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(1972).","npl_type":"a","external_id":["10.1530/acta.0.0700487","5068062"],"record_lens_id":"059-286-369-629-149","lens_id":["063-802-735-872-548","059-286-369-629-149","184-589-846-342-248"],"sequence":33,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":2,"text":"Andersen, D.K. et al., \"The Insulinotropic Effect of GIP: A Dose Response Comparison and Comparison to Glucagon-Like Peptide-1(7-37) amide (GLP),\" Diabetes 39(Suppl. 1):142A, Abstract No. 567, American Diabetes Association (May 1990).","npl_type":"a","external_id":[],"lens_id":[],"sequence":34,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":3,"text":"Andrews, P.C. and Ronner, P., \"Isolation and Structures of Glucagon and Glucagon-like Peptide from Catfish Pancreas,\" J. Biol. Chem. 260:3910-3914, The American Society for Biochemistry and Molecular Biology, Inc. (Apr. 1985).","npl_type":"a","external_id":["10.1016/s0021-9258(18)89208-0","3838546"],"record_lens_id":"130-721-313-168-722","lens_id":["149-031-703-018-019","130-721-313-168-722","198-215-622-675-483"],"sequence":35,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":4,"text":"Bell, G.I. et al., \"Hamster preproglucagon contains the sequence of glucagon and two related peptides,\" Nature 302:716-718, Macmillan Publishers Ltd. (1983).","npl_type":"a","external_id":["10.1038/302716a0","6835407"],"record_lens_id":"078-119-767-107-208","lens_id":["155-473-094-696-863","078-119-767-107-208","112-238-685-731-309"],"sequence":36,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":5,"text":"Blackmore, P.F. et al., \"Absence of insulinotropic glucagon-like peptide-I(7-37) receptors on isolated rat liver hepatocytes,\" FEBS Lett. 283:7-10, Elsevier Science Publishers B.V. (May 1991).","npl_type":"a","external_id":["1645298","10.1016/0014-5793(91)80541-a"],"record_lens_id":"042-161-035-344-729","lens_id":["166-011-869-884-310","042-161-035-344-729","098-024-682-241-823"],"sequence":37,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":6,"text":"Bromer, W.W. et al., \"Amino Acid Sequence of Bovine Glucagon,\" J. Biol. Chem. 246:2822-2827, American Society of Biological Chemists, Inc. (1971).","npl_type":"a","external_id":["5102927","10.1016/s0021-9258(18)62256-2"],"record_lens_id":"013-953-121-056-698","lens_id":["171-992-934-660-375","013-953-121-056-698","025-236-018-936-527"],"sequence":38,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":7,"text":"Buhl, T. et al., \"Naturally Occurring Products of Proglucagon 111-160 in the Porcine and Human Small Intestine,\" J. Biol. Chem. 263:8621-8624, The American Society for Biochemistry and Molecular Biology, Inc. (Jun. 1988).","npl_type":"a","external_id":["10.1016/s0021-9258(18)68350-4","3379036"],"record_lens_id":"123-282-441-465-582","lens_id":["180-267-025-175-991","123-282-441-465-582","168-243-131-867-990"],"sequence":39,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":8,"text":"Creutzfeldt, W. et al., \"Entero-Insular Axis 1988,\" in Diabetes 1988, Larkins, R. et al., eds., Elsevier Science Publishers B.V. (Biomedical Division), pp. 193-203 (May 1989).","npl_type":"a","external_id":[],"lens_id":[],"sequence":40,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":9,"text":"Dobbs, R. et al., \"Glucagon: Role in the Hyperglycemia of Diabetes Mellitus,\" Science 187:544-547, American Association for the Advancement of Science (1975).","npl_type":"a","external_id":["10.1126/science.1089999","1089999"],"record_lens_id":"054-685-450-909-208","lens_id":["124-512-295-737-11X","054-685-450-909-208","175-094-576-891-069"],"sequence":41,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":10,"text":"Dobs, A.S. et al., \"Regulation of Insulin Synthesis in an Insulin-Producing Cell Line (RINm5F): Long-Term Experiments,\" In Vitro Cell. Dev. Biol. 25:112-114, Society for In Vitro Biology (Feb. 1989).","npl_type":"a","external_id":["10.1007/bf02626166","2646270"],"record_lens_id":"024-813-180-137-02X","lens_id":["199-657-086-802-243","024-813-180-137-02X","071-956-640-446-222"],"sequence":42,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":11,"text":"Drucker, D.J. et al., \"Cell-specific Post-translational Processing of Preproglucagon Expressed from a Metallothionein-glucagon Fusion Gene,\" J. Biol. Chem. 261:9637-9643, The American Society of Biological Chemists, Inc. (Jul. 1986).","npl_type":"a","external_id":["3525530","10.1016/s0021-9258(18)67561-1"],"record_lens_id":"115-087-030-952-251","lens_id":["173-659-079-092-402","115-087-030-952-251","160-190-682-537-528"],"sequence":43,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":12,"text":"Drucker, D.J. et al., \"Glucagon-like Peptide I Increases Insulin mRNA Levels and Insulin Release in Rat Insulinoma Cells,\" Abstract No. 602, Programs and Abstracts book, 68
(1) H2N—X—CO—R1 \n\nwherein R1 is OH, OM, or —NR2R3;\nM is a pharmaceutically acceptable cation or a lower branched or unbranched alkyl group;\nR2 and R3 are the same or different and selected from the group consisting of hydrogen and a lower branched or unbranched alkyl group;\nX is a derivative of glucagon-like peptide-1 (7-37), (GLP-1 (7-37)), wherein the amino acid sequence of said derivative has the same number of amino acids as said GLP-1 (7-37), and has at least 80% amino acid identity to said GLP-1 (7-37);\nNH2 is the amine group of the amino terminus of X;\nCO is the carbonyl group of the carboxy terminus of X;\n
(2) the acid addition salts of (1);\n
(3) the amino or carboxyl protected form of (1);\n
(4) a pharmaceutically acceptable carboxylate salt of said peptide;\n
(5) a pharmaceutically acceptable lower alkyl ester of said peptide; or\n
(6) a pharmaceutically acceptable amide of said peptide;\nwherein said derivative has an insulinotropic activity that exceeds the insulinotropic activity of GLP-1 (1-37) and GLP-1 (1-36)."],"number":8,"annotation":false,"claim":true,"title":false},{"lines":["The derivative of claim 8, wherein said derivative has at least 90% amino acid identity to said GLP-1 (7-37)."],"number":9,"annotation":false,"claim":true,"title":false},{"lines":["The derivative of claim 8, wherein said derivative has at least 95% amino acid identity to said GLP-1 (7-37)."],"number":10,"annotation":false,"claim":true,"title":false},{"lines":["The derivative of claim 4, said derivative having the formula:\n
(1) H2N—X—CO—R1 \n\nwherein R1 is OH, OM, or —NR2R3;\nM is a pharmaceutically acceptable cation or a lower branched or unbranched alkyl group;\nR2 and R3 are the same or different and selected from the group consisting of hydrogen and a lower branched or unbranched alkyl group;\nX is a derivative of glucagon-like peptide-1 (7-37), (GLP-1 (7-37)), wherein the amino acid sequence of said derivative is that of GLP-1 (7-37) except that an amino acid residue has been substituted with a different amino acid residue;\nNH2 is the amine group of the amino terminus of X;\nCO is the carbonyl group of the carboxy terminus of X;\n
(2) the acid addition salts of (1);\n
(3) the amino or carboxyl protected form of (1);\n
(4) a pharmaceutically acceptable carboxylate salt of said peptide;\n
(5) a pharmaceutically acceptable lower alkyl ester of said peptide; or\n
(6) a pharmaceutically acceptable amide of said peptide;\nwherein said derivative has an insulinotropic activity that exceeds the insulinotropic activity of GLP-1 (1-37) and GLP-1 (1-36)."],"number":11,"annotation":false,"claim":true,"title":false},{"lines":["The derivative of claim 11, wherein a hydrophobic amino acid residue of GLP-1 (7-37) has been substituted with a different hydrophobic amino acid residue."],"number":12,"annotation":false,"claim":true,"title":false},{"lines":["The derivative of claim 11, wherein a basic amino acid residue of GLP-1 (7-37) has been substituted with a different basic amino acid residue."],"number":13,"annotation":false,"claim":true,"title":false},{"lines":["The derivative of claim 11, wherein an aromatic amino acid residue of GLP-1 (7-37) has been substituted with a different aromatic amino acid residue."],"number":14,"annotation":false,"claim":true,"title":false},{"lines":["A compound which is:\n
(A) a peptide having at least 80% homology with glucagon-like peptide-1 (7-37) (GLP-I (7-37)), with the proviso that the peptide is not GLP-I (7-34), GLP-I (7-35), GLP-I (7-36) or GLP-I (7-37); or\n
(B) a peptide which is \n\nwherein the compound is substantially free of natural contaminants, and has an insulinotropic activity which exceeds the insulinotropic activity of GLP-I (1-36) or GLP-1 (1-37)."],"number":15,"annotation":false,"claim":true,"title":false},{"lines":["A compound according to claim 15 having an insulinotropic activity at a concentration of at least 10−11 M."],"number":16,"annotation":false,"claim":true,"title":false},{"lines":["A compound according to claim 15, having an insulinotropic activity at a concentration of at least 10−10 M."],"number":17,"annotation":false,"claim":true,"title":false},{"lines":["An insulinotropic medicament comprising an insulinotropically effective amount of a compound according to claim 15 in combination with a pharmaceutically acceptable carrier."],"number":18,"annotation":false,"claim":true,"title":false},{"lines":["A compound which is:\n(i) a pharmaceutically acceptable acid addition salt of (A);\n(ii) a pharmaceutically acceptable carboxylate salt of (A);\n(iii) a pharmaceutically acceptable lower alkyl ester of (A); or\n(iv) a pharmaceutically acceptable amide, alkyl amide or dialkyl amide of (i), (ii), or (iii);\n
(A) a peptide having at least 80% homology with glucagon-like peptide-1 (7-36) (GLP-I (7-36)), with the proviso that the peptide is not GLP-I (7-34), GLP-I (7-35), GLP-I (7-36) or GLP-I (7-37); or\n
(B) a peptide which is \n\nwherein the compound is substantially free of natural contaminants, and has an insulinotropic activity which exceeds the insulinotropic activity of GLP-I (1-36) or GLP-I (1-37)."],"number":19,"annotation":false,"claim":true,"title":false},{"lines":["A compound according to claim 19 having an insulinotropic activity at a concentration of at least 10−11 M."],"number":20,"annotation":false,"claim":true,"title":false},{"lines":["A compound according to claim 19, having an insulinotropic activity at a concentration of at least 10−10 M."],"number":21,"annotation":false,"claim":true,"title":false},{"lines":["An insulinotropic medicament comprising an insulinotropically effective amount of a compound according to claim 19 in combination with a pharmaceutically acceptable carrier."],"number":22,"annotation":false,"claim":true,"title":false},{"lines":["A compound which is:\n(i) a pharmaceutically acceptable acid addition salt of (A);\n(ii) a pharmaceutically acceptable carboxylate salt of (A);\n(iii) a pharmaceutically acceptable lower alkyl ester of (A); or\n(iv) a pharmaceutically acceptable amide, alkyl amide or dialkyl amide of (i), (ii), or (iii);\n
(A) a peptide having at least 80% homology with glucagon-like peptide-1 (7-35) (GLP-I (7-35)) or glucagon-like peptide-1 (7-34) (GLP-I (7-34), with the proviso that the peptide is not GLP-I (7-34), GLP-I (7-35), GLP-I (7-36) or GLP-I (7-37); or\n
(B) a peptide which is \n\nwherein the compound is substantially free of natural contaminants, and has an insulinotropic activity which exceeds the insulinotropic activity of GLP-I (1-36) or GLP-1 (1-37)."],"number":23,"annotation":false,"claim":true,"title":false},{"lines":["A compound according to claim 23 having an insulinotropic activity at a concentration of at least 10−11 M."],"number":24,"annotation":false,"claim":true,"title":false},{"lines":["A compound according to claim 23, having an insulinotropic activity at a concentration of at least 10−10 M."],"number":25,"annotation":false,"claim":true,"title":false},{"lines":["An insulinotropic medicament comprising an insulinotropically effective amount of a compound according to claim 23 in combination with a pharmaceutically acceptable carrier."],"number":26,"annotation":false,"claim":true,"title":false}]}},"filters":{"npl":[],"notNpl":[],"applicant":[],"notApplicant":[],"inventor":[],"notInventor":[],"owner":[],"notOwner":[],"tags":[],"dates":[],"types":[],"notTypes":[],"j":[],"notJ":[],"fj":[],"notFj":[],"classIpcr":[],"notClassIpcr":[],"classNat":[],"notClassNat":[],"classCpc":[],"notClassCpc":[],"so":[],"notSo":[],"sat":[]},"sequenceFilters":{"s":"SEQIDNO","d":"ASCENDING","p":0,"n":10,"sp":[],"si":[],"len":[],"t":[],"loc":[]}}(i) a pharmaceutically acceptable acid addition salt of (A);\n(ii) a pharmaceutically acceptable carboxylate salt of (A);\n(iii) a pharmaceutically acceptable lower alkyl ester of (A); or\n(iv) a pharmaceutically acceptable amide, alkyl amide or dialkyl amide of (i), (ii), or (iii);\n