JP2008513498A5 - - Google Patents
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- JP2008513498A5 JP2008513498A5 JP2007532629A JP2007532629A JP2008513498A5 JP 2008513498 A5 JP2008513498 A5 JP 2008513498A5 JP 2007532629 A JP2007532629 A JP 2007532629A JP 2007532629 A JP2007532629 A JP 2007532629A JP 2008513498 A5 JP2008513498 A5 JP 2008513498A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hydrogen
- group
- independently selected
- rings
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 229910052739 hydrogen Inorganic materials 0.000 claims 74
- 239000001257 hydrogen Substances 0.000 claims 74
- 125000000217 alkyl group Chemical group 0.000 claims 53
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 46
- 125000003118 aryl group Chemical group 0.000 claims 40
- 125000000753 cycloalkyl group Chemical group 0.000 claims 40
- 125000001072 heteroaryl group Chemical group 0.000 claims 40
- 125000000623 heterocyclic group Chemical group 0.000 claims 40
- 125000003710 aryl alkyl group Chemical group 0.000 claims 33
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 33
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 33
- 150000001875 compounds Chemical class 0.000 claims 28
- 150000002431 hydrogen Chemical class 0.000 claims 28
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims 22
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 22
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 22
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 22
- 125000005020 hydroxyalkenyl group Chemical group 0.000 claims 22
- 125000003367 polycyclic group Chemical group 0.000 claims 18
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 16
- 125000001309 chloro group Chemical group Cl* 0.000 claims 16
- 125000001153 fluoro group Chemical group F* 0.000 claims 16
- 239000008194 pharmaceutical composition Substances 0.000 claims 15
- 125000004043 oxo group Chemical group O=* 0.000 claims 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims 8
- 201000010099 disease Diseases 0.000 claims 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 8
- 125000001188 haloalkyl group Chemical group 0.000 claims 8
- 239000000203 mixture Substances 0.000 claims 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 8
- 239000000651 prodrug Substances 0.000 claims 8
- 229940002612 prodrug Drugs 0.000 claims 8
- 150000003839 salts Chemical class 0.000 claims 8
- 101000631826 Homo sapiens Stearoyl-CoA desaturase Proteins 0.000 claims 6
- 102000055981 human SCD1 Human genes 0.000 claims 6
- 108010087894 Fatty acid desaturases Proteins 0.000 claims 4
- 102000016553 Stearoyl-CoA Desaturase Human genes 0.000 claims 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims 4
- 241000124008 Mammalia Species 0.000 claims 3
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 3
- 208000004930 Fatty Liver Diseases 0.000 claims 2
- 206010019708 Hepatic steatosis Diseases 0.000 claims 2
- 208000001145 Metabolic Syndrome Diseases 0.000 claims 2
- 208000008589 Obesity Diseases 0.000 claims 2
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- 208000010706 fatty liver disease Diseases 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 230000001404 mediated effect Effects 0.000 claims 2
- 208000008338 non-alcoholic fatty liver disease Diseases 0.000 claims 2
- 206010053219 non-alcoholic steatohepatitis Diseases 0.000 claims 2
- 235000020824 obesity Nutrition 0.000 claims 2
- 231100000240 steatosis hepatitis Toxicity 0.000 claims 2
- WFNHQQPAILHHHY-UHFFFAOYSA-N 6-[4-[5-fluoro-2-(trifluoromethyl)benzoyl]piperazin-1-yl]-n-(3-methylbutyl)imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound C1=CC2=NC(C(=O)NCCC(C)C)=CN2N=C1N(CC1)CCN1C(=O)C1=CC(F)=CC=C1C(F)(F)F WFNHQQPAILHHHY-UHFFFAOYSA-N 0.000 claims 1
- IJUINEMMNVBKSC-UHFFFAOYSA-N 6-[4-[5-fluoro-2-(trifluoromethyl)benzoyl]piperazin-1-yl]-n-hexylimidazo[1,2-b]pyridazine-2-carboxamide Chemical compound C1=CC2=NC(C(=O)NCCCCCC)=CN2N=C1N(CC1)CCN1C(=O)C1=CC(F)=CC=C1C(F)(F)F IJUINEMMNVBKSC-UHFFFAOYSA-N 0.000 claims 1
- CQKHBKHSSXUYNW-UHFFFAOYSA-N 6-[4-[5-fluoro-2-(trifluoromethyl)benzoyl]piperazin-1-yl]-n-pentylimidazo[1,2-b]pyridazine-2-carboxamide Chemical compound C1=CC2=NC(C(=O)NCCCCC)=CN2N=C1N(CC1)CCN1C(=O)C1=CC(F)=CC=C1C(F)(F)F CQKHBKHSSXUYNW-UHFFFAOYSA-N 0.000 claims 1
- 208000032928 Dyslipidaemia Diseases 0.000 claims 1
- 208000002705 Glucose Intolerance Diseases 0.000 claims 1
- 206010022489 Insulin Resistance Diseases 0.000 claims 1
- 208000017170 Lipid metabolism disease Diseases 0.000 claims 1
- CHANIKOYXKLUJA-UHFFFAOYSA-N [4-(2-butylimidazo[1,2-b]pyridazin-6-yl)piperazin-1-yl]-[2-(trifluoromethyl)phenyl]methanone Chemical compound C1=CC2=NC(CCCC)=CN2N=C1N(CC1)CCN1C(=O)C1=CC=CC=C1C(F)(F)F CHANIKOYXKLUJA-UHFFFAOYSA-N 0.000 claims 1
- PZGGHBAFDRRBJC-UHFFFAOYSA-N [4-(2-ethylimidazo[1,2-b]pyridazin-6-yl)piperazin-1-yl]-[2-(trifluoromethyl)phenyl]methanone Chemical compound C1=CC2=NC(CC)=CN2N=C1N(CC1)CCN1C(=O)C1=CC=CC=C1C(F)(F)F PZGGHBAFDRRBJC-UHFFFAOYSA-N 0.000 claims 1
- UWEIAULOMZAVFL-UHFFFAOYSA-N [4-(2-pentyl-3h-benzimidazol-5-yl)piperazin-1-yl]-[2-(trifluoromethyl)phenyl]methanone Chemical compound C=1C=C2NC(CCCCC)=NC2=CC=1N(CC1)CCN1C(=O)C1=CC=CC=C1C(F)(F)F UWEIAULOMZAVFL-UHFFFAOYSA-N 0.000 claims 1
- AECMFRRWQZBFCY-UHFFFAOYSA-N [4-(2-pentylimidazo[1,2-b]pyridazin-6-yl)piperazin-1-yl]-[2-(trifluoromethyl)phenyl]methanone Chemical compound C1=CC2=NC(CCCCC)=CN2N=C1N(CC1)CCN1C(=O)C1=CC=CC=C1C(F)(F)F AECMFRRWQZBFCY-UHFFFAOYSA-N 0.000 claims 1
- UKFUGRVXZDKAHC-UHFFFAOYSA-N [4-(2-propyl-3h-benzimidazol-5-yl)piperazin-1-yl]-[2-(trifluoromethyl)phenyl]methanone Chemical compound C=1C=C2NC(CCC)=NC2=CC=1N(CC1)CCN1C(=O)C1=CC=CC=C1C(F)(F)F UKFUGRVXZDKAHC-UHFFFAOYSA-N 0.000 claims 1
- UXIXHNZAEPVELV-UHFFFAOYSA-N butanamide 6-[4-[2-(trifluoromethyl)benzoyl]piperazin-1-yl]imidazo[1,2-b]pyridazine-2-carboxylic acid Chemical compound C(CCC)(=O)N.FC(C1=C(C(=O)N2CCN(CC2)C=2C=CC=3N(N2)C=C(N3)C(=O)O)C=CC=C1)(F)F UXIXHNZAEPVELV-UHFFFAOYSA-N 0.000 claims 1
- QRRCXKJNOUZZDS-UHFFFAOYSA-N butanamide 6-[4-[5-fluoro-2-(trifluoromethyl)benzoyl]piperazin-1-yl]imidazo[1,2-b]pyridazine-2-carboxylic acid Chemical compound C(CCC)(=O)N.FC=1C=CC(=C(C(=O)N2CCN(CC2)C=2C=CC=3N(N2)C=C(N3)C(=O)O)C1)C(F)(F)F QRRCXKJNOUZZDS-UHFFFAOYSA-N 0.000 claims 1
- LAFZMBWMUSXBPY-UHFFFAOYSA-N n-(3-cyclopropylpropyl)-6-[4-[5-fluoro-2-(trifluoromethyl)benzoyl]piperazin-1-yl]imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound FC1=CC=C(C(F)(F)F)C(C(=O)N2CCN(CC2)C2=NN3C=C(N=C3C=C2)C(=O)NCCCC2CC2)=C1 LAFZMBWMUSXBPY-UHFFFAOYSA-N 0.000 claims 1
- QNWVQJMOJXPWFC-UHFFFAOYSA-N n-(4-fluorophenyl)-6-[4-[2-(trifluoromethyl)benzoyl]piperazin-1-yl]imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CN(N=C(C=C2)N3CCN(CC3)C(=O)C=3C(=CC=CC=3)C(F)(F)F)C2=N1 QNWVQJMOJXPWFC-UHFFFAOYSA-N 0.000 claims 1
- PMFPUIKGZQZPBB-UHFFFAOYSA-N n-(5-chloropyridin-2-yl)-6-[4-[2-(trifluoromethyl)benzoyl]piperazin-1-yl]imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound FC(F)(F)C1=CC=CC=C1C(=O)N1CCN(C2=NN3C=C(N=C3C=C2)C(=O)NC=2N=CC(Cl)=CC=2)CC1 PMFPUIKGZQZPBB-UHFFFAOYSA-N 0.000 claims 1
- RWGDYMLWUNTSIJ-UHFFFAOYSA-N n-[(4-fluorophenyl)methyl]-6-[4-[2-(trifluoromethyl)benzoyl]piperazin-1-yl]imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound C1=CC(F)=CC=C1CNC(=O)C1=CN(N=C(C=C2)N3CCN(CC3)C(=O)C=3C(=CC=CC=3)C(F)(F)F)C2=N1 RWGDYMLWUNTSIJ-UHFFFAOYSA-N 0.000 claims 1
- SHBVWULGQNELRK-UHFFFAOYSA-N n-[(4-fluorophenyl)methyl]-6-[4-[5-fluoro-2-(trifluoromethyl)benzoyl]piperazin-1-yl]imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound C1=CC(F)=CC=C1CNC(=O)C1=CN(N=C(C=C2)N3CCN(CC3)C(=O)C=3C(=CC=C(F)C=3)C(F)(F)F)C2=N1 SHBVWULGQNELRK-UHFFFAOYSA-N 0.000 claims 1
- IPPLKHPXLPDXSZ-UHFFFAOYSA-N n-[2-(4-fluorophenyl)ethyl]-6-[4-[5-fluoro-2-(trifluoromethyl)benzoyl]piperazin-1-yl]imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound C1=CC(F)=CC=C1CCNC(=O)C1=CN(N=C(C=C2)N3CCN(CC3)C(=O)C=3C(=CC=C(F)C=3)C(F)(F)F)C2=N1 IPPLKHPXLPDXSZ-UHFFFAOYSA-N 0.000 claims 1
- HLNLHSIUBXRMAW-UHFFFAOYSA-N n-pentyl-6-[4-[2-(trifluoromethyl)benzoyl]piperazin-1-yl]imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound C1=CC2=NC(C(=O)NCCCCC)=CN2N=C1N(CC1)CCN1C(=O)C1=CC=CC=C1C(F)(F)F HLNLHSIUBXRMAW-UHFFFAOYSA-N 0.000 claims 1
- 201000009104 prediabetes syndrome Diseases 0.000 claims 1
- 0 CCNC(C(C)C(C)(C(*)C(*)(*)CCC(C)(*)C(C)C)*=C)C1CCCCC1 Chemical compound CCNC(C(C)C(C)(C(*)C(*)(*)CCC(C)(*)C(C)C)*=C)C1CCCCC1 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61164604P | 2004-09-20 | 2004-09-20 | |
| US60/611,646 | 2004-09-20 | ||
| PCT/US2005/033738 WO2006034312A1 (en) | 2004-09-20 | 2005-09-20 | Bicyclic heterocyclic derivatives and their use as inhibitors of stearoyl-coa-desaturase (scd) |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012133967A Division JP2012193188A (ja) | 2004-09-20 | 2012-06-13 | 二環式複素環誘導体およびステアロイル−CoAデサチュラーゼ(SCD)のインヒビターとしてのそれらの使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008513498A JP2008513498A (ja) | 2008-05-01 |
| JP2008513498A5 true JP2008513498A5 (cg-RX-API-DMAC10.html) | 2008-10-30 |
| JP5080256B2 JP5080256B2 (ja) | 2012-11-21 |
Family
ID=35623357
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007532629A Expired - Fee Related JP5080256B2 (ja) | 2004-09-20 | 2005-09-20 | 二環式複素環誘導体およびステアロイル−CoAデサチュラーゼ(SCD)のインヒビターとしてのそれらの使用 |
| JP2012133967A Withdrawn JP2012193188A (ja) | 2004-09-20 | 2012-06-13 | 二環式複素環誘導体およびステアロイル−CoAデサチュラーゼ(SCD)のインヒビターとしてのそれらの使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012133967A Withdrawn JP2012193188A (ja) | 2004-09-20 | 2012-06-13 | 二環式複素環誘導体およびステアロイル−CoAデサチュラーゼ(SCD)のインヒビターとしてのそれらの使用 |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US7547698B2 (cg-RX-API-DMAC10.html) |
| EP (1) | EP1804792A1 (cg-RX-API-DMAC10.html) |
| JP (2) | JP5080256B2 (cg-RX-API-DMAC10.html) |
| CN (1) | CN101083986A (cg-RX-API-DMAC10.html) |
| AR (1) | AR051294A1 (cg-RX-API-DMAC10.html) |
| AU (1) | AU2005286790A1 (cg-RX-API-DMAC10.html) |
| BR (1) | BRPI0515477A (cg-RX-API-DMAC10.html) |
| CA (1) | CA2580781A1 (cg-RX-API-DMAC10.html) |
| MX (1) | MX2007003329A (cg-RX-API-DMAC10.html) |
| TW (1) | TW200626148A (cg-RX-API-DMAC10.html) |
| WO (1) | WO2006034312A1 (cg-RX-API-DMAC10.html) |
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| EP1804799B1 (en) | 2004-09-20 | 2013-08-21 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
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| EP1799667B1 (en) * | 2004-09-20 | 2013-03-20 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as therapeutic agents |
| CN101084212A (zh) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | 杂环衍生物及其作为硬脂酰CoA去饱和酶介导剂的用途 |
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| AU2007288245A1 (en) | 2006-08-24 | 2008-02-28 | Novartis Ag | 2- (pyrazin-2-yl) -thiazole and 2- (1h-pyrazol-3-yl) -thiazole derivatives as well as related compounds as stearoyl-CoA desaturase (SCD) inhibitors for the treatment of metabolic, cardiovascular and other disorders |
| WO2008044767A1 (en) * | 2006-10-13 | 2008-04-17 | Takeda Pharmaceutical Company Limited | Aromatic amine derivative and use thereof |
| TW200826936A (en) | 2006-12-01 | 2008-07-01 | Merck Frosst Canada Ltd | Azacycloalkane derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
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| WO2008096746A1 (ja) | 2007-02-06 | 2008-08-14 | Takeda Pharmaceutical Company Limited | スピロ化合物およびその用途 |
| CA2687338A1 (en) * | 2007-05-23 | 2008-11-27 | Merck Frosst Canada Ltd. | Bicyclic heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
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2005
- 2005-09-20 CN CNA2005800396667A patent/CN101083986A/zh active Pending
- 2005-09-20 AU AU2005286790A patent/AU2005286790A1/en not_active Abandoned
- 2005-09-20 BR BRPI0515477-4A patent/BRPI0515477A/pt not_active IP Right Cessation
- 2005-09-20 AR ARP050103902A patent/AR051294A1/es unknown
- 2005-09-20 CA CA002580781A patent/CA2580781A1/en not_active Abandoned
- 2005-09-20 JP JP2007532629A patent/JP5080256B2/ja not_active Expired - Fee Related
- 2005-09-20 EP EP05808906A patent/EP1804792A1/en not_active Withdrawn
- 2005-09-20 US US11/575,643 patent/US7547698B2/en not_active Expired - Fee Related
- 2005-09-20 TW TW094132549A patent/TW200626148A/zh unknown
- 2005-09-20 WO PCT/US2005/033738 patent/WO2006034312A1/en not_active Ceased
- 2005-09-20 MX MX2007003329A patent/MX2007003329A/es unknown
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2009
- 2009-05-06 US US12/436,665 patent/US20110009414A9/en not_active Abandoned
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2012
- 2012-06-13 JP JP2012133967A patent/JP2012193188A/ja not_active Withdrawn