JP2016530283A5 - - Google Patents

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Publication number
JP2016530283A5
JP2016530283A5 JP2016539013A JP2016539013A JP2016530283A5 JP 2016530283 A5 JP2016530283 A5 JP 2016530283A5 JP 2016539013 A JP2016539013 A JP 2016539013A JP 2016539013 A JP2016539013 A JP 2016539013A JP 2016530283 A5 JP2016530283 A5 JP 2016530283A5
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Japan
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alkyl
membered monocyclic
optionally
cycloalkyl
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JP2016539013A
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JP2016530283A (ja
JP6371851B2 (ja
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Priority claimed from PCT/US2014/052600 external-priority patent/WO2015031295A1/en
Publication of JP2016530283A publication Critical patent/JP2016530283A/ja
Publication of JP2016530283A5 publication Critical patent/JP2016530283A5/ja
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JP2016539013A 2013-08-27 2014-08-26 Ido阻害剤 Expired - Fee Related JP6371851B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361870371P 2013-08-27 2013-08-27
US61/870,371 2013-08-27
PCT/US2014/052600 WO2015031295A1 (en) 2013-08-27 2014-08-26 Ido inhibitors

Publications (3)

Publication Number Publication Date
JP2016530283A JP2016530283A (ja) 2016-09-29
JP2016530283A5 true JP2016530283A5 (https=) 2017-10-12
JP6371851B2 JP6371851B2 (ja) 2018-08-08

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ID=51539339

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016539013A Expired - Fee Related JP6371851B2 (ja) 2013-08-27 2014-08-26 Ido阻害剤

Country Status (8)

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US (1) US9758492B2 (https=)
EP (1) EP3039020B1 (https=)
JP (1) JP6371851B2 (https=)
CN (1) CN105658643B (https=)
CA (1) CA2921199A1 (https=)
EA (1) EA029981B1 (https=)
MX (1) MX2016002075A (https=)
WO (1) WO2015031295A1 (https=)

Families Citing this family (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA031470B1 (ru) * 2013-03-15 2019-01-31 Бристол-Майерс Сквибб Компани Ингибиторы ido
GB201311888D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel compounds
GB201311891D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel compound
ES2707961T3 (es) * 2013-07-11 2019-04-08 Bristol Myers Squibb Co Inhibidores de IDO
US20180228907A1 (en) 2014-04-14 2018-08-16 Arvinas, Inc. Cereblon ligands and bifunctional compounds comprising the same
GB201419579D0 (en) 2014-11-03 2014-12-17 Iomet Pharma Ltd Pharmaceutical compound
KR20170134981A (ko) * 2015-04-03 2017-12-07 브리스톨-마이어스 스큅 컴퍼니 암의 치료를 위한 인돌아민-2,3-디옥시게나제의 억제제
WO2017051353A1 (en) * 2015-09-24 2017-03-30 Glaxosmithkline Intellectual Property (No.2) Limited Modulators of indoleamine 2,3-dioxygenase
TW201736373A (zh) * 2016-02-19 2017-10-16 Chia Tai Tianqing Pharmaceutical Group Co Ltd 作為免疫調節劑的三並環化合物
WO2017140835A1 (en) 2016-02-19 2017-08-24 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and pharmaceutical compositions for the treatment of obesity
KR20190004743A (ko) * 2016-05-04 2019-01-14 브리스톨-마이어스 스큅 컴퍼니 인돌아민 2,3-디옥시게나제의 억제제 및 그의 사용 방법
WO2017192844A1 (en) * 2016-05-04 2017-11-09 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
EP3452450A1 (en) * 2016-05-04 2019-03-13 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
EP3455220A1 (en) * 2016-05-12 2019-03-20 GlaxoSmithKline Intellectual Property Development Limited Modulators of indoleamine 2,3-dioxygenase
CN107556244B (zh) * 2016-07-01 2021-09-03 上海迪诺医药科技有限公司 并环化合物、其药物组合物及应用
WO2018036414A1 (zh) * 2016-08-23 2018-03-01 北京诺诚健华医药科技有限公司 稠杂环类衍生物、其制备方法及其在医学上的应用
KR20190040502A (ko) * 2016-08-26 2019-04-18 브리스톨-마이어스 스큅 컴퍼니 인돌아민 2,3-디옥시게나제의 억제제 및 그의 사용 방법
CN108017639B (zh) * 2016-11-01 2020-09-15 南京华威医药科技集团有限公司 Ido抑制剂及其制备方法和应用
CN114989205A (zh) 2016-12-22 2022-09-02 卡里塞拉生物科学股份公司 用于抑制精氨酸酶活性的组合物和方法
CA3047002A1 (en) 2017-01-17 2018-07-26 Board Of Regents, The University Of Texas System Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase
RU2764243C2 (ru) 2017-09-22 2022-01-14 ДЖУБИЛАНТ ЭПИПЭД ЭлЭлСи Гетероциклические соединения в качестве ингибиторов PAD
AU2018352142B2 (en) 2017-10-18 2022-08-25 Jubilant Epipad LLC Imidazo-pyridine compounds as PAD inhibitors
US11629135B2 (en) 2017-11-06 2023-04-18 Jubilant Prodell Llc Pyrimidine derivatives as inhibitors of PD1/PD-L1 activation
PT3704120T (pt) 2017-11-24 2024-07-03 Jubilant Episcribe Llc Compostos heterocíclicos como inibidores de prmt5
US11813280B2 (en) 2018-01-05 2023-11-14 Dicerna Pharmaceuticals, Inc. Reducing beta-catenin and IDO expression to potentiate immunotherapy
US11447449B2 (en) 2018-01-05 2022-09-20 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
EP3743063A4 (en) * 2018-01-26 2021-10-20 Nurix Therapeutics, Inc. CBL-B INHIBITORS AND THEIR METHODS OF USE
MX2020009517A (es) 2018-03-13 2021-01-20 Jubilant Prodel LLC Compuestos biciclicos como inhibidores de la interaccion/activacio n de pdl/pd-l1.
WO2020018670A1 (en) 2018-07-17 2020-01-23 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
CN111763164B (zh) * 2019-04-02 2023-03-10 中国医学科学院药物研究所 一类邻位羰基氨基取代苯衍生物的制备方法和用途
CA3136348A1 (en) 2019-04-09 2020-10-15 Nurix Therapeutics, Inc. 3-substituted piperidine compounds for cbl-b inhibition, and use of a cbl-b inhibitor in combination with a cancer vaccine and/or oncolytic virus
KR20220066950A (ko) 2019-09-25 2022-05-24 브리스톨-마이어스 스큅 컴퍼니 암 요법을 위한 복합 바이오마커
CN111153846B (zh) * 2020-01-17 2021-08-31 中国药科大学 吡咯类化合物、其制备方法和药物组合物与用途
CN111153850B (zh) * 2020-01-17 2021-08-13 中国药科大学 吲哚类化合物、其制备方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
CN116406266A (zh) * 2020-11-06 2023-07-07 勃林格殷格翰国际有限公司 2-[(噻吩-2-基)甲酰胺基]-n-(苯基)-2-甲基丙酰胺衍生物及其作为药物的用途
CN112206228A (zh) * 2020-11-24 2021-01-12 烟台大学 紫杉醇和ido1小分子抑制剂复方药物组合物及其用途
MX2023010371A (es) 2021-03-05 2024-02-12 Univ Basel Composiciones para el tratamiento de enfermedades o condiciones asociadas al veb.
EP4052705A1 (en) 2021-03-05 2022-09-07 Universität Basel Vizerektorat Forschung Compositions for the treatment of ebv associated diseases or conditions
CA3240263A1 (en) 2021-12-09 2023-06-15 Daniel L. Flynn Raf kinase inhibitors and methods of use thereof
WO2025067473A1 (zh) * 2023-09-28 2025-04-03 四川大学华西医院 一种含苯环的具有镇痛功效的化合物及其制备方法和用途

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1619184A3 (en) * 2000-08-15 2006-02-01 Amgen, Inc. Urea compounds as kinase inhibitors
US20020173507A1 (en) * 2000-08-15 2002-11-21 Vincent Santora Urea compounds and methods of uses
JP2003091058A (ja) * 2001-09-19 2003-03-28 Konica Corp ハロゲン化銀カラー写真感光材料
DE60304718T2 (de) * 2002-08-06 2007-04-26 Astrazeneca Ab Kondensierte pyridine und pyrimidine mit tie2 (tek) aktivität
CN101265254A (zh) * 2003-03-27 2008-09-17 兰肯瑙医学研究所 新型ido抑制剂及其使用方法
WO2005121132A1 (ja) * 2004-06-11 2005-12-22 Shionogi & Co., Ltd. 抗hcv作用を有する縮合ヘテロ環化合物
EP1858877B1 (en) * 2005-01-14 2014-03-12 Gilead Connecticut, Inc. 1,3 substituted diaryl ureas as modulators of kinase activity
US8450351B2 (en) 2005-12-20 2013-05-28 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
WO2008058178A1 (en) 2006-11-08 2008-05-15 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
WO2009076140A1 (en) * 2007-12-13 2009-06-18 Smithkline Beecham Corporation Thiazole and oxazole kinase inhibitors
WO2009078992A1 (en) * 2007-12-17 2009-06-25 Amgen Inc. Linear tricyclic compounds as p38 kinase inhibitors
JP2012500223A (ja) * 2008-08-15 2012-01-05 ローカス ファーマスーティカルズ,インコーポレイテッド Mapキナーゼインヒビターとしての尿素誘導体
EP2493862B1 (en) * 2009-10-28 2016-10-05 Newlink Genetics Corporation Imidazole derivatives as ido inhibitors
CA2834548C (en) 2011-04-28 2021-06-01 The Broad Institute, Inc. Inhibitors of histone deacetylase

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