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
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    • A61K38/00—Medicinal preparations containing peptides
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    • 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
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    • 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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Families Citing this family (478)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE417622T1 (en) 1996-08-08 2009-01-15 Amylin Pharmaceuticals Inc REGULATION OF GASTROINTESTINAL MOBILITY
US7235627B2 (en) 1996-08-30 2007-06-26 Novo Nordisk A/S Derivatives of GLP-1 analogs
US6458924B2 (en) 1996-08-30 2002-10-01 Novo Nordisk A/S Derivatives of GLP-1 analogs
US6268343B1 (en) 1996-08-30 2001-07-31 Novo Nordisk A/S Derivatives of GLP-1 analogs
HU227021B1 (en) * 1996-08-30 2010-05-28 Novo Nordisk As Glp-1 derivatives
UA65549C2 (en) 1996-11-05 2004-04-15 Елі Ліллі Енд Компані Use of glucagon-like peptides such as glp-1, glp-1 analog, or glp-1 derivative in methods and compositions for reducing body weight
US6380357B2 (en) 1997-12-16 2002-04-30 Eli Lilly And Company Glucagon-like peptide-1 crystals
DE69942306D1 (en) 1998-02-27 2010-06-10 Novo Nordisk As ABSTRACT OF GLP-1 ANALOG
AU2610599A (en) * 1998-02-27 1999-09-15 Novo Nordisk A/S N-terminally truncated glp-1 derivatives
EP1840134B1 (en) * 1998-02-27 2016-04-13 Novo Nordisk A/S GLP-1 derivatives
JP2003522099A (en) 1998-02-27 2003-07-22 ノボ ノルディスク アクティーゼルスカブ GLP-1 derivative of GLP-1 having a delayed action profile and exendin
AU2610799A (en) * 1998-02-27 1999-09-15 Novo Nordisk A/S Glp-1 derivatives with helix-content exceeding 25 per cent, forming partially structured micellar-like aggregates
WO1999043707A1 (en) 1998-02-27 1999-09-02 Novo Nordisk A/S N-terminally modified glp-1 derivatives
IL138214A0 (en) 1998-03-09 2001-10-31 Zealand Pharmaceuticals As Pharmacolgically active peptide conjugates having a reduced tendency towards enzymatic hydrolysis
EP1100530B1 (en) * 1998-07-31 2003-10-08 Novo Nordisk A/S In-vitro stimulation of beta cell proliferation
EA200100289A1 (en) * 1998-08-28 2001-10-22 Эли Лилли Энд Компани METHOD OF ADMINISTRATION OF INSULINOTROPIC PEPTIDES
EP1666054A1 (en) * 1998-08-28 2006-06-07 Eli Lilly &amp; Company Method for administering insulinotropic peptides
US6720407B1 (en) 1998-08-28 2004-04-13 Eli Lilly And Company Method for administering insulinotropic peptides
CN1317967A (en) 1998-09-17 2001-10-17 伊莱利利公司 Protein formulations
MY155270A (en) * 1998-09-24 2015-09-30 Lilly Co Eli Use of glp-1 or analogs in treatment of stroke
US6903186B1 (en) 1998-12-07 2005-06-07 Societe De Conseils De Recherches Et D'applications Scientifiques, S.A.S Analogues of GLP-1
CA2778047A1 (en) * 1998-12-07 2000-06-15 Ipsen Pharma S.A.S Analogues of glp-1
HUP0104579A3 (en) * 1998-12-07 2002-05-28 Univ Tulane Glp-1 analogues, pharmaceutical compositions comprising thereof and their use
NZ512663A (en) * 1999-01-14 2004-05-28 Amylin Pharmaceuticals Inc Novel exendin agonist formulations and methods of administration thereof
US6451987B1 (en) 1999-03-15 2002-09-17 Novo Nordisk A/S Ion exchange chromatography of proteins and peptides
EP2348044A1 (en) 1999-03-15 2011-07-27 Novo Nordisk A/S Ion exchange chromatography of GLP-1, analogs and derivatives thereof
US6444788B1 (en) 1999-03-15 2002-09-03 Novo Nordisk A/S Ion exchange chromatography of GLP-1, analogs and derivatives thereof
JP4949557B2 (en) * 1999-03-17 2012-06-13 ノヴォ ノルディスク アー／エス Peptide acylation method and novel acylating agent
US6451974B1 (en) 1999-03-17 2002-09-17 Novo Nordisk A/S Method of acylating peptides and novel acylating agents
AU3273500A (en) 1999-03-17 2000-10-04 Novo Nordisk A/S Method for acylating peptides and novel acylating agents
US6924264B1 (en) 1999-04-30 2005-08-02 Amylin Pharmaceuticals, Inc. Modified exendins and exendin agonists
AU775063C (en) * 1999-04-30 2005-05-12 Amylin Pharmaceuticals, Inc. Modified exendins and exendin agonists
US6514500B1 (en) 1999-10-15 2003-02-04 Conjuchem, Inc. Long lasting synthetic glucagon like peptide {GLP-!}
EP1180121B9 (en) 1999-05-17 2004-09-08 Conjuchem, Inc. Long lasting insulinotropic peptides
EP1076066A1 (en) * 1999-07-12 2001-02-14 Zealand Pharmaceuticals A/S Peptides for lowering blood glucose levels
US6528486B1 (en) 1999-07-12 2003-03-04 Zealand Pharma A/S Peptide agonists of GLP-1 activity
US6569832B1 (en) 1999-11-12 2003-05-27 Novo Nordisk A/S Inhibition of beta cell degeneration
JP2003516322A (en) * 1999-11-12 2003-05-13 ノボ ノルディスク アクティーゼルスカブ Use of a GLP-1 agonist for inhibiting beta-cell degeneration
US6844321B2 (en) * 2000-01-31 2005-01-18 Novo Nordisk A/S Crystallization of a GLP-1 analogue
EP1263458B1 (en) 2000-03-08 2005-11-16 Novo Nordisk A/S Lowering serum cholesterol
DE10013895A1 (en) 2000-03-21 2001-10-04 Dmc2 Degussa Metals Catalysts Cerdec Ag Water gas shift reaction, useful in mobile unit in vehicle for removing carbon monoxide from gas mixture containing hydrogen for fuel cell, uses catalyst based on noble metal coating on inert carrier
BR0113178A (en) * 2000-08-02 2004-04-06 Theratechnologies Inc Modified biological peptides with increased potency
CA2430934C (en) 2000-12-01 2011-06-21 Takeda Chemical Industries, Ltd. A method of producing sustained-release preparations of a bioactive substance using high-pressure gas
JP2004528014A (en) * 2000-12-07 2004-09-16 イーライ・リリー・アンド・カンパニー GLP-1 fusion protein
IL156548A0 (en) 2000-12-21 2004-01-04 Aventis Pharma Gmbh Diphenyl azetidinone derivatives, method for the production thereof, medicaments containing these compounds, and their use
RS50864B (en) 2000-12-21 2010-08-31 Sanofi-Aventis Deutschland Gmbh. Novel 1,2-diphenzylazetidinones, method for producing the same, medicaments containing said compounds, and the use thereof for treating disorders of the lipid metabolism
AU2002235731A1 (en) * 2001-03-07 2002-09-19 Novo Nordisk A/S Combined use of derivatives of glp-1 analogs and ppar ligands
US6573237B2 (en) 2001-03-16 2003-06-03 Eli Lilly And Company Protein formulations
US8981061B2 (en) 2001-03-20 2015-03-17 Novo Nordisk A/S Receptor TREM (triggering receptor expressed on myeloid cells) and uses thereof
DE10142660A1 (en) 2001-08-31 2003-03-20 Aventis Pharma Gmbh Use of derivatives of C2-substituted indan-1-ol systems for the preparation of medicaments for the prophylaxis or treatment of obesity
US6653492B2 (en) 2001-05-02 2003-11-25 Novo Nordick A/S Preparation of bile acids
JP2004529160A (en) * 2001-05-02 2004-09-24 ノボ・ノルデイスク・エー／エス Bile acid production
PE20021091A1 (en) 2001-05-25 2003-02-04 Aventis Pharma Gmbh DERIVATIVES OF PHENYLUREA SUBSTITUTED WITH CARBONAMIDE AND PROCEDURE FOR THEIR PREPARATION
US20030119734A1 (en) 2001-06-28 2003-06-26 Flink James M. Stable formulation of modified GLP-1
US7595172B2 (en) 2001-07-24 2009-09-29 Novo Nordisk A/S Method for making acylated polypeptides
US20030082671A1 (en) 2001-07-24 2003-05-01 Thomas Hoeg-Jensen Method for making acylated polypeptides
JP2005501861A (en) 2001-08-22 2005-01-20 アベンティス・ファーマ・ドイチユラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング Combinations of 1,4-benzothiepine 1,1-dioxide derivatives with other active substances and their use
DE10142662B4 (en) 2001-08-31 2004-07-08 Aventis Pharma Deutschland Gmbh Derivatives of C2-substituted indan-1-ol systems and their use as pharmaceuticals
DE10142667B4 (en) 2001-08-31 2004-06-09 Aventis Pharma Deutschland Gmbh C2-substituted indan-1-oles and their derivatives and their use as medicines
DE10142661B4 (en) 2001-08-31 2004-06-09 Aventis Pharma Deutschland Gmbh Poly-substituted indan-1-ol systems and their use as pharmaceuticals
DE10142663B4 (en) 2001-08-31 2004-08-19 Aventis Pharma Deutschland Gmbh C2-Disubstituted indan-1-ol systems
DE10142722A1 (en) 2001-08-31 2003-03-27 Aventis Pharma Gmbh C2-substituted indan-1-ones and their derivatives, processes for their preparation and their use as medicaments
DE10142659A1 (en) 2001-08-31 2003-03-20 Aventis Pharma Gmbh Use of multiply substituted indan-1-ol. Systems for the preparation of medicaments for the prophylaxis or treatment of obesity
DE10142665B4 (en) 2001-08-31 2004-05-06 Aventis Pharma Deutschland Gmbh C2-Disubstituted indan-1-ones and their derivatives
US6884812B2 (en) 2001-08-31 2005-04-26 Aventis Pharma Deutschland Gmbh Diarylcycloalkyl derivatives, processes for their preparation and their use as pharmaceuticals
US7399777B2 (en) 2001-08-31 2008-07-15 Sanofi-Aventis Deutschland Gmbh Diarylcycloalkyl derivatives, processes for their preparation and their use as pharmceuticals
DE10142668A1 (en) 2001-08-31 2003-03-20 Aventis Pharma Gmbh Use of C2-substituted indan-1-one systems for the preparation of medicaments for the prophylaxis or treatment of obesity
KR100915108B1 (en) 2001-08-31 2009-09-03 사노피-아벤티스 도이칠란트 게엠베하 Diarylcycloalkyl derivatives as PPAR activators and a pharmaceutical composition comprising the same
DE10142666A1 (en) 2001-08-31 2003-03-20 Aventis Pharma Gmbh Use of C2-substituted indan-1-ol systems for the preparation of medicaments for the prophylaxis or treatment of obesity
IL160983A0 (en) 2001-09-24 2004-08-31 Imp College Innovations Ltd Use of pyy for preparation of a medicament for modification of feeding behavior
EP1444219A1 (en) 2001-10-12 2004-08-11 Novo Nordisk A/S Substituted piperidines and their use for the treatment of diseases related to the histamine h3 receptor
US7238671B2 (en) 2001-10-18 2007-07-03 Bristol-Myers Squibb Company Human glucagon-like-peptide-1 mimics and their use in the treatment of diabetes and related conditions
EP1572892A4 (en) * 2001-10-18 2007-08-22 Bristol Myers Squibb Co Human glucagon-like-peptide-1 mimics and their use in the treatment of diabetes and related conditions
WO2003055482A1 (en) 2001-12-21 2003-07-10 Novo Nordisk A/S Amide derivatives as gk activators
AU2002351752A1 (en) 2001-12-29 2003-07-30 Novo Nordisk A/S Combined use of a glp-1 compound and another drug for treating dyslipidemia
WO2003058203A2 (en) * 2002-01-08 2003-07-17 Eli Lilly And Company Extended glucagon-like peptide-1 analogs
AU2003201998C1 (en) * 2002-01-10 2012-10-25 Imperial Innovations Limited Modification of feeding behavior
US8058233B2 (en) 2002-01-10 2011-11-15 Oregon Health And Science University Modification of feeding behavior using PYY and GLP-1
BR0307727A (en) 2002-02-20 2005-01-25 Lilly Co Eli Fomulation
US7223796B2 (en) 2002-04-11 2007-05-29 Sanofi-Aventis Deutschland Gmbh Acyl-4-carboxyphenylurea derivatives, processes for preparing them and their use
US7049341B2 (en) 2002-06-07 2006-05-23 Aventis Pharma Deutschland Gmbh N-benzoylureidocinnamic acid derivatives, processes for preparing them and their use
US7671047B2 (en) 2002-06-19 2010-03-02 Sanofi-Aventis Deutschland Gmbh Cationically substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use
US7176193B2 (en) 2002-06-19 2007-02-13 Sanofi-Aventis Deutschland Gmbh Acid-group-substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use
US7176194B2 (en) 2002-06-19 2007-02-13 Sanofi-Aventis Deutschland Gmbh Ring-substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use
EP1531815B1 (en) 2002-06-27 2014-09-24 Novo Nordisk A/S Glucokinase activators
ES2327328T3 (en) * 2002-07-04 2009-10-28 Zealand Pharma A/S GLP-1 AND PROCEDURES FOR THE TREATMENT OF DIABETES.
DE10231370B4 (en) 2002-07-11 2006-04-06 Sanofi-Aventis Deutschland Gmbh Thiophene glycoside derivatives, medicaments containing these compounds and methods of making these medicaments
US7262220B2 (en) 2002-07-11 2007-08-28 Sanofi-Aventis Deutschland Gmbh Urea- and urethane-substituted acylureas, process for their preparation and their use
PL373329A1 (en) 2002-07-12 2005-08-22 Sanofi-Aventis Deutschland Gmbh Heterocyclically substituted benzoylureas, method for their production and their use as medicaments
US7141561B2 (en) 2002-07-25 2006-11-28 Sanofi-Aventis Deutschland Gmbh Substituted diaryl heterocycles, process for their preparation and their use as medicaments
US8821915B2 (en) 2002-08-09 2014-09-02 Veroscience, Llc Therapeutic process for the treatment of the metabolic syndrome and associated metabolic disorders
US7273921B2 (en) 2002-09-25 2007-09-25 Novo Nordisk A/S Method for producing acylated peptides
MXPA05003002A (en) * 2002-09-25 2005-06-22 Novo Nordisk As Method for producing acylated peptides.
US7067488B2 (en) 2002-09-25 2006-06-27 Theratechnologies Inc. Modified GLP-1 peptides with increased biological potency
US20040157922A1 (en) 2002-10-04 2004-08-12 Aventis Pharma Deutschland Gmbh Carboxyalkoxy-substituted acyl-carboxyphenylurea derivatives and their use as medicaments
US7208504B2 (en) 2002-10-12 2007-04-24 Sanofi-Aventis Deutschland Gmbh Bicyclic inhibitors of hormone sensitive lipase
US7411039B2 (en) 2002-10-14 2008-08-12 Novo Nordisk A/S GLP-2 compounds, formulations, and uses thereof
DE10258007B4 (en) 2002-12-12 2006-02-09 Sanofi-Aventis Deutschland Gmbh Aromatic fluoroglycoside derivatives, medicaments containing these compounds and methods for the preparation of these medicaments
NZ541365A (en) 2002-12-27 2009-09-25 Diobex Inc Compositions and methods for the prevention and control of insulin-induced hypoglycemia
US7655618B2 (en) 2002-12-27 2010-02-02 Diobex, Inc. Compositions and methods for the prevention and control of insulin-induced hypoglycemia
GB0300571D0 (en) * 2003-01-10 2003-02-12 Imp College Innovations Ltd Modification of feeding behaviour
US20040242583A1 (en) 2003-01-20 2004-12-02 Aventis Pharma Deutschland Gmbh Pyrimido[5,4-e][1,2,4]triazine-5,7-diones, processes for preparing them and their use
US7179941B2 (en) 2003-01-23 2007-02-20 Sanofi-Aventis Deutschland Gmbh Carbonylamino-substituted acyl phenyl urea derivatives, process for their preparation and their use
DE602004031927D1 (en) 2003-02-04 2011-05-05 Novo Nordisk As INJECTION DEVICE WITH ROTATABLE DOSE ADJUSTMENT DEVICE
WO2004089470A2 (en) 2003-04-11 2004-10-21 Novo Nordisk A/S New amide derivatives and pharmaceutical use thereof
US7390814B2 (en) 2003-02-13 2008-06-24 Sanofi-Aventis Deutschland Gmbh Substituted hexahydropyrazino [1,2-a] pyrimidine-4,7-dione derivatives, process for their preparation and their use as medicaments
US7652007B2 (en) 2003-02-13 2010-01-26 Sanofi-Aventis Deutschland Gmbh Nitrogen-substituted hexahydropyrazino[1,2-A]pyrimidine-4,7-dione derivatives, processes for their preparation and their use as medicaments
DE10306250A1 (en) 2003-02-14 2004-09-09 Aventis Pharma Deutschland Gmbh Substituted N-aryl heterocycles, processes for their preparation and their use as pharmaceuticals
US7148246B2 (en) 2003-02-27 2006-12-12 Sanofi-Aventis Deutschland Gmbh Cycloalkyl derivatives having bioisosteric carboxylic acid groups, processes for their preparation and their use as pharmaceuticals
DE10308355A1 (en) 2003-02-27 2004-12-23 Aventis Pharma Deutschland Gmbh Aryl-cycloalkyl-substituted alkanoic acid derivatives, process for their preparation and their use as medicaments
DE10308353A1 (en) 2003-02-27 2004-12-02 Aventis Pharma Deutschland Gmbh Diarylcycloalkyl derivatives, processes for their preparation and their use as medicines
DE10308351A1 (en) 2003-02-27 2004-11-25 Aventis Pharma Deutschland Gmbh 1,3-substituted cycloalkyl derivatives having acidic, usually heterocyclic groups, processes for their preparation and their use as medicaments
DE10308352A1 (en) 2003-02-27 2004-09-09 Aventis Pharma Deutschland Gmbh Branched side chain arylcycloalkyl derivatives, process for their preparation and their use as medicaments
US7501440B2 (en) 2003-03-07 2009-03-10 Sanofi-Aventis Deutschland Gmbh Substituted benzoylureidopyridylpiperidine-and-pyrrolidinecarboxylic acid derivatives, processes for preparing them and their use
JP4548335B2 (en) 2003-03-07 2010-09-22 味の素株式会社 Inducing agent for converting intestinal cells into insulin-producing cells, and therapeutic agent for diabetes
BRPI0407936A (en) 2003-03-19 2006-02-21 Lilly Co Eli pegylated glp-1 compound, method of stimulating the glp-1 receptor in an individual, and use of pegylated glp-1 compound
CN102134577A (en) 2003-03-28 2011-07-27 独立行政法人农业生物资源研究所 Process for producing plant storage organ with high production of recombinant protein and novel recombinant protein
DE10314610A1 (en) 2003-04-01 2004-11-04 Aventis Pharma Deutschland Gmbh New diphenylazetidinone with improved physiological properties, process for its preparation, medicaments containing these compounds and its use
CA2523267C (en) 2003-04-23 2013-09-03 Biovalve Technologies, Inc. Hydraulically actuated pump for long duration medicament administration
BRPI0410972C1 (en) 2003-06-03 2021-05-25 Novo Nordisk As method for increasing the shelf life of a pharmaceutical composition, pharmaceutical composition, and method for treating hyperglycemia
JP2007524592A (en) 2003-06-03 2007-08-30 ノボ・ノルデイスク・エー／エス Stabilized pharmaceutical peptide composition
DE602004023626D1 (en) 2003-08-21 2009-11-26 Novo Nordisk As SEPARATION OF POLYPEPTIDES WITH A RACEMIZED AMINO ACID
WO2005023291A2 (en) * 2003-09-11 2005-03-17 Novo Nordisk A/S Use of glp1-agonists in the treatment of patients with type i diabetes
CN101380476A (en) * 2003-09-19 2009-03-11 诺沃挪第克公司 Albumin-binding derivatives of therapeutic peptides
JP4800959B2 (en) * 2003-11-13 2011-10-26 ノヴォ ノルディスク アー／エス Soluble pharmaceutical composition for parenteral administration comprising GLP-1 peptide and short-acting insulin peptide for the treatment of diabetes and bulimia
US20060287221A1 (en) 2003-11-13 2006-12-21 Novo Nordisk A/S Soluble pharmaceutical compositions for parenteral administration comprising a GLP-1 peptide and an insulin peptide of short time action for treatment of diabetes and bulimia
PT3300721T (en) 2003-11-20 2019-06-06 Novo Nordisk As Propylene glycol-containing peptide formulations which are optimal for production and for use in injection devices
JP4865565B2 (en) 2003-12-09 2012-02-01 ノヴォ ノルディスク アー／エス Controlling food selection using GLP-1 agonists
JP2007514752A (en) 2003-12-16 2007-06-07 ソシエテ・ドゥ・コンセイユ・ドゥ・ルシェルシュ・エ・ダプリカーション・シャンティフィック・エス・ア・エス GLP-1 pharmaceutical composition
EP1711523B1 (en) * 2003-12-16 2012-10-10 Ipsen Pharma Analogues of glp-1
ATE461217T1 (en) 2003-12-18 2010-04-15 Novo Nordisk As GLP-1 COMPOUNDS
US20060286129A1 (en) 2003-12-19 2006-12-21 Emisphere Technologies, Inc. Oral GLP-1 formulations
PT1723128E (en) 2004-01-06 2013-02-27 Novo Nordisk As Heteroaryl-ureas and their use as glucokinase activators
CA2552526A1 (en) 2004-01-08 2005-07-21 Theratechnologies Inc. Glucagon-like peptide-1 analogs with long duration of action
ATE550041T1 (en) 2004-01-21 2012-04-15 Novo Nordisk Healthcare Ag TRANSGLUTAMINASE-MEDIATED CONJUGATION OF PEPTIDES
US7241787B2 (en) 2004-01-25 2007-07-10 Sanofi-Aventis Deutschland Gmbh Substituted N-cycloexylimidazolinones, process for their preparation and their use as medicaments
US7470706B2 (en) 2004-01-31 2008-12-30 Sanofi-Aventis Deutschland Gmbh Cycloalkyl-substituted 7-amino-4-quinolone-3-carboxylic acid derivatives, process for their preparation and their use as medicaments
US7402674B2 (en) 2004-01-31 2008-07-22 Sanofi-Aventis Deutschland Gmbh, 7-Phenylamino-4-quinolone-3-carboxylic acid derivatives, process for their preparation and their use as medicaments
US7498341B2 (en) 2004-01-31 2009-03-03 Sanofi Aventis Deutschland Gmbh Heterocyclically substituted 7-amino-4-quinolone-3-carboxylic acid derivatives, process for their preparation and their use as medicaments
DE102004005172A1 (en) 2004-02-02 2005-08-18 Aventis Pharma Deutschland Gmbh Indazole derivatives as inhibitors of the hormone sensitive lipase
KR100564618B1 (en) 2004-03-11 2006-03-28 삼성전자주식회사 Method for searching between layers in a disc drive
GT200500063A (en) 2004-04-01 2005-10-14 METHOD FOR TREATMENT OF SCHIZOPHRENIA AND / OR GLUCOREGULATORY ABNORMALITIES
EP1586573B1 (en) 2004-04-01 2007-02-07 Sanofi-Aventis Deutschland GmbH Oxadiazolones, processes for their preparation and their use as pharmaceuticals
EP1604988A1 (en) 2004-05-18 2005-12-14 Sanofi-Aventis Deutschland GmbH Pyridazinone derivatives, methods for producing them and their use as pharmaceuticals
JP2008501765A (en) 2004-06-11 2008-01-24 ノボ　ノルディスク　アクティーゼルスカブ Neutralization of drug-induced obesity using GLP-1 agonists
US9089636B2 (en) 2004-07-02 2015-07-28 Valeritas, Inc. Methods and devices for delivering GLP-1 and uses thereof
WO2006024631A2 (en) 2004-08-31 2006-03-09 Novo Nordisk A/S Use of tris(hydroxymethyl) aminomethane for the stabilization of peptides, polypeptides and proteins
WO2006028970A1 (en) 2004-09-02 2006-03-16 Cengent Therapeutics, Inc. Derivatives of thiazole and thiadiazole inhibitors of tyrosine phosphatases
US7893017B2 (en) 2004-10-07 2011-02-22 Novo Nordisk A/S Protracted GLP-1 compounds
JP5107713B2 (en) 2004-10-07 2012-12-26 ノヴォ ノルディスク アー／エス Delayed exendin-4 compound
ES2458991T3 (en) * 2004-11-12 2014-05-07 Novo Nordisk A/S Stable insulinotropic peptide formulations
GB0426146D0 (en) 2004-11-29 2004-12-29 Bioxell Spa Therapeutic peptides and method
EP1824835A1 (en) 2004-12-03 2007-08-29 Novo Nordisk A/S Heteroaromatic glucokinase activators
TWI376234B (en) 2005-02-01 2012-11-11 Msd Oss Bv Conjugates of a polypeptide and an oligosaccharide
ES2490243T3 (en) 2005-02-02 2014-09-03 Novo Nordisk A/S Insulin derivatives
JP4933455B2 (en) 2005-02-02 2012-05-16 ノヴォ ノルディスク アー／エス New insulin derivatives
CN101128214A (en) 2005-03-18 2008-02-20 诺和诺德公司 Extended GLP-1 compounds
TWI362392B (en) * 2005-03-18 2012-04-21 Novo Nordisk As Acylated glp-1 compounds
US8512288B2 (en) 2006-08-23 2013-08-20 Medtronic Minimed, Inc. Infusion medium delivery device and method with drive device for driving plunger in reservoir
US8137314B2 (en) 2006-08-23 2012-03-20 Medtronic Minimed, Inc. Infusion medium delivery device and method with compressible or curved reservoir or conduit
US20080097291A1 (en) 2006-08-23 2008-04-24 Hanson Ian B Infusion pumps and methods and delivery devices and methods with same
US7569050B2 (en) 2005-05-06 2009-08-04 Medtronic Minimed, Inc. Infusion device and method with drive device in infusion device and method with drive device in separable durable housing portion
US8277415B2 (en) 2006-08-23 2012-10-02 Medtronic Minimed, Inc. Infusion medium delivery device and method with drive device for driving plunger in reservoir
US7905868B2 (en) 2006-08-23 2011-03-15 Medtronic Minimed, Inc. Infusion medium delivery device and method with drive device for driving plunger in reservoir
US8840586B2 (en) 2006-08-23 2014-09-23 Medtronic Minimed, Inc. Systems and methods allowing for reservoir filling and infusion medium delivery
JPWO2006126673A1 (en) * 2005-05-27 2008-12-25 第一三共株式会社 Antidiabetic drugs in combination
DE102005026762A1 (en) 2005-06-09 2006-12-21 Sanofi-Aventis Deutschland Gmbh Azolopyridin-2-one derivatives as inhibitors of lipases and phospholipases
AU2006265172B2 (en) 2005-06-30 2011-09-15 Vtv Therapeutics Llc Phenoxy acetic acids as PPAR delta activators
US8501739B2 (en) 2005-07-04 2013-08-06 High Point Pharmaceuticals, Llc Medicaments
US7884210B2 (en) 2005-07-14 2011-02-08 Novo Nordisk A/S Ureido-thiazole glucokinase activators
EP1910317B1 (en) 2005-07-20 2013-07-03 Eli Lilly And Company 1-amino linked compounds
ES2336575T3 (en) 2005-09-22 2010-04-14 Biocompatibles Uk Limited GLP-1 FUSION POLYPEPTIDES (PEPTIDE-1 SIMILAR TO GLUCAGON) WITH INCREASED RESISTANCE TO PEPTIDASE.
US8852164B2 (en) 2006-02-09 2014-10-07 Deka Products Limited Partnership Method and system for shape-memory alloy wire control
PT1951658E (en) 2005-11-17 2012-11-12 Lilly Co Eli Glucagon receptor antagonists, preparation and therapeutic uses
ES2390286T3 (en) 2005-12-16 2012-11-08 Nektar Therapeutics GLP-1 polymer conjugates
EA201101085A1 (en) 2005-12-22 2012-05-30 ХАЙ ПОЙНТ ФАРМАСЬЮТИКАЛЗ, ЭлЭлСи PHENOXYACIC ACIDS AS PPAR DELTA ACTIVATORS
CN101400363B (en) 2006-01-18 2012-08-29 昌达生物科技公司 Pharmaceutical compositions with enhanced stability
CN104162201A (en) 2006-02-09 2014-11-26 德卡产品有限公司 Peripheral system
US11478623B2 (en) 2006-02-09 2022-10-25 Deka Products Limited Partnership Infusion pump assembly
US11027058B2 (en) 2006-02-09 2021-06-08 Deka Products Limited Partnership Infusion pump assembly
US11497846B2 (en) 2006-02-09 2022-11-15 Deka Products Limited Partnership Patch-sized fluid delivery systems and methods
US11364335B2 (en) 2006-02-09 2022-06-21 Deka Products Limited Partnership Apparatus, system and method for fluid delivery
CN101443314B (en) 2006-03-13 2014-04-09 杏林制药株式会社 Aminoquinolones as GSK-3 inhibitors
EP1996224B1 (en) 2006-03-15 2012-11-07 Novo Nordisk A/S Mixtures of amylin and insulin
AU2007229492B2 (en) 2006-03-28 2011-11-03 High Point Pharmaceuticals, Llc Benzothiazoles having histamine H3 receptor activity
KR101361376B1 (en) 2006-03-30 2014-02-10 발레리타스 인코포레이티드 Multi-cartridge fluid delivery device
DK2049475T3 (en) 2006-04-24 2012-03-05 Lilly Co Eli Cyclohexyl-substituted pyrrolidinones as inhibitors of 11-beta-hydroxysteroid dehydrogenase1
DE602006009631D1 (en) 2006-05-10 2009-11-19 Biocompatibles Uk Ltd Spherical microcapsules containing GLP-1 peptides, their production and their use
KR20090040259A (en) 2006-05-29 2009-04-23 하이 포인트 파마슈티칼스, 엘엘씨 3-(1,3-benzodioxol-5-yl)-6-(4-cyclopropylpiperazin-1-yl)-pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist
DE102006028862A1 (en) 2006-06-23 2007-12-27 Merck Patent Gmbh 3-amino-imidazo [1,2-a] pyridine
BRPI0715469A2 (en) 2006-07-11 2013-03-12 Qps Llc Pharmaceutical compositions for sustained release of peptides
US20090325873A1 (en) 2006-07-18 2009-12-31 Centocor, Inc. Human glp-1 mimetibodies, compositions, methods and uses
RU2009108280A (en) 2006-08-08 2010-09-20 Санофи-Авентис (Fr) Arylamino-arylalkyl-substituted imidazolidine-2,4-dione, methods for their preparation containing these compounds and their use
US7811262B2 (en) 2006-08-23 2010-10-12 Medtronic Minimed, Inc. Systems and methods allowing for reservoir filling and infusion medium delivery
US7682338B2 (en) 2006-08-23 2010-03-23 Medtronic Minimed, Inc. Infusion medium delivery system, device and method with needle inserter and needle inserter device and method
US7828764B2 (en) 2006-08-23 2010-11-09 Medtronic Minimed, Inc. Systems and methods allowing for reservoir filling and infusion medium delivery
US7794434B2 (en) 2006-08-23 2010-09-14 Medtronic Minimed, Inc. Systems and methods allowing for reservoir filling and infusion medium delivery
US20100056428A1 (en) 2006-09-01 2010-03-04 Novo Nordisk Health Care Ag Modified proteins
EP2063890A1 (en) 2006-09-07 2009-06-03 Nycomed GmbH Combination treatment for diabetes mellitus
ES2377322T3 (en) 2006-11-15 2012-03-26 High Point Pharmaceuticals, Llc New 2- (2-hydroxyphenyl) benzothiadiazines useful for the treatment of obesity and diabetes
TWI428346B (en) 2006-12-13 2014-03-01 Imp Innovations Ltd Novel compounds and their effects on feeding behaviour
AU2008204530B2 (en) 2007-01-11 2013-08-01 Vtv Therapeutics Llc Urea glucokinase activators
DE102007002260A1 (en) 2007-01-16 2008-07-31 Sanofi-Aventis Use of substituted pyranonic acid derivatives for the preparation of medicaments for the treatment of the metabolic syndrome
DE102007005045B4 (en) 2007-01-26 2008-12-18 Sanofi-Aventis Phenothiazine derivatives, process for their preparation and their use as medicines
DE102007008420A1 (en) 2007-02-21 2008-08-28 Merck Patent Gmbh benzimidazole derivatives
EP1975176A1 (en) * 2007-03-27 2008-10-01 Biocompatibles UK Limited Novel glp-1 fusion peptides, their production and use
EP2146760B1 (en) 2007-04-30 2018-10-10 Medtronic MiniMed, Inc. Reservoir filling, bubble management, and infusion medium delivery systems and methods with same
US7959715B2 (en) 2007-04-30 2011-06-14 Medtronic Minimed, Inc. Systems and methods allowing for reservoir air bubble management
US7963954B2 (en) 2007-04-30 2011-06-21 Medtronic Minimed, Inc. Automated filling systems and methods
US8434528B2 (en) 2007-04-30 2013-05-07 Medtronic Minimed, Inc. Systems and methods for reservoir filling
US8597243B2 (en) 2007-04-30 2013-12-03 Medtronic Minimed, Inc. Systems and methods allowing for reservoir air bubble management
US8323250B2 (en) 2007-04-30 2012-12-04 Medtronic Minimed, Inc. Adhesive patch systems and methods
US8613725B2 (en) 2007-04-30 2013-12-24 Medtronic Minimed, Inc. Reservoir systems and methods
MX2009013354A (en) 2007-06-04 2010-07-06 Univ Ben Gurion Tri-aryl compounds and compositions comprising the same.
US20080319221A1 (en) 2007-06-22 2008-12-25 Bernd Junker Esters of Pentahydroxyhexylcarbamoyl Alkanoic Acids
JP2009019027A (en) * 2007-07-16 2009-01-29 Hanmi Pharmaceutical Co Ltd Insulin secretion peptide derivative in which amino acid of amino terminal is varied
JP5688969B2 (en) 2007-07-16 2015-03-25 ノボ・ノルデイスク・エー／エス Pegylated insulin analogues are stable against proteases
EP2025674A1 (en) 2007-08-15 2009-02-18 sanofi-aventis Substituted tetra hydro naphthalines, method for their manufacture and their use as drugs
EP2679597A1 (en) 2007-09-05 2014-01-01 Novo Nordisk A/S Glucagon-like peptide-1 derivatives and their pharmaceutical use
WO2009030774A1 (en) * 2007-09-05 2009-03-12 Novo Nordisk A/S Truncated glp-1 derivatives and their therapeutical use
ES2532116T3 (en) 2007-09-05 2015-03-24 Novo Nordisk A/S Peptides derived with A-B-C-D and their therapeutic uses
AU2008299903B2 (en) 2007-09-11 2013-08-29 Kyorin Pharmaceutical Co., Ltd Cyanoaminoquinolones and tetrazoloaminoquinolones as GSK-3 inhibitors
KR101597841B1 (en) 2007-09-12 2016-02-26 교린 세이야꾸 가부시키 가이샤 Spirocyclic aminoquinolones as gsk-3 inhibitors
DE102007048716A1 (en) 2007-10-11 2009-04-23 Merck Patent Gmbh Imidazo [1,2-a] pyrimidine derivatives
DE102007054497B3 (en) 2007-11-13 2009-07-23 Sanofi-Aventis Deutschland Gmbh New crystalline hydrate form of dodecanedioic acid 4-((2S,3R)-3-((S)-3-(4-fluoro-phenyl)-3-hydroxy-propyl)-2-(4-methoxy-phenyl)-4-oxo-azetidin-1-yl)-benzylamide ((2S,3R,4R,5R)-pentahydroxy-hexyl)-amide useful e.g. to treat hyperlipidemia
PL2597103T3 (en) 2007-11-16 2017-04-28 Novo Nordisk A/S Stable pharmaceutical compositions comprising liraglutide and degludec
US20100317057A1 (en) 2007-12-28 2010-12-16 Novo Nordisk A/S Semi-recombinant preparation of glp-1 analogues
US8881774B2 (en) 2007-12-31 2014-11-11 Deka Research & Development Corp. Apparatus, system and method for fluid delivery
BR122019016154B8 (en) 2007-12-31 2021-06-22 Deka Products Lp infusion pump set
US10188787B2 (en) 2007-12-31 2019-01-29 Deka Products Limited Partnership Apparatus, system and method for fluid delivery
US8900188B2 (en) 2007-12-31 2014-12-02 Deka Products Limited Partnership Split ring resonator antenna adapted for use in wirelessly controlled medical device
US9456955B2 (en) 2007-12-31 2016-10-04 Deka Products Limited Partnership Apparatus, system and method for fluid delivery
US10080704B2 (en) 2007-12-31 2018-09-25 Deka Products Limited Partnership Apparatus, system and method for fluid delivery
US8491570B2 (en) 2007-12-31 2013-07-23 Deka Products Limited Partnership Infusion pump assembly
DE102008025007A1 (en) 2008-05-24 2009-11-26 Sanofi-Aventis Deutschland Gmbh Insulin analogs which comprise A chain and B chain with disulfide bonds for use in treatment of diabetes and for cartilage regeneration
CA2711749A1 (en) 2008-01-09 2009-07-16 Sanofi-Aventis Deutschland Gmbh Novel insulin derivatives having an extremely delayed time-action profile
DE102008003566A1 (en) 2008-01-09 2009-07-16 Sanofi-Aventis Deutschland Gmbh New insulin analogs useful for treating diabetes
DE102008003568A1 (en) 2008-01-09 2009-07-16 Sanofi-Aventis Deutschland Gmbh New insulin analogs useful for treating diabetes
NZ586589A (en) 2008-01-09 2012-04-27 Sanofi Aventis Deutschland Novel insulin analogues having an extremely delayed time-action profile
DE102008025008A1 (en) 2008-05-24 2009-11-26 Sanofi-Aventis Deutschland Gmbh Insulin analogs which comprise A chain and B chain with disulfide bonds for use in treatment of diabetes
EP2259791A2 (en) * 2008-03-05 2010-12-15 Tel HaShomer Medical Research Infrastructure and Services Ltd. Glp-1 receptor agonists and related active pharmaceutical ingredients for treatment of cancer
PL2254906T3 (en) 2008-03-18 2017-04-28 Novo Nordisk A/S Protease stabilized, acylated insulin analogues
DE102008017590A1 (en) 2008-04-07 2009-10-08 Merck Patent Gmbh Glucopyranosidderivate
CN101555214B (en) 2008-04-08 2012-07-11 北京嘉事联博医药科技有限公司 Phenylcyclobutylacylamide derivative as well as optical isomer, preparation method and application thereof
WO2009158704A2 (en) 2008-06-27 2009-12-30 Duke University Therapeutic agents comprising elastin-like peptides
TW201014822A (en) 2008-07-09 2010-04-16 Sanofi Aventis Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof
BRPI0917000A2 (en) 2008-08-06 2016-02-16 Novo Nordisk Healthcare Ag protein conjugates with prolonged in vivo efficacy
US8637647B2 (en) 2008-09-12 2014-01-28 Novo Nordisk A/S Method of acylating a peptide or protein
JP6288903B2 (en) 2008-09-15 2018-03-07 デカ・プロダクツ・リミテッド・パートナーシップ Systems and methods for fluid delivery
LT2349324T (en) 2008-10-17 2017-12-27 Sanofi-Aventis Deutschland Gmbh Combination of an insulin and a glp-1 agonist
DE102008051834A1 (en) 2008-10-17 2010-04-22 Sanofi-Aventis Deutschland Gmbh Drug, useful e.g. for treating diabetes, preferably type-I or II and for controlling fasting, postprandial and/or postabsorptive plasma glucose concentration, comprises insulin and glucagon-like peptide-1 agonist
DE102009038210A1 (en) 2009-08-20 2011-03-03 Sanofi-Aventis Deutschland Gmbh Medicament, useful e.g. for treating diabetes, controlling fasting, postprandial or postabsorptive blood glucose concentration in diabetic patients and improving glucose tolerance, comprises insulin and glucagon-like peptide-1 agonist
DE102008053048A1 (en) 2008-10-24 2010-04-29 Sanofi-Aventis Deutschland Gmbh Medicament, useful e.g. for treating diabetes, controlling fasting, postprandial or postabsorptive blood glucose concentration in diabetic patients and improving glucose tolerance, comprises insulin and glucagon-like peptide-1 agonist
EP2344519B1 (en) 2008-11-07 2016-09-28 The General Hospital Corporation C-terminal fragments of glucagon-like peptide-1 (glp-1)
IT1392655B1 (en) 2008-11-20 2012-03-16 Bio Ker S R L SITE-SPECIFIC MONOCONJUGATED INSULINOTROPIC GLP-1 PEPTIDES.
US8927549B2 (en) 2008-11-21 2015-01-06 High Point Pharmaceuticals, Llc Adamantyl benzamide derivatives
AU2009322043A1 (en) 2008-12-05 2011-07-07 Angiochem Inc. Conjugates of neurotensin or neurotensin analogs and uses thereof
WO2010068601A1 (en) 2008-12-08 2010-06-17 Sanofi-Aventis A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof
JP5635531B2 (en) 2008-12-15 2014-12-03 ジーランド ファーマ アクティーゼルスカブ Glucagon analog
WO2010070252A1 (en) 2008-12-15 2010-06-24 Zealand Pharma A/S Glucagon analogues
MY160219A (en) 2008-12-15 2017-02-28 Zealand Pharma As Glucagon analogues
WO2010070255A1 (en) 2008-12-15 2010-06-24 Zealand Pharma A/S Glucagon analogues
EP2389389B1 (en) 2009-01-22 2015-04-15 Novo Nordisk Health Care AG Stable growth hormone compounds
CN102361647B (en) 2009-01-23 2018-02-16 诺沃-诺迪斯克有限公司 FGF21 derivatives and its application with albumin combination agent A B C D E
CN101824087A (en) * 2009-03-05 2010-09-08 连云港恒邦医药科技有限公司 Glucagon-like peptide-2 analog as well as preparation method and application thereof
MX2011009414A (en) 2009-03-11 2011-10-19 Kyorin Seiyaku Kk 7-cycloalkylaminoquinolones as gsk-3 inhibitors.
EP2437732B1 (en) * 2009-06-05 2018-05-09 VeroScience LLC Combination of dopamine agonists plus first phase insulin secretagouges for the treatment of metabolic disorders
US9352025B2 (en) 2009-06-05 2016-05-31 Veroscience Llc Combination of dopamine agonists plus first phase insulin secretagogues for the treatment of metabolic disorders
AU2014265118B2 (en) * 2009-06-05 2016-11-17 Veroscience Llc Combination of dopamine agonists plus first phase insulin secretagouges for the treatment of metabolic disorders
US20120172298A1 (en) * 2009-06-11 2012-07-05 Novo Nordisk A/S Glp-1 and fgf21 combinations for treatment of diabetes type 2
EA022816B1 (en) 2009-07-13 2016-03-31 Зилэнд Фарма А/С Acylated glucagon analogues
CA2768011C (en) 2009-07-15 2018-07-24 Deka Products Limited Partnership Apparatus, systems and methods for an infusion pump assembly
US8614182B2 (en) 2009-07-30 2013-12-24 Jiangsu Hansoh Pharmaceuticals Co., Ltd. GLP-1 analogues and their pharmaceutical salts and uses
CN101987868B (en) 2009-07-30 2013-09-04 江苏豪森医药集团有限公司 Derivative or pharmaceutically acceptable salt of GLP-1 analogue and application of derivative or pharmaceutically-acceptable salt of a GLP-1 analogue
US8841249B2 (en) 2009-08-06 2014-09-23 Novo Nordisk A/S Growth hormones with prolonged in-vivo efficacy
JP2013503135A (en) 2009-08-26 2013-01-31 サノフイ Novel crystalline heteroaromatic fluoroglycoside hydrate, pharmaceutical comprising the compound and use thereof
EP2482823A2 (en) 2009-10-02 2012-08-08 Sanofi Use of compounds with sglt-1/sglt-2 inhibitor activity for producing medicaments for treatment of bone diseases
WO2011048614A2 (en) 2009-10-22 2011-04-28 Cadila Healthcare Limited Short chain peptidomimetics based orally active glp-1 agonist and glucagon receptor antagonist
PL2498801T3 (en) 2009-11-13 2018-08-31 Sanofi Aventis Deutschland PHARMACEUTICAL COMPOSITION COMPRISING desPro36Exendin-4(1-39)-Lys6-NH2 AND METHIONINE
ES2534191T3 (en) 2009-11-13 2015-04-20 Sanofi-Aventis Deutschland Gmbh Pharmaceutical composition comprising a GLP-1 agonist, an insulin and methionine
ES2625735T3 (en) 2009-12-16 2017-07-20 Novo Nordisk A/S GLP-1 analogs and derivatives
CA2787895A1 (en) 2010-01-22 2011-07-28 Novo Nordisk Health Care Ag Stable growth hormone compounds
MX345736B (en) 2010-01-22 2017-02-14 Novo Nordisk Healthcare Ag Growth hormones with prolonged in-vivo efficacy.
BR112012021231A2 (en) 2010-02-26 2015-09-08 Basf Plant Science Co Gmbh method for enhancing plant yield, plant, construct, use of a construct, method for producing a transgenic plant, collectable parts of a plant, products derived from a plant, use of a nucleic acid and method for producing a product
US20130012432A1 (en) 2010-02-26 2013-01-10 Novo Nordisk A/S Peptides for Treatment of Obesity
US9422330B2 (en) * 2010-03-01 2016-08-23 Novo Nordisk A/S Preparative RP-HPLC method for purifying peptides
WO2011107494A1 (en) 2010-03-03 2011-09-09 Sanofi Novel aromatic glycoside derivatives, medicaments containing said compounds, and the use thereof
RU2559320C2 (en) 2010-03-26 2015-08-10 Ново Нордиск А/С Novel glucagon analogues
US9168288B2 (en) 2010-04-09 2015-10-27 Mount Sinai Hospital Methods for treating disorders of the gastrointestinal tract using a GLP-1 agonist
DE102010015123A1 (en) 2010-04-16 2011-10-20 Sanofi-Aventis Deutschland Gmbh New benzylamidic diphenylazetidinone compounds, useful for treating lipid disorders, hyperlipidemia, atherosclerotic manifestations or insulin resistance, and for reducing serum cholesterol levels
CA2797133C (en) 2010-04-27 2019-08-06 Zealand Pharma A/S Peptide conjugates of glp-1 receptor agonists and gastrin and their use
CN102869676A (en) 2010-04-30 2013-01-09 株式会社三和化学研究所 Peptide for improving in vivo stability of physiologically active substance or the like and physiologically active substance with improved in vivo stability
EP2582709B1 (en) 2010-06-18 2018-01-24 Sanofi Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases
US8530413B2 (en) 2010-06-21 2013-09-10 Sanofi Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments
AR081975A1 (en) 2010-06-23 2012-10-31 Zealand Pharma As GLUCAGON ANALOGS
EP2585482B1 (en) 2010-06-24 2019-03-27 Zealand Pharma A/S Glucagon analogues
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
HUE031181T2 (en) 2010-08-30 2017-06-28 Sanofi Aventis Deutschland Use of ave0010 for the manufacture of a medicament for the treatment of diabetes mellitus type 2
WO2012061466A2 (en) 2010-11-02 2012-05-10 The General Hospital Corporation Methods for treating steatotic disease
US9006178B2 (en) 2010-11-09 2015-04-14 Novo Nordisk A/S Double-acylated GLP-1 derivatives with a linker
JP5902194B2 (en) 2010-12-16 2016-04-13 ノヴォ ノルディスク アー／エス Solid composition comprising a GLP-1 agonist and a salt of N- (8- (2-hydroxybenzoyl) amino) caprylic acid
US20140004198A1 (en) 2011-01-19 2014-01-02 Novo Nordisk A/S Glp-1 particles and compositions
US20140045754A1 (en) 2011-01-19 2014-02-13 Joern Drustrup Glp-1 compositions
EP2665487A1 (en) 2011-01-20 2013-11-27 Zealand Pharma A/S Combination of acylated glucagon analogues with insulin analogues
WO2012104834A1 (en) 2011-02-03 2012-08-09 Pharmedica Ltd. New oral dissolving films for insulin administration, for treating diabetes
WO2012120054A1 (en) 2011-03-08 2012-09-13 Sanofi Di- and tri-substituted oxathiazine derivates, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
US8809324B2 (en) 2011-03-08 2014-08-19 Sanofi Substituted phenyl-oxathiazine derivatives, method for producing them, drugs containing said compounds and the use thereof
WO2012120051A1 (en) 2011-03-08 2012-09-13 Sanofi Benzyl-oxathiazine derivates substituted with adamantane or noradamantane, medicaments containing said compounds and use thereof
US8895547B2 (en) 2011-03-08 2014-11-25 Sanofi Substituted phenyl-oxathiazine derivatives, method for producing them, drugs containing said compounds and the use thereof
EP2683700B1 (en) 2011-03-08 2015-02-18 Sanofi Tetra-substituted oxathiazine derivatives, method for their preparation, their usage as medicament and medicament containing same and its use
EP2683701B1 (en) 2011-03-08 2014-12-24 Sanofi Oxathiazine derivatives substituted with benzyl or heteromethylene groups, method for their preparation, their usage as medicament, medicament containing same and its use
WO2012120053A1 (en) 2011-03-08 2012-09-13 Sanofi Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
WO2012120055A1 (en) 2011-03-08 2012-09-13 Sanofi Di- and tri-substituted oxathiazine derivates, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
EP2766349B1 (en) 2011-03-08 2016-06-01 Sanofi Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof
AU2012234276A1 (en) 2011-03-28 2013-08-29 Novo Nordisk A/S Novel glucagon analogues
ES2612278T3 (en) 2011-04-12 2017-05-16 Novo Nordisk A/S GLP-1 double-acylated derivatives
WO2012150503A2 (en) 2011-05-03 2012-11-08 Zealand Pharma A/S Glu-glp-1 dual agonist signaling-selective compounds
EP2707713A2 (en) 2011-05-10 2014-03-19 Zealand Pharma A/S Glu-glp-1 dual agonist signaling-selective compounds
US9821032B2 (en) 2011-05-13 2017-11-21 Sanofi-Aventis Deutschland Gmbh Pharmaceutical combination for improving glycemic control as add-on therapy to basal insulin
WO2013006692A2 (en) 2011-07-06 2013-01-10 The General Hospital Corporation Methods of treatment using a pentapeptide derived from the c-terminus of glucagon-like peptide 1 (glp-1)
CN108079281A (en) 2011-08-29 2018-05-29 赛诺菲-安万特德国有限公司 For the pharmaceutical composition of the glycemic control in diabetes B patient
AR087744A1 (en) 2011-09-01 2014-04-16 Sanofi Aventis Deutschland PHARMACEUTICAL COMPOSITION FOR USE IN THE TREATMENT OF A NEURODEGENERATIVE DISEASE
WO2013029279A1 (en) * 2011-09-03 2013-03-07 深圳市健元医药科技有限公司 Novel glp-i analogue, preparation method and use thereof
CN107266558A (en) 2011-09-06 2017-10-20 诺沃—诺迪斯克有限公司 The derivatives of GLP 1
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
EP2567959B1 (en) 2011-09-12 2014-04-16 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
JP6352806B2 (en) 2011-09-23 2018-07-04 ノヴォ ノルディスク アー／エス New glucagon analogues
US9458214B2 (en) 2011-09-26 2016-10-04 Novartis Ag Dual function fibroblast growth factor 21 proteins
WO2013045413A1 (en) 2011-09-27 2013-04-04 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
PL2763690T3 (en) 2011-10-04 2016-04-29 Sanofi Aventis Deutschland Lixisenatide for use in the treatment of stenosis or/and obstruction in the pancreatic duct system
EP2763691A1 (en) 2011-10-04 2014-08-13 Sanofi-Aventis Deutschland GmbH Glp-1 agonist for use in the treatment of stenosis or/and obstruction in the biliary tract
EA028951B9 (en) 2011-11-03 2018-05-31 Зилэнд Фарма А/С Peptide conjugates of gastrin and glucagon-like peptide 1 receptor agonist
JP2015500823A (en) 2011-12-09 2015-01-08 ノヴォ ノルディスク アー／エス GLP-1 agonist
RU2643515C2 (en) 2011-12-29 2018-02-02 Ново Нордиск А/С Dipeptide, containing nonproteinogenic amino acid
RS57827B1 (en) 2012-02-15 2018-12-31 Novo Nordisk As Antibodies that bind peptidoglycan recognition protein 1
EP3196214B1 (en) 2012-02-15 2019-07-31 Novo Nordisk A/S Antibodies that bind and block triggering receptor expressed on myeloid cells-1 (trem-1)
US9550830B2 (en) 2012-02-15 2017-01-24 Novo Nordisk A/S Antibodies that bind and block triggering receptor expressed on myeloid cells-1 (TREM-1)
WO2013134519A2 (en) 2012-03-07 2013-09-12 Deka Products Limited Partnership Apparatus, system and method for fluid delivery
JP6356660B2 (en) 2012-03-22 2018-07-11 ノヴォ ノルディスク アー／エス Compositions containing delivery agents and their preparation
ES2952874T3 (en) 2012-03-22 2023-11-06 Novo Nordisk As GLP-1 peptide compositions and preparation thereof
EA028665B1 (en) 2012-05-03 2017-12-29 Зилэнд Фарма А/С Gip-glp-1 dual agonist compounds and methods
JP6298044B2 (en) 2012-05-03 2018-03-20 ジーランド ファーマ アクティーゼルスカブ Glucagon-like peptide-2 (GLP-2) analog
US11274135B2 (en) * 2012-05-08 2022-03-15 Novo Nordisk A/S Double-acylated GLP-1 derivatives
WO2013167454A1 (en) 2012-05-08 2013-11-14 Novo Nordisk A/S Double-acylated glp-1 derivatives
EP2664374A1 (en) * 2012-05-15 2013-11-20 F. Hoffmann-La Roche AG Lysin-glutamic acid dipeptide derivatives
JP6517690B2 (en) 2012-06-20 2019-05-22 ノヴォ ノルディスク アー／エス Tablet formulation containing peptide and delivery agent
CA2877056A1 (en) 2012-07-01 2014-01-09 Novo Nordisk A/S Use of long-acting glp-1 peptides
EP2873422A4 (en) 2012-07-10 2015-12-30 Takeda Pharmaceutical Pharmaceutical preparation for injection
AR091866A1 (en) 2012-07-23 2015-03-04 Zealand Pharma As GLUCAGON ANALOGS
FR2994848B1 (en) 2012-08-30 2014-08-22 Univ Paris Curie TREATMENT OF ARTHROSIS BY INCRETINED HORMONES OR THEIR ANALOGUES
TWI608013B (en) 2012-09-17 2017-12-11 西蘭製藥公司 Glucagon analogues
UA116217C2 (en) 2012-10-09 2018-02-26 Санофі Exendin-4 derivatives as dual glp1/glucagon agonists
US20150273069A1 (en) 2012-10-17 2015-10-01 Novo Nordisk A/S Fatty acid acylated amino acids for oral peptide delivery
WO2014064215A1 (en) 2012-10-24 2014-05-01 INSERM (Institut National de la Santé et de la Recherche Médicale) TPL2 KINASE INHIBITORS FOR PREVENTING OR TREATING DIABETES AND FOR PROMOTING β-CELL SURVIVAL
US9867869B2 (en) 2012-12-12 2018-01-16 Massachusetts Institute Of Technology Insulin derivatives for diabetes treatment
JP2016503771A (en) 2012-12-21 2016-02-08 サノフイ Exendin-4 derivative
CN103059127B (en) * 2013-01-07 2014-12-17 天津嘉宏科技有限公司 GLP-1 analogs, and preparation method and application thereof
CN105007931B (en) 2013-03-01 2018-04-06 瓦尔德西布伦大学医院基金会研究所 Peptide is in retina neural degenerative disease, the particularly application in the local treatment for other retinal diseases that diabetic retinopathy early stage and neurodegeneration play an important role
EP4091624A1 (en) 2013-03-15 2022-11-23 Protagonist Therapeutics, Inc. Hepcidin analogues and uses thereof
JP6464145B2 (en) 2013-04-05 2019-02-06 ノヴォ・ノルディスク・ヘルス・ケア・アーゲー Growth hormone compound preparation
JP6594856B2 (en) 2013-04-18 2019-10-23 ノヴォ ノルディスク アー／エス Stable prolonged GLP-1 / glucagon receptor co-agonist for medical use
WO2015003145A1 (en) 2013-07-03 2015-01-08 Deka Products Limited Partnership Apparatus, system and method for fluid delivery
CN105451776B (en) * 2013-08-15 2020-04-17 诺和诺德股份有限公司 GLP-1 derivatives and uses thereof
GB201315335D0 (en) 2013-08-29 2013-10-09 Of Singapore Amino diacids containing peptide modifiers
ES2688708T3 (en) 2013-10-17 2018-11-06 Zealand Pharma A/S Acylated glucagon analogs
US9988429B2 (en) 2013-10-17 2018-06-05 Zealand Pharma A/S Glucagon analogues
US10111880B2 (en) 2013-11-05 2018-10-30 Ben-Gurion University Of The Negev Research And Development Authority Compounds for the treatment of diabetes and disease complications arising from same
CN105829339B (en) 2013-11-06 2021-03-12 西兰制药公司 glucagon-GLP-1-GIP triple agonist compounds
MX2016005556A (en) 2013-11-06 2016-07-15 Zealand Pharma As Gip-glp-1 dual agonist compounds and methods.
WO2015086730A1 (en) 2013-12-13 2015-06-18 Sanofi Non-acylated exendin-4 peptide analogues
EP3080150B1 (en) 2013-12-13 2018-08-01 Sanofi Exendin-4 peptide analogues as dual glp-1/gip receptor agonists
EP3080154B1 (en) 2013-12-13 2018-02-07 Sanofi Dual glp-1/gip receptor agonists
EP3080149A1 (en) 2013-12-13 2016-10-19 Sanofi Dual glp-1/glucagon receptor agonists
CN103884846B (en) * 2014-03-06 2016-06-08 杭州九源基因工程有限公司 A kind of detection method of Arg34Lys26-(N-EPSILON-(N-ALPHA-Palmitoyl-L-GAMMA-glutamyl))-GLP-1[7-37] biologic activity
TW201625668A (en) 2014-04-07 2016-07-16 賽諾菲公司 Exendin-4 derivatives as peptidic dual GLP-1/glucagon receptor agonists
TW201625669A (en) 2014-04-07 2016-07-16 賽諾菲公司 Peptidic dual GLP-1/glucagon receptor agonists derived from Exendin-4
TW201625670A (en) 2014-04-07 2016-07-16 賽諾菲公司 Dual GLP-1/glucagon receptor agonists derived from EXENDIN-4
WO2015155151A1 (en) * 2014-04-07 2015-10-15 Novo Nordisk A/S Double-acylated glp-1 compounds
CN106999553B (en) 2014-05-07 2021-11-26 诺和诺德股份有限公司 Treatment of type 1 diabetes using GLP-1 and anti-IL-21
DK3143037T3 (en) 2014-05-16 2021-09-20 Protagonist Therapeutics Inc ALPHA4BETA7-INTEGRIN-THIOETHER-PEPTIDE ANTAGONISTS
WO2015185640A1 (en) 2014-06-04 2015-12-10 Novo Nordisk A/S Glp-1/glucagon receptor co-agonists for medical use
US9932381B2 (en) 2014-06-18 2018-04-03 Sanofi Exendin-4 derivatives as selective glucagon receptor agonists
CN104987383A (en) * 2014-07-08 2015-10-21 四川百利药业有限责任公司 GLP-1 derivate
GB2528436A (en) 2014-07-15 2016-01-27 Lancaster Univ Business Entpr Ltd Treatment of neurological diseases
LT3172232T (en) 2014-07-17 2024-02-12 Novo Nordisk A/S Site directed mutagenesis of trem-1 antibodies for decreasing viscosity.
RU2736637C9 (en) 2014-07-17 2021-02-08 Протагонист Терепьютикс, Инк. Peptidic interleukin-23 receptor inhibitors for oral administration and use thereof for treating inflammatory intestinal diseases
EP3530671A3 (en) 2014-09-05 2019-11-13 University of Copenhagen Gip peptide analogues
JP2017535527A (en) 2014-10-01 2017-11-30 プロタゴニスト セラピューティクス， インコーポレイテッド Novel α4β7 peptide monomer and dimer antagonist
WO2016054445A1 (en) 2014-10-01 2016-04-07 Protagonist Therapeutics, Inc. Novel cyclic monomer and dimer peptides having integrin antagonist activity
DK3006045T3 (en) 2014-10-07 2017-07-17 Cyprumed Gmbh Pharmaceutical formulations for oral administration of peptide or protein drugs
JP6898231B6 (en) 2014-10-29 2021-07-28 ジーランド ファーマ アクティーゼルスカブ GIP agonist compounds and methods
WO2016083499A1 (en) 2014-11-27 2016-06-02 Novo Nordisk A/S Glp-1 derivatives and uses thereof
US9950039B2 (en) 2014-12-12 2018-04-24 Sanofi-Aventis Deutschland Gmbh Insulin glargine/lixisenatide fixed ratio formulation
TWI681966B (en) 2014-12-23 2020-01-11 丹麥商諾佛 儂迪克股份有限公司 Fgf21 derivatives and uses thereof
TWI748945B (en) 2015-03-13 2021-12-11 德商賽諾菲阿凡提斯德意志有限公司 Treatment type 2 diabetes mellitus patients
CA2979950A1 (en) 2015-03-18 2016-09-22 Zealand Pharma A/S Amylin analogues
TW201705975A (en) 2015-03-18 2017-02-16 賽諾菲阿凡提斯德意志有限公司 Treatment of type 2 diabetes mellitus patients
US10426818B2 (en) 2015-03-24 2019-10-01 Inserm (Institut National De La Sante Et De La Recherche Medicale) Method and pharmaceutical composition for use in the treatment of diabetes
AU2016247499B2 (en) 2015-04-16 2020-09-03 Zealand Pharma A/S Acylated glucagon analogue
AR105319A1 (en) 2015-06-05 2017-09-27 Sanofi Sa PROPHARMS THAT INCLUDE A DUAL AGONIST GLU-1 / GLUCAGON CONJUGATE HIALURONIC ACID CONNECTOR
AR105284A1 (en) 2015-07-10 2017-09-20 Sanofi Sa DERIVATIVES OF EXENDINA-4 AS SPECIFIC DUAL PEPTIDE AGONISTS OF GLP-1 / GLUCAGÓN RECEPTORS
US10787490B2 (en) 2015-07-15 2020-09-29 Protaganist Therapeutics, Inc. Peptide inhibitors of interleukin-23 receptor and their use to treat inflammatory diseases
AU2016335287A1 (en) 2015-10-07 2018-04-12 Cyprumed Gmbh Pharmaceutical formulations for the oral delivery of peptide drugs
CA3009834A1 (en) 2015-12-30 2017-07-06 Protagonist Therapeutics, Inc. Analogues of hepcidin mimetics with improved in vivo half lives
EP3205660A1 (en) 2016-02-10 2017-08-16 Polypeptide Laboratories Holding (PPL) AB Method for preparation of peptides with pswang linker
EP3196206A1 (en) 2016-01-20 2017-07-26 Lonza Ltd Method for preparation of liraglutide
WO2017127007A1 (en) 2016-01-20 2017-07-27 Poypeptide Laboratories Holding (Ppl) Ab METHOD FOR PREPARATION OF PEPTIDES WITH psWANG LINKER
EP3205664A1 (en) 2016-02-11 2017-08-16 Polypeptide Laboratories Holding (PPL) AB Method for preparation of liraglutide using bal linker
US10946074B2 (en) 2016-03-03 2021-03-16 Novo Nordisk A/S GLP-1 derivatives and uses thereof
CN108883159A (en) 2016-03-04 2018-11-23 诺和诺德股份有限公司 Liraglutide for diabetic foot ulcer
US20190091295A1 (en) 2016-03-04 2019-03-28 Novo Nordisk A/S Liraglutide in Renal Conditions
JP6991196B2 (en) 2016-03-23 2022-02-03 バッヘン・ホールディング・アクチエンゲゼルシャフト Methods for Producing Glucagon-Like Peptides
JP7011643B2 (en) 2016-03-23 2022-02-10 バッヘン・ホールディング・アクチエンゲゼルシャフト Purification of glucagon-like peptide 1 analog
US10407468B2 (en) 2016-03-23 2019-09-10 Protagonist Therapeutics, Inc. Methods for synthesizing α4β7 peptide antagonists
AR109514A1 (en) 2016-09-09 2018-12-19 Zealand Pharma As AMILINE ANALOGS
WO2018057977A1 (en) 2016-09-23 2018-03-29 Delpor, Inc. Stable compositions for incretin mimetic compounds
WO2018065634A1 (en) 2016-10-07 2018-04-12 Cyprumed Gmbh Pharmaceutical compositions for the nasal delivery of peptide or protein drugs
CN110022935A (en) 2016-11-28 2019-07-16 诺和诺德股份有限公司 Moral paddy insulin for the cardiovascular patient's condition
WO2018096164A1 (en) 2016-11-28 2018-05-31 Novo Nordisk A/S Insulin degludec for treating diabetes
EP3544682A1 (en) 2016-11-28 2019-10-02 Novo Nordisk A/S Insulin degludec for improvement of glycaemic control and reduction of acute and long-term diabetes complications
WO2018104263A1 (en) 2016-12-06 2018-06-14 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods of enhancing the potency of incretin-based drugs in subjects in need thereof
KR102502040B1 (en) 2016-12-09 2023-02-24 질랜드 파마 에이/에스 Acylated GLP-1/GLP-2 dual agonists
WO2018104558A1 (en) 2016-12-09 2018-06-14 Zealand Pharma A/S Acylated glp-1/glp-2 dual agonists
CN110099922A (en) 2016-12-09 2019-08-06 西兰制药公司 GLP-1/GLP-2 dual agonists
WO2018103868A1 (en) 2016-12-09 2018-06-14 Zealand Pharma A/S Acylated glp-1/glp-2 dual agonists
GB201621987D0 (en) 2016-12-22 2017-02-08 Archer Virgil L See Archer Sheri A Arecor Ltd Novel composition
JP2020514365A (en) 2017-03-15 2020-05-21 ノヴォ ノルディスク アー／エス Bicyclic compound capable of binding to melanocortin 4 receptor
WO2018210919A1 (en) 2017-05-17 2018-11-22 Novo Nordisk A/S Glp-1 compositions and uses thereof
US11572399B2 (en) 2017-05-31 2023-02-07 University Of Copenhagen Long-acting GIP peptide analogues
WO2019038412A1 (en) 2017-08-24 2019-02-28 Novo Nordisk A/S Glp-1 compositions and uses thereof
CN111163795A (en) 2017-09-10 2020-05-15 诺沃挪第克公司 MIC-1 and GLP-1 for the treatment of obesity
CA3073806A1 (en) 2017-09-11 2019-03-14 Protagonist Therapeutics, Inc. Opioid agonist peptides and uses thereof
JP2021514936A (en) 2017-12-19 2021-06-17 ノヴォ ノルディスク アー／エス Solubility of GLP-1 peptide
JP6898518B2 (en) 2018-02-02 2021-07-07 ノヴォ ノルディスク アー／エス A solid composition comprising a GLP-1 agonist, a salt of N- (8- (2-hydroxybenzoyl) amino) caprylic acid and a lubricant.
WO2019157268A1 (en) 2018-02-08 2019-08-15 Protagonist Therapeutics, Inc. Conjugated hepcidin mimetics
MX2020008902A (en) 2018-02-27 2020-12-03 Zp Spv 3 K/S Compstatin analogues and their medical uses.
JP2021519594A (en) 2018-04-02 2021-08-12 ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ Anti-TREM-1 antibody and its use
AU2019247936C1 (en) 2018-04-05 2023-06-15 Sun Pharmaceutical Industries Limited Novel GLP-1 analogues
US20210087250A1 (en) 2018-04-06 2021-03-25 Cyprumed Gmbh Pharmaceutical compositions for the transmucosal delivery of therapeutic peptides and proteins
WO2019200594A1 (en) 2018-04-19 2019-10-24 杭州先为达生物科技有限公司 Acylated glp-1 derivative
WO2019209963A1 (en) 2018-04-24 2019-10-31 Deka Products Limited Partnership Apparatus and system for fluid delivery
TWI829687B (en) 2018-05-07 2024-01-21 丹麥商諾佛 儂迪克股份有限公司 Solid compositions comprising a glp-1 agonist and a salt of n-(8-(2-hydroxybenzoyl)amino)caprylic acid
US20210221867A1 (en) 2018-05-15 2021-07-22 Novo Nordisk A/S Compounds Capable of Binding to Melanocortin 4 Receptor
WO2019222072A1 (en) * 2018-05-15 2019-11-21 Savior Lifetec Corporation Preparation method of liraglutide derivative
US10905738B2 (en) 2018-07-05 2021-02-02 Biozeus Desenvolvimento De Produtos Biofarmacêuticos Synthetic peptides, prodrugs, pharmaceutical compositions and uses
WO2020053414A1 (en) 2018-09-14 2020-03-19 Novo Nordisk A/S Bicyclic compounds capable of acting as melanocortin 4 receptor agonists
SG11202105586YA (en) 2018-12-03 2021-06-29 Antag Therapeutics Aps Modified gip peptide analogues
EP3938037A1 (en) 2019-03-15 2022-01-19 Diet4Life ApS Combination of dietary peptides
WO2020201280A1 (en) 2019-04-01 2020-10-08 Novo Nordisk A/S Antibodies directed against liraglutide and use thereof
EP3997105A4 (en) 2019-07-10 2023-09-13 Protagonist Therapeutics, Inc. Peptide inhibitors of interleukin-23 receptor and their use to treat inflammatory diseases
BR112022003760A2 (en) 2019-08-27 2022-05-31 Zp Spv 3 K/S Compstatin analogues and their medical uses
CN114728042A (en) 2019-11-06 2022-07-08 诺和诺德股份有限公司 GLP-1 receptor agonists for dementia
US20220395559A1 (en) 2019-11-07 2022-12-15 Novo Nordisk A/S Solid compositions comprising a glp-1 agonist, an sglt2 inhibitor and a salt of n-(8-(2-hydroxybenzoyl)amino)caprylic acid
WO2021105393A1 (en) 2019-11-29 2021-06-03 Novo Nordisk A/S Processes for obtaining stable glp-1 compositions
CN111040022B (en) 2019-12-23 2021-12-14 万新医药科技(苏州)有限公司 Triplex agonists directed to glucagon-like peptide-1 receptor, glucagon receptor, and pepstatin receptor
BR112022013042A2 (en) 2019-12-30 2022-10-18 Gan & Lee Pharmaceuticals Co Ltd FORMULA B COMPOUND, PHARMACEUTICAL FORMULATION, PHARMACEUTICAL COMPOSITION, METHOD TO TREAT OR PREVENT HYPERGLYCEMIA, DIABETES AND/OR OBESITY
CN118005737A (en) 2020-01-15 2024-05-10 詹森生物科技公司 Peptide inhibitors of interleukin-23 receptor and their use for the treatment of inflammatory diseases
AU2021207313A1 (en) 2020-02-18 2022-07-28 Novo Nordisk A/S Pharmaceutical formulations
EP4126003A1 (en) 2020-03-30 2023-02-08 Zealand Pharma A/S Glp-1/glp-2 dual agonists
US20230110689A1 (en) 2020-03-30 2023-04-13 Zealand Pharma A/S Agonist combination
US11478533B2 (en) 2020-04-27 2022-10-25 Novo Nordisk A/S Semaglutide for use in medicine
JP2023524695A (en) 2020-04-29 2023-06-13 ノヴォ ノルディスク アー／エス Solid composition comprising GLP-1 agonist and histidine
WO2021224338A1 (en) 2020-05-07 2021-11-11 Frederiksberg Hospital Treatment of hyperuricemia
EP4210680A1 (en) 2020-09-07 2023-07-19 Cyprumed GmbH Improved pharmaceutical formulations of glp-1 receptor agonists
CN115925995A (en) 2020-09-30 2023-04-07 北京质肽生物医药科技有限公司 Polypeptide Conjugates and Methods of Use
CA3202226A1 (en) 2020-11-20 2022-05-27 Janssen Pharmaceutica Nv Compositions of peptide inhibitors of interleukin-23 receptor
BR112023012422A2 (en) 2021-01-24 2023-12-12 Michael David Forrest ATP SYNTHASE INHIBITORS - COSMETIC AND THERAPEUTIC USES
FR3120189A1 (en) 2021-03-01 2022-09-02 Farid Bennis Pharmaceutical composition for oral administration of a GLP-1 receptor agonist
WO2023285347A1 (en) 2021-07-12 2023-01-19 Novo Nordisk A/S Novel fatty acid modified urocortin 2 derivatives and the uses thereof
WO2023012263A1 (en) 2021-08-04 2023-02-09 Novo Nordisk A/S Solid oral peptide formulations
CA3228429A1 (en) 2021-09-03 2023-03-09 Mikkel Askjar Agersnap Dosage regime
JPWO2023038039A1 (en) 2021-09-08 2023-03-16
WO2023192873A1 (en) * 2022-03-28 2023-10-05 Bristol-Myers Squibb Company Macrocyclic immunomodulators
WO2024061919A1 (en) 2022-09-19 2024-03-28 Zealand Pharma A/S Combination therapy
WO2024068848A1 (en) 2022-09-28 2024-04-04 Zealand Pharma A/S Methods for treating obesity
EP4345104A1 (en) 2022-09-30 2024-04-03 Bachem Holding AG Method for preparing liraglutide

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4683202A (en) 1985-03-28 1987-07-28 Cetus Corporation Process for amplifying nucleic acid sequences
EP1498425A1 (en) 1986-05-05 2005-01-19 The General Hospital Corporation Use of glucagone-like-peptide 1 (GLP-1) derivatives for the preparation of pharmaceutical compositions
NZ222907A (en) 1986-12-16 1990-08-28 Novo Industri As Preparation for intranasal administration containing a phospholipid absorption enhancing system
WO1991011457A1 (en) * 1990-01-24 1991-08-08 Buckley Douglas I Glp-1 analogs useful for diabetes treatment
DK36492D0 (en) 1992-03-19 1992-03-19 Novo Nordisk As PREPARATION
GB9409496D0 (en) * 1994-05-12 1994-06-29 London Health Ass Method for improving glycaemic control in diabetes
US5512549A (en) * 1994-10-18 1996-04-30 Eli Lilly And Company Glucagon-like insulinotropic peptide analogs, compositions, and methods of use
HU227021B1 (en) * 1996-08-30 2010-05-28 Novo Nordisk As Glp-1 derivatives

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