JP2018515438A5 - - Google Patents

Download PDF

Info

Publication number
JP2018515438A5
JP2018515438A5 JP2017551629A JP2017551629A JP2018515438A5 JP 2018515438 A5 JP2018515438 A5 JP 2018515438A5 JP 2017551629 A JP2017551629 A JP 2017551629A JP 2017551629 A JP2017551629 A JP 2017551629A JP 2018515438 A5 JP2018515438 A5 JP 2018515438A5
Authority
JP
Japan
Prior art keywords
optionally substituted
alkyl
compound according
optionally
phenyl
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.)
Withdrawn
Application number
JP2017551629A
Other languages
English (en)
Japanese (ja)
Other versions
JP2018515438A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2016/025531 external-priority patent/WO2016161269A1/en
Publication of JP2018515438A publication Critical patent/JP2018515438A/ja
Publication of JP2018515438A5 publication Critical patent/JP2018515438A5/ja
Withdrawn legal-status Critical Current

Links

JP2017551629A 2015-04-03 2016-04-01 癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法 Withdrawn JP2018515438A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562142589P 2015-04-03 2015-04-03
US62/142,589 2015-04-03
PCT/US2016/025531 WO2016161269A1 (en) 2015-04-03 2016-04-01 Inhibitors of indoleamine 2,3-dioxygenase for the treatment of cancer

Publications (2)

Publication Number Publication Date
JP2018515438A JP2018515438A (ja) 2018-06-14
JP2018515438A5 true JP2018515438A5 (enExample) 2019-05-09

Family

ID=55702190

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2017551628A Withdrawn JP2018519245A (ja) 2015-04-03 2016-04-01 癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法
JP2017551629A Withdrawn JP2018515438A (ja) 2015-04-03 2016-04-01 癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法
JP2017551647A Pending JP2018516238A (ja) 2015-04-03 2016-04-01 癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2017551628A Withdrawn JP2018519245A (ja) 2015-04-03 2016-04-01 癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2017551647A Pending JP2018516238A (ja) 2015-04-03 2016-04-01 癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法

Country Status (20)

Country Link
US (4) US10399933B2 (enExample)
EP (3) EP3277670A1 (enExample)
JP (3) JP2018519245A (enExample)
KR (3) KR20170134980A (enExample)
CN (3) CN108093636A (enExample)
AR (1) AR104176A1 (enExample)
AU (3) AU2016242978A1 (enExample)
BR (3) BR112017020999A2 (enExample)
CA (3) CA2981584A1 (enExample)
CL (1) CL2017002494A1 (enExample)
CO (1) CO2017011183A2 (enExample)
EA (3) EA201792186A1 (enExample)
HK (1) HK1247922A1 (enExample)
IL (3) IL254720A0 (enExample)
MX (3) MX2017012738A (enExample)
PE (1) PE20180117A1 (enExample)
SG (3) SG11201707948WA (enExample)
TW (1) TW201700453A (enExample)
UY (1) UY36601A (enExample)
WO (3) WO2016161286A1 (enExample)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK3105218T3 (da) 2014-02-13 2019-11-04 Incyte Corp Cyclopropylaminer som lsd1-inhibitorer
TWI720451B (zh) 2014-02-13 2021-03-01 美商英塞特控股公司 作為lsd1抑制劑之環丙胺
US9527835B2 (en) 2014-02-13 2016-12-27 Incyte Corporation Cyclopropylamines as LSD1 inhibitors
WO2016007736A1 (en) 2014-07-10 2016-01-14 Incyte Corporation Imidazopyrazines as lsd1 inhibitors
US9695168B2 (en) 2014-07-10 2017-07-04 Incyte Corporation Substituted imidazo[1,5-α]pyridines and imidazo[1,5-α]pyrazines as LSD1 inhibitors
WO2016007722A1 (en) 2014-07-10 2016-01-14 Incyte Corporation Triazolopyridines and triazolopyrazines as lsd1 inhibitors
SG11201707948WA (en) * 2015-04-03 2017-10-30 Bristol Myers Squibb Co Inhibitors of indoleamine 2,3-dioxygenase for the treatment of cancer
PE20180455A1 (es) 2015-04-03 2018-03-05 Incyte Corp Compuestos heterociclicos como inhibidores de lsd1
UA126277C2 (uk) 2015-08-12 2022-09-14 Інсайт Корпорейшн Солі інгібітору lsd1
CN108368049A (zh) * 2015-09-24 2018-08-03 葛兰素史克知识产权开发有限公司 吲哚胺2,3-双加氧酶的调节剂
EP3558966A1 (en) * 2016-12-20 2019-10-30 GlaxoSmithKline Intellectual Property Development Limited Modulators of indoleamine 2,3-dioxygenase
US10899754B2 (en) * 2016-12-20 2021-01-26 Glaxosmithkline Intellectual Property Development Limited Modulators of indoleamine 2,3-dioxygenase
ES2881395T3 (es) 2016-12-22 2021-11-29 Calithera Biosciences Inc Composiciones y métodos para inhibir la actividad de la arginasa
EP3570832A4 (en) 2017-01-17 2020-06-10 Board Of Regents, The University Of Texas System COMPOUNDS AS INHIBITORS OF INDOLAMINE-2,3-DIOXYGENASE AND / OR TRYPTOPHANE-DIOXYGENASE
WO2018201130A1 (en) * 2017-04-28 2018-11-01 The Brigham And Women's Hospital, Inc. Targeting gamma-delta t cells in obesity and cachexia
US11186554B2 (en) 2017-05-03 2021-11-30 Vivace Therapeutics, Inc. Non-fused tricyclic compounds
CN108976139B (zh) * 2017-06-02 2021-03-16 沈阳化工研究院有限公司 一种芳乙烯衍生物及其应用
US20210139467A1 (en) * 2017-06-28 2021-05-13 Glaxosmithkline Intellectual Property Development Limited Modulators of indoleamine 2,3-dioxygenase
CN107325019B (zh) * 2017-08-11 2019-11-22 石河子大学 芳胺基苯甲酰胺类化合物及n-芳基-芳胺基苯甲酰胺类化合物的制备方法
US11192865B2 (en) 2017-08-21 2021-12-07 Vivace Therapeutics, Inc. Benzosulfonyl compounds
US11180497B2 (en) * 2017-10-18 2021-11-23 Angex Pharmaceutical, Inc. Cyclic compounds as immunomodulating agents
CN109836356B (zh) * 2017-11-24 2022-03-08 沈阳化工研究院有限公司 一种芳甲醚衍生物及其应用
EP3720430A4 (en) 2017-12-06 2021-05-05 Vivace Therapeutics, Inc. BENZOCARBONYL COMPOUNDS
CN111587116A (zh) 2018-01-05 2020-08-25 迪克纳制药公司 降低β-连环蛋白和IDO表达以加强免疫疗法
WO2019136112A1 (en) * 2018-01-05 2019-07-11 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
US11661403B2 (en) 2018-05-16 2023-05-30 Vivace Therapeutics, Inc. Oxadiazole compounds
AU2019297428C1 (en) * 2018-07-06 2023-03-23 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
US11046649B2 (en) 2018-07-17 2021-06-29 Board Of Regents, The University Of Texas System Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase
US12059420B2 (en) * 2018-07-23 2024-08-13 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
WO2020047198A1 (en) 2018-08-31 2020-03-05 Incyte Corporation Salts of an lsd1 inhibitor and processes for preparing the same
CN109608334B (zh) * 2019-01-11 2021-07-13 盐城通海生物科技有限公司 一种合成4-甲氧基巴豆酸甲酯的方法
WO2020160365A1 (en) * 2019-02-01 2020-08-06 Glaxosmithkline Intellectual Property Development Limited Belantamab mafodotin in combination with pembrolizumab for treating cancer
KR102386849B1 (ko) * 2019-10-14 2022-04-13 포항공과대학교 산학협력단 면역치료를 위한 환경 반응형 접착성 항체전달체 및 이의 제조방법
WO2021102618A1 (en) * 2019-11-25 2021-06-03 InventisBio Co., Ltd. Novel salts of indoleamine 2,3-dioxygenase inhibitors
CN113214138A (zh) * 2020-02-04 2021-08-06 中国医学科学院药物研究所 苯丙酸类衍生物、及其制法和药物组合物与用途
US11839659B2 (en) 2020-07-02 2023-12-12 Northwestern University Proteolysis-targeting chimeric molecules (PROTACs) that induce degradation of indoleamine 2,3-dioxygenase (IDO) protein
CN112174891B (zh) * 2020-11-02 2022-02-01 浙江省农业科学院 一种氟唑菌苯胺代谢物的制备方法
JP2024016314A (ja) * 2020-12-24 2024-02-07 小野薬品工業株式会社 一般式(i-a)で示される化合物、その薬学的に許容される塩、またはそれらの水和物と免疫チェックポイント阻害薬および/またはep4受容体拮抗薬との組み合わせ
EP4052705A1 (en) 2021-03-05 2022-09-07 Universität Basel Vizerektorat Forschung Compositions for the treatment of ebv associated diseases or conditions
AU2022228701A1 (en) 2021-03-05 2023-09-14 Universität Basel Compositions for the treatment of ebv associated diseases or conditions

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3622337A (en) * 1968-08-02 1971-11-23 Gaf Corp Cyan color formers for color photography
US4252894A (en) * 1975-10-22 1981-02-24 Gaf Corporation Hydrophilic color coupler composition containing diepoxide
WO2003099276A1 (en) 2002-05-10 2003-12-04 Bristol-Myers Squibb Company 1,1-disubstituted cycloalkyl derivatives as factor xa inhibitors
CN101445469B (zh) * 2003-09-24 2013-02-13 梅特希尔基因公司 组蛋白脱乙酰基酶抑制剂
JP4809228B2 (ja) * 2003-09-24 2011-11-09 メチルジーン インコーポレイテッド ヒストンデアセチラーゼの阻害剤
TWI309240B (en) 2004-09-17 2009-05-01 Hoffmann La Roche Anti-ox40l antibodies
ES2432091T5 (es) 2005-03-25 2022-03-18 Gitr Inc Moléculas de unión GITR y usos de las mismas
EP2559690B1 (en) 2005-05-10 2016-03-30 Incyte Holdings Corporation Modulators of indoleamine 2,3-dioxygenase and methods of using the same
EA019344B1 (ru) 2005-07-01 2014-03-31 МЕДАРЕКС, Эл.Эл.Си. Человеческие моноклональные антитела против лиганда-1 запрограммированной гибели клеток (pd-l1) и их применения
TWI382974B (zh) 2005-12-20 2013-01-21 英塞特公司 作為吲哚胺2,3-二氧化酶調節劑之n-羥基甲脒基雜環化物
US8163746B2 (en) * 2006-04-19 2012-04-24 Astellas Pharma Inc. Azolecarboxamide derivative
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.
WO2008036642A2 (en) 2006-09-19 2008-03-27 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
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
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
EP2227233B1 (en) 2007-11-30 2013-02-13 Newlink Genetics Ido inhibitors
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
FI4209510T3 (fi) 2008-12-09 2024-03-22 Hoffmann La Roche Anti-PD-L1-vasta-aineita ja niiden käyttö T-solutoiminnan tehostamiseksi
RU2595409C2 (ru) 2009-09-03 2016-08-27 Мерк Шарп И Доум Корп., Анти-gitr-антитела
EP2493862B1 (en) 2009-10-28 2016-10-05 Newlink Genetics Corporation Imidazole derivatives as ido inhibitors
SI2510010T1 (sl) 2009-12-10 2016-02-29 F. Hoffmann-La Roche Ag Protitelesa, vezavna na ekstracelično domeno 4 humanega csf1r in njihova uporaba
PE20170779A1 (es) 2010-03-04 2017-07-04 Macrogenics Inc Anticuerpos reactivos con b7-h3, fragmentos inmunologicamente activos de los mismos y usos de los mismos
RU2617966C2 (ru) 2010-03-05 2017-04-28 Ф.Хоффманн-Ля Рош Аг Антитела против csf-1r человека и их применение
JP2013521765A (ja) 2010-03-05 2013-06-13 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト ヒトcsf−1rに対する抗体及びその使用
HRP20190047T1 (hr) 2010-05-04 2019-02-22 Five Prime Therapeutics, Inc. Protutijela koja se vežu na csf1r
PH12013500395B1 (en) 2010-09-09 2020-10-16 Pfizer 4-1bb binding molecules
NO2694640T3 (enExample) 2011-04-15 2018-03-17
RS57324B1 (sr) 2011-04-20 2018-08-31 Medimmune Llc Antitela i drugi molekuli koji vezuju b7-h1 i pd-1
EP3763741A1 (en) 2011-11-28 2021-01-13 Merck Patent GmbH Anti-pd-l1 antibodies and uses thereof
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
RU2670743C9 (ru) 2012-05-11 2018-12-19 Файв Прайм Терапьютикс, Инк. Способы лечения состояний антителами, которые связывают рецептор колониестимулирующего фактора 1 (csf1r)
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
SG10201906328RA (en) 2012-08-31 2019-08-27 Five Prime Therapeutics Inc Methods of treating conditions with antibodies that bind colony stimulating factor 1 receptor (csf1r)
ES2675022T3 (es) 2013-03-15 2018-07-05 Bristol-Myers Squibb Company Inhibidores de indolamina 2,3-dioxigenasa (IDO)
PE20151594A1 (es) * 2013-03-15 2015-11-19 Bristol Myers Squibb Co Inhibidores de indolamina 2-3 dioxigenasa
EA029981B1 (ru) * 2013-08-27 2018-06-29 Бристол-Майерс Сквибб Компани Ингибиторы ido
SG11201707948WA (en) * 2015-04-03 2017-10-30 Bristol Myers Squibb Co Inhibitors of indoleamine 2,3-dioxygenase for the treatment of cancer

Similar Documents

Publication Publication Date Title
JP2018515438A5 (enExample)
JP2018516238A5 (enExample)
JP2018519245A5 (enExample)
JP2016528197A5 (enExample)
JP2016518324A5 (enExample)
JP2017501237A5 (enExample)
JP2017526726A5 (enExample)
JP2017502940A5 (enExample)
JP2019529484A5 (enExample)
JP2017508782A5 (enExample)
JP2015535277A5 (enExample)
JP2017528498A5 (enExample)
JP2016520131A5 (enExample)
JP2016509583A5 (enExample)
JP2019501125A5 (enExample)
RU2019119893A (ru) Ингибиторы jak2 и alk2 и способы их использования
JP2016513660A5 (enExample)
JP2020517616A5 (enExample)
JP2016519147A5 (enExample)
JP2017509689A5 (enExample)
JP2016513661A5 (enExample)
RU2015143717A (ru) 2-Аминопиримидин-6-оны и аналоги, проявляющие противораковые и антипролиферативные действия
JP2009524670A5 (enExample)
JP2017512786A5 (enExample)
RU2016141647A (ru) ИНГИБИТОРЫ TrkA КИНАЗЫ, ОСНОВАННЫЕ НА НИХ КОМПОЗИЦИИ И СПОСОБЫ