JP6423371B2 - 強力なrock1およびrock2阻害剤としてのフェニルピラゾール誘導体 - Google Patents
強力なrock1およびrock2阻害剤としてのフェニルピラゾール誘導体 Download PDFInfo
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- JP6423371B2 JP6423371B2 JP2015560336A JP2015560336A JP6423371B2 JP 6423371 B2 JP6423371 B2 JP 6423371B2 JP 2015560336 A JP2015560336 A JP 2015560336A JP 2015560336 A JP2015560336 A JP 2015560336A JP 6423371 B2 JP6423371 B2 JP 6423371B2
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- pyrazol
- benzamide
- methoxy
- substituted
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- 0 *C(CC=C)c(c(F)ccc1)c1F Chemical compound *C(CC=C)c(c(F)ccc1)c1F 0.000 description 4
- GZBZEYZXHWDQPS-UHFFFAOYSA-N C=[O]C(c1ccc(-c2c[nH]nc2)c(OC(F)F)c1)=O Chemical compound C=[O]C(c1ccc(-c2c[nH]nc2)c(OC(F)F)c1)=O GZBZEYZXHWDQPS-UHFFFAOYSA-N 0.000 description 1
- FUCFRKDYPQBUBP-UHFFFAOYSA-N CC1NN=C(C)C1c(cc1)cc(OC)c1C(NC1(CC1)c1cccc(OC)c1)=O Chemical compound CC1NN=C(C)C1c(cc1)cc(OC)c1C(NC1(CC1)c1cccc(OC)c1)=O FUCFRKDYPQBUBP-UHFFFAOYSA-N 0.000 description 1
- OXTDXYQUHRWNOW-UHFFFAOYSA-N CN(C)c(cc(cc1)C(NC2(CC2)c(cc2)ccc2F)=O)c1-c1c[nH]nc1 Chemical compound CN(C)c(cc(cc1)C(NC2(CC2)c(cc2)ccc2F)=O)c1-c1c[nH]nc1 OXTDXYQUHRWNOW-UHFFFAOYSA-N 0.000 description 1
- UKFLJIHHRRIAMW-BZORFCIVSA-N COC(C(CC1)=CC(OC(F)F)=C1/C(/C=N)=C/N)=O Chemical compound COC(C(CC1)=CC(OC(F)F)=C1/C(/C=N)=C/N)=O UKFLJIHHRRIAMW-BZORFCIVSA-N 0.000 description 1
- VYOFPLOREOHCDP-UHFFFAOYSA-N COC(c(cc1)cc(O)c1Br)=O Chemical compound COC(c(cc1)cc(O)c1Br)=O VYOFPLOREOHCDP-UHFFFAOYSA-N 0.000 description 1
- ANIUCSFXFSEXMI-UHFFFAOYSA-N COC(c(cc1)cc(OCCO)c1Br)=O Chemical compound COC(c(cc1)cc(OCCO)c1Br)=O ANIUCSFXFSEXMI-UHFFFAOYSA-N 0.000 description 1
- GHEFZYZTGHKBBI-UHFFFAOYSA-N COC(c1cc(CBr)ccc1F)=O Chemical compound COC(c1cc(CBr)ccc1F)=O GHEFZYZTGHKBBI-UHFFFAOYSA-N 0.000 description 1
- NEKICXRETWFPGU-UHFFFAOYSA-N Cc1cccc(F)c1CCC=C Chemical compound Cc1cccc(F)c1CCC=C NEKICXRETWFPGU-UHFFFAOYSA-N 0.000 description 1
- KULBBOOLBGZMOE-UHFFFAOYSA-N OC(c(cc1)cc(OC(F)F)c1-c1c[nH]nc1)=O Chemical compound OC(c(cc1)cc(OC(F)F)c1-c1c[nH]nc1)=O KULBBOOLBGZMOE-UHFFFAOYSA-N 0.000 description 1
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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
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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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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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
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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
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- 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
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- 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
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- 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Ophthalmology & Optometry (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Urology & Nephrology (AREA)
- Gynecology & Obstetrics (AREA)
- Rheumatology (AREA)
- Reproductive Health (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361770508P | 2013-02-28 | 2013-02-28 | |
| US61/770,508 | 2013-02-28 | ||
| PCT/US2014/019237 WO2014134388A1 (en) | 2013-02-28 | 2014-02-28 | Phenylpyrazole derivatives as potent rock1 and rock2 inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016510032A JP2016510032A (ja) | 2016-04-04 |
| JP2016510032A5 JP2016510032A5 (enExample) | 2017-03-09 |
| JP6423371B2 true JP6423371B2 (ja) | 2018-11-14 |
Family
ID=50288312
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015560336A Expired - Fee Related JP6423371B2 (ja) | 2013-02-28 | 2014-02-28 | 強力なrock1およびrock2阻害剤としてのフェニルピラゾール誘導体 |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US9458110B2 (enExample) |
| EP (1) | EP2961745B1 (enExample) |
| JP (1) | JP6423371B2 (enExample) |
| CN (1) | CN105358547B (enExample) |
| AR (1) | AR094929A1 (enExample) |
| ES (1) | ES2624664T3 (enExample) |
| TW (1) | TW201444798A (enExample) |
| WO (1) | WO2014134388A1 (enExample) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2961746B1 (en) | 2013-02-28 | 2018-01-03 | Bristol-Myers Squibb Company | Phenylpyrazole derivatives as potent rock1 and rock2 inhibitors |
| US9902702B2 (en) | 2014-07-15 | 2018-02-27 | Bristol-Myers Squibb Company | Spirocycloheptanes as inhibitors of rock |
| CN107108581B (zh) | 2014-08-21 | 2020-06-23 | 百时美施贵宝公司 | 作为强效rock抑制剂的回接苯甲酰胺衍生物 |
| JP6779214B2 (ja) * | 2015-01-09 | 2020-11-04 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | Rock阻害剤としての環状ウレア |
| ES2730112T3 (es) | 2015-03-09 | 2019-11-08 | Bristol Myers Squibb Co | Lactamas como inhibidores de ROCK |
| TWI730032B (zh) | 2016-01-13 | 2021-06-11 | 美商必治妥美雅史谷比公司 | 作為rock抑制劑之螺庚烷水楊酸醯胺及相關化合物 |
| WO2017205709A1 (en) * | 2016-05-27 | 2017-11-30 | Bristol-Myers Squibb Company | Triazolones and tetrazolones as inhibitors of rock |
| ES2821877T3 (es) * | 2016-07-07 | 2021-04-28 | Bristol Myers Squibb Co | Espirolactamas como inhibidores de ROCK |
| JP7155102B2 (ja) | 2016-07-07 | 2022-10-18 | ブリストル-マイヤーズ スクイブ カンパニー | Rock阻害剤としてのスピロ縮合環尿素 |
| WO2018036414A1 (zh) * | 2016-08-23 | 2018-03-01 | 北京诺诚健华医药科技有限公司 | 稠杂环类衍生物、其制备方法及其在医学上的应用 |
| CN110099906B (zh) * | 2016-10-24 | 2022-07-26 | 转化药物开发有限责任公司 | 作为激酶抑制剂的酰胺化合物 |
| EP3548468B1 (en) * | 2016-11-30 | 2020-09-16 | Bristol-Myers Squibb Company | Tricyclic rho kinase inhibitors |
| EP3558992A4 (en) * | 2016-12-15 | 2020-12-02 | ONO Pharmaceutical Co., Ltd. | TREK CHANNEL ACTIVATOR (K + CHANNELS ASSOCIATED WITH TWIK) |
| WO2018108156A1 (zh) * | 2016-12-16 | 2018-06-21 | 成都先导药物开发有限公司 | Rock抑制剂及其应用 |
| CN110914257B (zh) | 2017-07-12 | 2023-05-26 | 百时美施贵宝公司 | 作为rock抑制剂的螺庚基乙内酰脲 |
| WO2019014300A1 (en) | 2017-07-12 | 2019-01-17 | Bristol-Myers Squibb Company | PHENYLACETAMIDES AS ROCK INHIBITORS |
| US12060341B2 (en) | 2017-07-12 | 2024-08-13 | Bristol-Myers Squibb Company | Spiroheptanyl hydantoins as ROCK inhibitors |
| TW201908293A (zh) | 2017-07-12 | 2019-03-01 | 美商必治妥美雅史谷比公司 | 作為rock抑制劑之5員及雙環雜環醯胺 |
| JP7234201B2 (ja) | 2017-07-12 | 2023-03-07 | ブリストル-マイヤーズ スクイブ カンパニー | 心不全の治療のためのrockの5員アミノヘテロ環および5,6-または6,6員二環式アミノヘテロ環の阻害剤 |
| US11230541B2 (en) | 2017-07-28 | 2022-01-25 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
| ES2937039T3 (es) | 2017-11-03 | 2023-03-23 | Bristol Myers Squibb Co | Inhibidores diazaespiro de ROCK |
| JP2021517137A (ja) | 2018-03-23 | 2021-07-15 | フォチョン・ファーマシューティカルズ・リミテッドFochon Pharmaceuticals, Ltd. | Rock阻害剤としての重水素化合物 |
| CN112020496B (zh) | 2018-04-18 | 2023-04-28 | 南京明德新药研发有限公司 | 作为rho激酶抑制剂的苯并吡唑类化合物 |
| JP7490569B2 (ja) * | 2018-04-24 | 2024-05-27 | トランスレイショナル・ドラッグ・ディベロップメント・エルエルシー | キナーゼ阻害剤としてのアミド化合物、組成物および処置方法 |
| CN109020977B (zh) * | 2018-10-26 | 2020-11-13 | 安庆奇创药业有限公司 | 一种Acalabrutinib的制备方法 |
| US12637418B2 (en) | 2019-01-24 | 2026-05-26 | Takeda Pharmaceutical Company Limited | Heterocyclic compounds as antagonist of NMDA |
| JP2021050161A (ja) | 2019-09-25 | 2021-04-01 | 武田薬品工業株式会社 | 複素環化合物及びその用途 |
| CN114555561B (zh) * | 2019-10-18 | 2023-08-11 | 南京明德新药研发有限公司 | 作为rho激酶抑制剂的苯并吡唑类化合物的盐型、晶型及其制备方法 |
| JP2021080177A (ja) | 2019-11-14 | 2021-05-27 | 武田薬品工業株式会社 | 複素環化合物及びその用途 |
| CN116438175B (zh) * | 2020-11-11 | 2025-07-22 | 南京明德新药研发有限公司 | 苯并脲环衍生物及其制备方法和应用 |
| JP2026507461A (ja) * | 2023-03-01 | 2026-03-04 | 成都先導薬物開発股▲フン▼有限公司 | 芳香環化合物及びその使用 |
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| PL173781B1 (pl) | 1992-02-05 | 1998-04-30 | Boehringer Ingelheim Kg | Sposób wytwarzania nowych pochodnych amidyny |
| CN1052224C (zh) | 1993-04-07 | 2000-05-10 | 大塚制药株式会社 | 哌啶衍生物、含有它的外周血管舒张剂及其应用 |
| CA2155662A1 (en) | 1993-12-27 | 1995-07-06 | Fumihiro Ozaki | Anthranilic acid derivative |
| GB9500580D0 (en) | 1995-01-12 | 1995-03-01 | Merck Sharp & Dohme | Therapeutic agents |
| US5763618A (en) | 1995-05-12 | 1998-06-09 | Konica Corporation | Manufacturing method of sulfides |
| DE19545878A1 (de) | 1995-12-08 | 1997-06-12 | Basf Ag | Pyridylcarbamate, Verfahren und Zwischenprodukte zu ihrer Herstellung und ihre Verwendung |
| ES2186874T3 (es) | 1996-02-22 | 2003-05-16 | Bristol Myers Squibb Pharma Co | Analogos de m-amidinofenilo como inhibidores del factor xa. |
| CA2249645A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| US6187797B1 (en) | 1996-12-23 | 2001-02-13 | Dupont Pharmaceuticals Company | Phenyl-isoxazoles as factor XA Inhibitors |
| CA2276034A1 (en) | 1996-12-23 | 1998-07-02 | Mimi Lifen Quan | Oxygen or sulfur containing 5-membered heteroaromatics as factor xa inhibitors |
| US6020357A (en) | 1996-12-23 | 2000-02-01 | Dupont Pharmaceuticals Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
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2014
- 2014-02-27 AR ARP140100640A patent/AR094929A1/es unknown
- 2014-02-27 TW TW103106886A patent/TW201444798A/zh unknown
- 2014-02-28 US US14/770,500 patent/US9458110B2/en active Active
- 2014-02-28 CN CN201480023844.6A patent/CN105358547B/zh not_active Expired - Fee Related
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| EP2961745A1 (en) | 2016-01-06 |
| US20140243338A1 (en) | 2014-08-28 |
| US9126944B2 (en) | 2015-09-08 |
| US20160016910A1 (en) | 2016-01-21 |
| JP2016510032A (ja) | 2016-04-04 |
| EP2961745B1 (en) | 2017-03-29 |
| CN105358547A (zh) | 2016-02-24 |
| TW201444798A (zh) | 2014-12-01 |
| AR094929A1 (es) | 2015-09-09 |
| ES2624664T3 (es) | 2017-07-17 |
| US9458110B2 (en) | 2016-10-04 |
| WO2014134388A1 (en) | 2014-09-04 |
| CN105358547B (zh) | 2018-04-03 |
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