WO2008105058A1 - スルホンアミド化合物 - Google Patents
スルホンアミド化合物 Download PDFInfo
- Publication number
- WO2008105058A1 WO2008105058A1 PCT/JP2007/053567 JP2007053567W WO2008105058A1 WO 2008105058 A1 WO2008105058 A1 WO 2008105058A1 JP 2007053567 W JP2007053567 W JP 2007053567W WO 2008105058 A1 WO2008105058 A1 WO 2008105058A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hydroxy
- alkyl
- hydrogen
- alkenyl
- halogeno
- 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.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Rhoキナーゼを強力に阻害する式(1)[Aは含窒素飽和環を示し;mは0~2の整数を示し;nは1~4の整数を示し;G1は水素原子、塩素原子、水酸基、アルコキシ基、又はアミノ基を示し;G2はハロゲン原子、水酸基、シアノ基、カルボキシ基、アルキル基、アルケニル基などを示し;G3は水素原子、ハロゲン原子、水酸基、シアノ基、カルボキシ基、アルキル基、アルケニル基などを示し;G4は水酸基、又は-N(R1)(R2)(R1及びR2は水素原子、アルキル基、アラルキル基、アルケニル基、アルキニル基、又は飽和ヘテロ環基を示す)を示し;G5はAの環構成炭素原子における置換基であり、水素原子、フッ素原子、又はアルキル基を示す]で表される化合物又はその塩、あるいはプロドラッグであるそれらの誘導体。
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/526,000 US8415372B2 (en) | 2007-02-27 | 2007-02-27 | Sulfonamide compound |
| PCT/JP2007/053567 WO2008105058A1 (ja) | 2007-02-27 | 2007-02-27 | スルホンアミド化合物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/JP2007/053567 WO2008105058A1 (ja) | 2007-02-27 | 2007-02-27 | スルホンアミド化合物 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2008105058A1 true WO2008105058A1 (ja) | 2008-09-04 |
Family
ID=39720904
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2007/053567 Ceased WO2008105058A1 (ja) | 2007-02-27 | 2007-02-27 | スルホンアミド化合物 |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US8415372B2 (ja) |
| WO (1) | WO2008105058A1 (ja) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7618984B2 (en) | 2005-08-30 | 2009-11-17 | Asahi Kasei Pharma Corporation | Sulfonamide compound |
| US7964613B2 (en) | 2007-02-28 | 2011-06-21 | Asahi Kasei Pharma Corporation | Sulfonamide compound |
| US8232292B2 (en) | 2007-07-02 | 2012-07-31 | Asahi Kasei Pharma Corporation | Sulfonamide compound and crystal thereof |
| WO2012105674A1 (ja) | 2011-02-04 | 2012-08-09 | 興和株式会社 | 緑内障予防又は治療のための薬物療法 |
| WO2014192915A1 (ja) * | 2013-05-30 | 2014-12-04 | 国立大学法人 千葉大学 | 抗ミオシン調節軽鎖ポリペプチド抗体を含む炎症疾患治療用組成物 |
| WO2017122666A1 (ja) * | 2016-01-12 | 2017-07-20 | 国立大学法人 千葉大学 | 抗Myl9抗体 |
| EP3461484B1 (en) | 2013-03-15 | 2020-11-18 | Aerie Pharmaceuticals, Inc. | Dimesylate salts of 4-(3-amino-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)benzyl, their combinations with prostaglandins and the use thereof in the treatment of ocular disorders |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2929545C (en) | 2009-05-01 | 2019-04-09 | Aerie Pharmaceuticals, Inc. | Dual mechanism inhibitors for the treatment of disease |
| WO2014199131A1 (en) * | 2013-06-13 | 2014-12-18 | Cipla Limited | Fixed Dose Pharmaceutical Composition |
| EP3138843B1 (en) * | 2014-04-28 | 2019-11-27 | Medshine Discovery Inc. | Isoquinolinesulfonyl derivative as rho kinase inhibitor |
| WO2018045091A1 (en) | 2016-08-31 | 2018-03-08 | Aerie Pharmaceuticals, Inc. | Ophthalmic compositions |
| KR20190135027A (ko) | 2017-03-31 | 2019-12-05 | 에어리 파마슈티컬즈, 인코포레이티드 | 아릴 시클로프로필-아미노-이소퀴놀리닐 아미드 화합물 |
| CA3112391A1 (en) | 2018-09-14 | 2020-03-19 | Aerie Pharmaceuticals, Inc. | Aryl cyclopropyl-amino-isoquinolinyl amide compounds |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05208973A (ja) * | 1991-07-31 | 1993-08-20 | Adir | 新規なn−(イソキノリン−5−イルスルホニル)アザシクロアルカン化合物 |
| JPH06100540A (ja) * | 1992-09-24 | 1994-04-12 | Asahi Chem Ind Co Ltd | 5−イソキノリンスルホン酸アミド誘導体 |
| JPH1087491A (ja) * | 1996-07-26 | 1998-04-07 | Asahi Chem Ind Co Ltd | 転写調節因子阻害剤 |
| WO1999064011A1 (en) * | 1998-06-11 | 1999-12-16 | Hiroyoshi Hidaka | Drugs |
| JP2001509780A (ja) * | 1995-12-21 | 2001-07-24 | アルコン ラボラトリーズ,インコーポレイテッド | 緑内障および眼虚血の治療のための特定のイソキノリンスルホニル化合物の使用 |
| JP2004107335A (ja) * | 2002-08-29 | 2004-04-08 | Santen Pharmaceut Co Ltd | Rhoキナーゼ阻害剤とプロスタグランジン類からなる緑内障治療剤 |
| JP2004182723A (ja) * | 2002-11-18 | 2004-07-02 | Santen Pharmaceut Co Ltd | Rhoキナーゼ阻害剤とβ遮断薬からなる緑内障治療剤 |
| WO2005080394A1 (en) * | 2004-02-24 | 2005-09-01 | Bioaxone Therapeutique Inc. | 4-substituted piperidine derivatives |
Family Cites Families (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4456757A (en) | 1981-03-20 | 1984-06-26 | Asahi Kasei Kogyo Kabushiki Kaisha | Isoquinolinesulfonyl derivatives and process for the preparation thereof |
| JPS57200366A (en) | 1981-06-01 | 1982-12-08 | Asahi Chem Ind Co Ltd | Isoquinoline compound |
| JPS57156463A (en) | 1981-03-20 | 1982-09-27 | Asahi Chem Ind Co Ltd | Isoquinoline derivative |
| JPH0667926B2 (ja) | 1985-11-12 | 1994-08-31 | 旭化成工業株式会社 | 環状のイソキノリンスルホンアミド誘導体 |
| CA2005741C (en) | 1988-12-26 | 1998-06-02 | Hiroyoshi Hidaka | Quinoline sulfonoamino compounds having vessel smooth muscle relaxation activity |
| JP2886225B2 (ja) | 1988-12-26 | 1999-04-26 | 弘義 日高 | アルキレンジアミン誘導体及びその製造方法 |
| US5245034A (en) | 1988-12-26 | 1993-09-14 | Kiroyoshi Hidaka | Compound having vessel smooth muscle relaxation activity |
| US5216150A (en) | 1988-12-26 | 1993-06-01 | Hiroyoshi Hidaka | Derivatives of isoquinoline (and naphthalene) sulfonamides |
| JP3408546B2 (ja) | 1991-02-19 | 2003-05-19 | 旭化成株式会社 | 抗喘息剤 |
| DK0602028T3 (da) | 1991-09-05 | 1996-02-12 | Pharno Wedropharm Gmbh | Aromatiske sulfonamidderivater, deres anvendelse som enzyminhibitorer og farmaceutiske præparater me d indhold deraf |
| CA2240271C (en) | 1995-12-21 | 2005-12-13 | Alcon Laboratories, Inc. | Use of certain isoquinolinesulfonyl compounds for the treatment of glaucoma and ocular ischemia |
| EP0885888B1 (en) | 1996-02-02 | 2003-08-13 | Dr.HIDAKA Hiroyoshi | Isoquinoline derivatives and drugs |
| IL128456A0 (en) | 1996-08-12 | 2000-01-31 | Yoshitomi Pharmaceutical | Compositions containing a Rho kinase inhibitor |
| JP4316794B2 (ja) | 1997-10-22 | 2009-08-19 | 株式会社デ・ウエスタン・セラピテクス研究所 | イソキノリン誘導体及び医薬 |
| EP1074545A4 (en) | 1998-04-23 | 2001-08-22 | Hiroyoshi Hidaka | ISOCHINOLINE SULPHONAMIDE DERIVATIVES AND MEDICINES CONTAINING IT AS AN ACTIVE INGREDIENT |
| US7217722B2 (en) | 2000-02-01 | 2007-05-15 | Kirin Beer Kabushiki Kaisha | Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same |
| DE60218138T2 (de) | 2001-03-23 | 2007-09-20 | Bayer Pharmaceuticals Corp., West Haven | Rho-kinase inhibitoren |
| US20030125344A1 (en) | 2001-03-23 | 2003-07-03 | Bayer Corporation | Rho-kinase inhibitors |
| JPWO2002100833A1 (ja) | 2001-06-12 | 2004-09-24 | 住友製薬株式会社 | Rhoキナーゼ阻害剤 |
| US7094789B2 (en) | 2002-07-22 | 2006-08-22 | Asahi Kasei Pharma Corporation | 5-substituted isoquinoline derivatives |
| AU2003281623B8 (en) | 2002-07-22 | 2009-06-11 | Asahi Kasei Pharma Corporation | 5-substituted isoquinoline derivative |
| CN100425241C (zh) | 2002-08-29 | 2008-10-15 | 参天制药株式会社 | 由Rho激酶抑制剂和前列腺素类物质构成的青光眼治疗剂 |
| CA2502583A1 (en) | 2002-09-12 | 2004-03-25 | Kirin Beer Kabushiki Kaisha | Isoquinoline derivatives having kinase inhibitory activity and medicament containing the same |
| MY140618A (en) | 2003-02-28 | 2009-12-31 | Kowa Co | Method for preparing acid addition salts of polyacidic basic compounds |
| US7160894B2 (en) | 2003-06-06 | 2007-01-09 | Asahi Kasei Pharma Corporation | Tricyclic compound |
| GB0317315D0 (en) | 2003-07-24 | 2003-08-27 | Astex Technology Ltd | Pharmaceutical compounds |
| JP2007008816A (ja) | 2003-10-15 | 2007-01-18 | Ube Ind Ltd | 新規イソキノリン誘導体 |
| JP2007015928A (ja) | 2003-10-15 | 2007-01-25 | Ube Ind Ltd | 新規オレフィン誘導体 |
| ES2426288T3 (es) | 2003-10-15 | 2013-10-22 | Ube Industries, Ltd. | Novedoso derivado de imidazol |
| JP2005232175A (ja) | 2004-01-21 | 2005-09-02 | Asahi Kasei Pharma Kk | 5−置換イソキノリン医薬 |
| US20060247266A1 (en) | 2004-11-26 | 2006-11-02 | Asahi Kasei Pharma Corporation | Nitrogen-containing tricyclic compounds |
| MY139797A (en) | 2004-11-29 | 2009-10-30 | Kowa Co | (s)-(-)-1-(4-fluoroisoquinolin-5-yl)sulfonyl-2-methyl-1, 4-homopiperazine hydrochloride dihydrate |
| EP1866298A2 (en) | 2005-03-31 | 2007-12-19 | Takeda San Diego, Inc. | Hydroxysteroid dehydrogenase inhibitors |
| DE602006005351D1 (de) | 2005-04-25 | 2009-04-09 | Western Therapeutics Inst Inc | Hochselektiver rho-kinase-inhibitor |
| WO2006115245A1 (ja) | 2005-04-25 | 2006-11-02 | D. Western Therapeutics Institute, Inc. | 4-エチニルイソキノリン誘導体及びこれを含有する医薬 |
| WO2006115244A1 (ja) | 2005-04-25 | 2006-11-02 | D. Western Therapeutics Institute, Inc. | 4-ブロモイソキノリン誘導体及びこれを含有する医薬 |
| JP2006348028A (ja) | 2005-05-19 | 2006-12-28 | Kowa Co | 緑内障予防又は治療剤 |
| CN101198354B (zh) | 2005-06-21 | 2012-01-11 | 兴和株式会社 | 青光眼的预防或治疗剂 |
| ES2416334T3 (es) | 2005-07-12 | 2013-07-31 | Kowa Company. Ltd. | Agente para la prevención o el tratamiento del glaucoma |
| KR101149954B1 (ko) | 2005-08-30 | 2012-06-01 | 아사히 가세이 파마 가부시키가이샤 | 술폰아미드 화합물 |
| JP2007238458A (ja) | 2006-03-06 | 2007-09-20 | D Western Therapeutics Institute Inc | 新規なイソキノリン誘導体及びこれを含有する医薬 |
| WO2008105442A1 (ja) | 2007-02-28 | 2008-09-04 | Asahi Kasei Pharma Corporation | スルホンアミド誘導体 |
| WO2009004792A1 (ja) | 2007-07-02 | 2009-01-08 | Asahi Kasei Pharma Corporation | スルホンアミド化合物及びその結晶 |
-
2007
- 2007-02-27 US US12/526,000 patent/US8415372B2/en not_active Expired - Fee Related
- 2007-02-27 WO PCT/JP2007/053567 patent/WO2008105058A1/ja not_active Ceased
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05208973A (ja) * | 1991-07-31 | 1993-08-20 | Adir | 新規なn−(イソキノリン−5−イルスルホニル)アザシクロアルカン化合物 |
| JPH06100540A (ja) * | 1992-09-24 | 1994-04-12 | Asahi Chem Ind Co Ltd | 5−イソキノリンスルホン酸アミド誘導体 |
| JP2001509780A (ja) * | 1995-12-21 | 2001-07-24 | アルコン ラボラトリーズ,インコーポレイテッド | 緑内障および眼虚血の治療のための特定のイソキノリンスルホニル化合物の使用 |
| JPH1087491A (ja) * | 1996-07-26 | 1998-04-07 | Asahi Chem Ind Co Ltd | 転写調節因子阻害剤 |
| WO1999064011A1 (en) * | 1998-06-11 | 1999-12-16 | Hiroyoshi Hidaka | Drugs |
| JP2004107335A (ja) * | 2002-08-29 | 2004-04-08 | Santen Pharmaceut Co Ltd | Rhoキナーゼ阻害剤とプロスタグランジン類からなる緑内障治療剤 |
| JP2004182723A (ja) * | 2002-11-18 | 2004-07-02 | Santen Pharmaceut Co Ltd | Rhoキナーゼ阻害剤とβ遮断薬からなる緑内障治療剤 |
| WO2005080394A1 (en) * | 2004-02-24 | 2005-09-01 | Bioaxone Therapeutique Inc. | 4-substituted piperidine derivatives |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7618984B2 (en) | 2005-08-30 | 2009-11-17 | Asahi Kasei Pharma Corporation | Sulfonamide compound |
| US7964613B2 (en) | 2007-02-28 | 2011-06-21 | Asahi Kasei Pharma Corporation | Sulfonamide compound |
| US8664243B2 (en) | 2007-07-02 | 2014-03-04 | Asahi Kasei Pharma Corporation | Sulfonamide compound and crystal thereof |
| US8232292B2 (en) | 2007-07-02 | 2012-07-31 | Asahi Kasei Pharma Corporation | Sulfonamide compound and crystal thereof |
| KR20180023041A (ko) | 2011-02-04 | 2018-03-06 | 코와 가부시키가이샤 | 녹내장 예방 또는 치료를 위한 약물 요법 |
| JPWO2012105674A1 (ja) * | 2011-02-04 | 2014-07-03 | 興和株式会社 | 緑内障予防又は治療のための薬物療法 |
| WO2012105674A1 (ja) | 2011-02-04 | 2012-08-09 | 興和株式会社 | 緑内障予防又は治療のための薬物療法 |
| EP3461484B1 (en) | 2013-03-15 | 2020-11-18 | Aerie Pharmaceuticals, Inc. | Dimesylate salts of 4-(3-amino-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)benzyl, their combinations with prostaglandins and the use thereof in the treatment of ocular disorders |
| WO2014192915A1 (ja) * | 2013-05-30 | 2014-12-04 | 国立大学法人 千葉大学 | 抗ミオシン調節軽鎖ポリペプチド抗体を含む炎症疾患治療用組成物 |
| JPWO2014192915A1 (ja) * | 2013-05-30 | 2017-02-23 | 国立大学法人 千葉大学 | 抗ミオシン調節軽鎖ポリペプチド抗体を含む炎症疾患治療用組成物 |
| WO2017122666A1 (ja) * | 2016-01-12 | 2017-07-20 | 国立大学法人 千葉大学 | 抗Myl9抗体 |
| CN108431037A (zh) * | 2016-01-12 | 2018-08-21 | 国立大学法人千叶大学 | 抗myl9抗体 |
| JPWO2017122666A1 (ja) * | 2016-01-12 | 2018-11-01 | 国立大学法人千葉大学 | 抗Myl9抗体 |
| US10513561B2 (en) | 2016-01-12 | 2019-12-24 | National University Corporation Chiba University | Anti-MYL9 antibody |
| CN108431037B (zh) * | 2016-01-12 | 2021-12-17 | 国立大学法人千叶大学 | 抗myl9抗体 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20100093789A1 (en) | 2010-04-15 |
| US8415372B2 (en) | 2013-04-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2008105058A1 (ja) | スルホンアミド化合物 | |
| WO2008105442A1 (ja) | スルホンアミド誘導体 | |
| TN2009000024A1 (en) | Prodrug of cinnamide compound | |
| TW200732306A (en) | Pyrimidine derivatives | |
| WO2008108378A3 (en) | Bicyclic oxomorpholine derivative | |
| WO2009001817A1 (ja) | 11β-HSD1阻害活性を有する化合物 | |
| AU2008303600A8 (en) | 1,1,1-trifluoro-2-hydroxy-3-phenylpropane derivatives | |
| WO2008108380A3 (en) | Pyrrole compounds | |
| WO2007084914A3 (en) | Phenoxy-substituted pyrimidines as adenosine receptor antagonists | |
| WO2005110410A3 (en) | Kinase inhibitors as therapeutic agents | |
| MX2009004920A (es) | Nuevos derivados de aminopirimidina como inhibidores de plk1. | |
| WO2009035150A3 (en) | 4-phenyl-5-hydroxy-3(2h)-pyridazinone derivatives as herbicides | |
| TNSN08407A1 (en) | Organic compounds | |
| WO2009107850A3 (en) | Fused heterocyclic derivative and use thereof | |
| WO2008096829A1 (ja) | 3環系化合物 | |
| EA017861B9 (ru) | Способ получения 4-оксохинолинового соединения | |
| WO2007133352A3 (en) | Macrocyclic kinase inhibitors | |
| WO2009057079A3 (en) | Novel pyrimidine derivatives | |
| WO2007103839A3 (en) | Pyrrolotriazine aniline prodrug compounds useful as kinase inhibitors | |
| WO2008078725A1 (ja) | チアゼピン誘導体 | |
| IN2014CN00532A (ja) | ||
| WO2008156094A1 (ja) | ピリダジノン誘導体及びそれらを有効成分とするpde阻害剤 | |
| WO2009038064A1 (ja) | I型11βヒドロキシステロイド脱水素酵素阻害活性を有する複素環誘導体 | |
| WO2008126901A1 (ja) | 含窒素複素環化合物およびそれを含有する医薬組成物 | |
| WO2009054439A1 (ja) | Pai-1産生抑制剤 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 07714960 Country of ref document: EP Kind code of ref document: A1 |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 12526000 Country of ref document: US |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 07714960 Country of ref document: EP Kind code of ref document: A1 |
|
| NENP | Non-entry into the national phase |
Ref country code: JP |