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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JP
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membered monocyclic
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JP2016539013A
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Japanese (ja)
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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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Expired - Fee Related legal-status Critical Current
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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 (enExample) 2017-10-12
JP6371851B2 JP6371851B2 (ja) 2018-08-08

Family

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 (enExample)
EP (1) EP3039020B1 (enExample)
JP (1) JP6371851B2 (enExample)
CN (1) CN105658643B (enExample)
CA (1) CA2921199A1 (enExample)
EA (1) EA029981B1 (enExample)
MX (1) MX2016002075A (enExample)
WO (1) WO2015031295A1 (enExample)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUE039339T2 (hu) * 2013-03-15 2018-12-28 Bristol Myers Squibb Co Indolamin-2,3-dioxigenáz (IDO) inhibitorai
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
CN105517999B (zh) * 2013-07-11 2019-06-28 百时美施贵宝公司 Ido抑制剂
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
MX2017012738A (es) * 2015-04-03 2017-11-15 Bristol Myers Squibb Co Inhibidores de indolamina 2.3-dioxigenasa (ido) para el tratamiento de cancer.
CN108260355A (zh) * 2015-09-24 2018-07-06 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
WO2017140272A1 (zh) * 2016-02-19 2017-08-24 正大天晴药业集团股份有限公司 作为免疫调节剂的三并环化合物
EP3416725A1 (en) 2016-02-19 2018-12-26 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and pharmaceutical compositions for the treatment of obesity
WO2017192844A1 (en) * 2016-05-04 2017-11-09 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
EP3452452A4 (en) * 2016-05-04 2019-10-30 Bristol-Myers Squibb Company INHIBITORS OF INDOLEAMINE-2,3-DIOXYGENASE AND METHOD FOR 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
CA3023034A1 (en) 2016-05-12 2017-11-16 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
JP2019528301A (ja) * 2016-08-26 2019-10-10 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company 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の使用方法
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
WO2018119440A1 (en) 2016-12-22 2018-06-28 Calithera Biosciences, Inc. Compositions and methods for inhibiting arginase activity
WO2018136437A2 (en) 2017-01-17 2018-07-26 Tesaro, Inc. 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
CN111225915B (zh) 2017-10-18 2023-03-07 朱比兰特埃皮帕德有限公司 作为pad抑制剂的咪唑并吡啶化合物
US11629135B2 (en) 2017-11-06 2023-04-18 Jubilant Prodell Llc Pyrimidine derivatives as inhibitors of PD1/PD-L1 activation
RS65576B1 (sr) 2017-11-24 2024-06-28 Jubilant Episcribe Llc Heterociklična jedinjenja kao inhibitori prmt5
AU2019205904A1 (en) 2018-01-05 2020-06-18 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
CN112105610B (zh) 2018-03-13 2024-01-26 朱比连特普罗德尔有限责任公司 作为pd1/pd-l1相互作用/活化的抑制剂的双环化合物
EP3823604A4 (en) 2018-07-17 2022-03-16 Board of Regents, The University of Texas System COMPOUNDS AS INHIBITORS OF INDOLAMINE-2,3-DIOXYGENASE AND/OR TRYPTOPHANE 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
KR102922115B1 (ko) 2019-04-09 2026-02-04 누릭스 테라퓨틱스 인코포레이티드 Cbl-b 억제용의 3-치환된 피페리딘 화합물, 및 암 백신 및/또는 종양용해 바이러스와 조합된 cbl-b 억제제의 용도
US12653809B2 (en) 2019-07-30 2026-06-16 Nurix Therapeutics, Inc. Urea, amide, and substituted heteroaryl compounds for CBL-B inhibition
CN114728070A (zh) 2019-09-25 2022-07-08 百时美施贵宝公司 用于癌症疗法的复合生物标记物
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
ES3068139T3 (es) * 2020-11-06 2026-05-27 Boehringer Ingelheim Int Derivados de 2¿[tiofen¿2-il)formamido]¿N¿(fenil)¿2-metilpropanamida y su uso como medicamento
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
EP4052705A1 (en) 2021-03-05 2022-09-07 Universität Basel Vizerektorat Forschung Compositions for the treatment of ebv associated diseases or conditions
BR112023017582A2 (pt) 2021-03-05 2023-12-05 Univ Basel Composições para o tratamento de doenças ou condições associadas ao ebv
US12319655B2 (en) 2021-12-09 2025-06-03 Deciphera Pharmaceuticals, Llc RAF kinase inhibitors and methods of use thereof
EP4786459A1 (en) * 2023-09-28 2026-08-05 West China Hospital, Sichuan University Benzene ring-containing compound having analgesic effect, preparation method therefor, and use thereof

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020173507A1 (en) * 2000-08-15 2002-11-21 Vincent Santora Urea compounds and methods of uses
SI1309589T1 (sl) * 2000-08-15 2006-06-30 Amgen Inc Secninske spojine in njihova uporaba
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
ATE323702T1 (de) * 2002-08-06 2006-05-15 Astrazeneca Ab Kondensierte pyridine und pyrimidine mit tie2 (tek) aktivität
CN1795187A (zh) * 2003-03-27 2006-06-28 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
ES2465469T3 (es) * 2005-01-14 2014-06-05 Gilead Connecticut, Inc. Diaril ureas 1,3-sustituidas como moduladores de la actividad quinasa
ES2540561T3 (es) 2005-12-20 2015-07-10 Incyte Corporation N-hidroxiamidinoheterociclos como moduladores de indolamina 2,3-dioxigenasa
US20080182882A1 (en) * 2006-11-08 2008-07-31 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
JP2011506454A (ja) * 2007-12-13 2011-03-03 グラクソスミスクライン エルエルシー チアゾールおよびオキサゾールキナーゼ阻害薬
WO2009078992A1 (en) * 2007-12-17 2009-06-25 Amgen Inc. Linear tricyclic compounds as p38 kinase inhibitors
US20100041642A1 (en) * 2008-08-15 2010-02-18 Locus Pharmaceuticals, Inc. Urea inhibitors of map kinases
EP2493862B1 (en) * 2009-10-28 2016-10-05 Newlink Genetics Corporation Imidazole derivatives as ido inhibitors
WO2012149540A1 (en) * 2011-04-28 2012-11-01 The Broad Institute Inc Inhibitors of histone deacetylase

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