JP2016528197A5 - - Google Patents

Download PDF

Info

Publication number
JP2016528197A5
JP2016528197A5 JP2016524305A JP2016524305A JP2016528197A5 JP 2016528197 A5 JP2016528197 A5 JP 2016528197A5 JP 2016524305 A JP2016524305 A JP 2016524305A JP 2016524305 A JP2016524305 A JP 2016524305A JP 2016528197 A5 JP2016528197 A5 JP 2016528197A5
Authority
JP
Japan
Prior art keywords
optionally substituted
alkyl
aryl
cycloalkyl
optionally
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.)
Ceased
Application number
JP2016524305A
Other languages
English (en)
Japanese (ja)
Other versions
JP2016528197A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2014/044992 external-priority patent/WO2015002918A1/en
Publication of JP2016528197A publication Critical patent/JP2016528197A/ja
Publication of JP2016528197A5 publication Critical patent/JP2016528197A5/ja
Ceased legal-status Critical Current

Links

JP2016524305A 2013-07-01 2014-07-01 Ido阻害剤 Ceased JP2016528197A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361841448P 2013-07-01 2013-07-01
US61/841,448 2013-07-01
PCT/US2014/044992 WO2015002918A1 (en) 2013-07-01 2014-07-01 Ido inhibitors

Publications (2)

Publication Number Publication Date
JP2016528197A JP2016528197A (ja) 2016-09-15
JP2016528197A5 true JP2016528197A5 (https=) 2017-07-06

Family

ID=51257587

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016524305A Ceased JP2016528197A (ja) 2013-07-01 2014-07-01 Ido阻害剤

Country Status (10)

Country Link
US (1) US9765018B2 (https=)
EP (1) EP3016932B1 (https=)
JP (1) JP2016528197A (https=)
CN (1) CN105473550B (https=)
BR (1) BR112015032595A8 (https=)
CA (1) CA2916615A1 (https=)
EA (1) EA029126B1 (https=)
ES (1) ES2719327T3 (https=)
MX (1) MX2015017486A (https=)
WO (1) WO2015002918A1 (https=)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HRP20160305T1 (hr) 2010-10-26 2016-07-01 Mars, Incorporated Borati kao inhibitori arginaze
NO2694640T3 (https=) 2011-04-15 2018-03-17
EA031470B1 (ru) * 2013-03-15 2019-01-31 Бристол-Майерс Сквибб Компани Ингибиторы ido
MX2015017486A (es) 2013-07-01 2016-03-21 Squibb Bristol Myers Co Inhibidores de indolamina 2,3-dioxigenasa (dio).
GB201311891D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel compound
GB201311888D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel compounds
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
CN107849024A (zh) * 2015-05-15 2018-03-27 吉利德科学公司 具有作为吲哚胺2,3‑二加氧酶抑制剂活性的苯并咪唑和咪唑并吡啶亚氨代甲酰胺化合物
TW201713332A (zh) 2015-07-14 2017-04-16 協和醱酵麒麟有限公司 包含與抗體組合投予之ido抑制物之腫瘤治療劑
EP4659747A2 (en) 2015-07-24 2025-12-10 Lumos Pharma, Inc. Salts and prodrugs of 1-methyl-d-tryptophan
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
WO2017051353A1 (en) * 2015-09-24 2017-03-30 Glaxosmithkline Intellectual Property (No.2) Limited Modulators of indoleamine 2,3-dioxygenase
WO2017133258A1 (zh) * 2016-02-04 2017-08-10 西华大学 1h-吲唑类衍生物及其作为ido抑制剂的用途
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
EP3452450A1 (en) * 2016-05-04 2019-03-13 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
WO2017192844A1 (en) * 2016-05-04 2017-11-09 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
JP7623784B2 (ja) 2016-10-13 2025-01-29 ジュノー セラピューティクス インコーポレイテッド トリプトファン代謝経路調節剤を含む免疫療法の方法および組成物
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
US10858351B2 (en) 2017-04-26 2020-12-08 Alberta Research Chemicals Inc. Substituted tetrahydropyridine derivatives as IDO-1 inhibitors and uses thereof
CN110709255B (zh) * 2017-06-08 2021-08-06 日本曹达株式会社 记录材料及化合物
US11813280B2 (en) 2018-01-05 2023-11-14 Dicerna Pharmaceuticals, Inc. Reducing beta-catenin and IDO expression to potentiate immunotherapy
CN110092750B (zh) 2018-01-29 2023-07-21 北京诺诚健华医药科技有限公司 五氟硫烷基取代的酰胺类化合物、其制备方法及其在医药学上的应用
CN110526898A (zh) 2018-05-25 2019-12-03 北京诺诚健华医药科技有限公司 3-吲唑啉酮类化合物、其制备方法及其在医药学上的应用
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
WO2020023356A1 (en) * 2018-07-23 2020-01-30 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
US12059420B2 (en) * 2018-07-23 2024-08-13 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
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
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
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

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001098268A2 (en) * 2000-06-21 2001-12-27 Bristol-Myers Squibb Pharma Company Piperidine amides as modulators of chemokine receptor activity
FR2878849B1 (fr) 2004-12-06 2008-09-12 Aventis Pharma Sa Indoles substitues, compositions les contenant, procede de fabrication et utilisation
WO2008058178A1 (en) 2006-11-08 2008-05-15 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
GB0806794D0 (en) * 2008-04-15 2008-05-14 Ludwig Inst Cancer Res Therapeutic compounds
WO2012087234A1 (en) * 2010-12-22 2012-06-28 Idogen Ab A composition comprising at least to compounds which induces indolamine 2,3-dioxygenase (ido), for the treatment of an autoimmune disorder or suffering from immune rejection of organs
EP2970114B1 (en) 2013-03-15 2019-05-15 Bristol-Myers Squibb Company Ido inhibitors
MX2015017486A (es) 2013-07-01 2016-03-21 Squibb Bristol Myers Co Inhibidores de indolamina 2,3-dioxigenasa (dio).
TWI582077B (zh) 2013-11-07 2017-05-11 必治妥美雅史谷比公司 作爲IL-12、IL-23及/或IFNα反應調節劑之經烷基-醯胺取代之吡啶化合物

Similar Documents

Publication Publication Date Title
JP2016528197A5 (https=)
JP2016530283A5 (https=)
JP2016523974A5 (https=)
JP2016519653A5 (https=)
US10774065B2 (en) 1-pyridazin-/triazin-3-yl-piper(-azine)/idine/pyrolidine derivatives and compositions thereof for inhibiting the activity of SHP2
JP2016518324A5 (https=)
JP2018519245A5 (https=)
JP2018516238A5 (https=)
JP2019529484A5 (https=)
JP6644792B2 (ja) ベンザゼピンスルホンアミド化合物
US9815813B2 (en) 1-(triazin-3-yl/pyridazin-3-yl)-piper(-azine)idine derivatives and compositions therefor for inhibiting the activity of SHP2
JP2019517487A5 (https=)
JP2022551668A5 (https=)
JP2015514056A5 (https=)
RU2018138828A (ru) Уменьшение массы опухоли путем введения ccr1 антагонистов в комбинации с pd-1 ингибиторами или pd-l1 ингибиторами
US12551482B2 (en) Aurora kinase inhibitors
RU2014152790A (ru) Пирролопиразоновые ингибиторы танкиразы
JP2014518544A5 (https=)
RU2013144571A (ru) Алинзамещенные хиназолины и способы их применения
AU2016298962A1 (en) Compounds and pharmaceutical composition associated with ubiquitination-proteasome system
JP2014513731A5 (https=)
JP2013127001A (ja) ピリミジルアミノベンズアミド化合物であるタンパク質キナーゼ阻害剤および17−aagのようなhsp90阻害剤を含む組合せ剤
JP2013035853A (ja) 増殖性疾患の処置または予防のためのピリミジルアミノベンズアミド化合物とイマチニブの組み合わせ
JP2012526793A5 (https=)
WO2015014283A1 (zh) 蛋白酪氨酸激酶抑制剂及其应用