HRP20110018T1 - Derivati pirido(2,1-a)-izokinolina kao inhibitori dpp-iv - Google Patents
Derivati pirido(2,1-a)-izokinolina kao inhibitori dpp-iv Download PDFInfo
- Publication number
- HRP20110018T1 HRP20110018T1 HR20110018T HRP20110018T HRP20110018T1 HR P20110018 T1 HRP20110018 T1 HR P20110018T1 HR 20110018 T HR20110018 T HR 20110018T HR P20110018 T HRP20110018 T HR P20110018T HR P20110018 T1 HRP20110018 T1 HR P20110018T1
- Authority
- HR
- Croatia
- Prior art keywords
- pyrido
- dimethoxy
- hexahydro
- amino
- isoquinolin
- Prior art date
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- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 22
- 125000000217 alkyl group Chemical group 0.000 claims abstract 16
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 8
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 7
- 239000001257 hydrogen Substances 0.000 claims abstract 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract 7
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 6
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims abstract 5
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract 5
- 229910052717 sulfur Chemical group 0.000 claims abstract 5
- 125000003342 alkenyl group Chemical group 0.000 claims abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 4
- 150000003839 salts Chemical class 0.000 claims abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 3
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims abstract 3
- 125000005842 heteroatom Chemical group 0.000 claims abstract 3
- 229920006395 saturated elastomer Polymers 0.000 claims abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract 2
- 125000003118 aryl group Chemical group 0.000 claims abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract 2
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 claims abstract 2
- 229910052736 halogen Inorganic materials 0.000 claims abstract 2
- 150000002367 halogens Chemical class 0.000 claims abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 2
- 239000001301 oxygen Chemical group 0.000 claims abstract 2
- 239000011593 sulfur Chemical group 0.000 claims abstract 2
- 201000010099 disease Diseases 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- NUBNLQCQSWLNCX-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-4-methylpyrrolidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CC(C)CC1=O NUBNLQCQSWLNCX-UHFFFAOYSA-N 0.000 claims 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 3
- 238000011321 prophylaxis Methods 0.000 claims 3
- -1 thiazolidin-3-yl Chemical group 0.000 claims 3
- 238000011282 treatment Methods 0.000 claims 3
- HVZDVNGFZKXGRM-UHFFFAOYSA-N (2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-(1,3-thiazolidin-3-yl)methanone Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1C(=O)N1CCSC1 HVZDVNGFZKXGRM-UHFFFAOYSA-N 0.000 claims 2
- ZFIBBFIUTCQDQR-ULQDDVLXSA-N (2s,3s,11bs)-3-(1,1-dioxothiazinan-2-yl)-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-2-amine Chemical compound N1([C@H]2CN3CCC=4C=C(C(=CC=4[C@@H]3C[C@@H]2N)OC)OC)CCCCS1(=O)=O ZFIBBFIUTCQDQR-ULQDDVLXSA-N 0.000 claims 2
- GUYMHFIHHOEFOA-STECZYCISA-N (4r)-1-[(2s,3s,11bs)-2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl]-4-(fluoromethyl)pyrrolidin-2-one Chemical compound N1([C@H]2CN3CCC=4C=C(C(=CC=4[C@@H]3C[C@@H]2N)OC)OC)C[C@H](CF)CC1=O GUYMHFIHHOEFOA-STECZYCISA-N 0.000 claims 2
- NUBNLQCQSWLNCX-ZCPGHIKRSA-N (4r)-1-[(2s,3s,11bs)-2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl]-4-methylpyrrolidin-2-one Chemical compound N1([C@H]2CN3CCC=4C=C(C(=CC=4[C@@H]3C[C@@H]2N)OC)OC)C[C@H](C)CC1=O NUBNLQCQSWLNCX-ZCPGHIKRSA-N 0.000 claims 2
- NUBNLQCQSWLNCX-STECZYCISA-N (4s)-1-[(2s,3s,11bs)-2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl]-4-methylpyrrolidin-2-one Chemical compound N1([C@H]2CN3CCC=4C=C(C(=CC=4[C@@H]3C[C@@H]2N)OC)OC)C[C@@H](C)CC1=O NUBNLQCQSWLNCX-STECZYCISA-N 0.000 claims 2
- YRRZMQVMDNBBLU-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-2,3-dihydropyridin-6-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CCC=CC1=O YRRZMQVMDNBBLU-UHFFFAOYSA-N 0.000 claims 2
- GUYMHFIHHOEFOA-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-4-(fluoromethyl)pyrrolidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CC(CF)CC1=O GUYMHFIHHOEFOA-UHFFFAOYSA-N 0.000 claims 2
- OXRRHYRRQWIHIV-UHFFFAOYSA-N 2,3-dihydro-1h-pyridin-6-one Chemical compound O=C1NCCC=C1 OXRRHYRRQWIHIV-UHFFFAOYSA-N 0.000 claims 2
- WXDAFCAAWAJFAG-UHFFFAOYSA-N 3-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-5-methyl-1,3-oxazolidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CC(C)OC1=O WXDAFCAAWAJFAG-UHFFFAOYSA-N 0.000 claims 2
- GUYMHFIHHOEFOA-ZCPGHIKRSA-N Carmegliptin Chemical compound N1([C@H]2CN3CCC=4C=C(C(=CC=4[C@@H]3C[C@@H]2N)OC)OC)C[C@@H](CF)CC1=O GUYMHFIHHOEFOA-ZCPGHIKRSA-N 0.000 claims 2
- 108010067722 Dipeptidyl Peptidase 4 Proteins 0.000 claims 2
- 102100025012 Dipeptidyl peptidase 4 Human genes 0.000 claims 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 229940079593 drug Drugs 0.000 claims 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 claims 2
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 2
- IDVRYJZZCUBUJS-UHFFFAOYSA-N (2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-(azetidin-1-yl)methanone Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1C(=O)N1CCC1 IDVRYJZZCUBUJS-UHFFFAOYSA-N 0.000 claims 1
- NWFBJRXBWCRZHR-UHFFFAOYSA-N (2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-pyrrolidin-1-ylmethanone Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1C(=O)N1CCCC1 NWFBJRXBWCRZHR-UHFFFAOYSA-N 0.000 claims 1
- NUBNLQCQSWLNCX-BASLNEPJSA-N (4r)-1-[(2r,3r,11br)-2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl]-4-methylpyrrolidin-2-one Chemical compound N1([C@@H]2CN3CCC=4C=C(C(=CC=4[C@H]3C[C@H]2N)OC)OC)C[C@H](C)CC1=O NUBNLQCQSWLNCX-BASLNEPJSA-N 0.000 claims 1
- NUBNLQCQSWLNCX-WBQNTZJQSA-N (4s)-1-[(2r,3r,11br)-2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl]-4-methylpyrrolidin-2-one Chemical compound N1([C@@H]2CN3CCC=4C=C(C(=CC=4[C@H]3C[C@H]2N)OC)OC)C[C@@H](C)CC1=O NUBNLQCQSWLNCX-WBQNTZJQSA-N 0.000 claims 1
- DDKJYXSAKVWFLS-LSKWAPIISA-N (4s)-1-[(2s,3s,11bs)-2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl]-4-(fluoromethyl)pyrrolidin-2-one;dihydrochloride Chemical compound Cl.Cl.N1([C@H]2CN3CCC=4C=C(C(=CC=4[C@@H]3C[C@@H]2N)OC)OC)C[C@@H](CF)CC1=O DDKJYXSAKVWFLS-LSKWAPIISA-N 0.000 claims 1
- OYELEBBISJGNHJ-UHFFFAOYSA-N 1,3-oxazinan-2-one Chemical compound O=C1NCCCO1 OYELEBBISJGNHJ-UHFFFAOYSA-N 0.000 claims 1
- UORKUFQLSBYWNL-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-3-methylpyrrolidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CCC(C)C1=O UORKUFQLSBYWNL-UHFFFAOYSA-N 0.000 claims 1
- RRMHXFUPTNJEEM-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-4-ethylpyrrolidin-2-one Chemical compound O=C1CC(CC)CN1C1C(N)CC2C3=CC(OC)=C(OC)C=C3CCN2C1 RRMHXFUPTNJEEM-UHFFFAOYSA-N 0.000 claims 1
- WVBKPWPUNZOWNG-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-4-methylpiperidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CCC(C)CC1=O WVBKPWPUNZOWNG-UHFFFAOYSA-N 0.000 claims 1
- DMHQAAKROHVXNB-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-5-methylpiperidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CC(C)CCC1=O DMHQAAKROHVXNB-UHFFFAOYSA-N 0.000 claims 1
- ARQNYGOILDZRGJ-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-5-methylpyrrolidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1C(C)CCC1=O ARQNYGOILDZRGJ-UHFFFAOYSA-N 0.000 claims 1
- HNCSYKUUKHXRCJ-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)azepan-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CCCCCC1=O HNCSYKUUKHXRCJ-UHFFFAOYSA-N 0.000 claims 1
- QSVZHKOHWFGXHF-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)piperidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CCCCC1=O QSVZHKOHWFGXHF-UHFFFAOYSA-N 0.000 claims 1
- INWWWTILZXHHJN-UHFFFAOYSA-N 1-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)pyrrolidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CCCC1=O INWWWTILZXHHJN-UHFFFAOYSA-N 0.000 claims 1
- QSVZHKOHWFGXHF-BRWVUGGUSA-N 1-[(2r,3r,11br)-2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl]piperidin-2-one Chemical compound N1([C@@H]2CN3CCC=4C=C(C(=CC=4[C@H]3C[C@H]2N)OC)OC)CCCCC1=O QSVZHKOHWFGXHF-BRWVUGGUSA-N 0.000 claims 1
- QSVZHKOHWFGXHF-ULQDDVLXSA-N 1-[(2s,3s,11bs)-2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl]piperidin-2-one Chemical compound N1([C@H]2CN3CCC=4C=C(C(=CC=4[C@@H]3C[C@@H]2N)OC)OC)CCCCC1=O QSVZHKOHWFGXHF-ULQDDVLXSA-N 0.000 claims 1
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 claims 1
- CCTPKHROVIWMRG-UHFFFAOYSA-N 3-(1,1-dioxo-1,2-thiazolidin-2-yl)-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-2-amine Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CCCS1(=O)=O CCTPKHROVIWMRG-UHFFFAOYSA-N 0.000 claims 1
- ZFIBBFIUTCQDQR-UHFFFAOYSA-N 3-(1,1-dioxothiazinan-2-yl)-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-2-amine Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CCCCS1(=O)=O ZFIBBFIUTCQDQR-UHFFFAOYSA-N 0.000 claims 1
- NSDPVRNHTOFONC-UHFFFAOYSA-N 3-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-1,3-oxazinan-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CCCOC1=O NSDPVRNHTOFONC-UHFFFAOYSA-N 0.000 claims 1
- KDYHKCSEXBPFCA-UHFFFAOYSA-N 3-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-1,3-oxazolidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CCOC1=O KDYHKCSEXBPFCA-UHFFFAOYSA-N 0.000 claims 1
- QFENECDXQMZEDF-UHFFFAOYSA-N 3-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)-5-(fluoromethyl)-1,3-oxazolidin-2-one Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1N1CC(CF)OC1=O QFENECDXQMZEDF-UHFFFAOYSA-N 0.000 claims 1
- AOCWQPKHSMJWPL-UHFFFAOYSA-N 3-methylpyrrolidin-2-one Chemical compound CC1CCNC1=O AOCWQPKHSMJWPL-UHFFFAOYSA-N 0.000 claims 1
- ZBCUGJNJBOSHIA-UHFFFAOYSA-N 4-ethylpyrrolidin-2-one Chemical compound CCC1CNC(=O)C1 ZBCUGJNJBOSHIA-UHFFFAOYSA-N 0.000 claims 1
- WKBDRRWUJFWHFP-UHFFFAOYSA-N 4-fluoro-1-methylpyrrolidin-2-one Chemical compound CN1CC(F)CC1=O WKBDRRWUJFWHFP-UHFFFAOYSA-N 0.000 claims 1
- PTSGHGGLRADEFP-UHFFFAOYSA-N 4-methylpiperidin-2-one Chemical compound CC1CCNC(=O)C1 PTSGHGGLRADEFP-UHFFFAOYSA-N 0.000 claims 1
- YRKRGYRYEQYTOH-UHFFFAOYSA-N 4-methylpyrrolidin-2-one Chemical compound CC1CNC(=O)C1 YRKRGYRYEQYTOH-UHFFFAOYSA-N 0.000 claims 1
- KMVXQRLMTSRFBF-UHFFFAOYSA-N 5-(fluoromethyl)-1,3-oxazolidin-2-one Chemical compound FCC1CNC(=O)O1 KMVXQRLMTSRFBF-UHFFFAOYSA-N 0.000 claims 1
- HBRXQSHUXIJOKV-UHFFFAOYSA-N 5-methyl-1,3-oxazolidin-2-one Chemical compound CC1CNC(=O)O1 HBRXQSHUXIJOKV-UHFFFAOYSA-N 0.000 claims 1
- NSRPFJGOCZUUHE-UHFFFAOYSA-N 5-methylpiperidin-2-one Chemical compound CC1CCC(=O)NC1 NSRPFJGOCZUUHE-UHFFFAOYSA-N 0.000 claims 1
- 206010009900 Colitis ulcerative Diseases 0.000 claims 1
- 208000011231 Crohn disease Diseases 0.000 claims 1
- 208000002705 Glucose Intolerance Diseases 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 1
- 208000001145 Metabolic Syndrome Diseases 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- 201000006704 Ulcerative Colitis Diseases 0.000 claims 1
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 claims 1
- 210000000227 basophil cell of anterior lobe of hypophysis Anatomy 0.000 claims 1
- 230000009286 beneficial effect Effects 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 239000002934 diuretic Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims 1
- YVIVRJLWYJGJTJ-UHFFFAOYSA-N gamma-Valerolactam Chemical compound CC1CCC(=O)N1 YVIVRJLWYJGJTJ-UHFFFAOYSA-N 0.000 claims 1
- RZLRUIOODAEHEX-UHFFFAOYSA-N n-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)butanamide Chemical compound C1CC2=CC(OC)=C(OC)C=C2C2N1CC(NC(=O)CCC)C(N)C2 RZLRUIOODAEHEX-UHFFFAOYSA-N 0.000 claims 1
- IYFPXHSCQNVJEU-UHFFFAOYSA-N n-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)cyclopropanecarboxamide Chemical compound NC1CC2C=3C=C(OC)C(OC)=CC=3CCN2CC1NC(=O)C1CC1 IYFPXHSCQNVJEU-UHFFFAOYSA-N 0.000 claims 1
- BPBNQPDORGSCJP-UHFFFAOYSA-N n-(2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1h-benzo[a]quinolizin-3-yl)propanamide Chemical compound C1CC2=CC(OC)=C(OC)C=C2C2N1CC(NC(=O)CC)C(N)C2 BPBNQPDORGSCJP-UHFFFAOYSA-N 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 201000009104 prediabetes syndrome Diseases 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- ALSCEGDXFJIYES-UHFFFAOYSA-N pyrrolidine-2-carbonitrile Chemical compound N#CC1CCCN1 ALSCEGDXFJIYES-UHFFFAOYSA-N 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
- A61K9/1623—Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
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EP03013404 | 2003-06-20 | ||
PCT/EP2004/006355 WO2005000848A1 (en) | 2003-06-20 | 2004-06-11 | Pyrido` 2, 1-a - isoquinoline derivatives as dpp-iv inhibitors |
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HRP20110018T1 true HRP20110018T1 (hr) | 2011-02-28 |
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HR20110018T HRP20110018T1 (hr) | 2003-06-20 | 2011-01-12 | Derivati pirido(2,1-a)-izokinolina kao inhibitori dpp-iv |
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EP (1) | EP1638970B1 (he) |
JP (1) | JP4160616B2 (he) |
KR (1) | KR100730867B1 (he) |
CN (1) | CN100374439C (he) |
AR (1) | AR044795A1 (he) |
AT (1) | ATE489387T1 (he) |
AU (1) | AU2004251830B8 (he) |
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CA (1) | CA2529443C (he) |
CO (1) | CO5640155A2 (he) |
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CY (1) | CY1111425T1 (he) |
DE (1) | DE602004030244D1 (he) |
DK (1) | DK1638970T3 (he) |
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EC (1) | ECSP056240A (he) |
ES (1) | ES2355105T3 (he) |
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HR (1) | HRP20110018T1 (he) |
IL (1) | IL172618A (he) |
MA (1) | MA27883A1 (he) |
MX (1) | MXPA05013904A (he) |
MY (1) | MY140039A (he) |
NO (1) | NO332126B1 (he) |
NZ (1) | NZ544221A (he) |
PL (1) | PL1638970T3 (he) |
PT (1) | PT1638970E (he) |
RS (1) | RS52397B (he) |
SI (1) | SI1638970T1 (he) |
TN (1) | TNSN05320A1 (he) |
TW (1) | TWI297011B (he) |
UA (1) | UA82242C2 (he) |
WO (1) | WO2005000848A1 (he) |
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EP3110449B1 (en) | 2014-02-28 | 2023-06-28 | Boehringer Ingelheim International GmbH | Medical use of a dpp-4 inhibitor |
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GB9313913D0 (en) | 1993-07-06 | 1993-08-18 | Smithkline Beecham Plc | Novel compounds |
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DE19616486C5 (de) | 1996-04-25 | 2016-06-30 | Royalty Pharma Collection Trust | Verfahren zur Senkung des Blutglukosespiegels in Säugern |
US6011155A (en) | 1996-11-07 | 2000-01-04 | Novartis Ag | N-(substituted glycyl)-2-cyanopyrrolidines, pharmaceutical compositions containing them and their use in inhibiting dipeptidyl peptidase-IV |
TW492957B (en) | 1996-11-07 | 2002-07-01 | Novartis Ag | N-substituted 2-cyanopyrrolidnes |
CA2819705C (en) | 1998-02-02 | 2014-07-08 | Trustees Of Tufts College | Method of regulating glucose metabolism, and reagents related thereto |
DE19834591A1 (de) * | 1998-07-31 | 2000-02-03 | Probiodrug Ges Fuer Arzneim | Verfahren zur Steigerung des Blutglukosespiegels in Säugern |
GB9817118D0 (en) | 1998-08-07 | 1998-10-07 | Glaxo Group Ltd | Pharmaceutical compounds |
CO5150173A1 (es) | 1998-12-10 | 2002-04-29 | Novartis Ag | Compuestos n-(glicilo sustituido)-2-cianopirrolidinas inhibidores de peptidasa de dipeptidilo-iv (dpp-iv) los cuales son efectivos en el tratamiento de condiciones mediadas por la inhibicion de dpp-iv |
US6110949A (en) | 1999-06-24 | 2000-08-29 | Novartis Ag | N-(substituted glycyl)-4-cyanothiazolidines, pharmaceutical compositions containing them and their use in inhibiting dipeptidyl peptidase-IV |
WO2001019805A1 (fr) | 1999-09-10 | 2001-03-22 | Takeda Chemical Industries, Ltd. | Composes heterocycliques et procede de preparation de ces derniers |
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AU2001233622A1 (en) | 2000-02-25 | 2001-09-03 | Novo-Nordisk A/S | Inhibition of beta cell degeneration |
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