JP2019517475A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2019517475A5 JP2019517475A5 JP2018562088A JP2018562088A JP2019517475A5 JP 2019517475 A5 JP2019517475 A5 JP 2019517475A5 JP 2018562088 A JP2018562088 A JP 2018562088A JP 2018562088 A JP2018562088 A JP 2018562088A JP 2019517475 A5 JP2019517475 A5 JP 2019517475A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- independently selected
- alkyl
- heterocyclyl
- cycloalkyl
- 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.)
- Granted
Links
- 125000000217 alkyl group Chemical group 0.000 claims 139
- 125000000623 heterocyclic group Chemical group 0.000 claims 72
- 229910052739 hydrogen Inorganic materials 0.000 claims 66
- 229910052799 carbon Inorganic materials 0.000 claims 53
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 29
- 229910052757 nitrogen Inorganic materials 0.000 claims 24
- 125000003118 aryl group Chemical group 0.000 claims 19
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 19
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 17
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 16
- 229910052717 sulfur Inorganic materials 0.000 claims 15
- -1 CN Inorganic materials 0.000 claims 14
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims 13
- 150000001875 compounds Chemical class 0.000 claims 13
- 125000001072 heteroaryl group Chemical group 0.000 claims 13
- 150000003839 salts Chemical class 0.000 claims 13
- 125000004452 carbocyclyl group Chemical group 0.000 claims 12
- 229910052760 oxygen Inorganic materials 0.000 claims 11
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims 9
- 125000006706 (C3-C6) carbocyclyl group Chemical group 0.000 claims 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 7
- 201000010099 disease Diseases 0.000 claims 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 208000024172 Cardiovascular disease Diseases 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 1
- 206010002383 Angina Pectoris Diseases 0.000 claims 1
- 201000001320 Atherosclerosis Diseases 0.000 claims 1
- 208000023275 Autoimmune disease Diseases 0.000 claims 1
- 241000239366 Euphausiacea Species 0.000 claims 1
- 206010019280 Heart failures Diseases 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 208000031481 Pathologic Constriction Diseases 0.000 claims 1
- 208000018262 Peripheral vascular disease Diseases 0.000 claims 1
- 208000006011 Stroke Diseases 0.000 claims 1
- 206010047163 Vasospasm Diseases 0.000 claims 1
- 230000002159 abnormal effect Effects 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 208000026106 cerebrovascular disease Diseases 0.000 claims 1
- 208000029078 coronary artery disease Diseases 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 230000003176 fibrotic effect Effects 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 claims 1
- 208000010125 myocardial infarction Diseases 0.000 claims 1
- 230000002981 neuropathic effect Effects 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 208000002815 pulmonary hypertension Diseases 0.000 claims 1
- 102000000568 rho-Associated Kinases Human genes 0.000 claims 1
- 108010041788 rho-Associated Kinases Proteins 0.000 claims 1
- 210000002460 smooth muscle Anatomy 0.000 claims 1
- 208000037804 stenosis Diseases 0.000 claims 1
- 230000036262 stenosis Effects 0.000 claims 1
- 0 C*C(N1C(*)c2ccccc2)=NN(C(C)=CC=C(C=C)C(c2c(N)[n]cc2)=I[Tl])C1=Cl Chemical compound C*C(N1C(*)c2ccccc2)=NN(C(C)=CC=C(C=C)C(c2c(N)[n]cc2)=I[Tl])C1=Cl 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662342441P | 2016-05-27 | 2016-05-27 | |
| US62/342,441 | 2016-05-27 | ||
| PCT/US2017/034613 WO2017205709A1 (en) | 2016-05-27 | 2017-05-26 | Triazolones and tetrazolones as inhibitors of rock |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019517475A JP2019517475A (ja) | 2019-06-24 |
| JP2019517475A5 true JP2019517475A5 (enExample) | 2020-07-02 |
| JP6987792B2 JP6987792B2 (ja) | 2022-01-05 |
Family
ID=59009815
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018562088A Active JP6987792B2 (ja) | 2016-05-27 | 2017-05-26 | Ｒｏｃｋ阻害剤としてのトリアゾロンおよびテトラゾロン |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10562887B2 (enExample) |
| EP (1) | EP3464262B1 (enExample) |
| JP (1) | JP6987792B2 (enExample) |
| KR (1) | KR102457933B1 (enExample) |
| CN (1) | CN109153663B (enExample) |
| ES (1) | ES2781309T3 (enExample) |
| WO (1) | WO2017205709A1 (enExample) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR107354A1 (es) | 2016-01-13 | 2018-04-18 | Bristol Myers Squibb Co | Salicilamidas espiroheptanos y compuestos relacionados como inhibidores de rock |
| ES2829550T3 (es) | 2016-07-07 | 2021-06-01 | Bristol Myers Squibb Co | Ureas cíclicas espiro-condensadas como inhibidores de ROCK |
| ES2814325T3 (es) | 2016-07-07 | 2021-03-26 | Bristol Myers Squibb Co | Derivados de lactama, urea cíclica y carbamato y de triazolona como inhibidores potentes y selectivos de ROCK |
| JP7113810B2 (ja) | 2016-07-07 | 2022-08-05 | 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ラクタム |
| WO2018102325A1 (en) | 2016-11-30 | 2018-06-07 | Bristol-Myers Squibb Company | Tricyclic rho kinase 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 |
| CN110869360B (zh) | 2017-07-12 | 2023-12-15 | 百时美施贵宝公司 | 作为rock抑制剂的苯乙酰胺类 |
| EP3652167B1 (en) | 2017-07-12 | 2021-06-02 | Bristol-Myers Squibb Company | Spiroheptanyl hydantoins as rock inhibitors |
| WO2019014303A1 (en) | 2017-07-12 | 2019-01-17 | Bristol-Myers Squibb Company | 5-OR 6,6-CHANNEL BICYCLIC CHAINS AND AMINOHETEROCYCLIC AMINOHETEROCYCLIC INHIBITORS FOR THE TREATMENT OF CARDIAC INSUFFICIENCY |
| US11192891B2 (en) | 2017-11-03 | 2021-12-07 | Bristol-Myers Squibb Company | Diazaspiro ROCK inhibitors |
| EP3886854A4 (en) | 2018-11-30 | 2022-07-06 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| WO2023041422A1 (en) | 2021-09-20 | 2023-03-23 | Basf Se | Heterocyclic compounds for the control of invertebrate pests |
| AU2022385051A1 (en) | 2021-11-11 | 2024-06-20 | Actualeyes Inc. | Cryopreservation preparation for corneal endothelial cells and method for producing said cryopreservation preparation |
| TW202409023A (zh) | 2022-07-14 | 2024-03-01 | 美商富曼西公司 | 除草苯并𠯤 |
| WO2024229406A1 (en) | 2023-05-04 | 2024-11-07 | Revolution Medicines, Inc. | Combination therapy for a ras related disease or disorder |
| CN119219603A (zh) * | 2023-06-28 | 2024-12-31 | 科辉智药(深圳)新药研究中心有限公司 | Sarm1酶活性抑制剂及其用途 |
| US20250049810A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| WO2025076010A1 (en) | 2023-10-01 | 2025-04-10 | Massachusetts Institute Of Technology | Site-selective conjugation of a pharmaceutical agent to an antibody using an affinity peptide |
| TW202530228A (zh) | 2023-10-12 | 2025-08-01 | 美商銳新醫藥公司 | Ｒａｓ抑制劑 |
| WO2025111184A1 (en) | 2023-11-21 | 2025-05-30 | Fmc Corporation | Substituted tetrahydroquinoline and tetrahydroquinoxaline herbicides |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| TW202547461A (zh) | 2024-05-17 | 2025-12-16 | 美商銳新醫藥公司 | Ｒａｓ抑制劑 |
| WO2025255438A1 (en) | 2024-06-07 | 2025-12-11 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| WO2025265060A1 (en) | 2024-06-21 | 2025-12-26 | Revolution Medicines, Inc. | Therapeutic compositions and methods for managing treatment-related effects |
| WO2026006747A1 (en) | 2024-06-28 | 2026-01-02 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2026015790A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015796A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015801A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015825A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Use of ras inhibitor for treating pancreatic cancer |
| WO2026050446A1 (en) | 2024-08-29 | 2026-03-05 | Revolution Medicines, Inc. | Ras inhibitors |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE186909T1 (de) | 1993-11-19 | 1999-12-15 | Du Pont | Cyclische fungizide amide |
| US20010020100A1 (en) * | 1994-06-14 | 2001-09-06 | G.D. Searle & Co. | N-substituted-1, 2, 4-triazolone compounds for treatment of cardiovascular disorders |
| US5607932A (en) * | 1994-07-12 | 1997-03-04 | Janssen Pharmaceutica N.V. | Heterocyclic derivatives of azolones |
| CA2211458A1 (en) | 1995-02-17 | 1996-08-22 | Kenji Okonogi | Azole compounds, their production and use |
| TW318841B (enExample) * | 1995-02-17 | 1997-11-01 | Takeda Pharm Industry Co Ltd | |
| JP3056412B2 (ja) * | 1995-02-17 | 2000-06-26 | 武田薬品工業株式会社 | アゾール化合物およびその用途 |
| JP2771334B2 (ja) | 1995-05-16 | 1998-07-02 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | 殺菌・殺カビ性環状アミド類 |
| WO2005074643A2 (en) | 2004-01-30 | 2005-08-18 | Smithkline Beecham Corporation | Benzamide compounds useful as rock inhibitors |
| BRPI0508514A (pt) * | 2004-03-10 | 2007-08-14 | Janssen Pharmaceutica Nv | aril piperidinas ou piperazinas substituìdas por heterociclos de 5-membros inibidoras de mtp |
| TW200612961A (en) | 2004-05-18 | 2006-05-01 | Fmc Corp | Substituted cyclic urea derivatives |
| BRPI0513433A (pt) * | 2004-07-16 | 2008-05-06 | Schering Corp | derivados de hidantoìna para o tratamento de distúrbios inflamatórios |
| WO2006048727A1 (en) | 2004-11-02 | 2006-05-11 | Pfizer Products Inc. | Piperazinylphenalkyl lactam/amine ligands for the 5ht1b receptor |
| CN101084201A (zh) * | 2004-12-21 | 2007-12-05 | 詹森药业有限公司 | 用作α2C－肾上腺素能受体拮抗剂的三唑酮、四唑酮和咪唑酮衍生物 |
| WO2007026920A2 (en) * | 2005-09-02 | 2007-03-08 | Astellas Pharma Inc. | Amide derivatives as rock inhibitors |
| JP5579170B2 (ja) | 2008-06-05 | 2014-08-27 | 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 | Ｄｇａｔ阻害剤とｐｐａｒ作動薬を含有する薬剤組み合わせ物 |
| EP2379075A4 (en) | 2008-12-16 | 2012-05-30 | Merck Sharp & Dohme | TRIAZOL DERIVATIVES FOR THE TREATMENT OF ALZHEIMER DISEASE |
| WO2013112722A1 (en) * | 2012-01-24 | 2013-08-01 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Inhibitors of rho associated protein kinases (rock) and methods of use |
| US9221767B2 (en) | 2013-01-18 | 2015-12-29 | Bristol-Myers Squibb Company | Substituted phthalazinones as rock inhibitors |
| TW201444798A (zh) * | 2013-02-28 | 2014-12-01 | 必治妥美雅史谷比公司 | 作爲強效ｒｏｃｋ１及ｒｏｃｋ２抑制劑之苯基吡唑衍生物 |
| EP2961746B1 (en) * | 2013-02-28 | 2018-01-03 | Bristol-Myers Squibb Company | Phenylpyrazole derivatives as potent rock1 and rock2 inhibitors |
| JP6522602B2 (ja) | 2013-07-02 | 2019-05-29 | ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ | Ｒｏｃｋ阻害剤としての三環式ピリド−カルボキサミド誘導体 |
| TW201506024A (zh) | 2013-07-02 | 2015-02-16 | 必治妥美雅史谷比公司 | 作為有效ｒｏｃｋ抑制劑的三環甲醯胺衍生物 |
| RU2016131875A (ru) | 2014-01-20 | 2018-02-26 | Ф. Хоффманн-Ля Рош Аг | Производные n-фениллактама, способные стимулировать нейрогенез, и их применение при лечении заболеваний нервной системы |
| US9902702B2 (en) | 2014-07-15 | 2018-02-27 | Bristol-Myers Squibb Company | Spirocycloheptanes as inhibitors of rock |
| US10112939B2 (en) | 2014-08-21 | 2018-10-30 | Bristol-Myers Squibb Company | Tied-back benzamide derivatives as potent rock inhibitors |
| AR103990A1 (es) | 2015-01-09 | 2017-06-21 | Bristol Myers Squibb Co | Ureas cíclicas como inhibidoras de rock |
| US10112929B2 (en) | 2015-03-09 | 2018-10-30 | Bristol-Myers Squibb Company | Lactams as inhibitors of rock |
| AR107354A1 (es) | 2016-01-13 | 2018-04-18 | Bristol Myers Squibb Co | Salicilamidas espiroheptanos y compuestos relacionados como inhibidores de rock |
| ES2814325T3 (es) | 2016-07-07 | 2021-03-26 | Bristol Myers Squibb Co | Derivados de lactama, urea cíclica y carbamato y de triazolona como inhibidores potentes y selectivos de ROCK |
| ES2829550T3 (es) | 2016-07-07 | 2021-06-01 | Bristol Myers Squibb Co | Ureas cíclicas espiro-condensadas como inhibidores de ROCK |
| JP7113810B2 (ja) | 2016-07-07 | 2022-08-05 | 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ラクタム |
| WO2018102325A1 (en) | 2016-11-30 | 2018-06-07 | Bristol-Myers Squibb Company | Tricyclic rho kinase inhibitors |
-
2017
- 2017-05-26 CN CN201780031569.6A patent/CN109153663B/zh active Active
- 2017-05-26 JP JP2018562088A patent/JP6987792B2/ja active Active
- 2017-05-26 KR KR1020187037221A patent/KR102457933B1/ko active Active
- 2017-05-26 EP EP17728029.4A patent/EP3464262B1/en active Active
- 2017-05-26 ES ES17728029T patent/ES2781309T3/es active Active
- 2017-05-26 WO PCT/US2017/034613 patent/WO2017205709A1/en not_active Ceased
- 2017-05-26 US US16/098,978 patent/US10562887B2/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2019517475A5 (enExample) | ||
| JP2019520398A5 (enExample) | ||
| JP2018501285A5 (enExample) | ||
| JP2019520396A5 (enExample) | ||
| JP2021501782A5 (enExample) | ||
| JP2019520402A5 (enExample) | ||
| JP2018538304A5 (enExample) | ||
| IL259947A (en) | The troirylhydroxypyrimidinones as apj receptor agonists | |
| JP2019518041A5 (enExample) | ||
| JP2019532072A5 (enExample) | ||
| HRP20201927T1 (hr) | PIRIMIDINONI KAO INHIBITORI FAKTORA XIa | |
| JP2020500869A5 (enExample) | ||
| JP2017504576A5 (enExample) | ||
| JP2019519476A5 (enExample) | ||
| JP2019094345A5 (enExample) | ||
| JP2019518766A5 (enExample) | ||
| JP2016510033A5 (enExample) | ||
| JP2014503574A5 (enExample) | ||
| JP2012513481A5 (enExample) | ||
| JP2019527682A5 (enExample) | ||
| JP2016505042A5 (enExample) | ||
| SI2906551T1 (en) | Crystalline forms of a factor xia inhibitor | |
| JP2013530237A5 (enExample) | ||
| HRP20161378T1 (hr) | Dihidropiridon kao faktor xia inhibitora | |
| JP2010524896A5 (enExample) |