JP2017527578A5 - - Google Patents

Download PDF

Info

Publication number
JP2017527578A5
JP2017527578A5 JP2017513450A JP2017513450A JP2017527578A5 JP 2017527578 A5 JP2017527578 A5 JP 2017527578A5 JP 2017513450 A JP2017513450 A JP 2017513450A JP 2017513450 A JP2017513450 A JP 2017513450A JP 2017527578 A5 JP2017527578 A5 JP 2017527578A5
Authority
JP
Japan
Prior art keywords
pharmaceutically acceptable
acceptable salt
compound
irritable bowel
bowel syndrome
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.)
Granted
Application number
JP2017513450A
Other languages
English (en)
Japanese (ja)
Other versions
JP6538154B2 (ja
JP2017527578A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2015/056905 external-priority patent/WO2016038552A1/en
Publication of JP2017527578A publication Critical patent/JP2017527578A/ja
Publication of JP2017527578A5 publication Critical patent/JP2017527578A5/ja
Application granted granted Critical
Publication of JP6538154B2 publication Critical patent/JP6538154B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017513450A 2014-09-10 2015-09-09 Ret(rearranged during transfection)キナーゼ阻害剤としてのピリジン誘導体 Expired - Fee Related JP6538154B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
CNPCT/CN2014/086197 2014-09-10
CN2014086197 2014-09-10
CNPCT/CN2015/086995 2015-08-14
CN2015086995 2015-08-14
PCT/IB2015/056905 WO2016038552A1 (en) 2014-09-10 2015-09-09 Pyridone derivatives as rearranged during transfection (ret) kinase inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2019102776A Division JP6728447B2 (ja) 2014-09-10 2019-05-31 Ret(rearranged during transfection)キナーゼ阻害剤としてのピリジン誘導体

Publications (3)

Publication Number Publication Date
JP2017527578A JP2017527578A (ja) 2017-09-21
JP2017527578A5 true JP2017527578A5 (enExample) 2018-10-25
JP6538154B2 JP6538154B2 (ja) 2019-07-03

Family

ID=54186249

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2017513450A Expired - Fee Related JP6538154B2 (ja) 2014-09-10 2015-09-09 Ret(rearranged during transfection)キナーゼ阻害剤としてのピリジン誘導体
JP2019102776A Expired - Fee Related JP6728447B2 (ja) 2014-09-10 2019-05-31 Ret(rearranged during transfection)キナーゼ阻害剤としてのピリジン誘導体

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2019102776A Expired - Fee Related JP6728447B2 (ja) 2014-09-10 2019-05-31 Ret(rearranged during transfection)キナーゼ阻害剤としてのピリジン誘導体

Country Status (36)

Country Link
US (4) US9918974B2 (enExample)
EP (2) EP3191450B1 (enExample)
JP (2) JP6538154B2 (enExample)
KR (1) KR20170045350A (enExample)
CN (1) CN107074768B (enExample)
AU (1) AU2015313841B2 (enExample)
BR (1) BR112017004900A2 (enExample)
CA (1) CA2960768A1 (enExample)
CL (1) CL2017000588A1 (enExample)
CO (1) CO2017002273A2 (enExample)
CR (1) CR20170093A (enExample)
CY (1) CY1121661T1 (enExample)
DK (1) DK3191450T3 (enExample)
DO (1) DOP2017000059A (enExample)
EA (1) EA033544B1 (enExample)
ES (2) ES2725704T3 (enExample)
HR (1) HRP20190815T1 (enExample)
HU (1) HUE044604T2 (enExample)
IL (1) IL250908B (enExample)
LT (1) LT3191450T (enExample)
MA (1) MA40581A (enExample)
ME (1) ME03432B (enExample)
MX (1) MX373863B (enExample)
MY (1) MY181913A (enExample)
PE (1) PE20170705A1 (enExample)
PH (1) PH12017500425A1 (enExample)
PL (1) PL3191450T3 (enExample)
PT (1) PT3191450T (enExample)
RS (1) RS58813B1 (enExample)
SG (1) SG11201701694QA (enExample)
SI (1) SI3191450T1 (enExample)
SM (1) SMT201900304T1 (enExample)
TW (1) TWI683807B (enExample)
UA (1) UA122213C2 (enExample)
UY (1) UY36293A (enExample)
WO (1) WO2016038552A1 (enExample)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2011256380C1 (en) 2010-05-20 2016-09-08 Array Biopharma Inc. Macrocyclic compounds as Trk kinase inhibitors
JP6538153B2 (ja) * 2014-09-10 2019-07-03 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited Rearranged during transfection(ret)阻害剤としての新規な化合物
RS58813B1 (sr) 2014-09-10 2019-07-31 Glaxosmithkline Ip Dev Ltd Piridonski derivati korišćeni kao inhibitori kinaze reorganizovane tokom transfekcije (ret)
US10202365B2 (en) 2015-02-06 2019-02-12 Blueprint Medicines Corporation 2-(pyridin-3-yl)-pyrimidine derivatives as RET inhibitors
JP6816100B2 (ja) 2015-07-16 2021-01-20 アレイ バイオファーマ、インコーポレイテッド RETキナーゼ阻害物質としての置換ピラゾロ[1,5−a]ピリジン化合物
TWI787018B (zh) 2015-11-02 2022-12-11 美商纜圖藥品公司 轉染過程重排之抑制劑
UY37155A (es) 2016-03-17 2017-10-31 Blueprint Medicines Corp Inhibidores de ret
US10227329B2 (en) 2016-07-22 2019-03-12 Blueprint Medicines Corporation Compounds useful for treating disorders related to RET
JP2018052878A (ja) * 2016-09-29 2018-04-05 第一三共株式会社 ピリジン化合物
JOP20190077A1 (ar) 2016-10-10 2019-04-09 Array Biopharma Inc مركبات بيرازولو [1، 5-a]بيريدين بها استبدال كمثبطات كيناز ret
TWI704148B (zh) 2016-10-10 2020-09-11 美商亞雷生物製藥股份有限公司 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物
WO2018136663A1 (en) 2017-01-18 2018-07-26 Array Biopharma, Inc. Ret inhibitors
ES2948194T3 (es) 2017-01-18 2023-09-01 Array Biopharma Inc Compuestos de pirazolo[1,5-a]pirazina sustituida como inhibidores de la cinasa RET
JOP20190213A1 (ar) 2017-03-16 2019-09-16 Array Biopharma Inc مركبات حلقية ضخمة كمثبطات لكيناز ros1
EP3624802A1 (en) 2017-05-15 2020-03-25 Blueprint Medicines Corporation Combinations of ret inhibitors and mtorc1 inhibitors and uses thereof for the treatment of cancer mediated by aberrant ret activity
TWI812649B (zh) 2017-10-10 2023-08-21 美商絡速藥業公司 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之調配物
TWI791053B (zh) 2017-10-10 2023-02-01 美商亞雷生物製藥股份有限公司 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之結晶形式及其醫藥組合物
US11603374B2 (en) 2018-01-18 2023-03-14 Array Biopharma Inc. Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors
JP6997876B2 (ja) 2018-01-18 2022-02-04 アレイ バイオファーマ インコーポレイテッド Retキナーゼ阻害剤としての置換ピラゾリル[4,3-c]ピリジン化合物
TW201938169A (zh) 2018-01-18 2019-10-01 美商亞雷生物製藥股份有限公司 作為RET激酶抑制劑之經取代吡唑并[3,4-d]嘧啶化合物
CA3096043A1 (en) 2018-04-03 2019-10-10 Blueprint Medicines Corporation Ret inhibitor for use in treating cancer having a ret alteration
CA3111984A1 (en) 2018-09-10 2020-03-19 Array Biopharma Inc. Fused heterocyclic compounds as ret kinase inhibitors
CA3183728A1 (en) 2020-05-29 2021-12-02 Blueprint Medicines Corporation Solid forms of pralsetinib
TWI786742B (zh) * 2020-07-23 2022-12-11 大陸商深圳晶泰科技有限公司 吡啶酮類化合物及其製備方法和應用
AU2023329563A1 (en) 2022-08-24 2025-02-27 Toray Industries, Inc. Medicament for treatment and/or prevention of cancer

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU739642B2 (en) 1997-12-22 2001-10-18 Bayer Healthcare Llc Inhibition of p38 kinase activity using substituted heterocyclic ureas
US20120046290A1 (en) 1997-12-22 2012-02-23 Jacques Dumas Inhibition of p38 kinase activity using substituted heterocyclic ureas
US20070244120A1 (en) 2000-08-18 2007-10-18 Jacques Dumas Inhibition of raf kinase using substituted heterocyclic ureas
CN100360507C (zh) 1997-12-22 2008-01-09 拜尔有限公司 用取代杂环脲抑制raf激酶
BR0013143A (pt) 1999-08-12 2002-06-11 Pharmacia Italia Spa Derivados de 3 (5) amino pirazol, processo para sua preparação e uso dos mesmos como agentes antitumorais
JP2004517840A (ja) * 2000-11-27 2004-06-17 フアルマシア・イタリア・エツセ・ピー・アー フェニルアセトアミド−ピラゾール誘導体およびそれの抗腫瘍薬としての使用
DE10201764A1 (de) 2002-01-18 2003-07-31 Bayer Cropscience Ag Substituierte 4-Aminopyridin-Derivate
PE20040522A1 (es) 2002-05-29 2004-09-28 Novartis Ag Derivados de diarilurea dependientes de la cinasa de proteina
WO2004024694A1 (ja) 2002-09-10 2004-03-25 Kyorin Pharmaceutical Co., Ltd. 4-置換アリール-5-ヒドロキシイソキノリノン誘導体
US20050148555A1 (en) 2003-08-22 2005-07-07 Boehringer Ingelheim Pharmaceuticals, Inc. Methods of treating COPD and pulmonary hypertension
TW200530236A (en) * 2004-02-23 2005-09-16 Chugai Pharmaceutical Co Ltd Heteroaryl phenylurea
KR101328273B1 (ko) * 2004-12-28 2013-11-14 키넥스 파마슈티컬즈, 엘엘씨 세포 증식 질환의 치료를 위한 조성물 및 방법
US7968574B2 (en) 2004-12-28 2011-06-28 Kinex Pharmaceuticals, Llc Biaryl compositions and methods for modulating a kinase cascade
GB0507575D0 (en) * 2005-04-14 2005-05-18 Novartis Ag Organic compounds
US8247556B2 (en) * 2005-10-21 2012-08-21 Amgen Inc. Method for preparing 6-substituted-7-aza-indoles
TW200804349A (en) * 2005-12-23 2008-01-16 Kalypsys Inc Novel substituted pyrimidinyloxy ureas as inhibitors of protein kinases
ES2500165T3 (es) 2006-06-29 2014-09-30 Kinex Pharmaceuticals, Llc Composiciones de biarilo y métodos para modular una cascada de quinasas
ES2565683T3 (es) * 2006-09-15 2016-04-06 Xcovery, Inc. Compuestos inhibidores de quinasa
CN101558068A (zh) * 2006-10-16 2009-10-14 诺瓦提斯公司 用作蛋白激酶抑制剂的苯乙酰胺类
WO2008058341A1 (en) 2006-11-15 2008-05-22 Cytopia Research Pty Ltd Inhibitors of kinase activity
CN102470127A (zh) 2009-08-19 2012-05-23 埃姆比特生物科学公司 联芳基化合物和其使用方法
WO2012082817A1 (en) 2010-12-16 2012-06-21 Boehringer Ingelheim International Gmbh Biarylamide inhibitors of leukotriene production
US8937071B2 (en) 2013-03-15 2015-01-20 Glaxosmithkline Intellectual Property Development Limited Compounds as rearranged during transfection (RET) inhibitors
UA115264C2 (uk) 2013-03-15 2017-10-10 Глаксосмітклайн Інтеллектьюел Проперті Девелопмент Лімітед Піридинові похідні як інгібітори реаранжованої у процесі трансфекції (ret) кінази
RS58813B1 (sr) * 2014-09-10 2019-07-31 Glaxosmithkline Ip Dev Ltd Piridonski derivati korišćeni kao inhibitori kinaze reorganizovane tokom transfekcije (ret)
JP6538153B2 (ja) 2014-09-10 2019-07-03 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited Rearranged during transfection(ret)阻害剤としての新規な化合物

Similar Documents

Publication Publication Date Title
JP2017527578A5 (enExample)
JP2017526711A5 (enExample)
HRP20190815T1 (hr) Piridonski derivati korišteni kao inhibitori kinaze reorganizirane tijekom transfekcije (ret)
JP2013543896A5 (enExample)
JP2017528503A5 (enExample)
JP2013527202A5 (enExample)
JP2017504635A5 (enExample)
JP2016503010A5 (enExample)
JP2015145426A5 (enExample)
NZ703941A (en) Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
JP2014525470A5 (enExample)
JP2015516434A5 (enExample)
JP2013526482A5 (enExample)
JP2015524472A5 (enExample)
JP2017528507A5 (enExample)
FI3699181T3 (fi) Kiteinen muoto (s)-n-(5-((r)-2-(2,5-diluorifenyyli)-pyrrolidin-1-yyli)-pyratsolo[1,5-a]pyrimidin-3-yyli)-3-hydroksipyrrolidiini-1-karboksamidivetyysulfaatista
NZ627750A (en) Carbamate compounds and of making and using same
JP2020510661A5 (enExample)
JP2009529541A5 (enExample)
JP2016516020A5 (enExample)
JP2014511892A5 (enExample)
JP2009541216A5 (enExample)
JP2014062126A5 (enExample)
RU2017116196A (ru) 2-амино-6-(дифторметил)-5,5-дифтор-6-фенил-3,4,5,6-тетрагидропиридины как ингибиторы васе1
JP2012507535A5 (enExample)