JP2014512406A5 - - Google Patents

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Publication number
JP2014512406A5
JP2014512406A5 JP2014506888A JP2014506888A JP2014512406A5 JP 2014512406 A5 JP2014512406 A5 JP 2014512406A5 JP 2014506888 A JP2014506888 A JP 2014506888A JP 2014506888 A JP2014506888 A JP 2014506888A JP 2014512406 A5 JP2014512406 A5 JP 2014512406A5
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JP
Japan
Prior art keywords
alkyl
het
group
aryl
heteroaryl
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
Application number
JP2014506888A
Other languages
English (en)
Japanese (ja)
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JP2014512406A (ja
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Publication date
Priority claimed from GBGB1107223.8A external-priority patent/GB201107223D0/en
Application filed filed Critical
Publication of JP2014512406A publication Critical patent/JP2014512406A/ja
Publication of JP2014512406A5 publication Critical patent/JP2014512406A5/ja
Ceased legal-status Critical Current

Links

JP2014506888A 2011-04-29 2012-04-27 新規のrock阻害剤 Ceased JP2014512406A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB1107223.8 2011-04-29
GBGB1107223.8A GB201107223D0 (en) 2011-04-29 2011-04-29 Novel rock inhibitors
PCT/EP2012/057785 WO2012146724A2 (en) 2011-04-29 2012-04-27 Novel rock inhibitors

Publications (2)

Publication Number Publication Date
JP2014512406A JP2014512406A (ja) 2014-05-22
JP2014512406A5 true JP2014512406A5 (enExample) 2015-04-23

Family

ID=44202979

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014506888A Ceased JP2014512406A (ja) 2011-04-29 2012-04-27 新規のrock阻害剤

Country Status (13)

Country Link
US (1) US9073905B2 (enExample)
EP (1) EP2702053A2 (enExample)
JP (1) JP2014512406A (enExample)
CN (1) CN103534249A (enExample)
AU (1) AU2012247455A1 (enExample)
BR (1) BR112013027241A2 (enExample)
CA (1) CA2834387A1 (enExample)
EA (1) EA201370230A1 (enExample)
GB (1) GB201107223D0 (enExample)
MX (1) MX2013012555A (enExample)
NZ (1) NZ616300A (enExample)
WO (1) WO2012146724A2 (enExample)
ZA (1) ZA201307496B (enExample)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA201500362A1 (ru) 2012-10-05 2015-08-31 Кадмон Корпорейшн, Ллк Ингибиторы rho-киназы
EA026629B1 (ru) * 2012-10-31 2017-04-28 пиЭйч ФАРМА Ко., ЛТД. Ингибиторы rock
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
AR094929A1 (es) 2013-02-28 2015-09-09 Bristol Myers Squibb Co Derivados de fenilpirazol como inhibidores potentes de rock1 y rock2
CN103127249A (zh) * 2013-03-02 2013-06-05 谭习达 一种治阑尾炎的药
US20170114323A1 (en) 2014-06-19 2017-04-27 Whitehead Institute For Biomedical Research Uses of kinase inhibitors for inducing and maintaining pluripotency
CN112969694B (zh) * 2018-11-09 2023-06-13 北京泰德制药股份有限公司 Rho相关蛋白激酶抑制剂、包含其的药物组合物及其用途
MX2021016068A (es) * 2019-06-21 2022-04-20 Guangzhou Ocusun Ophthalmic Biotechnology Co Ltd Derivados de isoquinolinona como inhibidores de la proteina quinasa rock y usos del mismo.
US12371667B2 (en) 2021-05-13 2025-07-29 Washington University Enhanced methods for inducing and maintaining naive human pluripotent stem cells
CA3238227A1 (en) 2021-11-11 2023-05-19 The Doshisha Cryopreservation preparation for corneal endothelial cells and method for producing said cryopreservation preparation
TW202508595A (zh) 2023-05-04 2025-03-01 美商銳新醫藥公司 用於ras相關疾病或病症之組合療法
WO2025034702A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Rmc-6291 for use in the treatment of ras protein-related disease or disorder
WO2025080946A2 (en) 2023-10-12 2025-04-17 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors
CN118304286B (zh) * 2024-06-07 2024-09-10 四川省医学科学院·四川省人民医院 芥子碱硫氰酸盐在制备治疗视网膜新生血管相关疾病的药物中的应用

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IS2334B (is) 1992-09-08 2008-02-15 Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) Aspartyl próteasi hemjari af nýjum flokki súlfonamíða
US6043358A (en) 1995-11-01 2000-03-28 Merck & Co., Inc. Hexahydro-5-imino-1,4-heteroazepine derivatives as inhibitors of nitric oxide synthases
GB9718913D0 (en) 1997-09-05 1997-11-12 Glaxo Group Ltd Substituted oxindole derivatives
US6369087B1 (en) 1999-08-26 2002-04-09 Robert R. Whittle Alkoxy substituted benzimidazole compounds, pharmaceutical preparations containing the same, and methods of using the same
US7217722B2 (en) 2000-02-01 2007-05-15 Kirin Beer Kabushiki Kaisha Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same
WO2007133622A2 (en) * 2006-05-12 2007-11-22 Vertex Pharmaceuticals Incorporated Selective inhibitors of rock protein kinase and uses thereof
WO2008049919A2 (en) * 2006-10-26 2008-05-02 Devgen N.V. Rho kinase inhibitors
US20100022517A1 (en) * 2006-12-18 2010-01-28 Richards Lori A Ophthalmic formulation of rho kinase inhibitor compound
US8071779B2 (en) * 2006-12-18 2011-12-06 Inspire Pharmaceuticals, Inc. Cytoskeletal active rho kinase inhibitor compounds, composition and use
US20090325959A1 (en) 2008-06-26 2009-12-31 Vittitow Jason L Method for treating ophthalmic diseases using rho kinase inhibitor compounds
US20090325960A1 (en) 2008-06-26 2009-12-31 Fulcher Emilee H Method for treating inflammatory diseases using rho kinase inhibitor compounds
WO2009158587A1 (en) 2008-06-26 2009-12-30 Inspire Pharmaceuticals, Inc. Method for treating pulmonary diseases using rho kinase inhibitor compounds
WO2010065782A1 (en) * 2008-12-04 2010-06-10 Inspire Pharmaceuticals, Inc. Method for treating pulmonary diseases using rho kinase inhibitor compounds
JP2013513664A (ja) * 2009-12-14 2013-04-22 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 架橋二環式rhoキナーゼ阻害化合物、組成および使用
WO2012015760A1 (en) * 2010-07-27 2012-02-02 Inspire Pharmaceuticals, Inc. Method for treating ophthalmic diseases using kinase inhibitor compounds in prodrug forms

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