JP2020531461A5 - - Google Patents

Download PDF

Info

Publication number
JP2020531461A5
JP2020531461A5 JP2020508623A JP2020508623A JP2020531461A5 JP 2020531461 A5 JP2020531461 A5 JP 2020531461A5 JP 2020508623 A JP2020508623 A JP 2020508623A JP 2020508623 A JP2020508623 A JP 2020508623A JP 2020531461 A5 JP2020531461 A5 JP 2020531461A5
Authority
JP
Japan
Prior art keywords
pharmaceutically acceptable
acceptable salt
compound according
composition
compound
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
JP2020508623A
Other languages
English (en)
Japanese (ja)
Other versions
JP2020531461A (ja
JP7269917B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2018/046957 external-priority patent/WO2019036657A1/en
Publication of JP2020531461A publication Critical patent/JP2020531461A/ja
Publication of JP2020531461A5 publication Critical patent/JP2020531461A5/ja
Application granted granted Critical
Publication of JP7269917B2 publication Critical patent/JP7269917B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2020508623A 2017-08-17 2018-08-17 Ahr阻害剤およびその使用 Active JP7269917B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201762546757P 2017-08-17 2017-08-17
US62/546,757 2017-08-17
US201862613141P 2018-01-03 2018-01-03
US62/613,141 2018-01-03
PCT/US2018/046957 WO2019036657A1 (en) 2017-08-17 2018-08-17 AHR INHIBITORS AND USES THEREOF

Publications (3)

Publication Number Publication Date
JP2020531461A JP2020531461A (ja) 2020-11-05
JP2020531461A5 true JP2020531461A5 (enExample) 2021-09-09
JP7269917B2 JP7269917B2 (ja) 2023-05-09

Family

ID=65360285

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2020508623A Active JP7269917B2 (ja) 2017-08-17 2018-08-17 Ahr阻害剤およびその使用

Country Status (12)

Country Link
US (2) US10696650B2 (enExample)
EP (1) EP3668496A4 (enExample)
JP (1) JP7269917B2 (enExample)
KR (1) KR20200051646A (enExample)
CN (1) CN111163766A (enExample)
AU (1) AU2018319016B2 (enExample)
BR (1) BR112020003116A2 (enExample)
CA (1) CA3073051A1 (enExample)
IL (1) IL272649B2 (enExample)
MX (1) MX2020001793A (enExample)
SG (1) SG11202001310SA (enExample)
WO (1) WO2019036657A1 (enExample)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2018300150A1 (en) 2017-07-11 2020-01-30 Vertex Pharmaceuticals Incorporated Carboxamides as modulators of sodium channels
CN111163766A (zh) 2017-08-17 2020-05-15 医肯纳肿瘤学公司 Ahr抑制剂和其用途
WO2020146682A1 (en) 2019-01-10 2020-07-16 Vertex Pharmaceuticals Incorporated Carboxamides as modulators of sodium channels
WO2020146612A1 (en) 2019-01-10 2020-07-16 Vertex Pharmaceuticals Incorporated Esters and carbamates as modulators of sodium channels
KR20220044753A (ko) * 2019-07-25 2022-04-11 큐라데브 파마 프라이버트 리미티드 아세틸 조효소 a 신테타제 단쇄 2(acss2)의 소분자 억제제
WO2021080015A1 (en) * 2019-10-24 2021-04-29 Ono Pharmaceutical Co., Ltd. Modulators of trek (twik related k+ channels) channel function
PH12022551379A1 (en) 2019-12-06 2023-05-03 Vertex Pharma Substituted tetrahydrofurans as modulators of sodium channels
BR112022013673A2 (pt) 2020-01-10 2022-09-13 Ikena Oncology Inc Inibidores de ahr e seus usos
IL296790B1 (en) 2020-03-30 2026-07-01 Hutchmed Ltd Amide compounds and their uses
WO2021236717A1 (en) 2020-05-20 2021-11-25 Senda Biosciences, Inc. Fused imidazole derivatives as ahr antagonists
CN114181212B (zh) * 2020-09-15 2023-06-06 山东轩竹医药科技有限公司 哒嗪酮类AhR抑制剂
CN114835687B (zh) * 2021-04-02 2023-09-05 北京华森英诺生物科技有限公司 AhR抑制剂
SI4347031T1 (sl) 2021-06-04 2026-01-30 Vertex Pharmaceuticals Incorporated N-(hidroksialkil (hetero)aril) tetrahidrofuran karboksamidi kot modulatorji natrijevih kanalčkov
CN115572282B (zh) * 2021-07-05 2024-07-09 华东理工大学 含芳杂环结构的吡唑酰胺类化合物及其制备方法和应用
CN116135850A (zh) * 2021-11-16 2023-05-19 深圳湾实验室 抗鼻咽癌的小分子抑制剂、化合物的制备方法及其应用
CN119707643A (zh) * 2023-09-28 2025-03-28 德明药泰生物技术(深圳)有限公司 AhR调节剂及其应用

Family Cites Families (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5403816A (en) * 1990-10-25 1995-04-04 Kumiai Chemical Industry Co., Ltd. Picolinic acid derivative and herbicidal composition
CA2254769A1 (en) 1996-05-20 1997-11-27 Merck & Co., Inc. Antagonists of gonadotropin releasing hormone
EP1208085B1 (en) * 1999-08-04 2007-12-05 Icagen, Inc. Benzanilides as potassium channel openers
US6608053B2 (en) 2000-04-27 2003-08-19 Yamanouchi Pharmaceutical Co., Ltd. Fused heteroaryl derivatives
US20040235877A1 (en) 2001-09-14 2004-11-25 Natsuki Ishizuka Novel use of tricyclic compound
CZ2004634A3 (cs) * 2001-10-25 2004-10-13 Takedaáchemicaláindustriesźáltd Chinolinová sloučeninaŹ způsob výroby a použití a farmaceutický přípravek
PL372295A1 (en) * 2002-02-04 2005-07-11 F.Hoffmann-La Roche Ag Quinoline derivatives as npy antagonists
TWI309240B (en) 2004-09-17 2009-05-01 Hoffmann La Roche Anti-ox40l antibodies
KR20070118068A (ko) 2004-11-23 2007-12-13 레디 유에스 테라퓨틱스 인코포레이티드 신규의 이원 헤테로고리 화합물, 그 제조방법 및 이들을포함하는 조성물
JP5238936B2 (ja) 2005-03-25 2013-07-17 ジーアイティーアール,インク. Gitr結合分子およびその使用
DK1879573T3 (da) 2005-05-10 2013-02-25 Incyte Corp Modulatorer af indolamin 2,3-dioxygenase og fremgangsmåder til anvendelse deraf
KR101704734B1 (ko) 2005-07-01 2017-02-09 이. 알. 스퀴부 앤드 선즈, 엘.엘.씨. 예정 사멸 리간드 1 (피디-엘1)에 대한 인간 모노클로날 항체
ES2540561T3 (es) 2005-12-20 2015-07-10 Incyte Corporation N-hidroxiamidinoheterociclos como moduladores de indolamina 2,3-dioxigenasa
AU2007211276B2 (en) * 2006-01-31 2013-06-06 Synta Pharmaceuticals Corp. Pyridylphenyl compounds for inflammation and immune-related uses
CA2663057C (en) 2006-09-19 2015-12-08 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
CL2007002650A1 (es) 2006-09-19 2008-02-08 Incyte Corp Compuestos derivados de heterociclo n-hidroxiamino; composicion farmaceutica, util para tratar cancer, infecciones virales y desordenes neurodegenerativos entre otras.
US7750007B2 (en) 2006-11-06 2010-07-06 Supergen, Inc. Imidazo[1,2-beta]pyridazine and pyrazolo[1,5-alpha]pyrimidine derivatives and their use as protein kinase inhibitors
EP1987839A1 (en) 2007-04-30 2008-11-05 I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale Cytotoxic anti-LAG-3 monoclonal antibody and its use in the treatment or prevention of organ transplant rejection and autoimmune disease
EA015952B1 (ru) * 2007-05-03 2011-12-30 Пфайзер Лимитед 2-пиридинкарбоксамидные производные в качестве модуляторов натриевых каналов
US8759348B2 (en) * 2007-05-17 2014-06-24 Helperby Therapeutics Limited Use of 4-(pyrrolidin-1-yl)quinoline compounds to kill clinically latent microorganisms
JP5352476B2 (ja) * 2007-06-05 2013-11-27 武田薬品工業株式会社 キナーゼ阻害剤としての二環式複素環化合物
PT2175884T (pt) 2007-07-12 2016-09-21 Gitr Inc Terapias de combinação empregando moléculas de ligação a gitr
EP2044949A1 (en) 2007-10-05 2009-04-08 Immutep Use of recombinant lag-3 or the derivatives thereof for eliciting monocyte immune response
WO2009073620A2 (en) 2007-11-30 2009-06-11 Newlink Genetics Ido inhibitors
AU2009243006B2 (en) * 2008-05-01 2013-03-21 Sirtris Pharmaceuticals, Inc. Quinolines and related analogs as sirtuin modulators
AR072999A1 (es) 2008-08-11 2010-10-06 Medarex Inc Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos
MX356367B (es) 2008-12-09 2018-05-25 Genentech Inc Anticuerpos anti-pd-l1 y su uso para mejorar la funcion de celulas t.
IN2015DN02826A (enExample) 2009-09-03 2015-09-11 Merck Sharp & Dohme
EP2493862B1 (en) 2009-10-28 2016-10-05 Newlink Genetics Corporation Imidazole derivatives as ido inhibitors
DK2510010T3 (en) 2009-12-10 2015-12-14 Hoffmann La Roche Antibodies that bind to human CSF1R extracellular domain 4 and their use
DK2542256T3 (da) 2010-03-04 2019-08-26 Macrogenics Inc Antistoffer reagerende med b7-h3, immunologisk aktive fragmenter deraf og anvendelser deraf
CN102918061B (zh) 2010-03-05 2016-06-08 霍夫曼-拉罗奇有限公司 针对人csf-1r的抗体及其用途
RU2617971C2 (ru) 2010-03-05 2017-04-28 Ф.Хоффманн-Ля Рош Аг Антитела против csf-1r человека и их применение
EP3943154A1 (en) 2010-05-04 2022-01-26 Five Prime Therapeutics, Inc. Antibodies that bind csf1r
NZ729044A (en) 2010-09-09 2020-07-31 Pfizer 4-1bb binding molecules
US8410107B2 (en) * 2010-10-15 2013-04-02 Hoffmann-La Roche Inc. N-pyridin-3-yl or N-pyrazin-2-yl carboxamides
PH12013501201A1 (en) 2010-12-09 2013-07-29 Univ Pennsylvania Use of chimeric antigen receptor-modified t cells to treat cancer
NO2694640T3 (enExample) 2011-04-15 2018-03-17
CA2833636A1 (en) 2011-04-20 2012-10-26 Amplimmune, Inc. Antibodies and other molecules that bind b7-h1 and pd-1
HK1201471A1 (en) 2011-09-07 2015-09-04 Deutsches Krebsforschungszentrum Means and methods for treating and/or preventing natural ahr ligand-dependent cancer
JP6165733B2 (ja) * 2011-09-16 2017-07-19 ノバルティス アーゲー N−置換ヘテロシクリルカルボキサミド類
WO2013059677A1 (en) * 2011-10-19 2013-04-25 Calcimedica, Inc. Compounds that modulate intracellular calcium
BR112014012819B1 (pt) 2011-11-28 2022-08-16 Merck Patent Gmbh Anticorpo anti-pd-l1 ou fragmento de ligação ao antígeno do mesmo e composição
MX356337B (es) 2011-12-15 2018-05-23 Hoffmann La Roche Anticuerpos contra csf-1r humano y sus usos.
MX2014008961A (es) 2012-02-06 2014-10-14 Genentech Inc Composiciones y metodos para utilizar inhibidores de csf1r.
AR090263A1 (es) 2012-03-08 2014-10-29 Hoffmann La Roche Terapia combinada de anticuerpos contra el csf-1r humano y las utilizaciones de la misma
KR20150018533A (ko) 2012-05-11 2015-02-23 파이브 프라임 테라퓨틱스, 인크. 콜로니 자극 인자 1 수용체(csf1r)에 결속하는 항체들에 의한 질병 상태의 치료 방법
AR091649A1 (es) 2012-07-02 2015-02-18 Bristol Myers Squibb Co Optimizacion de anticuerpos que se fijan al gen de activacion de linfocitos 3 (lag-3) y sus usos
CN107759690A (zh) 2012-08-31 2018-03-06 戊瑞治疗有限公司 用结合群落刺激因子1受体(csf1r)的抗体治疗病状的方法
WO2014138485A1 (en) 2013-03-08 2014-09-12 Irm Llc Ex vivo production of platelets from hematopoietic stem cells and the product thereof
KR20230146101A (ko) * 2014-12-31 2023-10-18 안트로제네시스 코포레이션 천연 킬러 세포 및 그의 용도
US11221329B2 (en) * 2015-10-30 2022-01-11 Lieber Institute, Inc. Treatment of neurological and neurodevelopmental diseases and disorders associated with aberrant ion channel expression and activity
WO2018085348A1 (en) * 2016-11-03 2018-05-11 Actavalon, Inc. Substituted quinolines and methods for treating cancer
US10457683B2 (en) 2017-04-12 2019-10-29 Magenta Therapeutics Inc. Aryl hydrocarbon receptor antagonists and uses thereof
MX2019012431A (es) 2017-04-21 2020-08-03 Ikena Oncology Inc Inhibidores del receptor de hidrocarburos de arilo (ahr) de indol y usos de los mismos.
WO2019018562A1 (en) 2017-07-19 2019-01-24 Ideaya Biosciences, Inc. AMIDO COMPOUND AS MODULATORS OF AHR
CN111163766A (zh) 2017-08-17 2020-05-15 医肯纳肿瘤学公司 Ahr抑制剂和其用途
US20190314407A1 (en) 2017-10-31 2019-10-17 Magenta Therapeutics Inc. Compositions and methods for the expansion of hematopoietic stem and progenitor cells
AU2018361971A1 (en) 2017-11-03 2020-06-04 Universite De Montreal Compounds and use thereof in the expansion of stem cells and/or progenitor cells
EP3713931B1 (en) 2017-11-21 2025-03-05 Deutsches Krebsforschungszentrum 3-oxo-6-heteroaryl-2-phenyl-2,3-dihydropyridazine-4-carboxamides
EP3713926B1 (en) 2017-11-21 2023-06-07 Bayer Aktiengesellschaft 2-hetarylpyrimidine-4-carboxamides as aryl hydrocarbon receptor anatgonists
WO2019101642A1 (en) 2017-11-21 2019-05-31 Bayer Aktiengesellschaft Sulphur substituted 3-oxo-2,3-dihydropyridazine-4-carboxamides
US11524944B2 (en) 2017-11-21 2022-12-13 Bayer Aktiengesellschaft 2-phenylpyrimidine-4-carboxamides as AHR inhibitors

Similar Documents

Publication Publication Date Title
JP2020517734A5 (enExample)
JP7710356B2 (ja) 5,10-メチレン-(6r)-テトラヒドロ葉酸のヘミ硫酸塩
ES2975263T3 (es) Formas cristalinas de un compuesto triazolopirimidínico
BR112021013050A2 (pt) Forma cristalina de um inibidor de cdk
US20100166881A1 (en) Novel IDO Inhibitors and Methods of Use Thereof
BR112019014756B1 (pt) Composto inibidor de ask1 e composição farmacêutica que o compreende
WO2007050963A1 (en) Novel ido inhibitors and methods of use thereof
ES2577391T3 (es) Polimorfos de un antagonista del receptor mglur5
CA2793413A1 (en) Crystal form of edoxaban tosylate monohydrate and method of producing same
Ashok et al. Synthesis and anti-leishmanial evaluation of 1-phenyl-2, 3, 4, 9-tetrahydro-1H-β-carboline derivatives against Leishmania infantum
AU2010224245A1 (en) Pyrrolo [2, 3-b] pyridine derivatives for the inhibition of Raf kinases
ES2699452T3 (es) Nuevo derivado de triazina
JP2016501192A (ja) プロテインキナーゼ阻害剤としてのチオエーテル誘導体
ES2325318T3 (es) Derivados de triazol como inhibidores de la ciclooxigenasa (cox).
JP2010507634A (ja) 新規フルオレン誘導体、これを含む組成物、およびタンパク質シャペロンhsp90の阻害剤としてのこれらの使用
JP6929299B2 (ja) インドール誘導体を含む医薬組成物、その調製方法及びその使用
US20160221991A1 (en) Novel triazine derivative
TH1901006700A (th) สารยับยั้ง ahr ชนิดอินโดลและการใช้สารดังกล่าว
CN112334470A (zh) 5-甲基-(6s)-四氢叶酸和氨基酸乙酯的结晶盐
JP7532336B2 (ja) 5-メチル(6s)-テトラヒドロ葉酸および4-(2-ヒドロキシエチル)-モルホリンを含む結晶塩
WO2025054386A1 (en) Cdk2 inhibitors and uses thereof
BR112017010938B1 (pt) Compostos hidrossolúveis derivados do benzimidazol, composição farmacêutica e uso da composição farmacêutica
SU795481A3 (ru) Способ получени производныхцЕфАлОСпОРиНА или иХ СОлЕй
HK40036063A (en) Crystalline salts of 5-methyl-(6s)-tetrahydrofolic acid and amino acid ethyl esters
HK1217018B (en) Hemisulfate salt of 5,10-methylene-(6r)-tetrahydrofolic acid