JPWO2020160537A5 - - Google Patents

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Publication number
JPWO2020160537A5
JPWO2020160537A5 JP2021544801A JP2021544801A JPWO2020160537A5 JP WO2020160537 A5 JPWO2020160537 A5 JP WO2020160537A5 JP 2021544801 A JP2021544801 A JP 2021544801A JP 2021544801 A JP2021544801 A JP 2021544801A JP WO2020160537 A5 JPWO2020160537 A5 JP WO2020160537A5
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JP
Japan
Prior art keywords
substituted
unsubstituted
deuterated
hydrogen
undeuterated
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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.)
Pending
Application number
JP2021544801A
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English (en)
Japanese (ja)
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JP2022523742A (ja
Publication date
Application filed filed Critical
Priority claimed from PCT/US2020/016394 external-priority patent/WO2020160537A1/fr
Publication of JP2022523742A publication Critical patent/JP2022523742A/ja
Publication of JPWO2020160537A5 publication Critical patent/JPWO2020160537A5/ja
Pending legal-status Critical Current

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JP2021544801A 2019-02-01 2020-02-03 二環式ピリジン組成物およびがんの治療にそれを使用する方法 Pending JP2022523742A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962800239P 2019-02-01 2019-02-01
US62/800,239 2019-02-01
PCT/US2020/016394 WO2020160537A1 (fr) 2019-02-01 2020-02-03 Compositions de pyridine bicyclique et procédés pour leur utilisation pour la thérapie du cancer

Publications (2)

Publication Number Publication Date
JP2022523742A JP2022523742A (ja) 2022-04-26
JPWO2020160537A5 true JPWO2020160537A5 (fr) 2023-02-13

Family

ID=71842384

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2021544801A Pending JP2022523742A (ja) 2019-02-01 2020-02-03 二環式ピリジン組成物およびがんの治療にそれを使用する方法

Country Status (7)

Country Link
US (1) US11572369B2 (fr)
EP (1) EP3917523B1 (fr)
JP (1) JP2022523742A (fr)
CN (1) CN113677341B (fr)
AU (1) AU2020216498A1 (fr)
CA (1) CA3128377A1 (fr)
WO (1) WO2020160537A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024193640A1 (fr) * 2023-03-22 2024-09-26 上海齐鲁制药研究中心有限公司 Inhibiteur de cdk

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4271723A (en) 1976-11-19 1981-06-09 Caterpillar Tractor Co. Power train with an auxiliary creeper drive system
GB9402029D0 (en) 1994-02-03 1994-03-30 Smithkline Beecham Plc Novel formulation
ME00355B (fr) 2002-06-06 2010-06-30 Ptp Group Ltd Polyethylene terephtalate cristallise contenant du silicone et procede de preparation
US7205308B2 (en) * 2002-09-04 2007-04-17 Schering Corporation Trisubstituted 7-aminopyrazolopyrimidines as cyclin dependent kinase inhibitors
MXPA06011799A (es) 2004-04-12 2006-12-15 Sankyo Co Derivados de tienopiridina.
US20070021920A1 (en) 2005-07-21 2007-01-25 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Selective resonance of chemical structures
WO2007103869A2 (fr) 2006-03-06 2007-09-13 Wyeth Préparations pharmaceutiques liquides et pâteuses et procédés associés
JP2008260693A (ja) * 2007-04-10 2008-10-30 Daiichi Sankyo Co Ltd チエノピリジン−2−カルボキサミド誘導体を含有する医薬組成物
US8598344B2 (en) 2009-11-30 2013-12-03 Senex Biotechnology CDKI pathway inhibitors and uses thereof
EP2489354A1 (fr) 2011-02-18 2012-08-22 Vironova AB Formulation pharmaceutique de B220 pour le traitement topique de l'herpès
EP2797598A4 (fr) 2011-09-13 2015-08-12 Igor Roninson Traitement de maladie ou de troubles causé(e)s par l'activité transcriptionnelle induite de nfkb
US9321737B2 (en) 2012-02-02 2016-04-26 Senex Biotechnology Inc CDK8-CDK19 selective inhibitors and their use in anti-metastatic and chemopreventative methods for cancer
CA2890108C (fr) * 2012-11-01 2021-03-02 University Of South Carolina Methode de traitement d'un cancer de la prostate
WO2014087240A2 (fr) * 2012-12-04 2014-06-12 Dalhousie University Compositions, procédés et coffrets de prévention, de réduction et d'élimination de métastase de cancer
CN103012428A (zh) * 2013-01-08 2013-04-03 中国药科大学 4-(五元杂环并嘧啶/吡啶取代)氨基-1H-3-吡唑甲酰胺类CDK/Aurora双重抑制剂及其用途
WO2014134169A1 (fr) * 2013-02-26 2014-09-04 Senex Biotechnology, Inc. Inhibiteurs de cdk8/19 pour utilisation dans le traitement du cancer du sein à récepteurs d'œstrogène positifs
US9216993B2 (en) * 2013-03-13 2015-12-22 The Regents Of The University Of Michigan Compositions comprising thienopyrimidine and thienopyridine compounds and methods of use thereof
WO2014194245A2 (fr) 2013-05-31 2014-12-04 Nimbus Iris, Inc. Inhibiteurs de cdk8 et leurs utilisations
US9937153B2 (en) 2013-08-30 2018-04-10 Merck Sharp & Dohme Ltd. Oral pharmaceutical formulation of omarigliptin
EA201891279A1 (ru) 2013-12-24 2019-01-31 Президент Энд Феллоус Оф Гарвард Колледж Аналоги кортистатина, их синтез и применения
US9566280B2 (en) * 2014-01-28 2017-02-14 Massachusetts Institute Of Technology Combination therapies and methods of use thereof for treating cancer
BR112016017781A2 (pt) * 2014-02-14 2017-08-08 Inception 2 Inc Compostos de pirazolona e usos dos mesmos
EP3154952A4 (fr) 2014-06-10 2018-03-14 University of South Carolina Méthodes et compositions pour traiter les cancers her positifs
WO2016009076A1 (fr) 2014-07-17 2016-01-21 Merck Patent Gmbh Nouvelles naphtyridines et isoquinoléines et leur utilisation à titre d'inhibiteurs de cdk8/19
WO2016041618A1 (fr) * 2014-09-15 2016-03-24 Merck Patent Gmbh Indazoles substitués et hétérocycles associés
CA2972771C (fr) 2014-12-18 2024-06-11 University Of South Carolina Suppression de formation neo-intimale suite a une chirurgie vasculaire, a l'aide d'inhibiteurs de cdk8
EP3370720A1 (fr) * 2015-11-03 2018-09-12 Lu License AB Composés destinés au traitement de désordres hyperprolifératifs
US11014906B2 (en) 2018-08-21 2021-05-25 University Of South Carolina Quinoline-based compounds and methods of inhibiting CDK8/19
US20220226343A1 (en) * 2019-05-21 2022-07-21 University Of South Carolina 3-amino-4-[4-[4 (dimethylcarbamoyl) phenyl]-1,4-diazepan-1-yl]thieno[2,3-b]pyridine-2-carboxamide for use in cancer therapy and formulations comprising the same

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