JP2014525425A5 - - Google Patents

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Publication number
JP2014525425A5
JP2014525425A5 JP2014527680A JP2014527680A JP2014525425A5 JP 2014525425 A5 JP2014525425 A5 JP 2014525425A5 JP 2014527680 A JP2014527680 A JP 2014527680A JP 2014527680 A JP2014527680 A JP 2014527680A JP 2014525425 A5 JP2014525425 A5 JP 2014525425A5
Authority
JP
Japan
Prior art keywords
alkyl
group
halo
alkoxy
amino
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.)
Pending
Application number
JP2014527680A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014525425A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2012/067016 external-priority patent/WO2013030365A1/en
Publication of JP2014525425A publication Critical patent/JP2014525425A/ja
Publication of JP2014525425A5 publication Critical patent/JP2014525425A5/ja
Pending legal-status Critical Current

Links

JP2014527680A 2011-08-31 2012-08-31 新規のrockキナーゼ阻害剤 Pending JP2014525425A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP11179491.3 2011-08-31
EP11179491 2011-08-31
PCT/EP2012/067016 WO2013030365A1 (en) 2011-08-31 2012-08-31 Novel rock kinase inhibitors

Publications (2)

Publication Number Publication Date
JP2014525425A JP2014525425A (ja) 2014-09-29
JP2014525425A5 true JP2014525425A5 (enExample) 2015-10-15

Family

ID=46796597

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2014527680A Pending JP2014525425A (ja) 2011-08-31 2012-08-31 新規のrockキナーゼ阻害剤
JP2014527681A Withdrawn JP2014525426A (ja) 2011-08-31 2012-08-31 新規のソフトrock阻害剤
JP2014527682A Withdrawn JP2014525427A (ja) 2011-08-31 2012-08-31 Rockキナーゼ阻害剤としてのビフェニルカルボキサミド

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2014527681A Withdrawn JP2014525426A (ja) 2011-08-31 2012-08-31 新規のソフトrock阻害剤
JP2014527682A Withdrawn JP2014525427A (ja) 2011-08-31 2012-08-31 Rockキナーゼ阻害剤としてのビフェニルカルボキサミド

Country Status (16)

Country Link
US (3) US9174939B2 (enExample)
EP (3) EP2751080B1 (enExample)
JP (3) JP2014525425A (enExample)
KR (2) KR20140072879A (enExample)
CN (3) CN103874683A (enExample)
AU (3) AU2012300834A1 (enExample)
BR (3) BR112014004435A2 (enExample)
CA (3) CA2846695A1 (enExample)
EA (3) EA201490515A1 (enExample)
ES (1) ES2560830T3 (enExample)
IL (2) IL231122A0 (enExample)
MX (3) MX2014002394A (enExample)
PT (1) PT2751080E (enExample)
SG (2) SG11201400058PA (enExample)
WO (3) WO2013030366A1 (enExample)
ZA (3) ZA201401416B (enExample)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10842669B2 (en) * 2008-11-13 2020-11-24 Gholam A. Peyman Ophthalmic drug delivery method
SG11201400058PA (en) * 2011-08-31 2014-03-28 Amakem Nv Novel rock kinase inhibitors
WO2014055996A2 (en) 2012-10-05 2014-04-10 Kadmon Corporation, Llc Rho kinase inhibitors
DK2951172T3 (en) 2013-01-29 2017-07-17 Redx Pharma Plc PYRIDINE DERIVATIVES LIKE SOFT ROCK INHIBITORS
US10092537B2 (en) 2013-04-15 2018-10-09 Renascience Co., Ltd. Use for PAI-1 inhibitor
SI3083554T1 (sl) * 2013-12-17 2019-04-30 Eli Lilly & Company Spojine dimetilbenzojske kisline
US20170114323A1 (en) 2014-06-19 2017-04-27 Whitehead Institute For Biomedical Research Uses of kinase inhibitors for inducing and maintaining pluripotency
WO2020047229A1 (en) 2018-08-29 2020-03-05 University Of Massachusetts Inhibition of protein kinases to treat friedreich ataxia
CN113801111B (zh) * 2020-06-12 2025-10-17 上海翰森生物医药科技有限公司 联苯类衍生物抑制剂及其制备方法和应用
US12371667B2 (en) 2021-05-13 2025-07-29 Washington University Enhanced methods for inducing and maintaining naive human pluripotent stem cells
EP4431596A1 (en) 2021-11-11 2024-09-18 The Doshisha Cryopreservation preparation for corneal endothelial cells and method for producing said cryopreservation preparation
KR20250057882A (ko) * 2022-09-08 2025-04-29 레드엑스 파마 리미티드 고체 형태의 rock 저해제
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
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
TW202530228A (zh) 2023-10-12 2025-08-01 美商銳新醫藥公司 Ras抑制劑
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
WO2025255438A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1990005723A1 (fr) 1988-11-24 1990-05-31 Yoshitomi Pharmaceutical Industries, Ltd. Composes de trans-4-amino(alkyl)-1-pyridylcarbamoylcyclohexane et leur utilisation en medecine
IS2334B (is) 1992-09-08 2008-02-15 Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) Aspartyl próteasi hemjari af nýjum flokki súlfonamíða
EG20677A (en) 1993-10-01 1999-11-30 Astra Ag Method and an apparatus for micronizing the particle size
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
GB0124928D0 (en) * 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
WO2005014599A1 (en) * 2003-06-04 2005-02-17 Cellular Genomics, Inc. Imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of bruton’s tyrosine kinase by such compounds
US7683097B2 (en) * 2004-05-27 2010-03-23 Propharmacon Inc. Topoisomerase inhibitors
US20100168102A9 (en) * 2005-07-11 2010-07-01 Devgen Nv Amide Derivatives as Kinase Inhibitors
CN101248046A (zh) * 2005-07-11 2008-08-20 德福根有限公司 作为激酶抑制剂的酰胺衍生物
WO2007006547A1 (en) * 2005-07-11 2007-01-18 Devgen N.V. Amide derivatives as kinase inhibitors
US20070042321A1 (en) * 2005-08-22 2007-02-22 Florman Michael J Grinder guard
HRP20100542T1 (hr) * 2005-09-16 2010-11-30 Arrow Therapeutics Limited Derivati bifenila i njihova uporaba za liječenje hepatitisa c
CN101287707A (zh) * 2005-10-13 2008-10-15 德福根有限公司 激酶抑制剂
CA2696793A1 (en) * 2007-08-17 2009-02-26 Eisai R&D Management Co., Ltd. Novel preparation for external use
GB201018996D0 (en) * 2010-11-10 2010-12-22 Amakem Nv Novel ROCK inhibitors
EA031616B1 (ru) 2010-03-02 2019-01-31 пиЭйч ФАРМА Ко., ЛТД. Новые ингибиторы rock
US8921383B2 (en) * 2011-03-28 2014-12-30 Hoffmann-La Roche Inc. Thiazolopyrimidine compounds
GB201114854D0 (en) * 2011-08-29 2011-10-12 Amakem Nv Novel rock inhibitors
SG11201400058PA (en) * 2011-08-31 2014-03-28 Amakem Nv Novel rock kinase inhibitors
CA2846768A1 (en) * 2011-09-13 2013-03-21 Novartis Ag Combinations comprising a s1p receptor modulator

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