JP2006526660A - Vr1レセプターのモジュレーター - Google Patents
Vr1レセプターのモジュレーター Download PDFInfo
- Publication number
- JP2006526660A JP2006526660A JP2006515204A JP2006515204A JP2006526660A JP 2006526660 A JP2006526660 A JP 2006526660A JP 2006515204 A JP2006515204 A JP 2006515204A JP 2006515204 A JP2006515204 A JP 2006515204A JP 2006526660 A JP2006526660 A JP 2006526660A
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- JP
- Japan
- Prior art keywords
- ring
- compound
- optionally substituted
- pain
- heteroatoms
- 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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- 0 CC(*)(CC1)CC*=CCCC1IC(CC(C(O1)=C2)NC1=O)=C2I Chemical compound CC(*)(CC1)CC*=CCCC1IC(CC(C(O1)=C2)NC1=O)=C2I 0.000 description 4
- ZGQROMIOSKXRPR-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1C(NCC(C=C1N2)=CCC1NC2=O)=O Chemical compound CC(C)(C)c(cc1)ccc1C(NCC(C=C1N2)=CCC1NC2=O)=O ZGQROMIOSKXRPR-UHFFFAOYSA-N 0.000 description 1
- QKUSKDFFXMRJGR-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1NC(c(cc1N2)ccc1NC2=O)=O Chemical compound CC(C)(C)c(cc1)ccc1NC(c(cc1N2)ccc1NC2=O)=O QKUSKDFFXMRJGR-UHFFFAOYSA-N 0.000 description 1
- PEZLPZKGBHTJAV-UHFFFAOYSA-N CC(C1)=C(C(Nc(cc2N3)ccc2NC3=O)=O)SC1c1cc(C(F)(F)F)ccc1 Chemical compound CC(C1)=C(C(Nc(cc2N3)ccc2NC3=O)=O)SC1c1cc(C(F)(F)F)ccc1 PEZLPZKGBHTJAV-UHFFFAOYSA-N 0.000 description 1
- FEAIKCGBMAGONW-UHFFFAOYSA-N CC(C=C1)NC(Oc(cc2)ccc2F)=C1C(Nc(cc1N2)ccc1NC2=O)=O Chemical compound CC(C=C1)NC(Oc(cc2)ccc2F)=C1C(Nc(cc1N2)ccc1NC2=O)=O FEAIKCGBMAGONW-UHFFFAOYSA-N 0.000 description 1
- UEIRQFMQUVLQCZ-UHFFFAOYSA-N COc(cc1)ccc1-c1ccc(C(Nc(cc2N3)ccc2NC3=O)=O)[s]1 Chemical compound COc(cc1)ccc1-c1ccc(C(Nc(cc2N3)ccc2NC3=O)=O)[s]1 UEIRQFMQUVLQCZ-UHFFFAOYSA-N 0.000 description 1
- ADSJYAMRIHIPHH-UHFFFAOYSA-N Cc([o]c(-c1ccccc1)c1)c1C(Nc(cc1N2)ccc1NC2=O)=O Chemical compound Cc([o]c(-c1ccccc1)c1)c1C(Nc(cc1N2)ccc1NC2=O)=O ADSJYAMRIHIPHH-UHFFFAOYSA-N 0.000 description 1
- JYTVGQIDFHLYNB-UHFFFAOYSA-N Cc1c(C(Nc(cc2N3)ccc2NC3=O)=O)[s]c(-c2ccc(C(F)(F)F)cc2)n1 Chemical compound Cc1c(C(Nc(cc2N3)ccc2NC3=O)=O)[s]c(-c2ccc(C(F)(F)F)cc2)n1 JYTVGQIDFHLYNB-UHFFFAOYSA-N 0.000 description 1
- JPBZRJMGYMJOBL-UHFFFAOYSA-N Cc1c(C(Nc(cc2N3)ccc2NC3=O)=O)[s]c(-c2ccc(C)cc2)n1 Chemical compound Cc1c(C(Nc(cc2N3)ccc2NC3=O)=O)[s]c(-c2ccc(C)cc2)n1 JPBZRJMGYMJOBL-UHFFFAOYSA-N 0.000 description 1
- AUJPIGJXJNSBDN-UHFFFAOYSA-N Cc1c(C(Nc(cc2N3)ccc2NC3=O)=O)[s]c(-c2ccccc2)n1 Chemical compound Cc1c(C(Nc(cc2N3)ccc2NC3=O)=O)[s]c(-c2ccccc2)n1 AUJPIGJXJNSBDN-UHFFFAOYSA-N 0.000 description 1
- DGNVFUPBQAXPSN-UHFFFAOYSA-N O=C(C(C=CCN1)=C1Sc(cc1)ccc1Cl)Nc(cc1N2)ccc1NC2=O Chemical compound O=C(C(C=CCN1)=C1Sc(cc1)ccc1Cl)Nc(cc1N2)ccc1NC2=O DGNVFUPBQAXPSN-UHFFFAOYSA-N 0.000 description 1
- HVBRQYOJEMPFSV-UHFFFAOYSA-N O=C(CCC1CCCC1)Nc(cc1N2)ccc1NC2=O Chemical compound O=C(CCC1CCCC1)Nc(cc1N2)ccc1NC2=O HVBRQYOJEMPFSV-UHFFFAOYSA-N 0.000 description 1
- AREMXLKETQTKKU-UHFFFAOYSA-N O=C(c1c[s]c(-c2c(C(F)(F)F)cccc2)n1)Nc(cc1N2)ccc1NC2=O Chemical compound O=C(c1c[s]c(-c2c(C(F)(F)F)cccc2)n1)Nc(cc1N2)ccc1NC2=O AREMXLKETQTKKU-UHFFFAOYSA-N 0.000 description 1
- HFSLHAYBBWFRIW-UHFFFAOYSA-N O=C(c1c[s]c(-c2ccccc2)n1)NC(CC=C1N2)C=C1NC2=O Chemical compound O=C(c1c[s]c(-c2ccccc2)n1)NC(CC=C1N2)C=C1NC2=O HFSLHAYBBWFRIW-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
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- A61K31/423—Oxazoles condensed with carbocyclic rings
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- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
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- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
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- Thiazole And Isothizaole Compounds (AREA)
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- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US47645703P | 2003-06-05 | 2003-06-05 | |
| PCT/US2004/017779 WO2004108133A2 (en) | 2003-06-05 | 2004-06-04 | Modulators of vr1 receptor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006526660A true JP2006526660A (ja) | 2006-11-24 |
| JP2006526660A5 JP2006526660A5 (enExample) | 2007-07-26 |
Family
ID=33511790
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006515204A Pending JP2006526660A (ja) | 2003-06-05 | 2004-06-04 | Vr1レセプターのモジュレーター |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20050004133A1 (enExample) |
| EP (1) | EP1628661A2 (enExample) |
| JP (1) | JP2006526660A (enExample) |
| WO (1) | WO2004108133A2 (enExample) |
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| JP2010523726A (ja) * | 2007-04-16 | 2010-07-15 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | 新規バニロイド受容体リガンド及び医薬の製造におけるその使用 |
| WO2011118812A1 (ja) * | 2010-03-26 | 2011-09-29 | 国立大学法人北海道大学 | 神経変性疾患治療薬 |
| JP2013523663A (ja) * | 2010-03-30 | 2013-06-17 | ファルメステ ソシエタ ア レスポンサビリタ リミタータ | 二環式部分を持つtrpv1バニロイド受容体拮抗薬 |
| JP2017518348A (ja) * | 2014-06-20 | 2017-07-06 | オーリジーン ディスカバリー テクノロジーズ リミテッドAurigene Discovery Technologies Limited | Irak4阻害剤としての置換インダゾール化合物 |
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Citations (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62215589A (ja) * | 1986-03-17 | 1987-09-22 | Sumitomo Chem Co Ltd | ベンゾチアゾロン誘導体およびそれを有効成分とする除草剤 |
| JPS6423255A (en) * | 1987-07-20 | 1989-01-25 | Fuji Photo Film Co Ltd | Silver halide photographic sensitive material |
| JPH0311062A (ja) * | 1989-05-12 | 1991-01-18 | Schering Ag | 2―フエニル―ペルヒドロ―イソインドール‐1‐オン及び‐1‐チオン、その製法、該化合物を含有する除草作用を有する薬剤及び該薬剤の製法 |
| JPH0375744A (ja) * | 1989-08-18 | 1991-03-29 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料の処理方法 |
| JPH10500960A (ja) * | 1994-05-28 | 1998-01-27 | スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー | 5ht1d−アンタゴニスト活性を有するアミド誘導体 |
| WO2000018744A1 (en) * | 1998-09-25 | 2000-04-06 | Fujisawa Pharmaceutical Co., Ltd. | Oxazole compounds as prostaglandin e2 agonists or antagonists |
| WO2000020358A2 (en) * | 1998-08-20 | 2000-04-13 | Agouron Pharmaceuticals, Inc. | NON-PEPTIDE GnRH AGENTS, METHODS AND INTERMEDIATES FOR THEIR PREPARATION |
| WO2000027819A2 (de) * | 1998-11-10 | 2000-05-18 | Schering Aktiengesellschaft | Anthranilsäureamide und deren verwendung als arzneimittel |
| WO2001057002A1 (fr) * | 2000-02-02 | 2001-08-09 | Les Laboratoires Servier | Derives d'azoles condenses et leur utilisation comme agents hypoglycemiants |
| US6291476B1 (en) * | 1999-05-12 | 2001-09-18 | Ortho-Mcneil Pharmaceutical, Inc. | Pyrazole carboxamides useful for the treatment of obesity and other disorders |
| WO2001068619A1 (en) * | 2000-03-15 | 2001-09-20 | Warner-Lambert Company | 5-amide substituted diarylamines as mex inhibitors |
| WO2001085719A1 (de) * | 2000-05-09 | 2001-11-15 | Schering Aktiengesellschaft | Ortho substituierte anthranilsäureamide und deren verwendung als arzneimittel |
| WO2002046170A2 (en) * | 2000-12-06 | 2002-06-13 | Signal Pharmaceuticals, Inc. | Anilinopyrimidine derivatives as jnk pathway inhibitors and compositions and methods related thereto |
| WO2002090352A2 (de) * | 2001-05-08 | 2002-11-14 | Schering Aktiengesellschaft | Selektive anthranylamidpyridinamide als vegfr-2 und vegfr-3 inhibitoren |
| WO2002100833A1 (en) * | 2001-06-12 | 2002-12-19 | Sumitomo Pharmaceuticals Company, Limited | Rho KINASE INHIBITORS |
| US20030078252A1 (en) * | 2001-05-11 | 2003-04-24 | Pfizer Inc. | Thiazole derivatives |
| WO2003037274A2 (en) * | 2001-11-01 | 2003-05-08 | Icagen, Inc. | Pyrazole-amides and-sulfonamides |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002047287A (ja) * | 2000-05-25 | 2002-02-12 | Kyowa Hakko Kogyo Co Ltd | 芳香族誘導体 |
| US7105682B2 (en) * | 2001-01-12 | 2006-09-12 | Amgen Inc. | Substituted amine derivatives and methods of use |
-
2004
- 2004-06-04 EP EP04754390A patent/EP1628661A2/en not_active Withdrawn
- 2004-06-04 US US10/861,788 patent/US20050004133A1/en not_active Abandoned
- 2004-06-04 JP JP2006515204A patent/JP2006526660A/ja active Pending
- 2004-06-04 WO PCT/US2004/017779 patent/WO2004108133A2/en not_active Ceased
Patent Citations (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62215589A (ja) * | 1986-03-17 | 1987-09-22 | Sumitomo Chem Co Ltd | ベンゾチアゾロン誘導体およびそれを有効成分とする除草剤 |
| JPS6423255A (en) * | 1987-07-20 | 1989-01-25 | Fuji Photo Film Co Ltd | Silver halide photographic sensitive material |
| JPH0311062A (ja) * | 1989-05-12 | 1991-01-18 | Schering Ag | 2―フエニル―ペルヒドロ―イソインドール‐1‐オン及び‐1‐チオン、その製法、該化合物を含有する除草作用を有する薬剤及び該薬剤の製法 |
| JPH0375744A (ja) * | 1989-08-18 | 1991-03-29 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料の処理方法 |
| JPH10500960A (ja) * | 1994-05-28 | 1998-01-27 | スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー | 5ht1d−アンタゴニスト活性を有するアミド誘導体 |
| WO2000020358A2 (en) * | 1998-08-20 | 2000-04-13 | Agouron Pharmaceuticals, Inc. | NON-PEPTIDE GnRH AGENTS, METHODS AND INTERMEDIATES FOR THEIR PREPARATION |
| WO2000018744A1 (en) * | 1998-09-25 | 2000-04-06 | Fujisawa Pharmaceutical Co., Ltd. | Oxazole compounds as prostaglandin e2 agonists or antagonists |
| WO2000027819A2 (de) * | 1998-11-10 | 2000-05-18 | Schering Aktiengesellschaft | Anthranilsäureamide und deren verwendung als arzneimittel |
| US6291476B1 (en) * | 1999-05-12 | 2001-09-18 | Ortho-Mcneil Pharmaceutical, Inc. | Pyrazole carboxamides useful for the treatment of obesity and other disorders |
| WO2001057002A1 (fr) * | 2000-02-02 | 2001-08-09 | Les Laboratoires Servier | Derives d'azoles condenses et leur utilisation comme agents hypoglycemiants |
| WO2001068619A1 (en) * | 2000-03-15 | 2001-09-20 | Warner-Lambert Company | 5-amide substituted diarylamines as mex inhibitors |
| WO2001085719A1 (de) * | 2000-05-09 | 2001-11-15 | Schering Aktiengesellschaft | Ortho substituierte anthranilsäureamide und deren verwendung als arzneimittel |
| WO2002046170A2 (en) * | 2000-12-06 | 2002-06-13 | Signal Pharmaceuticals, Inc. | Anilinopyrimidine derivatives as jnk pathway inhibitors and compositions and methods related thereto |
| WO2002090352A2 (de) * | 2001-05-08 | 2002-11-14 | Schering Aktiengesellschaft | Selektive anthranylamidpyridinamide als vegfr-2 und vegfr-3 inhibitoren |
| US20030078252A1 (en) * | 2001-05-11 | 2003-04-24 | Pfizer Inc. | Thiazole derivatives |
| WO2002100833A1 (en) * | 2001-06-12 | 2002-12-19 | Sumitomo Pharmaceuticals Company, Limited | Rho KINASE INHIBITORS |
| WO2003037274A2 (en) * | 2001-11-01 | 2003-05-08 | Icagen, Inc. | Pyrazole-amides and-sulfonamides |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007518816A (ja) * | 2004-01-23 | 2007-07-12 | アムジエン・インコーポレーテツド | バニロイド受容体リガンド及び炎症性及び神経因性疼痛の治療におけるこれらの使用 |
| JP2010523726A (ja) * | 2007-04-16 | 2010-07-15 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | 新規バニロイド受容体リガンド及び医薬の製造におけるその使用 |
| US8642775B2 (en) | 2007-04-16 | 2014-02-04 | Gruenenthal Gmbh | Vanilloid receptor ligands, pharmaceutical compositions containing them, process for making them, and use thereof for treating pain and other conditions |
| US8791268B2 (en) | 2007-04-16 | 2014-07-29 | Gruenenthal Gmbh | Vanilloid receptor ligands, pharmaceutical compositions containing them, process for making them, and use thereof for treating pain and other conditions |
| WO2011118812A1 (ja) * | 2010-03-26 | 2011-09-29 | 国立大学法人北海道大学 | 神経変性疾患治療薬 |
| JP5733839B2 (ja) * | 2010-03-26 | 2015-06-10 | 国立大学法人北海道大学 | 神経変性疾患治療薬 |
| JP2013523663A (ja) * | 2010-03-30 | 2013-06-17 | ファルメステ ソシエタ ア レスポンサビリタ リミタータ | 二環式部分を持つtrpv1バニロイド受容体拮抗薬 |
| JP2017518348A (ja) * | 2014-06-20 | 2017-07-06 | オーリジーン ディスカバリー テクノロジーズ リミテッドAurigene Discovery Technologies Limited | Irak4阻害剤としての置換インダゾール化合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004108133A2 (en) | 2004-12-16 |
| US20050004133A1 (en) | 2005-01-06 |
| WO2004108133A3 (en) | 2005-03-31 |
| EP1628661A2 (en) | 2006-03-01 |
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