WO2002100833A1 - Rho KINASE INHIBITORS - Google Patents
Rho KINASE INHIBITORS Download PDFInfo
- Publication number
- WO2002100833A1 WO2002100833A1 PCT/JP2002/005609 JP0205609W WO02100833A1 WO 2002100833 A1 WO2002100833 A1 WO 2002100833A1 JP 0205609 W JP0205609 W JP 0205609W WO 02100833 A1 WO02100833 A1 WO 02100833A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- substituted
- hydrogen
- unsubstituted alkyl
- rho kinase
- kinase inhibitors
- 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
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- 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A61P11/00—Drugs for disorders of the respiratory system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
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- A61P13/08—Drugs for disorders of the urinary system of the prostate
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P9/08—Vasodilators for multiple indications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Reproductive Health (AREA)
- Endocrinology (AREA)
- Urology & Nephrology (AREA)
- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
- Pulmonology (AREA)
- Gynecology & Obstetrics (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Oncology (AREA)
- Virology (AREA)
- Hospice & Palliative Care (AREA)
- Communicable Diseases (AREA)
- Pregnancy & Childbirth (AREA)
- Rheumatology (AREA)
- AIDS & HIV (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Vascular Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Tropical Medicine & Parasitology (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02733352A EP1403255A4 (en) | 2001-06-12 | 2002-06-06 | RHO KINASE INHIBITORS |
| US10/480,526 US7199147B2 (en) | 2001-06-12 | 2002-06-06 | Rho kinase inhibitors |
| JP2003503602A JPWO2002100833A1 (ja) | 2001-06-12 | 2002-06-06 | Rhoキナーゼ阻害剤 |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001176826 | 2001-06-12 | ||
| JP2001-176826 | 2001-06-12 | ||
| JP2001398992 | 2001-12-28 | ||
| JP2001-398992 | 2001-12-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2002100833A1 true WO2002100833A1 (en) | 2002-12-19 |
Family
ID=26616749
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2002/005609 Ceased WO2002100833A1 (en) | 2001-06-12 | 2002-06-06 | Rho KINASE INHIBITORS |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US7199147B2 (ja) |
| EP (1) | EP1403255A4 (ja) |
| JP (1) | JPWO2002100833A1 (ja) |
| WO (1) | WO2002100833A1 (ja) |
Cited By (100)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003064397A1 (en) * | 2002-01-25 | 2003-08-07 | Vertex Pharmaceuticals Incorporated | Indazole compounds useful as protein kinase inhibitors |
| WO2004039366A1 (en) * | 2002-11-01 | 2004-05-13 | Pharmacia & Upjohn Company Llc | Nicotinic acetylcholine agonists in the treatment of glaucoma and retinal neuropathy |
| WO2004085406A1 (en) | 2003-03-24 | 2004-10-07 | F. Hoffmann-La Roche Ag | Benzyl-pyridazinons as reverse transcriptase inhibitors |
| WO2004062666A3 (en) * | 2003-01-16 | 2004-10-07 | Univ London | Use of rho-kinase inhibitorrs for treatment of benign prostatic hyperplasia |
| WO2004091605A1 (ja) * | 2003-04-17 | 2004-10-28 | Toyama Chemical Co., Ltd. | アルキルエーテル誘導体またはその塩を含有する網膜神経疾患の予防・治療剤 |
| WO2004091662A1 (ja) * | 2003-04-18 | 2004-10-28 | Senju Pharmaceutical Co. Ltd. | 角膜知覚回復剤 |
| WO2005035506A1 (ja) | 2003-10-15 | 2005-04-21 | Ube Industries, Ltd. | 新規インダゾール誘導体 |
| WO2005082890A1 (en) | 2004-02-20 | 2005-09-09 | Smithkline Beecham Corporation | Novel compounds |
| JP2006517574A (ja) * | 2003-02-14 | 2006-07-27 | グラクソ グループ リミテッド | カルボキサミド誘導体 |
| WO2006112313A1 (ja) * | 2005-04-13 | 2006-10-26 | Ube Industries, Ltd. | インダゾール誘導体を有効成分として含む網膜神経細胞保護剤 |
| US7135575B2 (en) * | 2003-03-03 | 2006-11-14 | Array Biopharma, Inc. | P38 inhibitors and methods of use thereof |
| JP2006526660A (ja) * | 2003-06-05 | 2006-11-24 | バーテックス ファーマシューティカルズ インコーポレイテッド | Vr1レセプターのモジュレーター |
| WO2007039563A1 (en) | 2005-09-30 | 2007-04-12 | N.V. Organon | 9-azabicyclo [3 . 3 . 1] nonane derivatives as monoamine reuptake inhibitors |
| JP2007513901A (ja) * | 2003-12-09 | 2007-05-31 | バイエル・ヘルスケア・アクチェンゲゼルシャフト | ヘテロアリール置換ベンゼン |
| JP2007516173A (ja) * | 2003-06-19 | 2007-06-21 | スミスクライン ビーチャム コーポレーション | 化合物 |
| US7271190B2 (en) | 2001-10-25 | 2007-09-18 | Asahi Kasei Pharma Corporation | Indazole compounds as β3 adrenoceptor agonist |
| WO2007142323A1 (ja) | 2006-06-08 | 2007-12-13 | Ube Industries, Ltd. | 側鎖にスピロ環構造を有する新規インダゾール誘導体 |
| JP2008516929A (ja) * | 2004-10-14 | 2008-05-22 | ラボラトワール テラメックス | インダゾール、ベンゾイソオキサゾールおよびベンゾイソチアゾール、その製造方法、医薬組成物およびエストロゲン様物質としての使用 |
| US7396833B2 (en) | 2003-12-22 | 2008-07-08 | Memory Pharmaceuticals Corporation | Indoles, 1H-indazoles, 1,2-benzisoxazoles, and 1,2-benzisothiazoles, and preparation and uses thereof |
| WO2008105442A1 (ja) | 2007-02-28 | 2008-09-04 | Asahi Kasei Pharma Corporation | スルホンアミド誘導体 |
| US7429664B2 (en) | 2002-09-25 | 2008-09-30 | Memory Pharmaceuticals Corporation | Indazoles, benzothiazoles, and benzoisothiazoles, and preparation and uses thereof |
| JP2008543956A (ja) * | 2005-06-28 | 2008-12-04 | サノフィ−アベンティス | Rho−キナーゼの阻害剤としてのイソキノリン誘導体 |
| JP2008545008A (ja) * | 2005-06-30 | 2008-12-11 | プロシディオン・リミテッド | Gpcrアゴニスト |
| US7473701B2 (en) | 2002-03-11 | 2009-01-06 | Aventis Pharma S.A. | Substituted indazoles, compositions containing them, method of production and use |
| JP2009502829A (ja) * | 2005-07-26 | 2009-01-29 | サノフィ−アベンティス | Rho−キナーゼ阻害剤としてのピペリジニル置換されたイソキノロン誘導体 |
| JP2009502830A (ja) * | 2005-07-26 | 2009-01-29 | サノフィ−アベンティス | Rho−キナーゼ阻害剤としてのシクロヘキシルアミンイソキノロン誘導体 |
| US7488737B2 (en) | 2004-04-22 | 2009-02-10 | Memory Pharmaceutical Corporation | Indoles, 1H-indazoles, 1,2-benzisoxazoles, 1,2-benzoisothiazoles, and preparation and uses thereof |
| WO2009028631A1 (ja) | 2007-08-29 | 2009-03-05 | Senju Pharmaceutical Co., Ltd. | 角膜内皮細胞接着促進剤 |
| US7521447B2 (en) | 2003-03-03 | 2009-04-21 | Array Biopharma Inc. | P38 inhibitors and methods of use thereof |
| US7524958B2 (en) * | 2004-06-18 | 2009-04-28 | Neurosearch A/S | Certain 9-aza-bicyclo[3.3.1] nonane derivatives and their use as monoamine neurotransmitter re-uptake inhibitors |
| US7563800B2 (en) | 2006-12-19 | 2009-07-21 | Roche Palo Alto Llc | Substituted pyrazolo[3,4-D]pyrimidines as p38 map kinase inhibitors |
| JP2009530345A (ja) * | 2006-03-22 | 2009-08-27 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Mdm2及びp53間の相互作用のインヒビターとしての環式アルキルアミン誘導体 |
| US7601726B2 (en) | 2005-08-25 | 2009-10-13 | Roche Palo Alto Llc | Substituted pyrazolo[3,4-d]pyrimidines as p38 MAP kinase inhibitors |
| US7605170B2 (en) | 2005-12-01 | 2009-10-20 | N.V. Organon | 8-azabicyclo[3.2.1]octane derivatives |
| US7618984B2 (en) | 2005-08-30 | 2009-11-17 | Asahi Kasei Pharma Corporation | Sulfonamide compound |
| JP2009541377A (ja) * | 2006-07-01 | 2009-11-26 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | Hsp90誘発疾患を治療するためのインダゾール誘導体 |
| US7625924B2 (en) | 2004-12-22 | 2009-12-01 | Memory Pharmaceuticals Corporation | Nicotinic alpha-7 receptor ligands and preparation and uses thereof |
| US7632831B2 (en) | 2004-05-07 | 2009-12-15 | Memory Pharmaceuticals Corporation | 1H-indazoles, benzothiazoles, 1,2-benzoisoxazoles, 1,2-benzoisothiazoles, and chromones and preparation and uses thereof |
| US7652135B2 (en) | 2003-09-23 | 2010-01-26 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of protein kinases |
| US7655662B2 (en) | 2005-12-22 | 2010-02-02 | Alcon Research, Ltd. | (Indazol-5-yl)-pyrazines and (1,3-dihydro-indol-2-one)-pyrazines for treating glaucoma and controlling intraocular pressure |
| JP2010513319A (ja) * | 2006-12-18 | 2010-04-30 | インスパイアー ファーマシューティカルズ,インコーポレイティド | 細胞骨格活性rhoキナーゼインヒビター化合物、組成物及び使用 |
| JP2010514718A (ja) * | 2006-12-27 | 2010-05-06 | サノフィ−アベンティス | シクロアルキルアミン置換イソキノロン及びイソキノリノン誘導体 |
| JP2010514719A (ja) * | 2006-12-27 | 2010-05-06 | サノフィ−アベンティス | シクロアルキルアミン置換イソキノリン誘導体 |
| JP2010514715A (ja) * | 2006-12-27 | 2010-05-06 | サノフィ−アベンティス | Rhoキナーゼ阻害剤としての置換イソキノロン及びイソキノリノン誘導体 |
| JP2010514717A (ja) * | 2006-12-27 | 2010-05-06 | サノフィ−アベンティス | 置換イソキノリン及びイソキノリノン誘導体 |
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| Publication number | Publication date |
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| EP1403255A1 (en) | 2004-03-31 |
| US7199147B2 (en) | 2007-04-03 |
| EP1403255A4 (en) | 2005-04-06 |
| JPWO2002100833A1 (ja) | 2004-09-24 |
| US20040138286A1 (en) | 2004-07-15 |
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