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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Publication date
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
Active legal-status Critical Current
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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)

Families Citing this family (21)

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ES2900243T3 (es) 2008-10-22 2022-03-16 Array Biopharma Inc Compuestos de pirazolo[1,5-a]pirimidina sustituidos como inhibidores de trk quinasa
AR077468A1 (es) 2009-07-09 2011-08-31 Array Biopharma Inc Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa
MX2012013467A (es) 2010-05-20 2013-04-29 Array Biopharma Inc Compuestos macrociclicos como inhibidores de trk cinasa.
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
JP2017531037A (ja) * 2014-10-06 2017-10-19 フラットレー ディスカバリー ラブ,エルエルシー トリアゾロピリジン化合物および嚢胞性線維症の治療のための方法
US10799505B2 (en) 2014-11-16 2020-10-13 Array Biopharma, Inc. 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
EP3233840B1 (en) 2014-12-16 2018-11-21 Eudendron S.r.l. Heterocyclic derivatives modulating activity of certain protein kinases
EP3368039A1 (en) 2015-10-26 2018-09-05 The Regents of The University of Colorado, A Body Corporate 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
HUE068971T2 (hu) 2016-04-04 2025-02-28 Loxo Oncology Inc (S)-N-(5-((R)-2-(2,5-difluorofenil)-pirrolidin-1-il)-pirazolo[1,5-A]pirimidin-3-il) -3-hidroxipirrolidin-1-karboxamid folyékony készítményei
PT3800189T (pt) 2016-05-18 2023-07-27 Array Biopharma Inc Preparação de (s)-n-(5-((r)-2-(2,5- difluoropenil)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
AU2019264078A1 (en) * 2018-05-02 2020-12-17 Jw Pharmaceutical Corporation Novel heterocycle derivative
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
TW202448883A (zh) * 2023-05-24 2024-12-16 大陸商長春金賽藥業有限責任公司 Fgfr2/3選擇性抑制劑、藥物組合物及其用途

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ID24653A (id) 1997-03-19 2000-07-27 Basf Ag Zat-zat terapi
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
EP1292586B1 (en) 2000-06-22 2004-08-04 Pfizer Limited 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
BRPI0614884A2 (pt) * 2005-08-25 2011-04-19 Hoffmann La Roche inibidores de p38 map cinase e métodos para uso dos mesmos
AU2007275816A1 (en) 2006-07-17 2008-01-24 Merck Sharp & Dohme Corp. 1-hydroxy naphthyridine compounds as anti-HIV agents
CN101594862B (zh) * 2006-12-20 2015-11-25 内尔维阿诺医学科学有限公司 作为激酶抑制剂的取代吲唑衍生物
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
CA2693901C (en) 2007-07-20 2015-12-29 Nerviano Medical Sciences S.R.L. Substituted indazole derivatives active as kinase inhibitors
ES2630026T3 (es) * 2008-12-18 2017-08-17 Nerviano Medical Sciences S.R.L. Derivados indazólicos sustituidos activos como inhibidores de cinasa
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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