JP2015522650A5 - - Google Patents

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Publication number
JP2015522650A5
JP2015522650A5 JP2015523576A JP2015523576A JP2015522650A5 JP 2015522650 A5 JP2015522650 A5 JP 2015522650A5 JP 2015523576 A JP2015523576 A JP 2015523576A JP 2015523576 A JP2015523576 A JP 2015523576A JP 2015522650 A5 JP2015522650 A5 JP 2015522650A5
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JP
Japan
Prior art keywords
group
pharmaceutical composition
composition according
atom
pain
Prior art date
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Application number
JP2015523576A
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English (en)
Japanese (ja)
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JP2015522650A (ja
JP6456823B2 (ja
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Priority claimed from EP12305922.2A external-priority patent/EP2689778A1/en
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Publication of JP2015522650A publication Critical patent/JP2015522650A/ja
Publication of JP2015522650A5 publication Critical patent/JP2015522650A5/ja
Application granted granted Critical
Publication of JP6456823B2 publication Critical patent/JP6456823B2/ja
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JP2015523576A 2012-07-27 2013-07-29 疼痛を治療するためのアザインダゾールまたはジアザインダゾール型の誘導体 Active JP6456823B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP12305922.2A EP2689778A1 (en) 2012-07-27 2012-07-27 Derivatives of azaindoles or diazaindoles for treating pain
EP12305922.2 2012-07-27
PCT/EP2013/065907 WO2014016433A1 (en) 2012-07-27 2013-07-29 Derivatives of azaindazole or diazaindazole type for treating pain

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2018200317A Division JP6732855B2 (ja) 2012-07-27 2018-10-24 疼痛を治療するためのアザインダゾールまたはジアザインダゾール型の誘導体

Publications (3)

Publication Number Publication Date
JP2015522650A JP2015522650A (ja) 2015-08-06
JP2015522650A5 true JP2015522650A5 (enExample) 2016-09-15
JP6456823B2 JP6456823B2 (ja) 2019-01-23

Family

ID=48948392

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2015523576A Active JP6456823B2 (ja) 2012-07-27 2013-07-29 疼痛を治療するためのアザインダゾールまたはジアザインダゾール型の誘導体
JP2018200317A Active JP6732855B2 (ja) 2012-07-27 2018-10-24 疼痛を治療するためのアザインダゾールまたはジアザインダゾール型の誘導体

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2018200317A Active JP6732855B2 (ja) 2012-07-27 2018-10-24 疼痛を治療するためのアザインダゾールまたはジアザインダゾール型の誘導体

Country Status (28)

Country Link
US (1) US9381195B2 (enExample)
EP (2) EP2689778A1 (enExample)
JP (2) JP6456823B2 (enExample)
KR (1) KR102120505B1 (enExample)
CN (1) CN104684554B (enExample)
AU (1) AU2013294920B2 (enExample)
BR (1) BR112015001502B1 (enExample)
CA (1) CA2879595C (enExample)
CY (1) CY1118478T1 (enExample)
DK (1) DK2877177T3 (enExample)
ES (1) ES2612349T3 (enExample)
HR (1) HRP20170104T1 (enExample)
HU (1) HUE032919T2 (enExample)
IL (1) IL236917A (enExample)
LT (1) LT2877177T (enExample)
MA (1) MA37866B1 (enExample)
MX (1) MX363605B (enExample)
MY (1) MY183398A (enExample)
NZ (1) NZ705253A (enExample)
PL (1) PL2877177T3 (enExample)
PT (1) PT2877177T (enExample)
RS (1) RS55646B1 (enExample)
RU (1) RU2640046C2 (enExample)
SI (1) SI2877177T1 (enExample)
TN (1) TN2015000034A1 (enExample)
UA (1) UA116107C2 (enExample)
WO (1) WO2014016433A1 (enExample)
ZA (1) ZA201501209B (enExample)

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PT3106463T (pt) 2008-10-22 2018-05-18 Array Biopharma Inc Compostos de pirazolo[1,5-]pirimidina substituídos como inibidores de cinase trk
AR077468A1 (es) 2009-07-09 2011-08-31 Array Biopharma Inc Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa
RU2735545C2 (ru) 2010-05-20 2020-11-03 Эррэй Биофарма Инк. Макроциклические соединения в качестве ингибиторов киназы trk
EP2689778A1 (en) * 2012-07-27 2014-01-29 Pierre Fabre Medicament Derivatives of azaindoles or diazaindoles for treating pain
WO2015143652A1 (en) * 2014-03-26 2015-10-01 Merck Sharp & Dohme Corp. TrkA KINASE INHIBITORS,COMPOSITIONS AND METHODS THEREOF
US9573948B2 (en) 2014-10-06 2017-02-21 Flatley Discovery Lab Triazolopyridine compounds and methods for the treatment of cystic fibrosis
EP3218380B1 (en) 2014-11-16 2021-03-17 Array Biopharma, Inc. Preparation of a crystalline form of (s)-n-(5-((r)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate
WO2016096709A1 (en) 2014-12-16 2016-06-23 Eudendron S.R.L. Heterocyclic derivatives modulating activity of certain protein kinases
TN2019000271A1 (en) 2015-10-26 2021-01-07 Univ Colorado Regents Point mutations in trk inhibitor-resistant cancer and methods relating to the same
US10045991B2 (en) 2016-04-04 2018-08-14 Loxo Oncology, Inc. Methods of treating pediatric cancers
IL304018A (en) 2016-04-04 2023-08-01 Loxo Oncology Inc Liquid formulations of (S)-N-(5-((R)-2-(5,2-difluorophenyl)-pyrrolidine-1-yl)-pyrazolo[5,1-A]pyrimidin-3-yl)-3 -hydroxypyrrolidine-1-carboxamide
ES2952056T3 (es) 2016-05-18 2023-10-26 Loxo Oncology Inc Preparación de (s)-n-(5-((r)-2-(2,5-difluorofenil)pirrolidin-1-il)pirazolo[1,5-a]pirimidin-3-il)-3-hidroxipirrolidina-1-carboxamida
WO2018049271A1 (en) * 2016-09-09 2018-03-15 Flx Bio, Inc. Chemokine receptor modulators and uses thereof
JOP20190092A1 (ar) 2016-10-26 2019-04-25 Array Biopharma Inc عملية لتحضير مركبات بيرازولو[1، 5-a]بيريميدين وأملاح منها
WO2018079759A1 (ja) * 2016-10-31 2018-05-03 塩野義製薬株式会社 TrkA阻害活性を有する縮合複素環および縮合炭素環誘導体
JOP20190213A1 (ar) 2017-03-16 2019-09-16 Array Biopharma Inc مركبات حلقية ضخمة كمثبطات لكيناز ros1
WO2019212256A1 (ko) * 2018-05-02 2019-11-07 제이더블유중외제약 주식회사 신규한 헤테로 사이클 유도체
KR102129114B1 (ko) * 2018-07-26 2020-07-02 주식회사 온코파마텍 TrkA 저해 활성을 갖는 화합물 및 이를 유효성분으로 함유하는 통증의 예방 또는 치료용 약학적 조성물
EP3725777A1 (en) * 2019-04-17 2020-10-21 Rottapharm Biotech S.r.l. Benzo- and pyrido-pyrazoles as protein kinase inhibitors
CN110105356B (zh) * 2019-05-31 2022-04-01 四川国康药业有限公司 一种氮杂吲哚类化合物及其制备方法和用途
CN121358733A (zh) * 2023-05-24 2026-01-16 长春金赛药业有限责任公司 Fgfr2/3选择性抑制剂、药物组合物及其应用

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ATE242245T1 (de) * 1997-03-19 2003-06-15 Basf Ag Pyrrolo(2,3-d)pyrimidine und ihre verwendung als tyrosinkinase-inhibitoren
EP1215208B1 (en) 1997-10-27 2006-07-12 Agouron Pharmaceuticals, Inc. 4-Aminothiazole derivatives, their preparation and their use as inhibitors of cyclin-dependent kinases
HUP0301183A3 (en) 2000-06-22 2006-02-28 Pfizer Process for the preparation of pyrazolopyrimidinones
SE0301906D0 (sv) * 2003-06-26 2003-06-26 Astrazeneca Ab New compounds
DE102004061288A1 (de) * 2004-12-14 2006-06-29 Schering Ag 3-Amino-Pyrazolo[3,4b]pyridine als Inhibitoren von Proteintyrosinkinasen, deren Herstellung und Verwendung als Arzneimittel
AU2006283940A1 (en) * 2005-08-25 2007-03-01 F. Hoffmann-La Roche Ag P38 MAP kinase inhibitors and methods for using the same
WO2008010964A1 (en) 2006-07-17 2008-01-24 Merck & Co., Inc. 1-hydroxy naphthyridine compounds as anti-hiv agents
ES2509820T3 (es) 2006-12-20 2014-10-20 Nerviano Medical Sciences S.R.L. Derivados de indazol como inhibidores de la cinasa para el tratamiento del cáncer
US20080194557A1 (en) * 2007-01-18 2008-08-14 Joseph Barbosa Methods and compositions for the treatment of pain, inflammation and cancer
WO2008112695A2 (en) * 2007-03-12 2008-09-18 Irm Llc Pyrazolo [3,4-d] pyrimidines and 1, 2, 5, 6-tetraaza- as- indacenes as protein kinase inhibitors for cancer treatment
EA018503B1 (ru) 2007-07-20 2013-08-30 НЕРВИАНО МЕДИКАЛ САЙЕНСИЗ С.р.л. Замещенные производные индазола, активные как ингибиторы киназы
US8354399B2 (en) * 2008-12-18 2013-01-15 Nerviano Medical Sciences S.R.L. Substituted indazole derivatives active as kinase inhibitors
FR2970967B1 (fr) * 2011-01-27 2013-02-15 Pf Medicament Derives de type azaindazole ou diazaindazole comme medicament
EP2689778A1 (en) * 2012-07-27 2014-01-29 Pierre Fabre Medicament Derivatives of azaindoles or diazaindoles for treating pain

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