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
Classifications
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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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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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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- 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
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- 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
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- 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)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Ophthalmology & Optometry (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Vascular Medicine (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Gynecology & Obstetrics (AREA)
- Endocrinology (AREA)
- Reproductive Health (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 (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105102448B (zh) | 2013-02-28 | 2018-03-06 | 百时美施贵宝公司 | 作为rock1和rock2抑制剂的苯基吡唑衍生物 |
| US9902702B2 (en) | 2014-07-15 | 2018-02-27 | Bristol-Myers Squibb Company | Spirocycloheptanes as inhibitors of rock |
| WO2016028971A1 (en) | 2014-08-21 | 2016-02-25 | Bristol-Myers Squibb Company | Tied-back benzamide derivatives as potent rock inhibitors |
| TW201630899A (zh) * | 2015-01-09 | 2016-09-01 | 必治妥美雅史谷比公司 | 作為rock抑制劑的環狀脲類 |
| TW201706265A (zh) * | 2015-03-09 | 2017-02-16 | 必治妥美雅史谷比公司 | 做為Rho激酶(ROCK)抑制劑之內醯胺 |
| 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 |
| KR102457933B1 (ko) * | 2016-05-27 | 2022-10-24 | 브리스톨-마이어스 스큅 컴퍼니 | Rock의 억제제로서의 트리아졸론 및 테트라졸론 |
| US10787450B2 (en) | 2016-07-07 | 2020-09-29 | Bristol-Myers Squibb Company | Spiro-fused cyclic ureas as inhibitors of rock |
| KR102491994B1 (ko) * | 2016-07-07 | 2023-01-25 | 브리스톨-마이어스 스큅 컴퍼니 | Rock의 억제제로서의 스피로락탐 |
| CN109689652B (zh) * | 2016-08-23 | 2022-04-26 | 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 |
| IL266150B2 (en) * | 2016-10-24 | 2023-12-01 | Translational Drug Dev Llc | 3-substituted benzamide derivatives as kinase inhibitors |
| KR102511441B1 (ko) * | 2016-11-30 | 2023-03-16 | 브리스톨-마이어스 스큅 컴퍼니 | 트리시클릭 Rho 키나제 억제제 |
| US11046683B2 (en) | 2016-12-15 | 2021-06-29 | Ono Pharmaceutical Co., Ltd. | Activator of TREK (TWIK RElated K+ channels) channels |
| CN108203433B (zh) * | 2016-12-16 | 2020-07-03 | 成都先导药物开发股份有限公司 | 一种rock抑制剂及其应用 |
| US12060341B2 (en) | 2017-07-12 | 2024-08-13 | Bristol-Myers Squibb Company | Spiroheptanyl hydantoins as ROCK inhibitors |
| US11299488B2 (en) | 2017-07-12 | 2022-04-12 | Bristol-Myers Squibb Company | Five membered-aminoheterocycle and 5,6-or 6,6-membered bicyclic aminoheterocyclic inhibitors of rock for the treatment of heart failure |
| US11306081B2 (en) | 2017-07-12 | 2022-04-19 | Bristol-Myers Squibb Company | Phenylacetamides as inhibitors of rock |
| 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 |
| KR102644889B1 (ko) | 2017-07-12 | 2024-03-06 | 브리스톨-마이어스 스큅 컴퍼니 | Rock 억제제로서의 스피로헵타닐 히단토인 |
| US11230541B2 (en) | 2017-07-28 | 2022-01-25 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
| US11192891B2 (en) | 2017-11-03 | 2021-12-07 | Bristol-Myers Squibb Company | Diazaspiro ROCK inhibitors |
| EP3768661B1 (en) * | 2018-03-23 | 2024-05-01 | Fochon Pharmaceuticals, Ltd. | Deuterated compounds as rock inhibitors |
| JP7187575B2 (ja) | 2018-04-18 | 2022-12-12 | メッドシャイン ディスカバリー インコーポレイテッド | Rhoキナーゼ阻害剤としてのベンゾピラゾール系化合物 |
| EP3784226B1 (en) | 2018-04-24 | 2024-08-14 | Translational Drug Development Llc | Pyrazole-phenylamide derivatives as inhibitors of the rho-associated protein kinase rock1 and rock2 for the treatment of cancer |
| 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 |
| 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 |
| WO2021073592A1 (zh) | 2019-10-18 | 2021-04-22 | 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 |
| 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 |
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| KR100238346B1 (ko) | 1993-04-07 | 2000-03-02 | 오쓰까 아끼히꼬 | 피페리딘 유도체를 유효성분으로 하는 말초혈관확장제 |
| 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 |
| EP0892780B1 (en) | 1996-02-22 | 2002-11-20 | Bristol-Myers Squibb Pharma Company | M-AMIDINO PHENYL ANALOGS AS FACTOR Xa INHIBITORS |
| CA2249645A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| DE69720773T2 (de) | 1996-12-23 | 2004-01-29 | Bristol Myers Squibb Pharma Co | SAUERSTOFF ODER SCHWEFEL ENTHALTENDE 5-GLIEDRIGE HETEROAROMATISHE DERIVATIVE ALS FACTOR Xa HEMMER |
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| EP0946508B1 (en) | 1996-12-23 | 2009-09-23 | Bristol-Myers Squibb Pharma 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 WO PCT/US2014/019237 patent/WO2014134388A1/en not_active Ceased
- 2014-02-28 EP EP14710732.0A patent/EP2961745B1/en active Active
- 2014-02-28 US US14/770,500 patent/US9458110B2/en active Active
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| WO2014134388A1 (en) | 2014-09-04 |
| AR094929A1 (es) | 2015-09-09 |
| EP2961745B1 (en) | 2017-03-29 |
| US20160016910A1 (en) | 2016-01-21 |
| EP2961745A1 (en) | 2016-01-06 |
| US9458110B2 (en) | 2016-10-04 |
| CN105358547B (zh) | 2018-04-03 |
| US20140243338A1 (en) | 2014-08-28 |
| ES2624664T3 (es) | 2017-07-17 |
| US9126944B2 (en) | 2015-09-08 |
| CN105358547A (zh) | 2016-02-24 |
| JP2016510032A (ja) | 2016-04-04 |
| TW201444798A (zh) | 2014-12-01 |
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