JP2002371059A5 - - Google Patents
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- Publication number
- JP2002371059A5 JP2002371059A5 JP2001145691A JP2001145691A JP2002371059A5 JP 2002371059 A5 JP2002371059 A5 JP 2002371059A5 JP 2001145691 A JP2001145691 A JP 2001145691A JP 2001145691 A JP2001145691 A JP 2001145691A JP 2002371059 A5 JP2002371059 A5 JP 2002371059A5
- Authority
- JP
- Japan
- Prior art keywords
- substituent
- ring
- compound according
- group
- nitrogen
- 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.)
- Withdrawn
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- 125000001424 substituent group Chemical group 0.000 description 36
- 150000001875 compounds Chemical class 0.000 description 26
- 150000003839 salts Chemical class 0.000 description 15
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 14
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 13
- 125000000623 heterocyclic group Chemical group 0.000 description 11
- 125000006850 spacer group Chemical group 0.000 description 11
- 125000004429 atom Chemical group 0.000 description 10
- 125000001183 hydrocarbyl group Chemical group 0.000 description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 description 8
- 125000004122 cyclic group Chemical group 0.000 description 7
- 239000003814 drug Substances 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 5
- 150000001555 benzenes Chemical group 0.000 description 5
- 229940124597 therapeutic agent Drugs 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 239000008194 pharmaceutical composition Substances 0.000 description 4
- 239000000651 prodrug Substances 0.000 description 4
- 229940002612 prodrug Drugs 0.000 description 4
- 101800002739 Melanin-concentrating hormone Proteins 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- ORRDHOMWDPJSNL-UHFFFAOYSA-N melanin concentrating hormone Chemical compound N1C(=O)C(C(C)C)NC(=O)C(CCCNC(N)=N)NC(=O)CNC(=O)C(C(C)C)NC(=O)C(CCSC)NC(=O)C(NC(=O)C(CCCNC(N)=N)NC(=O)C(NC(=O)C(NC(=O)C(N)CC(O)=O)C(C)O)CCSC)CSSCC(C(=O)NC(CC=2C3=CC=CC=C3NC=2)C(=O)NC(CCC(O)=O)C(=O)NC(C(C)C)C(O)=O)NC(=O)C2CCCN2C(=O)C(CCCNC(N)=N)NC(=O)C1CC1=CC=C(O)C=C1 ORRDHOMWDPJSNL-UHFFFAOYSA-N 0.000 description 3
- 102000047659 melanin-concentrating hormone Human genes 0.000 description 3
- 125000005915 C6-C14 aryl group Chemical group 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000003667 hormone antagonist Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000069 prophylactic effect Effects 0.000 description 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 description 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 description 1
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 description 1
- SPCXCXWTBGVFJF-UHFFFAOYSA-N 4,5-dihydro-3h-azepine Chemical compound C1CC=CN=CC1 SPCXCXWTBGVFJF-UHFFFAOYSA-N 0.000 description 1
- 206010003210 Arteriosclerosis Diseases 0.000 description 1
- 0 CCCCC(C=C1)=C(CCCCC*C)C=C*1[N+](C)[O-] Chemical compound CCCCC(C=C1)=C(CCCCC*C)C=C*1[N+](C)[O-] 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 125000002015 acyclic group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000001887 anti-feedant effect Effects 0.000 description 1
- 208000011775 arteriosclerosis disease Diseases 0.000 description 1
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 1
- -1 biphenylyl Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001145691A JP2002371059A (ja) | 2000-05-16 | 2001-05-15 | メラニン凝集ホルモン拮抗剤 |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000148647 | 2000-05-16 | ||
| JP2001116219 | 2001-04-13 | ||
| JP2001-116219 | 2001-04-13 | ||
| JP2000-148647 | 2001-04-13 | ||
| JP2001145691A JP2002371059A (ja) | 2000-05-16 | 2001-05-15 | メラニン凝集ホルモン拮抗剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002371059A JP2002371059A (ja) | 2002-12-26 |
| JP2002371059A5 true JP2002371059A5 (https=) | 2008-06-26 |
Family
ID=27343435
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001145691A Withdrawn JP2002371059A (ja) | 2000-05-16 | 2001-05-15 | メラニン凝集ホルモン拮抗剤 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2002371059A (https=) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2468015A1 (en) | 2001-11-27 | 2003-06-05 | Merck & Co., Inc. | 2-aminoquinoline compounds |
| EP2133340B1 (en) * | 2002-12-20 | 2013-01-16 | Glaxo Group Limited | Novel benzazepine derivatives |
| US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
| US7727998B2 (en) | 2003-02-10 | 2010-06-01 | Banyu Pharmaceutical Co., Ltd. | Melanin-concentrating hormone receptor antagonists containing piperidine derivatives as the active ingredient |
| CN100418965C (zh) * | 2003-08-15 | 2008-09-17 | 万有制药株式会社 | 咪唑并吡啶衍生物 |
| US7902356B2 (en) * | 2004-12-17 | 2011-03-08 | Eli Lilly And Company | Thiazolopyridinone derivates as MCH receptor antagonists |
| GB0504314D0 (en) * | 2005-03-02 | 2005-04-06 | Glaxo Group Ltd | Novel polymorph |
| WO2007028131A1 (en) * | 2005-09-01 | 2007-03-08 | Eli Lilly And Company | 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO[d]AZEPINES AS 5-HT2C RECEPTOR AGONISTS |
| JP5249031B2 (ja) * | 2005-09-01 | 2013-07-31 | イーライ リリー アンド カンパニー | ５−ＨＴ２Ｃ受容体アゴニストとしての６−Ｎ結合型へテロ環置換された２，３，４，５−テトラヒドロ−１Ｈ−ベンゾ［ｄ］アゼピン |
| MX2010011288A (es) * | 2008-04-23 | 2010-11-09 | Rigel Pharmaceuticals Inc | Compuestos de carboxamida para el tratamiento de trastornos metabolicos. |
| ES2350077B1 (es) * | 2009-06-04 | 2011-11-04 | Laboratorios Salvat, S.A. | Compuestos inhibidores de 11beta-hidroxiesteroide deshidrogenasa de tipo 1. |
| US8895596B2 (en) | 2010-02-25 | 2014-11-25 | Merck Sharp & Dohme Corp | Cyclic benzimidazole derivatives useful as anti-diabetic agents |
| US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
| CA2848877A1 (en) * | 2011-09-15 | 2013-03-21 | Taipei Medical University | Use of indolyl and indolinvl hvdroxamates for treating heart failure or neuronal injury |
-
2001
- 2001-05-15 JP JP2001145691A patent/JP2002371059A/ja not_active Withdrawn
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