTION OF THE INVENTION1015202530CA 02264243 1999-02-25W0 98/08871 PCT/DK97/0034031To obtain a satisfactory protracted profile of action of the GLP~1 derivative, the lipophilicsubstituent attached to the GLP-1 moiety preferably comprises 4-40 carbon atoms, inparticular 8-25 carbon atoms. The lipophilic substituent may be attached to an amino groupof the GLP-1 moiety by means of a carboxyl group of the lipophilic substituent which formsan amide bond with an amino group of the amino acid residue to which it is attached.Alternatively, the lipophilic substituent may be attached to said amino acid residue in such away that an amino group of the lipophilic substituent forms an amide bond with a carboxylgroup of the amino acid residue. As a further option, the lipophilic substituent may be linkedto the GLP-1 moiety via an ester bond. Formally, the ester can be formed either by reactionbetween a carboxyl group of the GLP-1 moiety and a hydroxyl group of the substituent-to-beor by reaction between a hydroxyl group of the GLP-1 moiety and a carboxyl group of thesubstituent-to-be. As a further alternative, the lipophilic substituent can be an alkyl groupwhich is introduced into a primary amino group of the GLP-1 moiety.In one preferred embodiment of the invention, the lipophilic substituent is attached to theGLP-1 moiety by means of a spacer in such a way that a carboxyl group of the spacer formsan amide bond with an amino group of the GLP-1 moiety. Examples of suitable spacers aresuccinic acid, Lys, Glu or Asp, or a dipeptide such as Gly-Lys. When the spacer is succinicacid, one carboxyl group thereof may form an amide bond with an amino group of the aminoacid residue, and the other carboxyl group thereof may form an amide bond with an aminogroup of the lipophilic substituent. When the spacer is Lys, Glu or Asp, the carboxyl groupthereof may form an amide bond with an amino group of the amino acid residue, and theamino group thereof may form an amide bond with a carboxyl group of the lipophilicsubstituent. When Lys is used as the spacer, a further spacer may in some instances beinserted between the e-amino group of Lys and the lipophilic substituent. In one preferredembodiment, such a further spacer is succinic acid which forms an amide bond with the 5-amino group of Lys and with an amino group present in the lipophilic substituent. in anotherpreferred embodiment such a further spacer is Glu or Asp which forms an amide bond withthe e-amino group of Lys and another amide bond with a carboxyl group present in thelipophilic substituent, that is, the lipophilic substituent is a N‘-acylated lysine residue.in another preferred embodiment of the present invention, the lipophilic substituent has agroup which can be negatively charged. One preferred group which can be negatively..i._.................. ....... .. ... ..,.i...i,........................_N, .1015202530CA 02264243 1999-02-25W0 98/0887] PCT/DK97/0034032charged is a carboxylic acid group.The parent peptide can be produced by a method which comprises culturing a host cellcontaining a DNA sequence encoding the polypeptide and capable of expressing thepolypeptide in a suitable nutrient medium under conditions permitting the expression of thepeptide, after which the resulting peptide is recovered from the culture.The medium used to culture the cells may be any conventional medium suitable for growingthe host cells, such as minimal or complex media containing appropriate supplements. Suit-able media are available from commercial suppliers or may be prepared according topublished recipes (e.g. in catalogues of the American Type Culture Collection). The peptideproduced by the cells may then be recovered from the culture medium by conventionalprocedures including separating the host cells from the medium by centrifugation or filtration,precipitating the proteinaceous components of the supernatant or filtrate by means of a salt,e.g. ammonium sulphate, purification by a variety of chromatographic procedures, e.g. ionexchange chromatography, gel filtration chromatography, affinity chromatography, or the like,dependent on the type of peptide in question.The DNA sequence encoding the parent peptide may suitably be of genomic or cDNA origin,for instance obtained by preparing a genomic or cDNA library and screening for DNAsequences coding for all or part of the peptide by hybridisation using syntheticoligonucleotide probes in accordance with standard techniques (see, for example,Sambrook, J, Fritsch, EF and Maniatis, T, Molecular Cloning: A Laboratory Manual, ColdSpring Harbor Laboratory Press, New York, 1989). The DNA sequence encoding the peptidemay also be prepared synthetically by established standard methods, e.g. thephosphoamidite 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 specificprimers, 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 torecombinant DNA procedures, and the choice of vector will often depend on the host cell intowhich it is to be introduced. Thus, the vector may be an autonomously replicating vector, i.e.1015202530CA 02264243 1999-02-25WO 93103371 PCT/DK97/0034033a vector which exists as an extrachromosomal entity, the replication of which is independentof chromosomal replication, e.g. a plasmid. Alternatively, the vector maybe one which, whenintroduced into a host cell, is integrated into the host cell genome and replicated togetherwith the chromosome(s) into which it has been integrated.The vector is preferably an expression vector in which the DNA sequence encoding thepeptide is operably linked to additional segments required for transcription of the DNA, suchas a promoter. The promoter may be any DNA sequence which shows transcriptional activityin the host cell of choice and may be derived from genes encoding proteins eitherhomologous or heterologous to the host cell. Examples of suitable promoters for directing thetranscription of the DNA encoding the peptide of the invention in a variety of host cells arewell known in the art, cf. for instance Sambrook et a/., supra.The DNA sequence encoding the peptide may also, if necessary, be operably connected to asuitable terminator, polyadenylation signals, transcriptional enhancer sequences, andtranslational enhancer sequences. The recombinant vector of the invention may furthercomprise a DNA sequence enabling the vector to replicate in the host cell in question.The vector may also comprise a selectable marker, e.g. a gene the product of whichcomplements a defect in the host cell or one which confers resistance to a drug, e.g.ampicillin, kanamycin, tetracyclin, chloramphenicol, neomycin, hygromycin or methotrexate.To direct a parent peptide of the present invention into the secretory pathway of the hostcells, a secretory signal sequence (also known as a leader sequence, prepro sequence orpre 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. Secretorysignal 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 befrom a gene encoding another secreted protein.The procedures used to ligate the DNA sequences coding for the present peptide, thepromoter and optionally the terminator and/or secretory signal sequence, respectively, and toinsert them into suitable vectors containing the information necessary for replication, are wellknown to persons skilled in the art (cf., for instance, Sambrook et al.., supra).1015202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/0034034The host cell into which the DNA sequence or the recombinant vector is introduced may beany cell which is capable of producing the present peptide and includes bacteria, yeast, fungiand higher eukaryotic cells. Examples of suitable host cells well known and used in the artare, without limitation, E. coli, Saccharomyces cerevisiae, or mammalian BHK or CHO celllines.Examples of compounds which can be useful as GLP-1 moieties according to the presentinvention are described in international Patent Application No. WO 87/06941 (The GeneralHospital Corporation) which relates to a peptide fragment which comprises GLP-1(7-37) andfunctional derivatives thereof and to its use as an insulinotropic agent.Further GLP-1 analogues are described in international Patent Application No. 90/11296(The General Hospital Corporation) which relates to peptide fragments which compriseGLP-1(7-36) and functional derivatives thereof and have an insulinotropic activity whichexceeds the insulinotropic activity of GLP-1(l-36) or GLP-1(1-37) and to their use asinsulinotropic agents.International Patent Application No. 91/1145? (Buckley et aI..) discloses analogues of theactive GLP-1 peptides 7-34, 7-35, 7-36, and 7-37 which can also be useful as GLP-1moieties according to the present invention.Pharmaceutical compositionsPharmaceutical compositions containing a GLP-1 derivative according to the presentinvention may be administered parenterally to patients in need of such a treatment.Parenteral administration may be performed by subcutaneous, intramuscular or intravenousinjection by means of a syringe, optionally a pen—like syringe. Alternatively, parenteraladministration can be performed by means of an infusion pump. A further option is acomposition which may be a powder or a liquid for the administration of the GLP-1 derivativein the form of a nasal or pulmonal spray. As a still further option, the GLP-1 derivatives of theinvention can also be administered transdermally, eg. from a patch, optionally aiontophoretic patch, or transmucosally, e.g. bucally.1015202530CA 02264243 1999-02-25W0 98/08871 PCTIDK97/0034035Pharmaceutical compositions containing a GLP-1 derivative of the present invention may beprepared by conventional techniques, e.g. as described in Remington's PharmaceuticalSciences, 1985 or in Remington: The Science and Practice of Pharmacy, 19"‘ edition, 1995.Thus, the injectable compositions of the GLP-1 derivative of the invention can be preparedusing the conventional techniques of the pharmaceutical industry which involves dissolvingand mixing the ingredients as appropriate to give the desired end product.According to one procedure, the GLP-1 derivative is dissolved in an amount of water which issomewhat less than the final volume of the composition to be prepared. An isotonic agent, apreservative and a buffer is added as required and the pH value of the solution is adjusted - ifnecessary - using an acid, e.g. hydrochloric acid, or a base, e.g. aqueous sodium hydroxideas needed. Finally, the volume of the solution is adjusted with water to give the desiredconcentration of the ingredients.Examples of isotonic agents are sodium chloride, mannitol and glycerol.Examples of preservatives are phenol, m-cresol, methyl p-hydroxybenzoate and benzylalcohol.Examples of suitable buffers are sodium acetate and sodium phosphate.Further to the above-mentioned components, solutions containing a GLP-1 derivativeaccording to the present invention may also contain a surfactant in order to improve thesolubility and/or the stability of the GLP-1 derivative.A composition for nasal administration of certain peptides may, for example, be prepared asdescribed in European Patent No. 272097 (to Novo Nordisk A/S) or in WO 93/18785.According to one preferred embodiment of the present invention, the GLP-1 derivative isprovided in the form of a composition suitable for administration by injection. Such acomposition can either be an injectable solution ready for use or it can be an amount of asolid composition, e.g. a lyophilised product, which has to be dissolved in a solvent before it1015202530CA 02264243 1999-02-25W0 98l08871 PCT/DK97/0034036can be injected. The injectable solution preferably contains not less than about 2 mg/ml,preferably not less than about 5 mg/ml, more preferred not less than about 10 mg/ml of theGLP-1 derivative and, preferably, not more than about 100 mg/ml of the GLP-1 derivative.The GLP-1 derivatives of this invention can be used in the treatment of various diseases.The particular GLP-1 derivative to be used and the optimal dose level for any patient willdepend on the disease to be treated and on a variety of factors including the efficacy of thespecific peptide derivative employed, the age. body weight, physical activity, and diet of thepatient, on a possible combination with other drugs, and on the severity of the case. it isrecommended that the dosage of the GLP-1 derivative of this invention be determined foreach individual patient by those skilled in the art.in particular, it is envisaged that the GLP-1 derivative will be useful for the preparation of amedicament with a protracted profile of action for the treatment of non-insulin dependentdiabetes mellitus and/or for the treatment of obesity.The present invention is further illustrated by the following examples which, however, are notto be construed as limiting the scope of protection. The features disclosed in the foregoingdescription and in the following examples may, both separately and in any combinationthereof. be material for realising the invention in diverse forms thereof.EXAMPLESThe following acronyms for commercially available chemicals are used:DMF : N,N—Dimethylformamide.NMP 2 N-Methyl-2-pyrrolidone.EDPA : N-Ethyl—N,N-diisopropylamine.EGTA : Ethylene glycol—bis(B-aminoethyl ether)~N,N,N’,N’-tetraaceticacid.GTP Guanosine 5’—triphosphate.TFA : Trifluoroacetic acid.THF : Tetrahyd rofuran101520253035CA 02264243 1999-02-25wo 98/08871 PCT/DK97/0034037Myr-ONSu: Tetradecanoic acid 2,5-dioxopyrrolidin-1-yl ester.Pal-ONSu: Hexadecanoic acid 2,5-dioxopyrrolidin-1-yl ester.Ste-ONSu Octadecanoic acid 2,5-dioxopyrrolidin-1~yl ester.HOOC~(CH_,_)6-COONSu:HOOC—(CH2),0-COONSu:HOOC-(CH2)12-COONSU:HOOC-(CH2),4-COONSU:HOOC-(CH2),6-COONSu:HOOC-(CH2).8-COONSu:o)—Carboxyheptanoic acid 2,5-dioxopyrrolidin-1-yl ester.co—Carboxyundecanoic acid 2,5-dioxopyrrolidin-1-yl ester.cn—Carboxytridecanoic acid 2,5-dioxopyrrolidin-1-yl ester.co—Carboxypentadecanoic acid 2,5-dioxopyrrolidin-1-yl ester.co—Carboxyheptadecanoic acid 2,5~dioxopyrro|idin—1-yl ester.co—Carboxynonadecanoic acid 2.5-dioxopyrrolidin-1-yl ester.Abbreviations:PDMS: Plasma Desorption Mass SpectrometryMALDl-MS: Matrix Assisted Laser Desorption/ionisation Mass SpectrometryHPLC: High Performance Liquid Chromatographyamu: atomic mass unitsAnalyticalPlasma Desorption Mass SpectrometrySample preparation:The sample is dissolved in 0.1 % TFAlEtOH (1:1) at a concentration of 1 pg/pl. Thesample solution (5-10 ul) is placed on a nitrocellulose target (Bio-ion AB, Uppsala.Sweden) and allowed to adsorb to the target surface for 2 minutes. The target issubsequently rinsed with 2x25 ul 0.1 % TFA and spin-dried. Finally, the nitrocellulosetarget is placed in a target carrousel and introduced into the mass spectrometer.M I is:PDMS analysis was carried out using a Bio-ion 20 time-of flight instrument (Bio-ion NordicAB, Uppsala, Sweden). An acceleration voltage of 15 kV was applied and molecular ionsformed by bombardment of the nitrocellulose surface with 252-Cf fission fragments wereaccelerated towards a stop detector. The resulting time-of—flight spectrum was calibrated.. .......,..,,............................._.,........,.............. _.......... ................................................... . . .. . .10152530CA 02264243 2001-05-28W0 98/082371 PCT /DK97I0034038into a true mass spectrum using the H’ and NO’ ions at mlz 1 and 30, respectively. Massspectra were generally accumulated for 1.0x10° fission events corresponding to 15-20minutes. Resulting assigned masses all correspond to isotopically averaged molecularmasses. The accuracy of mass assignment is generally better than 0.1 %.MALDI-MSMALDI-TOF MS analysis_was carried out using a Voyagerm RP instrument (perSeptiveBiosystems Inc, Framingham, MA) equipped with delayed extraction and operated inlinear mode. Alpha—cyano—4-hydroxy-cinnamic acid was used as matrix, and massassignments were based on external calibration.Example 1Synthesis of Lys’°(N‘-tetradecanoyl)-GLP-1(7-37).The title compound was synthesised from GLP-1(7-37). A mixture of GLP—1(7-37) (25 mg.7.45 pm), EDPA (26.7 mg, 208 pm), NMP (520 pl) and water (260 pl) was gently shakenfor 5 min. at room temperature. To the resulting mixture was added a solution of Myr-ONSu (2.5 mg, 7.67 pm) in NMP (62.5 pl). the reaction mixture was gently.shaken for 5min. at room temperature and then allowed to stand for 20 min. An additional amount ofMyr-ONSu (2.5 mg. 7.67 pm) in NMP (62.5 pl) was added and the resulting mixture gentlyshaken for 5 min. After a total reaction time of 40 min. the reaction was quenched by theaddition of a solution of glycine (12.5 mg. 166 pmol) in 50% aqueous ethanol (12.5 ml).The title compound was isolated from the reaction mixture by HPLC using a cyanopropylcolumn (Zorbax"" 300SB-CN) and a standard acetonitrile/T FA system, yield: 1.3 mg(corresponding to 4.9% of the theoretical yield). The column was heated to 65°C and theacetonitrile gradient was 0-100% in 60 minutes. The isolated product was analysed byPDMS and the mlz value for the protonated molecular ion was found to be 3567.913. Theresulting molecular weight is thus 3566.9-:3 amu (theoretical value: 3565.9 amu). Theposition of acylation (Lys26) was verified by enzymatic cleavage of the title compound withStaphylococcus aureus V8 protease and subsequent mass determination of the peptidefragments by PDMS.1015202530CA 02264243 1999-02-25wo 93/03371 PCT/DK97/0034039In addition to the title compound two other GLP-1 derivatives were isolated from thereaction mixture by using the same chromatographic column and a more shallow gradient(35-38% acetonitrile in 60 minutes), see Examples 2 and 3.Example 2Synthesis of Lys3“(N‘-tetradecanoyl)-GLP-1 (7-37).The title compound was isolated by HPLC from the reaction mixture described in Example1. PDMS analysis yielded a protonated molecular ion at m/z 3567.7i3. The molecularweight is thus found to be 3566.713 amu (theoretical value: 3565.9 amu). The acylationsite was determined on the basis of the fragmentation pattern.Example 3Synthesis of Lys"'”“—bis(N‘-tetradecanoyl)-GLP-1(7-37).The title compound was isolated by HPLC from the reaction mixture described in Example1. PDMS analysis yielded a protonated molecular ion at m/z 3778.4.t3. The molecularweight is thus found to be 3777.413 amu (theoretical value: 3776.1 amu).Example 4Synthesis of Lys25(N‘-tetradecanoyl)Arg3"-GLP-1(7-37).The title compound was synthesised from Arg“-GLP-1(7-37). A mixture of Arg“-GLP-1(7-37) (5 mg, 1.47 pm), EDPA (5.3 mg, 41.1 um), NMP (105 pl) and water (50 ul) was gentlyshaken for 5 min. at room temperature. To the resulting mixture was added a solution ofMyr-ONSu (0.71 mg, 2.2 pm) in NMP (17.8 pl), the reaction mixture was gently shaken for5 min. at room temperature and then allowed to stand for 20 min. After a total reactiontime of 30 min. the reaction was quenched by the addition of a solution of glycine (25 mg,33.3 pm) in 50% aqueous ethanol (2.5 ml). The reaction mixture was purified by HPLC asdescribed in Example 1. PDMS analysis yielded a protonated molecular ion at m/z3594.913. The molecular weight is thus found to be 3593.9-.l:3 amu (theoretical value:3593.9 amu)...s.........w_.,.m.. ...... ........_.........-...»..... ........... .. .c.m.._..._......._.,.,. .... .1015202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/0034040Example 5Synthesis of Gly“Arg’°'3‘Lys“‘(N‘-tetradecanoyl)-GLP-1 (7-37).The title compound was synthesised from Gly“Arg25'3‘Lys35-GLP—1(7-37) which waspurchased from QCB. A mixture of Gly"Arg25"*“Lys°‘"’-GLP-1 (7-37) (1.3 mg, 0.39 pm), EDPA(1.3 mg, 10 pm), NMP (125 pl) and water (30 pl) was gently shaken for 5 min. at roomtemperature. To the resulting mixture was added a solution of Myr-ONSu (0.14 mg, 0.44pm) in NMP (3.6 ml), the reaction mixture was gently shaken for 15 min. at roomtemperature. The reaction was quenched by the addition of a solution of glycine (0.1 mg,1.33 pm) in 50% aqueous ethanol (10 pl). The reaction mixture was purified by HPLC, andthe title compound (60 pg, 4%) was isolated.Example 6Synthesis of Arg2“‘Lys35 (Nfitetradecanoyl)-GLP-1(7-37)-OH.A mixture of Arg2”‘Lys35-GLP-1(7-37)-OH (5.0 mg, 1.477 pmol), EDPA (5.4 mg, 41.78pmol), NMP (105 pl) and water (50 pl) was gently shaken for 5 min. at room temperature. .To the resulting mixture was added a solution of Myr-ONSu (0.721 mg, 2.215 pmol) inNMP (18 pl). The reaction mixture was gently shaken for 5 min. at room temperature, andthen allowed to stand for an additional 45 min. at room temperature. The reaction wasquenched by the addition of a solution of glycine (2.5 mg, 33.3 pmol) in 50% aqueousethanol (250 pl). The reaction mixture was purified by column chromatography using acyanopropyl column (Zorbax 300SB—CN) and a standard acetonitrile/TFA system. Thecolumn was heated to 65°C and the acetonitrile gradient was 0-100% in 60 minutes. Thetitle compound ( 1.49 mg. 28 %) was isolated, and the product was analysed by PDMS.The m/z value for the protonated molecular ion was found to be 3595 : 3. The resultingmolecular weight is thus 3594 1 3 amu (theoretical value 3594 amu).Example 7Synthesis of Lys25'3“bis(N‘-(co—carboxynonadecanoyl))-GLP-1(7-37)-OH.A mixture of GLP-1(7-37)—OH (70 mg, 20.85 pmol), EDPA (75.71 mg, 585.8 pmol), NMP(1.47 ml) and water (700 pL) was gently shaken for 10 min. at room temperature. To the1015202530CA 02264243 1999-02-25wo 93/03371 PCT/DK97/0034041resulting mixture was added a solution of HOOC-(CH2),,,-COONSU (27.44 mg, 62.42 umol)in NMP (686 iii), the reaction mixture was gently shaken for 5 min. at room temperature,and then allowed to stand for an additional 50 min. at room temperature. The reaction wasquenched by the addition of a solution of glycine (34.43 mg, 458.? umol) in 50% aqueousethanol (3.44 ml). The reaction mixture was purified by column chromatography using acyanopropyl column (Zorbax 30OSB-CN) and a standard acetonitrile/T FA system. Thecolumn was heated to 65°C and the acetonitrile gradient was 0-100"/o in 60 minutes. Thetitle compound ( 8.6 mg, 10 °/o) was isolated, and the product was analysed by PDMS. Them/z value for the protonated molecular ion was found to be 4006 i 3. The resultingmolecular weight is thus 4005 i 3 amu (theoretical value 4005 amu).Example 8Synthesis of Arg2“‘Lys3“(N‘-(orcarboxynonadecanoyl))-GLP—1(7-36)-OH.A mixture of Arg”-°‘Lys35-GLP-1(7-36)-OH (5.06 mg, 1.52 umol), EDPA (5.5 mg, 42.58umol), NMP (106 pl) and water (100 pl) was gently shaken for 5 min. at room temperature.To the resulting mixture was added a solution of HOOC-(CH2),,,—COONSu (1.33 mg, 3.04umol) in NMP (33.2 pl), the reaction mixture was gently shaken for 5 min. at roomtemperature, and then allowed to stand for an additional 2.5 h at room temperature. Thereaction was quenched by the addition of a solution of glycine (2.50 mg, 33.34 umol) in50% (250 ul). The reaction mixture was purified by columnchromatography using a cyanopropyl column (Zorbax 30088-CN) and a standardacetonitrilefl" FA system. The column was heated to 65°C and the acetonitrile gradient wasaqueous ethanol0-100% in 60 minutes. The title compound ( 0.46 mg, 8 %) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3652 i 3. The resulting molecular weight is thus 3651 : 3 amu (theoretical value 3651amu).Example 9Synthesis of Argzs-3‘Lys3°(N‘-(u)-carboxynonadecanoyl))-GLP-1(7-38)-OH.A mixture of Argze-3‘Lys3°-GLP-1(7~38)—OH (5.556 mg, 1.57umol), EDPA (5.68 mg, 43.96umol), NMP (116.6 pi) and water (50 pl) was gently shaken for 10 min. at roomtemperature. To the resulting mixturewas added a solution HOOC-(CH2),,,-COONSu (1.381015202530CA 02264243 1999-02-25W0 98/08871 PCT/DK97I0034042mg, 3.14 umol) in NMP (34.5 pl), the reaction mixture was gently shaken for 5 min. atroom temperature, and then allowed to stand for an additional 2.5 h at room temperature.The reaction was quenched by the addition of a solution of glycine (2.5 mg, 33.3 umol) in50% aqueous ethanol (250 pl). The reaction mixture was purified by columnchromatography using a cyanopropyl column (Zorbax 3OOSB-CN) and a standardacetonitrile/T FA system. The column was heated to 65°C and the acetonitrile gradient was0—100% in 60 minutes. The m_<a_cQmpgmg (0.7 mg, 12 %) was isolated. and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3866 : 3. The resulting molecular weight is thus 3865 : 3 amu (theoretical value 3865amu).Example 10Synthesis of Arg3‘Lys25 (N‘-(u)—carboxynonadecanoyl))-GLP-1(7-37)-OH.A mixture of Arg“-GLP-1(7-37)-OH (5.04 mg, 1.489 umol), EDPA (5.39 mg, 41.70 umol),NMP (105 pi) and water (50 pl) was gently shaken for 10 min. at room temperature. To theresulting mixture was added a solution HOOC-(CH2)15-COONSU (1.31 mg, 2.97 umol) inNMP (32.8 ul), the reaction mixture was gently shaken for 5 min. at room temperature, andthen allowed to stand for an additional 30 min. at room temperature. The reaction wasquenched by the addition of a solution of glycine (2.46 mg, 32.75 umol) in 50% aqueousethanol (246 pl). The reaction mixture was purified by column chromatography using acyanopropyl column (Zorbax 3OOSB-CN) and a standard acetonitrilefl”FA system. Thecolumn was heated to 65°C and the acetonitrile gradient was 0—100% in 60 minutes. Thetitle ggmpgund ( 1.2 mg, 22 %) was isolated, and the product was analysed by PDMS. Them/z value for the protonated molecular ion was found to be 3709 :r 3. The resultingmolecular weight is thus 3708 1 3 amu (theoretical value 3708 amu).Example 11Synthesis of Arg3“i_ys2" (N‘-(co—carboxyheptadecanoyl))—GLP-1(7-37)-OH.A mixture of Arg“-GLP-1(7-37)-OH (5.8 mg, 1.714 umol), EDPA (6.20 mg, 47.99 pmol).NMP (121.8 pl) and water (58 ul) was gently shaken for 10 min. at room temperature. Tothe resulting mixture was added a solution HOOC-(CH2),5-COONSu (2.11 mg, 5.142 pmol)in NMP (52.8 pl), the reaction mixture was gently shaken for 5 min. at room temperature,1015202530CA 02264243 1999-02-25wo 93/03371 PCT/DK97I0034043and then allowed to stand for an additional 2 h at room temperature. The reaction wasquenched by the addition of a solution of glycine (2.83 mg, 37.70 pmol) in 50% aqueousethanol (283 pl). The reaction mixture was purified by column chromatography using acyanopropyl column (Zorbax 300SB-CN) and a standard acetonitrile/'l' FA system. Thecolumn was heated to 65°C and the acetonitrile gradient was 0-100% in 60 minutes. The d (0.81 mg, 13 %) was isolated, and the product was analysed by PDMS.The m/z value for the protonated molecular ion was found to be 3681 i 3. The resultingmolecular weight is thus 3680 : 3 amu (theoretical value 3680 amu).Example 12Synthesis of Arg26'3‘Lys3“ (N‘-(u)—carboxyheptadecanoyl))—GLP-1(7-37)-OH.A mixture of ArgZ°'°‘Lys35-GLP-1(7-37)-OH (3.51 mg. 1.036 pmol), EDPA (3.75 mg, 29.03pmol), NMP (73.8 pi) and water (35 pl) was gently shaken for 10 min. at roomtemperature. To the resulting mixture was added a solution HOOC-(CH2),,,-COONSu (1.27mg, 3.10 pmol) in NMP (31.8 pl), the reaction mixture was gently shaken for 5 min. atroom temperature, and then allowed to stand for an additional 2 h and 10 min. at roomtemperature. The reaction was quenched by the addition of a solution of glycine (1.71 mg,22.79 pmol) in 50% aqueous ethanol (171 pl). The reaction mixture was purified by columnchromatography using a cyanopropyl column (Zorbax 3008B-CN) and a standardacetonitrileff FA system. The column was heated to 65°C and the acetonitrile gradient wasO-100% in 60 minutes. The title gomggund (0.8 mg, 21 %) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3682 : 3. The resulting molecular weight is thus 3681 t 3 amu (theoretical value3681amu).Example 13Synthesis of Argm‘Lys”(N‘-(cn—carboxyheptadecanoyl))-GLP-1(7-38)-OH.A mixture of Arg2“'3‘Lys”-GLP-1(7-38)-OH (5.168 mg, 1.459 pmol), EDPA (5.28 mg, 40.85pmol), NMP (108.6 pl) and water (51.8 pl) was gently shaken for 10 min. at roomtemperature. To the resulting mixture was added a solution HOOC-(CH2),6-COONSu (1.80mg, 4.37 pmol) in NMP (45 pl), the reaction mixture was gently shaken for 10 min. at roomtemperature, and then allowed to stand for an additional 2 h and 15 min. at room1015202530CA 02264243 1999-02-25WO 98108871 PCT/DK97/0034044temperature. The reaction was quenched by the addition of a solution of glycine (2.41 mg,32.09 pmol) in 50% aqueous ethanol (241 pl). The reaction mixture was purified by columnchromatography using a cyanopropyl column (Zorbax 300SB-CN) and a standardacetonitrile/TFA system. The column was heated to 65°C and the acetonitrile gradient was0-100% in 60 minutes. The title c m nd (0.8 mg, 14 °/o) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3838 i 3. The resulting molecular weight is thus 3837 : 3 amu (theoretical value 3837amu).Example 14Synthesis of Arg25'3‘Lys35 (N‘-(co—carboxyheptadecanoyl))—GLP-1(7-36)-OH.A mixture of Arg2“'3‘Lys35—GLP-1(7-36)-OH (24.44 mg, 7.34 pmol), EDPA (26.56 mg,205.52 pmol), NMP (513 pl) and water (244.4 pl) was gently shaken for 5 min. at roomtemperature. To the resulting mixture was added a solution HOOC-(CH2),5-COONSU (9.06mg, 22.02 pmol) in NMP (1.21 ml), the reaction mixture was gently shaken for 5 min. atroom temperature, and then allowed to stand for an additional 30 min. at roomtemperature. The reaction was quenched by the addition of a solution of glycine (12.12mg, 161.48 pmol) in 50% aqueous ethanol (1.21 ml). The reaction mixture was purified bycolumn chromatography using a cyanopropyl column (Zorbax 300SB—CN) and a standardacetonitrile/TFA system. The column was heated to 65°C and the acetonitrile gradient was0-100% in 60 minutes. The title compound (7.5 mg, 28 %) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3625 1 3. The resulting molecular weight is thus 3624 :r 3 amu (theoretical value 3624amu).Example 15Synthesis of Argzfi-“Lys” (N‘—(co—carboxyundecanoyl))—GLP-1(7-37)—OH.A mixture of Argze-“Lyssa-GLP-1(7-37)-OH (4.2 mg, 1.24 pmol), EDPA (4.49 mg, 34.72pmol), NMP (88.2 pl) and water (42 pl) was gently shaken for 10 min. at roomtemperature. To the resulting mixture was added a solution HOOC-(CH2),o-COONSu (1.21mg, 3.72 pmol) in NMP (30.25 pl), the reaction mixture was gently shaken for 5 min. atroom temperature, and then allowed to stand for an additional 40 min. at room1015202530CA 02264243 1999-02-25WO 98/08371 PCT/DK97/0034045temperature. The reaction was quenched by the addition of a solution of glycine (2.04 mg,27.28 pmol) in 50% aqueous ethanol (204 pl). The reaction mixture was purified by columnchromatography using a cyanopropyl column (Zorbax 300SB-CN) and a standardacetonitrile/T FA system. The column was heated to 65°C and the acetonitrile gradient was0-100% in 60 minutes. The title compound (0.8 mg, 18 %) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3598 i 3. The resulting molecular weight is thus 3597 i 3 amu (theoretical value 3597amu).Example 16Synthesis of Argm‘Lys3°(N‘—(w—carboxyundecanoyl))-GLP-1(7-38)—OH.A mixture of Arg2‘""3‘Lys3“-GLP-1(7-38)-OH (5.168 mg, 1.46 pmol), EDPA (5.28 mg, 40.88pmol), NMP (108.6 pl) and water (51.7 pl) was gently shaken for 10 min. at roomtemperature. To the resulting mixture was added a solution HOOC—(CH2),,,-COONSu (1.43mg, 4.38 pmol) in NMP (35.8 pl), the reaction mixture was gently shaken for 5 min. atroom temperature, and then allowed to stand for an additional 50 min. at roomtemperature. The reaction was quenched by the addition of a solution of glycine (2.41 mg,32.12 pmol) in 50% aqueous ethanol (241 pl). The reaction mixture was purified by columnchromatography using a cyanopropyl column (Zorbax 300SB—CN) and a standardacetonitrile/TFA system. The column was heated to 65°C and the acetonitrile gradient wasO-100% in 60 minutes. The title compgund (0.85 mg, 16 %) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3753 i 3. The resulting molecular weight is thus 3752 : 3 amu (theoretical value 3752amu).Example 17Synthesis of Lys2““bis(N‘-(co—carboxyundecanoyl))-GLP-1(7-37)-OH.A mixture of GLP-1(7-37)-OH (10.0 mg, 2.98 pmol), EDPA (10.8 mg, 83.43 pmol), NMP(210 pl) and water (100 pl) was gently shaken for 10 min. at room temperature. To theresulting mixture was added a solution HOOC-(CH2),,,-COONSu (2.92 mg, 8.94 pmol) inNMP (73 pl), the reaction mixture was gently shaken for 5 min. at room temperature, andthen allowed to stand for an additional 50 min. at room temperature. The reaction was1015202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/0034046quenched by the addition of a solution of glycine (4.92 mg, 65.56 pmol) in 50% aqueousethanol (492 pl). The reaction mixture was purified by column chromatography using acyanopropyl column (Zorbax 3OOSB-CN) and a standard acetonitrilefl'FA system. Thecolumn was heated to 65°C and the acetonitrile gradient was 0-100% in 60 minutes. Thetitle compound (1.0 mg, 9 %) was isolated, and the product was analysed by PDMS. Them/z value for the protonated molecular ion was found to be 3781 i 3. The resultingmolecular weight is thus 3780 : 3 amu (theoretical value 3780amu).Example 18Synthesis of Arg2°'3‘Lys35 (N‘-(cwcarboxyundecanoyl))-GLP-1(7—36)—OH.A mixture of Arg2“~3‘Lys35-GLP-1(7-36)-OH (15.04 mg, 4.52 pmol), EDPA (16.35 mg,126.56 pmol), NMP (315.8 pl) and water (150.4 pl) was gently shaken for 10 min. at roomtemperature. To the resulting mixture was added a solution HOOC-(CH2),o-COONSu (4.44mg, 1356 pmol) in NMP (111 pl), the reaction mixture was gently shaken for 5 min. atroom temperature, and then allowed to stand for an additional 40 min. at roomtemperature. The reaction was quenched by the addition of a solution of glycine (7.5 mg,99.44 pmol) in 50% aqueous ethanol (750 pl). The reaction mixture was purified by columnchromatography using a cyanopropyl column (Zorbax 3OOSB-CN) and a standardacetonitrilefTFA system. The column was heated to 65°C and the acetonitrile gradient wasO-100% in 60 minutes. The title compound (3.45 mg, 22 %) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3540 i 3. The resulting molecular weight is thus 3539 1 3 amu (theoretical value 3539amu).Example 19Synthesis of Arg3“Lys26 (N‘-(u>—carboxyundecanoyl))-GLP-1(7-37)-OH.A mixture of Arg3“-GLP-1(7-37)-OH (5.87 mg, 1.73 pmol), EDPA (6.27 mg, 48.57 pmol),NMP (123.3 pl) and water (58.7 pl) was gently shaken for 10 min. at room temperature. Tothe resulting mixture was added a solution HOOC-(CH2),0-COONSU (1.70 mg, 5.20 pmol)in NMP (42.5 pl), the reaction mixture was gently shaken for 5 min. at room temperature,and then allowed to stand for an additional 40 min. at room temperature. The reaction wasquenched by the addition of a solution of glycine (2.86 mg, 286 pmol) in 50% aqueous1015202530CA 02264243 1999-02-25W0 93/03371 PCT/DK97/0034047ethanol (286 pl). The reaction mixture was purified by column chromatography using acyanopropyl column (Zorbax 300SB-CN) and a standard acetonitrile/T FA system. Thecolumn was heated to 65°C and the acetonitrile gradient was 0-100% in 60 minutes. Thetitle compound (1.27 mg, 20 %) was isolated, and the product was analysed by PDMS.The m/z value for the protonated molecular ion was found to be 3597 1 3. The resultingmolecular weight is thus 3596 i 3 amu (theoretical value 3596 amu).Example 20Synthesis of Arg3“Lys2° (N‘-(co—carboxyheptanoyl))-GLP-1(7-37)-OH.A mixture of Arg“-GLP-1(7-37)-OH (4.472 mg, 1.32 pmol), EDPA (4.78 mg, 36.96 pmol),NMP (94 pl) and water (44.8 pl) was gently shaken for 5 min. at room temperature. To theresulting mixture was added a solution HOOC-(CH2)5-COONSU (1.07 mg, 3.96 pmol) inNMP (26.8 pl), the reaction mixture was gently shaken for 5 min. at room temperature, andthen allowed to stand for an additional 1 h and 50 min. at room temperature. The reactionwas quenched by the addition of a solution of glycine (2.18 mg, 29.04 pmol) in 50%aqueous ethanol (218 pl). The reaction mixture was purified by column chromatographyusing a cyanopropyl column (Zorbax 300SB—CN) and a standard acetonitrile/T FA system.The column was heated to 65°C and the acetonitrile gradient was 0-100% in 60 minutes.The title compound (0.5 mg, 11 %) was isolated, and the product was analysed by PDMS.The m/z value for the protonated molecular ion was found to be 3540 : 3. The resultingmolecular weight is thus 3539 : 3 amu (theoretical value 3539 amu).Example 21Synthesis of Arg25'3‘Lys°‘(N‘-(co—carboxyheptanoy|))-GLP-1(7-38)-OH.A mixture of Argze-3‘Lys3°-GLP—1(7-38)-OH (5.168 mg, 1.459 pmol), EDPA (5.28 mg, 40.85pmol), NMP (108.6 pl) and water (51.6 pl) was gently shaken for 10 min. at roomtemperature. To the resulting mixture was added a solution HOOC—(CH2)5-COONSu (1.18mg, 4.37 pmol) in NMP (29.5 pl), the reaction mixture was gently shaken for 5 min. atroom temperature, and then allowed to stand for an additional 1 h and 50 min. at roomtemperature. The reaction was quenched by the addition of a solution of glycine (2.40 mg,32.09 pmol) in 50% aqueous ethanol (240 pl). The reaction mixture was purified by columnchromatography using a cyanopropyl column (Zorbax 30088-CN) and a standard1015202530CA 02264243 1999-02-25W0 98/08871 PCT/DK97/0034048acetonitrile/T FA system. The column was heated to 65°C and the acetonitrile gradient was0-100% in 60 minutes. The t_itIe_c_Q_r_r_1p9ur_ig (0.5 mg, 9 %) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3697 : 3. The resulting molecular weight is thus 3695 i 3 amu (theoretical value 3695amu).Example 22Synthesis of Arg2““Lys“6 (N‘-(co—carboxyheptanoyl))-GLP-1(7-37)—OH.A mixture of Arg2°'3‘Lys35—GLP-1(7-37)-OH (5.00 mg, 1.47 pmol), EDPA (5.32 mg, 41.16umol), NMP (105 pi) and water (50 pl) was gently shaken for 5 min. at room temperature.To the resulting mixture was added a solution HOOC-(CH2)6-COONSu (1.19 mg, 4.41umol) in NMP (29.8 pl), the reaction mixture was gently shaken for 5 min. at roomtemperature, and then allowed to stand for an additional 2 h at room temperature. Thereaction was quenched by the addition of a solution of glycine (2.42 mg, 32.34 pmol) in50% (242 pl).chromatography using a cyanopropyl column (Zorbax 300SB—CN) and a standardaqueous ethanol The reaction mixture was purified by columnacetonitrile/T FA system. The column was heated to 65°C and the acetonitrile gradient was0-100% in 60 minutes. The title compound (0.78 mg, 15 °/0) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3542 i 3. The resulting molecular weight is thus 3541 : 3 amu (theoretical value 3541amu).Example 23Synthesis of Arg”-3‘Lys35 (N‘-(co—carboxyheptanoyl))-GLP-1(7-36)-OH.A mixture of Arg2“""Lys3'5-GLP—1(7-36)—OH (5.00 mg, 1.50 pmol), EDPA (5.44 mg, 42.08pmol), NMP (210 pi) and water (50 pl) was gently shaken for 5 min. at room temperature.To the resulting mixture was added a solution HOOC-(CH2)6-COONSu (1.22 mg, 4.5 pmol)in NMP (30.5 pl), the reaction mixture was gently shaken for 5 min. at room temperature,and then allowed to stand for an additional 2 h at room temperature. The reaction wasquenched by the addition of a solution of glycine (2.47 mg, 33.0 pmol) in 50% aqueousethanol (247 pl). The reaction mixture was purified by column chromatography using a1015202530CA 02264243 1999-02-25wo 98/08871 PCT/DK97/0034049cyanopropyl column (Zorbax 30OSB-CN) and a standard acetonitrile/T FA system. Thecolumn was heated to 65°C and the acetonitrile gradient was 0-100% in 60 minutes. Thetitle compound (0.71 mg, 14 %) was isolated, and the product was analysed by PDMS.The m/z value for the protonated molecular ion was found to be 3484 i 3. The resultingmolecular weight is thus 3483 J_r 3 amu (theoretical value 3483 amu).Example 24Synthesis of Lys2°'3“bis(N‘-(o>—carboxyheptanoy|))-GLP—1(7-37)-OH.A mixture of GLP-1(7-37)-OH (10 mg, 2.5 pmol), EDPA (10.8 mg, 83.56 pmol), NMP (210pi) and water (100 pl) was gently shaken for 10 min. at room temperature. To the resultingmixture was added a solution HOOC—(CH2)6-COONSu (2.42 mg, 8.92 pmol) in NMP (60.5ul), the reaction mixture was gently shaken for 5 min. at room temperature, and thenallowed to stand for an additional 2 h and 35 min. at room temperature. The reaction wasquenched by the addition of a solution of glycine (4.92 mg, 65.54 umol) in 50% aqueousethanol (492 pl). The reaction mixture was purified by column chromatography using acyanopropyl column (Zorbax 30OSB-CN) and a standard acetonitrile/T FA system. Thecolumn was heated to 65°C and the acetonitrile gradient was O-100% in 60 minutes. Thetitle compound (2.16 mg, 24 %) was isolated, and the product was analysed by PDMS.The m/z value for the protonated molecular ion was found to be 3669 : 3. The resultingmolecular weight is thus 3668 : 3 amu (theoretical value 3668 amu).Example 25Synthesis of Arg3“Lys’5 (N‘-(m—carboxypentadecanoy|))—GLP-1(7-37)-OH.A mixture of Arg“-GLP-1(7-37)-OH (4.472 mg, 1.321 umol), EDPA (4.78 mg, 36.99 pmol),NMP (93.9 pl) and water (44.7 pl) was gently shaken for 10 min. at room temperature. Tothe resulting mixture was added a solution HOOC—(CH2),.—COONSu (1.519 mg, 3.963umol) in NMP (38 pl), the reaction mixture was gently shaken for 5 min. at roomtemperature, and then allowed to stand for an additional 1 h at room temperature. Thereaction was quenched by the addition of a solution of glycine (2.18 mg, 29.06 pmol) in50%chromatography using a cyanopropyl column (Zorbax 30OSB-CN) and a standardaqueous ethanol (218 pl). The reaction mixture was purified by columnacetonitrile/T FA system. The column was heated to 65°C and the acetonitrile gradient was1015202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/00340500-100% in 60 minutes. The title comggund (0.58 mg, 12 %) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3654 i 3. The resulting molecular weight is thus 3653 -_t 3 amu (theoretical value 3653amu).Example 26Synthesis of Arg2°'3“Lys3° (N‘-(cn—carboxyheptanoy|))-GLP-1(7-36)-OH.A mixture of Arg26'3‘Lys35—GLP-1(7-36)-OH (5.00 mg, 1.50 umol), EDPA (5.44 mg. 42.08umol), NMP (210 pi) and water (50 ul) was gently shaken for 5 min. at room temperature.To the resulting mixture was added a solution HOOC-(CH2),.,-COONSu (1.72 mg, 4.5umol) in NMP (43 ul), the reaction mixture was gently shaken for 5 min. at roomtemperature, and then allowed to stand for an additional 1 h at room temperature. Thereaction was quenched by the addition of a solution of glycine (2.48 mg, 33 umol) in 50%aqueous ethanol (248 pl). The reaction mixture was purified by column chromatographyusing a cyanopropyl column (Zorbax 300SB—CN) and a standard acetonitrilefT FA system.The column was heated to 65°C and the acetonitrile gradient was 0-100% in 60 minutes.The title compound (0.58 mg, 11 %) was isolated, and the product was analysed byPDMS. The m/z value for the protonated molecular ion was found to be 3596 i 3. Theresulting molecular weight is thus 3595 i 3 amu (theoretical value 3595 amu).Example 27Synthesis of lithocholic acid 2,5-dioxo-pyrrolidin-1-yl ester.To a mixture of lithocholic acid (5.44 g, 14.34 mmol), N-hydroxysuccinimide (1.78 g, 15.0mmol), anhydrous THF (120 ml) and anhydrous acetonitrile (30 ml). kept at to 10 °C, wasadded a solution of N,N'-dicyclohexylcarbodiimide (3.44 g, 16.67 mmol) in anhydrous THF.The reaction mixture was stirred at ambient temperature for 16 h, filtered and concentratedin vaguo. The residue was dissolved in dichloromethane (450 ml), washed with a 10%aqueous Na2CO3 solution (2x150 ml) and water (2x150 ml), and dried (MgSO,,). Filteredand the filtrate concentrated in vagug to give a crystalline residue. The residue wasrecrystallised from a mixture of dichloromethane (30 ml) and n—heptane (30 ml to give thetitle compound (3.46 g, 51%) as a crystalline solid.1015202530CA 02264243 1999-02-25wo 93/03371 PCT/DK97/0034051Example 28Synthesis of Arg“Lys25(N‘-llthocholyl)-GLP-1(7-37)-OH.A mixture of Arg“-GLP-1(7-37)-OH (4.472 mg, 1.32 pmol), EDPA (4.78 mg, 36.96 pmol),NMP (94 pi) and water (44.8 pl) was gently shaken for 10 min. at room temperature. Tothe resulting mixture was added a solution of lithocholic acid 2,5-dioxo—pyrrolidin-1-yl ester(1.87 mg, 3.96 pmol) in NMP (46.8 pl), the reaction mixture was gently shaken for 5 min.at room temperature, and then allowed to stand for an additional 1 h at room temperature.The reaction was quenched by the addition of a solution of glycine (2.18 mg, 2904 pmol)in 50% aqueous ethanol (218 pl). The reaction mixture was purified by columnchromatography using a cyanopropyl column (Zorbax 3OOSB—CN) and a standardacetonitrile/TFA system. The column was heated to 65°C and the acetonitrile gradient was0-100% in 60 minutes. The title compound (1.25 mg, 25 %) was isolated, and the productwas analysed by PDMS. The m/2 value for the protonated molecular ion was found to be3744 +- 3. The resulting molecular weight is thus 3743 +- 3 amu (theoretical value 3743amu).Example 29Synthesis of N“-tetradecanoyl-Glu(ONSu)-OBu‘.To a suspension of H-Glu(OH)-OBu‘ (2.5 g, 12.3 mmol), DMF (283 ml) and EDPA (1.58 g,12.3 mmol) was added drop by drop a solution of Myr-ONSu (4.0 g, 12.3 mmol) in DMF(59 ml). The reaction mixture was stirred for 16 h at room temperature and thenconcentrated in vaggo to a total volume of 20 ml. The residue was partitioned between 5%aqueous citric acid (250 ml) and ethyl acetate (150 ml), and the phases were separated.The organic phase was concentrated in vague and the residue dissolved in DMF (40 ml).The resulting solution was added drop by drop to a 10% aqueous solution of citric acid(300 ml) kept at 0 “C. The precipitated compound was collected and washed with icedwater and dried in a vacuum drying oven. The dried compound was dissolved in DMF (23ml) and HONSu (1.5 g, 13 mmol) was added. To the resulting mixture was added asolution of N,N’-dicyclohexylcarbodiimide (2.44 g, 11.9 mmol) in dichloromethane (47 ml).The reaction mixture was stirred for 16 h at room temperature, and the precipitatedcompound was filtered off. The precipitate was recrystallised from n-heptane/2-propanol togive the title compound (3.03 g, 50%).1015202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/0034052Example 30Synthesis of Glu”-23'3°Arg25'3‘Lys“(N‘-(y-glutamyl(N“-tetradecanoyl)))-GLP-1 (7-38)-OH.A mixture of GIu22'23'3°Arg2“‘Lys”-GLP-1(7-38)-OH (1.0 mg, 0.272 pmol), EDPA (0.98 mg,7.62 pmol), NMP (70 pi) and water (70 pl) was gently shaken for 5 min. at roomtemperature. To the resulting mixture was added a solution of N"-tetradecanoyl-G|u(ONSu)-OBu‘, prepared as described in Example 29, (0.41 mg, 0.816 pmol) in NMP(10.4 pl), the reaction mixture was gently shaken for 5 min. at room temperature, and thenallowed to stand for an additional 45 min. at room temperature. The reaction wasquenched by the addition of a solution of glycine (0.448 mg, 5.98 pmol) in 50% aqueousethanol (45 pl). A 0.5 % aqueous solution of ammonium acetate (0.9 ml) was added, andthe resulting mixture was immobilised on a Varian 500 mg C8 Mega Bond Elut® cartridge,the immobilised compound washed with 5% aqueous acetonitrile (10 ml), and finallyliberated from the cartridge by elution with TFA (10 ml). The eluate was concentrated ig@QLI_O, and the reaction mixture was purified by column chromatography using acyanopropyl column (Zorbax 300SB-CN) and a standard acetonitrilefl'FA system. Thecolumn was heated to 65°C and the acetonitrile gradient was 0-100"/o in 60 minutes. Thetitle compound (0.35 mg, 32 %) was isolated, and the product was analysed by PDMS.The m/z value for the protonated molecular ion was found to be 4012 i 3. The resultingmolecular weight is thus 4011 1 3 amu (theoretical value 4011 amu).Example 31Synthesis of Glu23'2°Arg““Lys3“(N‘—(y-glutamy|(N“-tetradecanoyl)))-GLP-1 (7-38)-OH.A mixture of Glu23'2“Arg°“‘Lys“"-GLP-1(7-38)-OH (6.07 mg, 1.727 pmol), EDPA (6.25 mg,48.36 pmol), NMP (425 pl) and water (425 pl) was gently shaken for 5 min. at roomtemperature. To the resulting mixture was added a solution of N°‘-tetradecanoy|-Glu(ONSu)-OBu‘ , prepared as described in example 29, (2.65 mg, 5.18 pmol) in NMP(66.3 pl), the reaction mixture was gently shaken for 5 min. at room temperature, and thenallowed to stand for an additional 45 min. at room temperature. The reaction wasquenched by the addition of a solution of glycine (2.85 mg, 38.0 pmol) in 50% aqueousethanol (285 pl). A 0.5 % aqueous solution of ammonium acetate (5.4 ml) was added, andthe resulting mixture was immobilised on a Varian 500 mg C8 Mega Bond Elut® cartridge,1015202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/0034053the immobilised compound washed with 5% aqueous acetonitrile (10 ml), and finallyliberated from the cartridge by elution with TFA (10 ml). The eluate was concentrated i_n_vacuo, and the reaction mixture was purified by column chromatography using acyanopropyl column (Zorbax 30088-CN) and a standard acetonitrile/T FA system. Thecolumn was heated to 65°C and the acetonitrile gradient was O-100% in 60 minutes. Thetitl com nd (0.78 mg, 12 %) was isolated, and the product was analysed by PDMS.The m/z value for the protonated molecular ion was found to be 3854 i 3. The resultingmolecular weight is thus 3853 i 3 amu (theoretical value 3853 amu).Example 32Synthesis of Lysm‘-bis(N‘-(cu-carboxytridecanoyl))-GLP-1(7-37)-OH.A mixture of GLP-1(7-37)-OH (30 mg, 8.9 umol), EDPA (32.3 mg, 250 pmol), NMP (2.1ml) and water (2.1 ml) was gently shaken for 5 min. at room temperature. To the resultingmixture was added a solution HOOC-(CH2),2-COONSU (12.7 mg, 35.8 umol) in NMP (318pl), the reaction mixture was gently shaken for 1 h and 40 min. at room temperature. Thereaction was quenched by the addition of a solution of glycine (3.4 mg, 44.7 umol) in 50%aqueous ethanol (335 pl). The reaction mixture was purified by column chromatographyusing a cyanopropyl column (Zorbax 3008B-CN) and a standard acetonitrile/T FA system.The column was heated to 85°C and the acetonitrile gradient was 0-100% in 60 minutes.The title compound (10 mg, 29 °/0) was isolated, and the product was analysed by PDMS.The m/z value for the protonated molecular ion was found to be 3840 1 3. The resultingmolecular weight is thus 3839 t 3 amu (theoretical value 3839 amu).Example 33Synthesis of Lys25'3“-bis(N‘-(y-gIutamyl(N“-tetradecanoyl)))-GLP-1(7-37)-OH. (NNC 90-1167).A mixture of GLP-1(7-37)-OH (300 mg, 79.8 umol), EDPA (288.9 mg, 2.24 mmol), NMP(21 ml) and water (21 ml) was gently shaken for 5 min. at room temperature. To theresulting mixture was added a solution of N“-tetradecanoyl-Glu(ONSu)-OBu‘, prepared asdescribed in Example 29, (163 mg, 319.3 pmol) in NMP (4.08 ml), the reaction mixturewas gently shaken for 5 min. at room temperature, and then allowed to stand for anadditional 1 h at room temperature. The reaction was quenched by the addition of a........_.....................—..u-.-................«__.-,..., . . . ......_...........».......i..-......_......».«....._., ... . .1015202530CA 02264243 1999-02-25wo 93/03371 PCT/DK97/0034054solution of glycine (131.8 mg, 1.76 mmol) in 50% aqueous ethanol (13.2 ml). A 0.5 %aqueous solution of ammonium-acetate (250 ml) was added, and the resulting mixture wasdivided into four equal portions. Each portion was eluted onto a Varian 500 mg C8 MegaBond Elut® cartridge, the immobilised compound washed with 0.1% aqueous TFA (3.5 ml),and finally liberated from the cartridge by elution with 70% aqueous acetonitrile (4 ml). Thecombined eluates were diluted with 0.1% aqueous TFA (300 ml). The precipitatedcompound was collected by centrifugation, washed with 0.1% aqueous TFA (50 ml), andfinally isolated by centrifugation. To the precipitate was added TFA (60 ml), and theresulting reaction mixture was stirred for 1 h and 30 min. at room temperature. ExcessTFA was removed in vacuo, and the residue was poured into water (50 ml). Theprecipitated compound was purified by column chromatography using a cyanopropylcolumn (Zorbax 3OOSB—CN) and a standard acetonitrile/TFA system. The column washeated to 65°C and the acetonitrile gradient was O-100% in 60 minutes. The titlecompound (27.3 mg, 8 %) was isolated, and the product was analysed by PDMS. The m/zvalue for the protonated molecular ion was found to be 4036 : 3. The resulting molecularweight is thus 4035 i 3 amu (theoretical value 4035 amu).Example 34Synthesis of Arg25'°“Lys3°(N‘-(arcarboxypentadecanoyl))-GLP-1(7-38)—OH.A mixture of Arg2““Lys°°-GLP-1(7-38)-OH (30 mg, 8.9 umol), EDPA (32.3 mg, 250 umol),NMP (2.1 ml) and water (2.1 ml) was gently shaken for 5 min. at room temperature. To theresulting mixture was added a solution HOOC-(CH2)1,,-COONSU (13.7 mg, 35.8 umol) inNMP (343 pl), the reaction mixture was gently shaken for 1 h at room temperature. Thereaction was quenched by the addition of a solution of glycine (3.4 mg, 44.7 umol) in 50%aqueous ethanol (335 pl). The reaction mixture was purified by column chromatographyusing a cyanopropyl column (Zorbax 3OOSB—CN) and a standard acetonitrile/T FA system.The column was heated to 65°C and the acetonitrile gradient was 0-100% in 60 minutes.The title compound (4.8 mg, 14 %) was isolated. and the product was analysed by PDMS.The m/z value for the protonated molecular ion was found to be 3894 : 3. The resultingmolecular weight is thus 3893 1 3 amu (theoretical value 3893 amu).1015202530CA 02264243 1999-02-25wo 93/03371 PCT/DK97l0034055Example 35Synthesis of N“-hexadecanoyl-Glu(ONSu)-OBU‘.To a suspension of H-Glu(OH)-OBu‘ (4.2 g, 20.6 mmol), DMF (500 ml) and EDPA (2.65 g,20.6 mmol) was added drop by drop a solution of Pal-ONSu (7.3 g, 20.6 mmol) in DMF(100 ml). The reaction mixture was stirred for 64 h at room temperature and thenconcentrated L/;i_v_a&Q to a total volume of 20 ml. The residue was partitioned between10% aqueous citric acid (300 ml) and ethyl acetate (250 ml), and the phases wereseparated. The organic phase was concentrated in vacuo and the residue dissolved inDMF (50 ml). The resulting solution was added drop by drop to a 10% aqueous solution ofcitric acid (500 ml) kept at 0 °C. The precipitated compound was collected and washedwith iced water and dried in a vacuum drying oven. The dried compound was dissolved inDMF (45 ml) and HONSu (2.15 g, 18.7 mmol) was added. To the resulting mixture wasadded a solution of N,N'-dicyclohexylcarbodiimide (3.5 g, 17 mmol) in dichloromethane (67ml). The reaction mixture was stirred for 16 h at room temperature, and the precipitatedcompound was filtered off. The precipitate was recrystallised from n—heptane/2-propanol togive the title compound (6.6 g, 72%).Example 36Synthesis of Lys2“""‘-bis(N‘-(y-glutamyl(N“-hexadecanoyl)))-GLP-1(7-37)-OH.A mixture of GLP-1(7-37)-OH (10 mg, 2.9 umol). EDPA (10.8 mg, 83.4 umol), NMP (0.7ml) and water (0.7 ml) was gently shaken for 5 min. at room temperature. To the resultingmixture was added a solution of N“-hexadecanoyl-Glu(ONSu)—OBu‘ , prepared asdescribed in Example 33, (163 mg, 319.3 umol) in NMP (4.08 ml), the reaction mixturewas gently shaken 1 h and 20 min. at room temperature. The reaction was quenched bythe addition of a solution of glycine (4.9 mg, 65.6 pmol) in 50% aqueous ethanol (492 pl).A 0.5 % aqueous solution of ammonium-acetate (9 ml) was added, and the resultingmixture eluted onto a Varian 1g C8 Mega Bond Elut® cartridge, the immobilised compoundwashed with 5% aqueous acetonitrile (10 ml). and finally liberated from the cartridge byelution with TFA (10 ml). The eluate was concentrated in vacuo, and the residue purifiedby column chromatography using a cyanopropyl column (Zorbax 30OSB—CN) and astandard acetonitrile/T FA system. The column was heated to 65°C and the acetonitrile1015202530CA 02264243 1999-02-25W0 98/08871 PCT/DK97/0034056gradient was O—100% in 60 minutes. The Qm;m (2.4 mg, 20 %) was isolated, andthe product was analysed by PDMS. The m/z value for the protonated molecular ion wasfound to be 4092 i 3. The resulting molecular weight is thus 4091 : 3 amu (theoreticalvalue 4091 amu).Example 37Synthesis of Arg3“Lys25(N‘-(y-glutamyl(N“-hexadecanoyl)))-GLP—1 (7-37)-OH.A mixture of Arg3“—GLP-1(7-37)-OH (3.7 mg, 1.1 umol), EDPA (4.0 mg, 30.8 umol),acetonitrile (260 pi) and water (260 pl) was gently shaken for 5 min. at room temperature.To the resulting mixture was added a solution of N“-hexadecanoyl-Glu(ONSu)-OBu‘ ,prepared as described in Example 35, (1.8 mg, 3.3 umol) in acetonitrile (44.2 pi), and thereaction mixture was gently shaken for 1 h and 20 min. at room temperature. The reactionwas quenched by the addition of a solution of glycine (1.8 mg, 24.2 umol) in 50% aqueousethanol (181 pl). A 0.5 % aqueous solution of ammonium-acetate (12 ml) and NMP (300pl) were added, and the resulting mixture eluted onto a Varian 1g C8 Mega Bond Elut®cartridge, the immobilised compound washed with 5% aqueous acetonitrile (10 ml), andfinally liberated from the cartridge by elution with TFA (6 ml). The eluate was allowed tostand for 2 h at room temperature and then concentrated in vacuo. The residue waspurified by column chromatography using a cyanopropyl column (Zorbax 30OSB-CN) and astandard acetonitrile/TFA system. The column was heated to 65°C and the acetonitrilegradient was 0-100% in 60 minutes. The title compound (0.23 mg, 6 %) was isolated, andthe product was analysed by PDMS. The m/z value for the protonated molecular ion wasfound to be 3752 i 3. The resulting molecular weight is thus 3751 : 3 amu (theoreticalvalue 3751 amu).Example 38Synthesis of Arg25~3‘Lys3°(N‘-(y-glutamy|(N“-tetradecanoyl)))-GLP—1(7-38)-OH.A mixture of Arg“-"“Lys3"-GLP-1(7-38)-OH (14 mg, 4.0 umol), EDPA (14.3 mg, 110.6pmol), NMP (980 pl) and water (980 pl) was gently shaken for 5 min. at room temperature.To the resulting mixture was added a solution of N“-tetradecanoyl-Glu(ONSu)-OBu’ ,prepared as described in Example 29, (12.1 mg, 23.7 umol) in NMP (303 pl), and thereaction mixture was gently shaken for 2 h at room temperature. The reaction was1015202530CA 02264243 1999-02-25wo 98108871 PCT/DK97/0034057quenched by the addition of a solution of glycine (6.5 mg, 86.9 mmol) in 50% aqueousethanol (652 pl). A 0.5 % aqueous solution of ammonium-acetate (50 (ml) was added, andthe resulting mixture eluted onto a Varian 1g C8 Mega Bond E|ut® cartridge, theimmobilised compound washed with 5% aqueous acetonitrile (15 ml), and finally liberatedfrom the cartridge by elution with TFA (6 ml). The eluate was allowed to stand for 1 h and45 min. at room temperature and then concentrated in_\4aooo. The residue was purified bycolumn chromatography using a cyanopropyl column (Zorbax 300SB-CN) and a standardacetonitrile/T FA system. The column was heated to 65°C and the acetonitrile gradient was0-100% in 60 minutes. The title compound (3.9 mg, 26 %) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3881 i 3. The resulting molecular weight is thus 3880 1 3 amu (theoretical value 3880amu).Example 39Synthesis of Argm“Lys°"(N‘-(co-carboxypentadecanoyl))-GLP-1(7-38)—OH.A mixture of Arg25'3‘Lys3“-GLP-1(7-38)-OH (14 mg, 4.0 pmol), EDPA (14.3 mg, 111 pmol),NMP (980 pl) and water (980 pl) was gently shaken for 5 min. at room temperature. To theresulting mixture was added a solution of HOOC-(CH2)...-COONSu (4.5 mg, 11.9 pmol) inNMP (114 pl), the reaction mixture was gently shaken for 1 h and 45 min. at roomtemperature. An additional solution of HOOC-(CH2),.,-COONSu (4.0 mg, 10.4 pmol) inNMP (100 pl) was added, and the resulting mixture was gently shaken for an additional 1 hand 30 min. at room temperature. The reaction was quenched by the addition of a solutionof glycine (1.5 mg, 19.8 pmol) in 50% aqueous ethanol (148 pl). The reaction mixture waspurified by column chromatography using a cyanopropyl column (Zorbax 300SB-CN) and astandard acetonitrilefl” FA system. The column was heated to 65°C and the acetonitrilegradient was 0-100% in 60 minutes. The title comoound (3.9 mg, 26 %) was isolated, andthe product was analysed by PDMS. The m/z value for the protonated molecular ion wasfound to be 3809 1: 3. The resulting molecular weight is thus 3808 i 3 amu (theoreticalvalue 3808 amu).. . ..........................._.....e......... -.. .. .1015202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/0034058Example 40Synthesis of Arg25'3‘Lys"”(N‘-(y—glutamyl(N“-hexadecanoyl)))—GLP—1 (7-3'8)-OH.A mixture of Arg2°'3‘Lys°°—GLP-1(7-38)-OH (14 mg, 4.0 umol), EDPA (14.3 mg, 110.6pmol), NMP (980 pl) and water (980 ul) was gently shaken for 5 min. at room temperature.To the resulting mixture was added a solution of N“-hexadecanoyl-G|u(ONSu)-OBu‘ ,prepared as described in Example 35. (6.4 mg, 11.9 umol) in NMP (160 pi), and thereaction mixture was gently shaken for 1 h and 20 min. at room temperature. The reactionwas quenched by the addition of a solution of glycine (6.5 mg, 87 mmol) in 50% aqueousethanol (653 pl). A 0.5 % aqueous solution of ammonium-acetate (50 ml) was added, andthe resulting mixture eluted onto a Varian 1g C8 Mega Bond Elut® cartridge, theimmobilised compound washed with 5% aqueous acetonitrile (10 ml), and finally liberatedfrom the cartridge by elution with TFA (6 ml). The eluate was allowed to stand for 1 h and30 min. at room temperature and then concentrated in vacuo. The residue was purified bycolumn chromatography using a cyanopropyl column (Zorbax 300SB-CN) and a standardacetonitrile/TFA system. The column was heated to 65°C and the acetonitrile gradient was0-100% in 60 minutes. The title compound (7.2 mg, 47 %) was isolated, and the productwas analysed by PDMS. The m/z value for the protonated molecular ion was found to be3881 i 3. The resulting molecular weight is thus 3880 1 3 amu (theoretical value 3880amu).Example 41Synthesis of Arg""23-26'3°'3“Lys3”(N‘-hexadecanoyl)-GLP-1(7-38)-OH.A mixture of Arg‘“3'2“'°°'3“Lys°“’—GLP-1(7-38)-OH (1.0 mg, 0.27 umol), EDPA (0.34 mg, 2.7umol) and DMSO (600 pl) was gently shaken for 5 min. at room temperature. To theresulting mixture was added a solution of Pal—ONSu (0.28 mg, 0.8 umol) in NMP (7 ul).The reaction mixture was gently shaken for 5 min. at room temperature, and then allowedto stand for an additional 6 h at room temperature. The reaction was quenched by theaddition of a solution of glycine (1.6 mg, 21.7 pmol) in 50% aqueous ethanol (163 pl). Thereaction mixture was purified by column chromatography using a cyanopropyl column(Zorbax 300SB-CN) and a standard acetonitrile/T FA system. The column was heated to65°C and the acetonitrile gradient was 0-100% in 60 minutes. The title comggimd ( 0.17mg, 16 %) was isolated, and the product was analysed by MALDI-MS. The m/z value for51015202530CA 02264243 1999-02-25wo 93/03371 PCT/DK97/0034059the protonated molecular ion was found to be 3961 i 3. The resulting molecular weight isthus 3960 t 3 amu (theoretical value 3960 amu).Example 42Synthesis of Arg”-3‘Lys”(N‘-(tn-carboxytridecanoyl))-GLP-1(7-38)-OH.A mixture of Arg’°'3“Lys3"-GLP-1(7-38)—OH (14 mg, 4.0 umol), EDPA (14.3 mg, 111 umol),NMP (980 pi) and water (980 pl) was gently shaken for 5 min. at room temperature. To theresulting mixture was added a solution of HOOC-(CH2),2-COONSu (4.2 mg, 11.9 umol) inNMP (105 pl), the reaction mixture was gently shaken for 1 h and 50 min. at roomtemperature. The reaction was quenched by the addition of a solution of glycine (6.5 mg,87 umol) in 50% aqueous ethanol (652 pl). The reaction mixture was purified by columnchromatography using a cyanopropyl column (Zorbax 3OOSB-CN) and a standardacetonitri|efT FA system. The column was heated to 65°C and the acetonitrile gradient was0-100% in 60 minutes. The title compound (5.8 mg, 39 %) was isolated, and the productwas analysed by MALDl—MS. The m/z value for the protonated molecular ion was found tobe 3780 i 3. The resulting molecular weight is thus 3779 : 3 amu (theoretical value 3781amu).Example 43Synthesis of Arg3‘Lys26(N‘-(y-glutamyl(N“—tetradecanoyl)))-GLP-1(7-37)—OH.A mixture of Arg3“-GLP-1(7-37)-OH (15 mg, 4.4 umol), EDPA (16 mg, 124 umol), NMP (2ml) and water (4.8 ml ) was gently shaken for 5 min. at room temperature. To the resultingmixture was added a solution of N“-tetradecanoyl—Glu(ONSu)-OBu‘ , prepared asdescribed in Example 29, (12.1 mg, 23.7 umol) in NMP (303 pi), and the reaction mixturewas gently shaken for 2 h at room temperature. The reaction was quenched by theaddition of a solution of glycine (6.5 mg, 86.9 umol) in 50% aqueous ethanol (652 pl). A0.5 % aqueous solution of ammonium-acetate (50 ml) was added, and the resultingmixture eluted onto a Varian 1g C8 Mega Bond Elut® cartridge, the immobilised compoundwashed with 5% aqueous acetonitrile (15 ml), and finally liberated from the cartridge byelution with TFA (6 ml). The eluate was allowed to stand for 1 h and 45 min. at roomtemperature and then concentrated in vacuo. The residue was purified by column..........w..l..u.......A.....__.......—........_....._.. .. .1015202530CA 02264243 1999-02-25WO 98/08871 PCT/DK97/0034060chromatography using a cyanopropyl column (Zorbax 300SB-CN) and a standardacetonitrilefTFA system. The column was heated to 65°C and the acetonitrile gradient was0-100% in 60 minutes. The title compound (3.9 mg, 26 %) was isolated, and the productwas analysed by MALDI-MS. The m/z value for the protonated molecular ion was found tobe 3723 i 3. The resulting molecular weight is thus 3722 :5 3 amu (theoretical value 3723amu).Example 44Synthesis of N“-octadecanoyl-Glu(ONSu)-OBu‘.To a suspension of H-Glu(OH)-OBu‘(2.82 g, 13.9 mmol), DMF (370 ml) and EDPA (1.79 g,13.9 mmol) was added drop by drop a solution of Ste-ONSu (5.3 g, 13.9 mmol) in DMF (60ml). Dichloromethane (35 ml) was added, and the reaction mixture was stirred for 24 h atroom temperature and then concentrated in vaguo. The residue was partitioned between10% aqueous citric acid (330 ml) and ethyl acetate (200 ml), and the phases wereseparated. The organic phase was concentrated in vagug and the residue dissolved inDMF (60 ml). The resulting solution was added drop by drop to a 10% aqueous solution ofcitric acid (400 ml) kept at 0 °C. The precipitated compound was collected and washedwith iced water and dried in a vacuum drying oven. The dried compound was dissolved inDMF (40 ml) and HONSu (1.63 g, 14.2 mmol) was added. To the resulting mixture wasadded a solution of DCC (2.66 g, 12.9 mmol) in dichloromethane (51 ml). The reactionmixture was stirred for 64 h at room temperature, and the precipitated compound wasfiltered off. The precipitate was recrystallised from n-heptane/2-propanol to give the flt_le_compound (4.96 g, 68 %).Example 45Synthesis of Argze-3‘Lys3°(N‘-(y-glutamyl(N“-octadecanoyl)))-GLP-1(7-38)-OH.A mixture of Arg2°'3‘—GLP-1(7-38)—OH (28 mg, 7.9 pmol), EDPA (28.6 mg, 221.5 pmol),NMP (1.96 ml) and water (1.96 ml )was gently shaken for 5 min. at room temperature. Tothe resulting mixture was added a solution of N“-octadecanoyl-GIu(ONSu)-OBu‘ (17.93 g,31.6 pmol), prepared as described in Example 44, in NMP (448 pl), and the reactionmixture was gently shaken for 2 h at room temperature. The reaction was quenched by theaddition of a solution of glycine (13.1 mg, 174 pmol) in 50% aqueous ethanol (1.3 ml). A1015202530CA 02264243 1999-02-25wo 93/03371 PCT/DK97/00340610.5 % aqueous solution of ammonium—acetate (120 ml) was added, and the resultingmixture was divided into two equal portions. Each portion was eluted onto a Varian 5 g C8Mega Bond Elut® cartridge, the immobilised compound washed with 5% aqueousacetonitrile (25 ml), and finally liberated from the cartridge by elution TFA (25 ml). Thecombined eluates were allowed to stand for 1 h and 25 min. at room temperature and thenconcentrated in vaggg. The residue was purified by column chromatography using acyanopropyl column (Zorbax 300SB-CN) and a standard acetonitrile/T FA system. Thecolumn was heated to 65°C and the acetonitrile gradient was 0-100% in 60 minutes. Thetitle compound (3.6 mg, 11 %) was isolated, and the product was analysed by MALDI-MS.The m/z value for the protonated molecular ion was found to be 3940 i 3. The resultingmolecular weight is thus 3939 i 3 amu (theoretical value 3937 amu).BIOLOGICAL FINDINGSProtraction of GLP-1 derivatives after s.c. administrationThe protraction of a number GLP-1 derivatives of the invention was determined bymonitoring the concentration thereof in plasma after so administration to healthy pigs,using the method described below. For comparison also the concentration in plasma ofGLP-1(7-37) after so. administration was followed. The results are given in Table 1. Theprotraction of other GLP-1 derivatives of the invention can be determined in the same way.Pigs (50% Duroc, 25% Yorkshire, 25% Danish Landrace, app 40 kg) were fasted from thebeginning of the experiment. To each pig 0.5 nmol of test compound per kg body weightwas administered in a 50 pM isotonic solution (5 mM phosphate, pH 7.4, 0.02% Tween®-20 (Merck), 45 mg/ml mannitol (pyrogen free, Novo Nordisk). Blood samples were drawnfrom a catheter in vena jugularis at the hours indicated in Table 1. 5 ml of the bloodsamples were poured into chilled glasses containing 175 pl of the following solution: 0.18M EDTA, 1500 KIE/ml aprotinin (Novo Nordisk) and 3% bacitracin (Sigma), pH 7.4. Within30 min, the samples were centrifuged for 10 min at 5-6000*g. Temperature was kept at4°C. The supernatant was pipetted into different glasses and kept at minus 20°C until use.The plasma concentrations of the peptides were determined by RIA using a monoclonalantibody specific for the N-terminal region of GLP-1(7-37). The cross reactivities were lessCA 02264243 2001-05-28WO 98/08871 PCT/DK97/0034062than 1% with GLP-1(1-37) and GLP-1(8-36)amide and < 0.1% with GLP-1(9-37), GLP-1(10-36)amide and GLP—1(11~36)arnide. The entire procedure was carried out at 4°C.The assay was carried out as follows: 100 pl plasma was mixed with 271 pl 96% ethanol,.3 mixed using a vortex mixer and centrifuged at 2600'g for 30 min. The supernatantwasdecanted into Minisorp” tubes and evaporated completely (Savant speedvacw As290)_ Theevaporation residue was reconstituted in the assay buffer consisting of 80 mMNaH2PO./Na2HPO.. 0.1 % HSA (Orpha 20/21, Behring), 10 mM EDTA, 0.6 mM thiomersal(Sigma), pH 7.5. Samples were reconstituted in volumes suitable for their expected10 concentrations, and were allowed to reconstitute for 30 min. To 300 pl sample, 100 plantibody solution in -dilution buffer containing 40 mM NaH2PO./Na,HPO., 0.1 % HSA, 0.6mM thiomersal. pH 7.5, was added. A non-specific sample was prepared by mixing 300 plbuffer with 100 pl dilution buffer. Individual standards were prepared from freeze driedstocks, dissolved in 300 pl assay buffer. All samples were pre-incubated in Minisorp tubes15 with antibody as described above for 72 h. 200 pl tracer in dilution buffer containing 6-7000CPM was added, samples were mixed and incubated for 48 h. 1.5 ml of a suspension of200 ml per litre of heparin-stabilised bovine plasma and 18 g per litre of activated carbon(Merck) in 40 mM NaH2F’O./Na,HPO.. 0.6 mM thiomersal. pH 7.5, was added to eachtube. Before use, the suspension was mixed and allowed to stand for 2 h at 4°C. All210 samples were incubated for 1 h at 4°C and then centrifuged at 3400"g for 25 min.Immediately after the centrifugation. the supernatant was decanted and counted in a y-counter. The concentration in the samples was calculated from individual standard curves.The following plasma concentrations were found, calculated as % of the maximumconcentration for the individual compounds (n=2):2535101520CA 02264243 1999-02-25WO 98/08871 PCT/DK97/0034063Table 1Test Hours after so. administrationcompound"0.75 1 2 4 6 8 10 12 24GLP-1 (7-37) 100 9 1Example 25 73 92 100 98 82 24 16 16 16Example 17 76 71 91 100 84 68 30 9Example 43 39 71 93 100 91 59 50 17Example 37 26 38 97 100 71 81 80 45Example 11 24 47 59 71 100 94 100 94Example 12 36 54 65 94 80 100 85 93Example 32 55 53 90 83 88 70 98 100 100Example 14 18 25 32 47 98 83 97 100Example 13 15 22 38 59 97 85 100 76Example 38 60 53 100 66 48 39 25 29 0Example 39 38 100 70 47 33 33 18 27 14Example 40 47 19 50 100 51 56 34 14 0Example 34 19 32 44 84 59 66 83 84 100"The test compounds are the title compounds of the examples with the numbers givenAs it appears from Table 1, the GLP-1 derivatives of the invention have a protracted profileof action relative to GLP-1(7-37) and are much more persistent in plasma than GLP-1(7-37). it also appears from Table 1 that the time at which the peak concentration in plasma isachieved varies within wide limits, depending on the particular GLP-1 derivative selected.Stimulation of cAMP formation in a cell line expressing the cloned human GLP-1receptorIn order to demonstrate efficacy of the GLP-1 derivatives, their ability to stimulateformation of CAMP in a cell line expressing the cloned human GLP-1 receptor was tested.An EC5,, was calculated from the dose-response curve.Baby hamster kidney (BHK) cells expressing the human pancreatic GLP-1 receptor wereused (Knudsen and Pridal, 1996, Eur. J. Pharm. 318, 429-435). Plasma membranes wereprepared (Adelhorst et al, 1994, J. Biol. Chem. 269, 6275) by homogenisation in buffer (10mmol/l Tris-HCl and 30 mmol/l NaCl pH 7.4, containing, in addition, 1 mmol/l dithiothreitol, 5mg/l leupeptin (Sigma, St. Louis, MO, USA), 5 mg/l pepstatin (Sigma, St. Louis, MO, USA),100 mg/l bacitracin (Sigma, St. Louis, MO, USA), and 16 mg/l aprotinin (Novo Nordisk A/S,CA 02264243 1999-02-25W0 98/08871 PCT/DK97/0034064Bagsvaerd, Denmark)). The homogenate was centrifuged on top of a layer of 41 w/v%sucrose. The white band between the two layers was diluted in buffer and centrifuged.Plasma membranes were stored at -80°C until used.5 The assay was carried out in 96-well microtiter plates in a total volume of 140 pl. The bufferused was 50 mmol/I Tris-HCl, pH 7.4 with the addition of 1 mmol/l EGTA, 1.5 mmol/l MgSO,,.1.7 mmol/l ATP, 20 mM GTP, 2 mmol/I 3-isobutyl-1-methylxanthine, 0.01 % Tween-20 and0.1 % human serum albumin (Reinst, Behringwerke AG, Marburg, Germany). Compounds tobe tested for agonist activity were dissolved and diluted in buffer, added to the membrane10 preparation and the mixture was incubated for 2 h at 37°C. The reaction was stopped by theaddition of 25 ul of 0.05 mol/l HCl. Samples were diluted 10 fold before analysis for cAMP bya scintillation proximity assay (RPA 538, Amersham, UK). The following results were found:Test compound" EC50, pM Test compound" EC:-,0, pMGLP-1 (7-37) 61 Example 31 96Example 45 120 Example 30 41Example 43 24 Example 26 8.8Example 40 55 Example 25 99Example 39 5.1 Example 19 79Example 38 54 Example 16 3.5Example 37 6015 " The test compounds are the title compounds of the examples with the numbers given.CA 02264243 1999-08-2564aSEQUENCE LISTING(1) GENERAL INFORMATION:(i) APPLICANT: NOVO NORDISK A/S(ii) TITLE OF INVENTION: GLP-l DERIVATIVES(iii) NUMBER OF SEQUENCES: 96(iV) CORRESPONDENCE ADDRESS:(A) ADDRESSEE: SWABEY OGILVY RENAULT(B) STREET: 1981 McGill College Avenue, Suite 1600(C) CITY: Montréal(D) STATE: QC(E) COUNTRY: CANADA(F) ZIP: H3A 2Y3(V) COMPUTER READABLE FORM:(A) MEDIUM TYPE: Diskette(B) COMPUTER: IBM Compatible(C) OPERATING SYSTEM: Windows(D) SOFTWARE: FastSEQ for Windows Version 2.0b(vi) CURRENT APPLICATION DATA:(A) APPLICATION NUMBER: 2,264,243(B) FILING DATE: 22-AUG-1997(C) CLASSIFICATION:(Vii) PRIOR APPLICATION DATA:(A) APPLICATION NUMBER: DK 0931/96(B) FILING DATE: 30-AUG-1996(A) APPLICATION NUMBER: DK 1259/96(B) FILING DATE: 08—NOV—l996(A) APPLICATION NUMBER: DK 1470/96(B) FILING DATE: 20—DEC-1996(viii) ATTORNEY/AGENT INFORMATION:(A) NAME: Cété, France(B) REGISTRATION NUMBER: 4166(C) REFERENCE/DOCKET NUMBER: 11667-10 FC/ntb(ix) TELECOMMUNICATION INFORMATION:(A) TELEPHONE: 514-845-7126(B) TELEFAX: 514-288-8389(C) TELEX:(2) INFORMATION FOR SEQ ID NO:1:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acidCA 02264243 1999-08-2564b(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Lys Gly Arg Gly20 25 30(2) INFORMATION FOR SEQ ID NO:2:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly20 25 30(2) INFORMATION FOR SEQ ID NO:3:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu Val Lys Gly Lys Gly20 25 30(2) INFORMATION FOR SEQ ID NO:4:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: proteinCA 02264243 1999-08-2564c(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly20 25 30(2) INFORMATION FOR SEQ ID NO:5:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 32 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly Arg20 25 30(2) INFORMATION FOR SEQ ID NO:6:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30Lys(2) INFORMATION FOR SEQ ID NO:7:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 34 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:CA 02264243 1999-08-2564dHis Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30Arg Lys(2) INFORMATION FOR SEQ ID NO:8:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Lys Gly Lys Gly20 25 30(2) INFORMATION FOR SEQ ID N029:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:9:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly20 25 30(2) INFORMATION FOR SEQ ID NO:l0:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:l0:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15CA 02264243 1999-08-2564eGln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Lys Gly Arg Gly Arg20 25 30Lys(2) INFORMATION FOR SEQ ID NO:ll:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 34 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:ll:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30Arg Lys(2) INFORMATION FOR SEQ ID NO:l2:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:12:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly Arg20 25 30Lys(2) INFORMATION FOR SEQ ID NO:l3:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 34 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:l3:CA 02264243 1999-08-2564fHis Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly Arg20 25 30Arg Lys(2) INFORMATION FOR SEQ ID NO:l4:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:l4:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Lys Gly Arg Gly20 25 30(2) INFORMATION FOR SEQ ID NO:15:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:15:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly20 25 30(2) INFORMATION FOR SEQ ID NO:l6:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:l6:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15CA 02264243 1999-08-2564gGln Ala Ala Lys Glu Phe Ile Ala Trp Leu Val Lys Gly Lys Gly20 25 30(2) INFORMATION FOR SEQ ID NO:17:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:17:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly20 25 30(2) INFORMATION FOR SEQ ID NO:l8:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:l8:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30Lys(2) INFORMATION FOR SEQ ID NO:l9:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 34 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:l9:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30Arg LysCA 02264243 1999-08-2564h(2) INFORMATION FOR SEQ ID NO:20:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:20:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Lys Gly Lys Gly20 25 30(2) INFORMATION FOR SEQ ID NO:21:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:21:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Glyl 5 10 15Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly20 25 30(2) INFORMATION FOR SEQ ID NO:22:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:22:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Lys Gly Arg Gly Arg20 25 30Lys(2) INFORMATION FOR SEQ ID NO:23:CA 02264243 1999-08-2564i(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 34 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:23:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30Arg Lys(2) INFORMATION FOR SEQ ID NO:24:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:24:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly Arg20 25 30Lys(2) INFORMATION FOR SEQ ID NO:25:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 34 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:25:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly Arg20 25 30Arg LysCA 02264243 1999-08-25543'(2) INFORMATION FOR SEQ ID NO:26:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 32 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:26:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Lys20 25 30(2) INFORMATION FOR SEQ ID NO:27:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:27:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30Lys(2) INFORMATION FOR SEQ ID NO:28:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 34 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:28:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30Arg Lys(2) INFORMATION FOR SEQ ID NO:29:CA 02264243 1999-08-2564k(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 35 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:29:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly15301 5 10Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25Arg Glu Lys35(2) INFORMATION FOR SEQ ID NO:30:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 36 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:30:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly15301 5 10Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25Arg Glu Phe Lys35(2) INFORMATION FOR SEQ ID NO:3l:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 37 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:3l:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 1015Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25Arg Glu Phe Pro Lys3530CA 02264243 1999-08-25641(2) INFORMATION FOR SEQ ID NO:32:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 38 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:32:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Glyl 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30Arg Glu Phe Pro Glu Lys35(2) INFORMATION FOR SEQ ID NO:33:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 39 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:33:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Glyl 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30Arg Glu Phe Pro Glu Glu Lys35(2) INFORMATION FOR SEQ ID NO:34:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 38 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:34:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Arg Gly Arg Gly Lys35CA 02264243 1999-08-2564m(2) INFORMATION FOR SEQ ID NO:35:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 39 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear‘(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:35:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Arg Gly Arg Gly Arg Lys35(2) INFORMATION FOR SEQ ID NO:36:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 40 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:36:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Arg Gly Arg Gly Arg Arg Lys35 40(2) INFORMATION FOR SEQ ID NO:37:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 41 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:37:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30CA 02264243 1999-08-2564nVal Arg Gly Arg Gly Arg Arg Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:38:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 42 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:38:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Arg Gly Arg Gly Arg Arg Glu Phe Lys35 40(2) INFORMATION FOR SEQ ID NO:39:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 43 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:39:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Arg Gly Arg Gly Arg Arg Glu Phe Pro Lys35 40(2) INFORMATION FOR SEQ ID NO:40:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 44 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:40:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15CA 02264243 1999-08-25640Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Arg Gly Arg Gly Arg Arg Glu Phe Pro Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:4l:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 45 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:41:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Arg Gly Arg Gly Arg Arg Glu Phe Pro Glu Glu Lys35 40 45(2) INFORMATION FOR SEQ ID NO:42:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 37 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:42:Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser1 5 10 15Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val20 25 30Arg Gly Arg Gly Lys35(2) INFORMATION FOR SEQ ID NO:43:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 38 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:43:CA 02264243 1999-08-2564pAsp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser1 5 10 15Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val20 25 30Arg Gly Arg Gly Arg Lys35(2) INFORMATION FOR SEQ ID NO:44:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 39 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:44:Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser1 5 10 15Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val20 25 30Arg Gly Arg Gly Arg Arg Lys35(2) INFORMATION FOR SEQ ID NO:45:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 40 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:45:Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser1 5 10 15Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val20 25 30Arg Gly Arg Gly Arg Arg Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:46:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 41 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: proteinCA 02264243 1999-08-2564q(xi) SEQUENCE DESCRIPTION: SEQ ID NO:46:Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser1 5 10 15Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val20 25 30Arg Gly Arg Gly Arg Arg Glu Phe Lys35 40(2) INFORMATION FOR SEQ ID NO:47:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 42 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:47:Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser1 5 10 15Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val20 25 30Arg Gly Arg Gly Arg Arg Glu Phe Pro Lys35 40(2) INFORMATION FOR SEQ ID NO:48:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 43 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:48:Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser1 5 10 15Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val20 25 30Arg Gly Arg Gly Arg Arg Glu Phe Pro Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:49:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 44 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: proteinCA 02264243 1999-08-2564r(xi) SEQUENCE DESCRIPTION: SEQ ID NO:49:Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser1 5 1015Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val20 25Arg Gly Arg Gly Arg Arg Glu Phe Pro Glu Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:50:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 36 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:50:30Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser15301 5 10Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg20 25Gly Arg Gly Lys35(2) INFORMATION FOR SEQ ID NO:51:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 37 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:51:Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser1530l 5 10Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg20 25Gly Arg Gly Arg Lys35(2) INFORMATION FOR SEQ ID NO:52:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 38 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linearCA 02264243 1999-08-25645(ii) MOLECULE TYPE: peptide(xi) SEQUENCE DESCRIPTION: SEQ ID NO:52:Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser1 5 10 15Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg20 25 30Gly Arg Gly Arg Arg Lys35(2) INFORMATION FOR SEQ ID NO:53:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 39 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:53:Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser1 5 10 15Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg20 25 30Gly Arg Gly Arg Arg Glu Lys35(2) INFORMATION FOR SEQ ID NO:54:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 40 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:54:Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser1 5 10 15Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg20 25 30Gly Arg Gly Arg Arg Glu Phe Lys35 40(2) INFORMATION FOR SEQ ID NO:55:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 41 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linearCA 02264243 1999-08-2564t(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:55:Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser1 5 10 15Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg20 25 30Gly Arg Gly Arg Arg Glu Phe Pro Lys35 40(2) INFORMATION FOR SEQ ID NO:56:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 42 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID N0:56:Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser1 5 10 15Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg20 25 30Gly Arg Gly Arg Arg Glu Phe Pro Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:57:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 43 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:57:Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser1 5 10 15Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg20 25 30Gly Arg Gly Arg Arg Glu Phe Pro Glu Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:58:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 35 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: singleCA 02264243 1999-08-2564u(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:58:Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr1 5 10 15Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly20 25 30Arg Gly Lys35(2) INFORMATION FOR SEQ ID NO:59:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 36 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:59:Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr1 5 10 15Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly20 25 30Arg Gly Arg Lys35(2) INFORMATION FOR SEQ ID NO 60:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 37 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:60:Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyrl 5 10 15Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly20 25 30Arg Gly Arg Arg Lys35(2) INFORMATION FOR SEQ ID NO:6l:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 38 amino acids(B) TYPE: amino acidCA 02264243 1999-08-2564V(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:6l:Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyrl 5 10 15Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly20 25 30Arg Gly Arg Arg Glu Lys35(2) INFORMATION FOR SEQ ID NO:62:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 39 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:62:Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr1 5 10 15Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly20 25 30Arg Gly Arg Arg Glu Phe Lys35(2) INFORMATION FOR SEQ ID NO:63:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 40 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: Single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:63:Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr1 5 10 15Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly20 25 30Arg Gly Arg Arg Glu Phe Pro Lys35 40(2) INFORMATION FOR SEQ ID NO:64:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 41 amino acidsCA 02264243 1999-08-2564w(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:64:Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr1 5 10 15Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly20 25 30Arg Gly Arg Arg Glu Phe Pro Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:65:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 42 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:65:Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr1 5 10 15Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly20 25 30Arg Gly Arg Arg Glu Phe Pro Glu Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:66:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 34 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:66:Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu1 5 10 15Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg20 25 30Gly Lys(2) INFORMATION FOR SEQ ID NO:67:(i) SEQUENCE CHARACTERISTICS:CA 02264243 1999-08-2564x(A) LENGTH: 35 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:67:Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu1 5 10 15Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg20 25 30Gly Arg Lys35(2) INFORMATION FOR SEQ ID NO:68:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 36 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:68:Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu1 5 10 15Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg20 25 30Gly Arg Arg Lys35(2) INFORMATION FOR SEQ ID NO:69:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 37 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: peptide(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:69:Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu1 5 10 15Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg20 25 30Gly Arg Arg Glu Lys35(2) INFORMATION FOR SEQ ID NO:70:CA 02264243 1999-08-2564y(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 38 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: peptide(xi) SEQUENCE DESCRIPTION: SEQ ID NO:70:Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu1 5 10 15Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg20 25 30Gly Arg Arg Glu Phe Lys35(2) INFORMATION FOR SEQ ID NO:7l:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 39 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:7l:Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu1 5 10 15Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg20 25 30Gly Arg Arg Glu Phe Pro Lys35(2) INFORMATION FOR SEQ ID NO:72:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 40 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:72:Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu1 5 10 15Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg20 25 30Gly Arg Arg Glu Phe Pro Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:73:CA 02264243 1999-08-25642(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 41 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:73:Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu1 5 10 15Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg20 25 30Gly Arg Arg Glu Phe Pro Glu Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:74:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:74:Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu1 5 10 15Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly20 25 30Lys(2) INFORMATION FOR SEQ ID NO:75:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 34 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:75:Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu1 5 10 15Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly20 25 30Arg LysCA 02264243 1999-08-2564aa(2) INFORMATION FOR SEQ ID NO:76:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 35 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:76:Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu1 5 10 15Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly20 25 30Arg Arg Lys35(2) INFORMATION FOR SEQ ID NO:77:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 36 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:77:Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu1 5 10 15Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly20 25 30Arg Arg Glu Lys35(2) INFORMATION FOR SEQ ID NO:78:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 37 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:78:Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu1 S 10 15Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly20 25 30Arg Arg Glu Phe Lys35CA 02264243 1999-08-2564bb(2) INFORMATION FOR SEQ ID NO:79:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 38 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:79:Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu1 5 10 15Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly20 25 30Arg Arg Glu Phe Pro Lys35(2) INFORMATION FOR SEQ ID NO:80:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 39 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:80:Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu1 5 10 15Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly20 25 30Arg Arg Glu Phe Pro Glu Lys35(2) INFORMATION FOR SEQ ID NO:81:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 40 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:8l:Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu1 5 10 15Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly20 25 30CA 02264243 1999-08-2564ccArg Arg Glu Phe Pro Glu Glu Lys35 40(2) INFORMATION FOR SEQ ID NO:82:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 38 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:82:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Lys Gly Arg Gly Lys35(2) INFORMATION FOR SEQ ID NO:83:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 38 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:83:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu20 ~ 25 30Val Arg Gly Arg Gly Lys35(2) INFORMATION FOR SEQ ID NO:84:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 38 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:84:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15CA 02264243 1999-08-2564ddSer Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Arg Gly Lys Gly Lys35(2) INFORMATION FOR SEQ ID NO:85:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 32 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:85:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Lys Gly Arg Gly Lys20 25 30(2) INFORMATION FOR SEQ ID NO:86:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 32 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:86:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Lys20 25 30(2) INFORMATION FOR SEQ ID NO:87:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 32 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:87:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly Lys20 25 30CA 02264243 1999-08-2564ee(2) INFORMAT'ION FOR SEQ ID NO:88:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 32 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:88:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Lys20 25 30(2) INFORMATION FOR SEQ ID NO:89:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 39 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: s ingle(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:89:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Lys Gly Arg Gly Arg Lys35(2) INFORMATION FOR SEQ ID NO:90:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 39 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:90:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu20 25 30Val Arg Gly Arg Gly Arg Lys35(2) INFORMATION FOR SEQ ID NO:91:CA 02264243 1999-08-2564ff(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 39 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:91:His Asp Glu Phe Glu Arg His Ala Glu Gly Thr Phe Thr Ser Asp Val1 5 10 15Ser Ser Tyr Leu Glu Gly Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu20 25 30Val Arg Gly Lys Gly Arg Lys35(2) INFORMATION FOR SEQ ID NO:92:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:92:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Lys Gly Arg Gly Arg20 25 30Lys(2) INFORMATION FOR SEQ ID NO:93:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:93:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Lys Glu Phe Ile Ala Trp Leu Val Arg Gly Arg Gly Arg20 25 30LysCA 02264243 1999-08-256499(2) INFORMAT'ION FOR SEQ ID NO:94:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:94:His Ala Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly Arg20 25 30Lys(2) INFORMATION FOR SEQ ID N0:95:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 32 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID N0:95:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Lys Gly Arg Gly Lys20 25 30(2) INFORMATION FOR SEQ ID NO:96:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 32 amino acids(B) TYPE: amino acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(Xi) SEQUENCE DESCRIPTION: SEQ ID NO:96:His Gly Glu Gly Thr Phe Thr Ser Asp Val Ser Ser Tyr Leu Glu Gly1 5 10 15Gln Ala Ala Arg Glu Phe Ile Ala Trp Leu Val Arg Gly Lys Gly Lys20 25 30

Claims (40)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. A GLP-1 derivative of formula I (SEQ ID NO:2):

His-Xaa-Xaa-Gly-Xaa-Phe-Thr-Xaa-Asp-Xaa-Xaa Xaa-Xaa-Xaa-Xaa-Xaa-Xaa-Xaa-Xaa-Xaa-Xaa-Phe Ile-Xaa-Xaa-Xaa-Xaa-Xaa-Xaa-Xaa-Xaa wherein Xaa at position 8 is Ala, Xaa at position 9 is Glu, Xaa at position 11 is Thr, Xaa at position 14 is Ser, Xaa at position 16 is Val, Xaa at position 17 is Ser, Xaa at position 18 is Ser, Xaa at position 19 is Tyr, Xaa at position 20 is Leu, Xaa at position 21 is Glu, Xaa at position 22 is Gly, Xaa at position 23 is Gln, Xaa at position 24 is Ala, Xaa at position 25 is Ala, Xaa at position 26 is Lys, Xaa at position 27 is Glu, Xaa at position 30 is Ala, Xaa at position 31 is Trp, Xaa at position 32 is Leu, Xaa at position 33 is Val, Xaa at position 34 is Arg, Xaa at position 35 is Gly, Xaa at position 36 is Arg, and Xaa at position 37 is Gly, wherein (a) the .epsilon.-amino group of Lys at position 26 is substituted with a lipophilic substituent, optionally via a spacer, (b) the lipophilic substituent is (i) CH3(CH2)n CO - wherein n is 6, 8, 10, 12, 14, 16, 18, 20 or 22, (ii) HOOC(CH2)m CO - wherein m is 10, 12, 14, 16, 18, 20 or 22, or (iii) lithochoyl, and (c) the spacer is (i) an unbranched alkane .alpha.,.omega.-dicarboxylic acid group having from 1 to 7 methylene groups, (ii) an amino acid residue except Cys, or (iii) .gamma.-aminobutanoyl.
2. The GLP-1 derivative of claim 1, wherein the lipophilic substituent is linked to the .omega.-amino group of Lys via a spacer.
3. The GLP-1 derivative of claim 2, wherein the spacer is .gamma.-glutamyl.
4. The GLP-1 derivative of claim 2, wherein the spacer is .beta.-asparagyl.
5. The GLP-1 derivative of claim 2, wherein the spacer is glycyl.
6. The GLP-1 derivative of claim 2, wherein the .gamma.-aminobutanoyl.
7. The GLP-1 derivative of claim 2, wherein the .beta.-alanyl.
8. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon.-tetradecanoyl), Arg34-GLP-1(7-37).
9. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon.-(.omega.-carboxynonadecanoyl)), Arg34-GLP-1(7-37).
10. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.omega.-carboxyheptadecanoyl)), Arg34-GLP-1(7-37).
11. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.omega.-carboxyundecanoyl)), Arg34-GLP-1(7-37).
12. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.omega.-carboxypentadecanoyl)), Arg34-GLP-1(7-37).
13. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -lithochoyl),Arg34-GLP-1(7-37).
14. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.gamma.-glutamyl(N.alpha.-hexadecanoyl))), Arg34-GLP-1(7-37).
15. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.gamma.glutamyl(N.alpha. tetradecanoyl))), Arg34-GLP-1(7-37).
16. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.gamma.glutamyl(N.alpha. lithochoyl))), Arg34-GLP-1(7-37).
17. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.gamma.glutamyl(N.alpha. octadecanoyl))), Arg34-GLP-1(7-37).
18. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -decanoyl), Arg34-GLP-1(7-37).
19. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -hexadecanoyl), Arg34-GLP-1(7-37).
20. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -octanoyl), Arg34-GLP-1(7-37).
21. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -dodecanoyl), Arg34-GLP-1(7-37).
22. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. (N68 (.gamma.aminobutyroyl-(N.gamma.-hexadecanoyl))), Arg34-GLP-1(7-37).
23. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.gamma.-D
glutamyl(N.alpha.hexadecanoyl))), Arg34 -GLP-1(7-37).
24. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.gamma.glutamyl(N.alpha.-dodecanoyl))), Arg34-GLP-1(7-37).
25. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.beta.alanyl(N.alpha.-hexadecanoyl))), Arg34-GLP-1(7-37).
26. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.alpha.-glutamyl(N.alpha.-hexadecanoyl))), Arg34-GLP-1(7-37).
27. The GLP-1 derivative of claim 1, which is Lys26 (N.epsilon. -(.gamma.-glutamyl(N.alpha.-decanoyl))), Arg34-GLP-1(7-37).
28. A pharmaceutical composition comprising a GLP-1 derivative of claim 1 and a pharmaceutically acceptable vehicle or carrier.
29. A pharmaceutical composition of claim 28, further comprising an isotonic agent, a preservative and a buffer.
30. A pharmaceutical composition of claim 29, wherein the isotonic agent is sodium chloride, mannitol and glycerol.
31. A pharmaceutical composition of claim 29, wherein the preservative is phenol, m-cresol, methyl p-hydroxybenzoate or benzyl alcohol.
32. A pharmaceutical composition of claim 29, wherein the buffer is sodium acetate or sodium phosphate.
33. A pharmaceutical composition of claim 28, further comprising a surfactant.
34. A pharmaceutical composition of claim 28, further comprising zinc.
35. A pharmaceutical composition of claim 28, further comprising another antidiabetic agent.
36. A pharmaceutical composition of claim 35, wherein the antidiabetic agent is human insulin.
37. A pharmaceutical composition of claim 35, wherein the antidiabetic agent is a hypoglycemic agent.
38. A pharmaceutical composition of claim 28, further comprising another antiobesity agent.
39. Use of a derivative of any one of claims 1-27 for the preparation of a medicament for the treatment of diabetes.
40. Use of a derivative of any one of claims 1-27 for the preparation of a medicament for the treatment of obesity.
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