JP2018516917A5 - - Google Patents

Download PDF

Info

Publication number
JP2018516917A5
JP2018516917A5 JP2017561810A JP2017561810A JP2018516917A5 JP 2018516917 A5 JP2018516917 A5 JP 2018516917A5 JP 2017561810 A JP2017561810 A JP 2017561810A JP 2017561810 A JP2017561810 A JP 2017561810A JP 2018516917 A5 JP2018516917 A5 JP 2018516917A5
Authority
JP
Japan
Prior art keywords
compound
cancer
pharmaceutically acceptable
stereoisomer
acceptable salt
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
JP2017561810A
Other languages
English (en)
Japanese (ja)
Other versions
JP6750806B2 (ja
JP2018516917A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2016/053267 external-priority patent/WO2016193939A1/en
Publication of JP2018516917A publication Critical patent/JP2018516917A/ja
Publication of JP2018516917A5 publication Critical patent/JP2018516917A5/ja
Application granted granted Critical
Publication of JP6750806B2 publication Critical patent/JP6750806B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017561810A 2015-06-04 2016-06-03 Cdk阻害剤としての置換型ヘテロシクリル誘導体 Active JP6750806B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
IN2803/CHE/2015 2015-06-04
IN2803CH2015 2015-06-04
IN6214/CHE/2015 2015-11-18
IN6214CH2015 2015-11-18
PCT/IB2016/053267 WO2016193939A1 (en) 2015-06-04 2016-06-03 Substituted heterocyclyl derivatives as cdk inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2020131775A Division JP7033764B2 (ja) 2015-06-04 2020-08-03 Cdk阻害剤としての置換型ヘテロシクリル誘導体

Publications (3)

Publication Number Publication Date
JP2018516917A JP2018516917A (ja) 2018-06-28
JP2018516917A5 true JP2018516917A5 (enExample) 2019-07-04
JP6750806B2 JP6750806B2 (ja) 2020-09-02

Family

ID=57440798

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2017561810A Active JP6750806B2 (ja) 2015-06-04 2016-06-03 Cdk阻害剤としての置換型ヘテロシクリル誘導体
JP2020131775A Expired - Fee Related JP7033764B2 (ja) 2015-06-04 2020-08-03 Cdk阻害剤としての置換型ヘテロシクリル誘導体
JP2022024039A Active JP7482918B2 (ja) 2015-06-04 2022-02-18 Cdk阻害剤としての置換型ヘテロシクリル誘導体

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2020131775A Expired - Fee Related JP7033764B2 (ja) 2015-06-04 2020-08-03 Cdk阻害剤としての置換型ヘテロシクリル誘導体
JP2022024039A Active JP7482918B2 (ja) 2015-06-04 2022-02-18 Cdk阻害剤としての置換型ヘテロシクリル誘導体

Country Status (20)

Country Link
US (3) US10689347B2 (enExample)
EP (2) EP3302448B1 (enExample)
JP (3) JP6750806B2 (enExample)
KR (1) KR102691467B1 (enExample)
CN (2) CN113773257A (enExample)
AU (3) AU2016272908B2 (enExample)
CA (1) CA2987552A1 (enExample)
CU (1) CU24496B1 (enExample)
DK (1) DK3302448T3 (enExample)
EA (1) EA037236B1 (enExample)
FI (1) FI3302448T3 (enExample)
HR (1) HRP20240101T1 (enExample)
IL (2) IL255960B (enExample)
LT (1) LT3302448T (enExample)
MX (2) MX375639B (enExample)
MY (2) MY198769A (enExample)
PH (1) PH12017502179B1 (enExample)
SI (1) SI3302448T1 (enExample)
WO (1) WO2016193939A1 (enExample)
ZA (1) ZA201800022B (enExample)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2972239A1 (en) 2014-12-23 2016-06-30 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
JP6789962B2 (ja) * 2015-03-09 2020-11-25 オーリジーン ディスカバリー テクノロジーズ リミテッドAurigene Discovery Technologies Limited CDK阻害剤としてのピラゾロ[1,5−a][1,3,5]トリアジンとピラゾロ[1,5−a]ピリミジン誘導体
EP3302448B1 (en) 2015-06-04 2023-10-25 Aurigene Oncology Limited Substituted heterocyclyl derivatives as cdk inhibitors
GB201617548D0 (en) 2016-10-17 2016-11-30 Linnane Pharma Ab Novel biological factor
TWI703149B (zh) 2017-11-16 2020-09-01 美商美國禮來大藥廠 用於抑制cdk7之化合物
KR20200104873A (ko) 2017-12-06 2020-09-04 린 바이오사이언스, 피티와이 엘티디. 튜불린 억제제
US11472774B2 (en) 2018-02-01 2022-10-18 The University Of Sydney Anti-cancer compounds
SMT202400346T1 (it) * 2018-03-29 2024-11-15 Takeda Pharmaceuticals Co Composto eterociclico
CA3095987A1 (en) * 2018-04-04 2019-10-10 Aurigene Discovery Technologies Limited Substituted pyrazole derivatives as selective cdk12/13 inhibitors
WO2019213403A1 (en) 2018-05-02 2019-11-07 Kinnate Biopharma Inc. Inhibitors of cyclin-dependent kinases
CN110590747B (zh) * 2018-06-12 2022-03-22 隆泰申医药科技(南京)有限公司 一种化合物、其制备方法、药物组合物和应用
JP7590185B2 (ja) 2018-06-25 2024-11-26 ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド Taireファミリーキナーゼインヒビターおよびそれらの使用
JP2021529740A (ja) 2018-06-29 2021-11-04 キネート バイオファーマ インク. サイクリン依存性キナーゼの阻害剤
UA125427C2 (uk) * 2018-09-17 2022-03-02 Юнґдзин Фарм. Ко., Лтд. Похідні тіазолу і їх фармацевтично прийнятні солі
EP3902542A4 (en) 2018-12-28 2022-09-07 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 and uses thereof
WO2020202001A1 (en) 2019-04-01 2020-10-08 Aurigene Discovery Technologies Limited Substituted 5-cyclopropyl-1h-pyrazol-3-yl-amine derivatives as selective cdk12/13 inhibitors
CN110845474B (zh) * 2019-11-07 2021-01-12 四川大学 一种靶向i型prmt的化合物及其制备方法和应用
CN115485274A (zh) * 2020-03-13 2022-12-16 永进药品株式会社 包含噻唑衍生物或其药学上可接受的盐的用于预防或治疗癌症的药物组合物
WO2021182914A1 (ko) * 2020-03-13 2021-09-16 영진약품 주식회사 신규한 cdk7 억제 화합물 및 이의 약제학적으로 허용가능한 염
TWI783480B (zh) 2020-05-27 2022-11-11 美商美國禮來大藥廠 用於抑制cdk7之化合物
WO2022084930A2 (en) * 2020-10-22 2022-04-28 Aurigene Discovery Technologies Limited Cancer therapy using a combination of cdk7 inhibitor with an anti-microtubule agent
MX2023007218A (es) * 2020-12-18 2023-07-27 Aurigene Oncology Ltd Cocristal de un inhibidor de cinasa dependiente de ciclina (cdk).
CA3215788A1 (en) * 2021-04-27 2022-11-03 Aurigene Oncology Limited Process for preparing a cdk inhibitor
WO2022249141A2 (en) * 2021-05-28 2022-12-01 Aurigene Discovery Technologies Limited Cancer therapy using a combination of cdk7 inhibitor with an anti-cancer agent
MX2023015245A (es) * 2021-06-16 2024-01-19 Blueprint Medicines Corp Pirimidinil-pirazoles sustituidos como inhibidores de cdk2.
UY39832A (es) 2021-06-28 2023-01-31 Blueprint Medicines Corp Inhibidores de cdk2
TW202327583A (zh) * 2021-12-06 2023-07-16 美商艾克塞里克斯公司 使用cdk7抑制劑治療癌症之方法
US12084453B2 (en) 2021-12-10 2024-09-10 Incyte Corporation Bicyclic amines as CDK12 inhibitors
CN118973401B (zh) 2022-05-11 2025-12-02 株式会社前川制作所 削切装置及工件的削切方法
WO2023224961A1 (en) 2022-05-16 2023-11-23 Exelixis, Inc. Cancer therapy using a combination of a cdk7 inhibitor with an oral serd
CN115093397B (zh) * 2022-06-07 2023-09-05 自贡市第三人民医院 一种用于治疗肿瘤的化合物、合成方法及应用
WO2024066984A1 (zh) * 2022-09-30 2024-04-04 楚浦创制(武汉)医药科技有限公司 三并环类衍生物、药物组合物以及应用
WO2024140653A1 (zh) * 2022-12-27 2024-07-04 南京圣和药业股份有限公司 选择性cdk12/13抑制剂及其应用
TW202508595A (zh) 2023-05-04 2025-03-01 美商銳新醫藥公司 用於ras相關疾病或病症之組合療法
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
WO2025080946A2 (en) 2023-10-12 2025-04-17 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025217307A1 (en) 2024-04-09 2025-10-16 Revolution Medicines, Inc. Methods for predicting response to a ras(on) inhibitor and combination therapies
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57169465A (en) * 1981-04-13 1982-10-19 Showa Denko Kk Pyrazole derivative, its preparation and herbicide
AU4166400A (en) 1999-02-11 2000-08-29 Cor Therapeutics, Inc. Alkenyl and alkynyl compounds as inhibitors of factor xa
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
KR100423899B1 (ko) 2000-05-10 2004-03-24 주식회사 엘지생명과학 세포 증식 억제제로 유용한 1,1-디옥소이소티아졸리딘을갖는 인다졸
EE05405B1 (et) * 2000-08-10 2011-04-15 Pharmacia Italia S.P.A. Kinaasi inhibiitoritena toimivad bitskloprasoolid, nende valmistamismeetod, kasutamine ja neid sisaldavad farmatseutilised kompositsioonid
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
US6455559B1 (en) 2001-07-19 2002-09-24 Pharmacia Italia S.P.A. Phenylacetamido-pyrazole derivatives, process for their preparation and their use as antitumor agents
DE10148618B4 (de) * 2001-09-25 2007-05-03 Schering Ag Substituierte N-(1,4,5,6-Tetrahydro-cyclopentapyrazol-3-yl)-Derivate, deren Herstellung und Verwendung als Arzneimittel
JP4553899B2 (ja) 2003-08-21 2010-09-29 メルク フロスト カナダ リミテツド カテプシンシステインプロテアーゼ阻害剤
JP5507049B2 (ja) 2004-12-30 2014-05-28 アステックス、セラピューティックス、リミテッド 医薬品
JP2008526723A (ja) * 2004-12-30 2008-07-24 アステックス、セラピューティックス、リミテッド Cdk、gsk及びオーロラキナーゼの活性を調節するピラゾール誘導体
US8404718B2 (en) 2005-01-21 2013-03-26 Astex Therapeutics Limited Combinations of pyrazole kinase inhibitors
JP2008528469A (ja) 2005-01-21 2008-07-31 アステックス・セラピューティクス・リミテッド ピラゾールキナーゼ阻害剤およびさらなる抗癌剤の組合せ剤
GT200600457A (es) 2005-10-13 2007-04-27 Aventis Pharma Inc Sal de fosfato dihidrogeno como antagonistas del receptor de prostaglandina d2
EP2089394B1 (en) 2006-10-11 2011-06-29 Nerviano Medical Sciences S.r.l. Substituted pyrrolo-pyrazole derivatives as kinase inhibitors
WO2010002472A1 (en) * 2008-07-02 2010-01-07 Ambit Biosciences Corporation Jak kinase modulating compounds and methods of use thereof
ATE544063T1 (de) 2008-07-17 2012-02-15 Koninkl Philips Electronics Nv Nanoporenvorrichtung und verfahren zur nukleinsäureanalyse
US8541424B2 (en) 2008-12-23 2013-09-24 Abbott Laboratories Anti-viral compounds
FR2943058B1 (fr) 2009-03-11 2011-06-03 Centre Nat Rech Scient Derives de pyrazolo°1,5-a!-1,3,5-triazines, leur preparation et leur application en therapeutique.
EP2241619A1 (en) * 2009-04-17 2010-10-20 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Development of fluorescently P-loop labeled kinases for screening of inhibitors
JP6106685B2 (ja) * 2011-11-17 2017-04-05 ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド C−jun−n−末端キナーゼ(jnk)の阻害剤
US10112927B2 (en) * 2012-10-18 2018-10-30 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
WO2014201073A1 (en) 2013-06-13 2014-12-18 Bristol-Myers Squibb Company Macrocyclic factor viia inhibitors
RU2016111675A (ru) 2013-08-30 2017-10-04 Эмбит Байосайенсиз Корпорейшн Соединения биарилацетамида и способы их применения
CA2926207C (en) 2013-10-21 2022-06-21 Merck Patent Gmbh Heteroaryl compounds as btk inhibitors and uses thereof
AU2015240518A1 (en) 2014-04-05 2016-10-20 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
FR3025075A1 (fr) * 2014-08-28 2016-03-04 Oreal Nouveau dispositif de soin et/ou maquillage comprenant une composition d’architecture gel/gel
CA2972239A1 (en) 2014-12-23 2016-06-30 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
EP3302448B1 (en) * 2015-06-04 2023-10-25 Aurigene Oncology Limited Substituted heterocyclyl derivatives as cdk inhibitors

Similar Documents

Publication Publication Date Title
JP2018516917A5 (enExample)
JP2018507877A5 (enExample)
HRP20240101T1 (hr) Supstituirani heterociklil derivati kao cdk inhibitori
JP2012082234A5 (enExample)
JP2008505167A5 (enExample)
JP2020007311A5 (enExample)
CN107548391A (zh) 嘧啶或吡啶类化合物、其制备方法和医药用途
RU2016141934A (ru) Ингибиторы циклин-зависимой киназы 7 (cdk7)
WO2016105528A3 (en) Inhibitors of cyclin-dependent kinase 7 (cdk7)
JP2017509586A5 (enExample)
WO2016160617A3 (en) Inhibitors of cyclin-dependent kinases
JP2019517487A5 (enExample)
WO2017044858A3 (en) Inhibitors of cyclin-dependent kinases
RU2018119173A (ru) Производное бензофурана, способ его получения и его применение в медицине
JP2014511892A5 (enExample)
JP2013544846A5 (enExample)
RU2016118753A (ru) Производные пиридилкетона, способ их получения и их фармацевтическое применение
JP2016533379A5 (enExample)
JP2016501191A5 (enExample)
JP2013507448A5 (enExample)
JP2015514806A5 (enExample)
JP2008528467A5 (enExample)
HRP20221207T1 (hr) Supstituirani biciklički heterociklički spojevi kao inhibitori prmt5
JP2015535277A5 (enExample)
JP2018526413A5 (enExample)