JP2022523742A5 - - Google Patents

Info

Publication number
JP2022523742A5
JP2022523742A5 JP2021544801A JP2021544801A JP2022523742A5 JP 2022523742 A5 JP2022523742 A5 JP 2022523742A5 JP 2021544801 A JP2021544801 A JP 2021544801A JP 2021544801 A JP2021544801 A JP 2021544801A JP 2022523742 A5 JP2022523742 A5 JP 2022523742A5
Authority
JP
Japan
Prior art keywords
substituted
unsubstituted
deuterated
hydrogen
undeuterated
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
JP2021544801A
Other languages
English (en)
Japanese (ja)
Other versions
JP2022523742A (ja
JP7628252B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2020/016394 external-priority patent/WO2020160537A1/en
Publication of JP2022523742A publication Critical patent/JP2022523742A/ja
Publication of JP2022523742A5 publication Critical patent/JP2022523742A5/ja
Application granted granted Critical
Publication of JP7628252B2 publication Critical patent/JP7628252B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

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 Active JP7628252B2 (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 (en) 2019-02-01 2020-02-03 Bicyclic pyridine compositions and methods of using the same for cancer therapy

Publications (3)

Publication Number Publication Date
JP2022523742A JP2022523742A (ja) 2022-04-26
JP2022523742A5 true JP2022523742A5 (enExample) 2023-02-13
JP7628252B2 JP7628252B2 (ja) 2025-02-10

Family

ID=71842384

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2021544801A Active JP7628252B2 (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 (8)

Country Link
US (1) US11572369B2 (enExample)
EP (1) EP3917523B1 (enExample)
JP (1) JP7628252B2 (enExample)
CN (1) CN113677341B (enExample)
AU (1) AU2020216498B2 (enExample)
CA (1) CA3128377A1 (enExample)
ES (1) ES2991429T3 (enExample)
WO (1) WO2020160537A1 (enExample)

Families Citing this family (1)

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

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
DE60325051D1 (de) 2002-06-06 2009-01-15 Boehringer Ingelheim Pharma SUBSTITUIERTE 3-AMINO-THIENO(2,3-b)PYRIDINE-2-AMIDE UND HERSTELLUNGSVERFAHREN SOWIE DEREN VERWENDUNG
US7205308B2 (en) * 2002-09-04 2007-04-17 Schering Corporation Trisubstituted 7-aminopyrazolopyrimidines as cyclin dependent kinase inhibitors
EP1764367A1 (en) * 2004-04-12 2007-03-21 Sankyo Company, Limited Thienopyridine derivatives
US20070021927A1 (en) 2005-07-21 2007-01-25 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Selective resonance of chemical structures
US20070207201A1 (en) 2006-03-06 2007-09-06 Wyeth Liquid and Semi-Solid Pharmaceutical Formulations and Processes
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 (en) 2011-02-18 2012-08-22 Vironova AB Pharmaceutical formulation of B220 for topical treatment of herpes
EA027531B1 (ru) 2011-09-13 2017-08-31 Игорь Ронинсон ЛЕЧЕНИЕ ЗАБОЛЕВАНИЙ И НАРУШЕНИЙ, ВЫЗВАННЫХ АКТИВНОСТЬЮ ТРАНСКРИПЦИОННОГО ФАКТОРА NF-κB
KR20150023223A (ko) 2012-02-02 2015-03-05 세넥스 바이오테크놀러지 인코포레이티드 Cdk8/cdk19 선택성 억제제 및 암에 대한 항-전이 및 화학예방 방법에서 이들의 용도
KR20160014568A (ko) * 2012-11-01 2016-02-11 유니버시티 오브 싸우스 캐롤라이나 전립선암을 치료하는 방법
WO2014087240A2 (en) * 2012-12-04 2014-06-12 Dalhousie University Compositions, methods and kits for preventing, reducing, and eliminating cancer metastasis
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 (en) * 2013-02-26 2014-09-04 Senex Biotechnology, Inc. Inhibitors of cdk8/19 for use in treating estrogen receptor positive breast cancer
WO2014164543A1 (en) * 2013-03-13 2014-10-09 The Regents Of The University Of Michigan Compositions comprising thienopyrimidine and thienopyridine compounds and methods of use thereof
WO2014194245A2 (en) 2013-05-31 2014-12-04 Nimbus Iris, Inc. Cdk8 inhibitors and uses thereof
US9937153B2 (en) 2013-08-30 2018-04-10 Merck Sharp & Dohme Ltd. Oral pharmaceutical formulation of omarigliptin
AU2014369834B2 (en) 2013-12-24 2018-12-20 President And Fellows Of Harvard College Cortistatin analogues and syntheses and uses thereof
US9566280B2 (en) * 2014-01-28 2017-02-14 Massachusetts Institute Of Technology Combination therapies and methods of use thereof for treating cancer
NZ722345A (en) * 2014-02-14 2018-02-23 Inception 2 Inc Pyrazolone compounds and uses thereof
WO2016018511A2 (en) 2014-06-10 2016-02-04 University Of South Carolina Methods and compositions for treatment of her-positive cancers
JP2017522324A (ja) * 2014-07-17 2017-08-10 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung 新規ナフチリジン及びイソキノリンならびにcdk8/19阻害剤としてのその使用
WO2016041618A1 (en) * 2014-09-15 2016-03-24 Merck Patent Gmbh Substituted indazoles and related heterocycles
US20210322651A1 (en) 2014-12-18 2021-10-21 Senex Biotechnology, Inc. Suppression of neointimal formation following vascular surgeru using cdk8 inhibitors
AU2016348659B2 (en) * 2015-11-03 2022-07-28 Apriligen, Inc. Compounds for treatment of hypoproliferative disorders
US11014906B2 (en) 2018-08-21 2021-05-25 University Of South Carolina Quinoline-based compounds and methods of inhibiting CDK8/19
WO2020237014A1 (en) * 2019-05-21 2020-11-26 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

Similar Documents

Publication Publication Date Title
AU2016317521A1 (en) Novel pyrazolo[3,4-d]pyrimidine compound or salt thereof
PH12015501004B1 (en) AMIDE-SUBSTITUTED HETEROCYCLIC COMPOUNDS USEFUL AS MODULATORS OF IL-12, IL-23 AND/OR IFN ALPHa RESPONSES
JP7187449B2 (ja) Ehmt2阻害剤としての置換された融合二環式または三環式複素環化合物
CN116354901B (zh) 一种噻唑烷二酮类化合物及其制备方法和应用
MX2014012992A (es) Derivado de quinazolindiona.
KR20020047331A (ko) 인데노-, 나프토- 및 벤조사이클로헵타-디하이드로티아졸유도체, 이의 제조 및 식욕억제성 의약으로서의 이의 용도
JP2024073409A (ja) 抗癌剤としての置換されたアルキニレン化合物
AU2009275929B2 (en) Nitrogenated derivatives of pancratistatin
CA3188350A1 (en) Processes for making serd tricyclic compounds having a substituted phenyl or pyridinyl moiety
TW202340166A (zh) 多環化合物
WO2020068950A1 (en) Hdac1,2 inhibitors
JP2022523742A5 (enExample)
ES2349753T3 (es) Derivados de piperidina como profármacos de inhibidores de los canales de potasio.
Xin et al. Synthesis and pharmacological evaluation of trifluoromethyl containing 4-(2-pyrimidinylamino) benzamides as Hedgehog signaling pathway inhibitors
US7211588B2 (en) N-substituted indolyl-3-glyoxylamides, their use as medicaments and process for their preparation
KR102313230B1 (ko) 항종양 활성을 갖는 벤조-n-하이드록시 아미드 화합물
US20230017312A1 (en) Centrally active p38alpha inhibiting compounds
AU2006334364B2 (en) Imidazo (1,2-a)pyridin-3-yl-acetic acid hydrazides, processes for their preparation and pharmaceutical uses thereof
Somani et al. Synthesis and antibacterial activity of some new 2, 5‐disubstituted‐1, 3, 4‐oxadiazole derivatives
EP4663628A1 (en) New compound and pharmaceutical composition comprising same
CN110963991A (zh) 一种pi3k抑制剂及其制备方法和应用
WO2002098871A1 (en) Phenylcarboxamides and process for preparation thereof
WO2025194094A1 (en) Small molecule modulators of sirt5 and uses thereof
CA3233731A1 (en) Synthesis of mavorixafor and intermediates thereof
IL303795A (en) Chemical compounds useful for inhibition of NAV1.8 voltage-gated sodium channels and treatment of NAV1.8-mediated diseases