JP2015522607A5 - - Google Patents

Download PDF

Info

Publication number
JP2015522607A5
JP2015522607A5 JP2015523009A JP2015523009A JP2015522607A5 JP 2015522607 A5 JP2015522607 A5 JP 2015522607A5 JP 2015523009 A JP2015523009 A JP 2015523009A JP 2015523009 A JP2015523009 A JP 2015523009A JP 2015522607 A5 JP2015522607 A5 JP 2015522607A5
Authority
JP
Japan
Prior art keywords
phenyl
isoquinoline
carboxamide
amino
trifluoromethyl
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.)
Withdrawn
Application number
JP2015523009A
Other languages
English (en)
Japanese (ja)
Other versions
JP2015522607A (ja
Filing date
Publication date
Priority claimed from KR1020120078904A external-priority patent/KR20140011780A/ko
Application filed filed Critical
Publication of JP2015522607A publication Critical patent/JP2015522607A/ja
Publication of JP2015522607A5 publication Critical patent/JP2015522607A5/ja
Withdrawn legal-status Critical Current

Links

JP2015523009A 2012-07-19 2013-07-17 プロテインキナーゼに対する阻害活性を有するイソキノリン−5−カルボキサミド誘導体 Withdrawn JP2015522607A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
KR1020120078904A KR20140011780A (ko) 2012-07-19 2012-07-19 단백질 키나아제 저해활성을 갖는 이소퀴놀린-5-카복스아미드 유도체
KR10-2012-0078904 2012-07-19
PCT/KR2013/006392 WO2014014270A1 (ko) 2012-07-19 2013-07-17 단백질 키나아제 저해활성을 갖는 이소퀴놀린-5-카복스아미드 유도체

Publications (2)

Publication Number Publication Date
JP2015522607A JP2015522607A (ja) 2015-08-06
JP2015522607A5 true JP2015522607A5 (enExample) 2016-08-18

Family

ID=49949038

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015523009A Withdrawn JP2015522607A (ja) 2012-07-19 2013-07-17 プロテインキナーゼに対する阻害活性を有するイソキノリン−5−カルボキサミド誘導体

Country Status (6)

Country Link
US (1) US9388165B2 (enExample)
EP (1) EP2876107A4 (enExample)
JP (1) JP2015522607A (enExample)
KR (1) KR20140011780A (enExample)
CN (1) CN104487420A (enExample)
WO (1) WO2014014270A1 (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3201174A4 (en) * 2014-10-03 2018-06-06 The Royal Institution for the Advancement of Learning / McGill University Urea and bis-urea based compounds and analogues thereof useful in the treatment of androgen receptor mediated diseases or disorders
ES2908602T3 (es) 2017-07-29 2022-05-03 Lutris Pharma Ltd Nuevos inhibidores de BRaf y uso de los mismos para el tratamiento de reacciones cutáneas
EP3717492B1 (en) 2017-11-30 2023-05-24 Hanmi Pharm. Co., Ltd. Thieno[3,2-d]pyrimidine compound having inhibitory activity for protein kinase
US12274703B2 (en) 2017-12-21 2025-04-15 Gliapharm Sa Compositions and methods of treatment for neurological disorders comprising a dementia
US12310967B2 (en) 2017-12-21 2025-05-27 Gliapharm Sa Compositions and methods of treatment for neurological disorders comprising motor neuron diseases
CA3104808A1 (en) * 2018-07-02 2020-01-09 Ecole Polytechnique Federale De Lausanne (Epfl) Lactate enhancing compounds and uses thereof
WO2020132378A2 (en) 2018-12-22 2020-06-25 Gliapharm Sa Compositions and methods of treatment for neurological disorders comprising depression
RS64618B1 (sr) 2019-02-12 2023-10-31 Lutris Pharma Ltd Upotreba lokalnih kompozicija braf inhibitorа za lečenje radijacijskog dermatitisa
WO2021231191A1 (en) * 2020-05-12 2021-11-18 Merck Sharp & Dohme Corp. Factor xi activation inhibitors

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL341356A1 (en) * 1997-12-22 2001-04-09 Bayer Ag Raf kinase inhibition employing aryl- and heteroaryl-substituted heterocyclic ureas
GB0005357D0 (en) 2000-03-06 2000-04-26 Smithkline Beecham Plc Compounds
DE60230044D1 (de) * 2001-06-11 2009-01-08 Vertex Pharma Isochinolin-inhibitoren von p38
WO2003022832A1 (en) * 2001-09-05 2003-03-20 Smithkline Beecham P.L.C. Pyridylfurans and pyrroles as raf kinase inhibitors
JP2005504793A (ja) * 2001-09-05 2005-02-17 スミスクライン ビーチャム パブリック リミテッド カンパニー Rafキナーゼ阻害剤としてのヘテロサイクルカルボキサミド誘導体
WO2005105777A1 (en) * 2004-05-05 2005-11-10 Pharmacia & Upjohn Company Llc Substituted thiophene amide compounds for the treatment of inflammation
SE0401345D0 (sv) 2004-05-25 2004-05-25 Astrazeneca Ab Therapeutic compounds: Pyridine as scaffold
SE0401342D0 (sv) * 2004-05-25 2004-05-25 Astrazeneca Ab Therapeutic compounds
SG182361A1 (en) * 2010-01-29 2012-08-30 Hanmi Science Co Ltd THIENO[3,2-d]PYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY ON PROTEIN KINASES

Similar Documents

Publication Publication Date Title
JP2015522607A5 (enExample)
JP2019517487A5 (enExample)
JP2014511892A5 (enExample)
JP2018138577A5 (enExample)
JP2017537948A5 (enExample)
JP2005535586A5 (enExample)
RU2017121044A (ru) Производные амидотиадиазола в качестве ингибиторов надфн-оксидазы
RU2016134751A (ru) Соединения
RU2019106484A (ru) Гетероциклическое соединение
JP2014511891A5 (enExample)
JP2017502940A5 (enExample)
JP2013527202A5 (enExample)
JP2017527578A5 (enExample)
JP2013532727A5 (enExample)
JP2013510122A5 (enExample)
JP2009536620A5 (enExample)
JP2016513660A5 (enExample)
JP2018516238A5 (enExample)
JP2018519245A5 (enExample)
JP2016523923A5 (enExample)
JP2009513703A5 (enExample)
IL264982B (en) (hetero)aryl cyclopropylamine compounds as lsd1 inhibitors
NZ627750A (en) Carbamate compounds and of making and using same
RU2014131390A (ru) ПРОИЗВОДНЫЕ ТИЕНО[3,2-d]ПИРИМИДИНА, ОБЛАДАЮЩИЕ ИНГИБИРУЮЩЕЙ АКТИВНОСТЬЮ В ОТНОШЕНИИ ПРОТЕИНКИНАЗ
RU2019136279A (ru) C5 -Анилинохиназолиновые соединения и их использование в лечении рака