JP2018516238A5 - - Google Patents

Download PDF

Info

Publication number
JP2018516238A5
JP2018516238A5 JP2017551647A JP2017551647A JP2018516238A5 JP 2018516238 A5 JP2018516238 A5 JP 2018516238A5 JP 2017551647 A JP2017551647 A JP 2017551647A JP 2017551647 A JP2017551647 A JP 2017551647A JP 2018516238 A5 JP2018516238 A5 JP 2018516238A5
Authority
JP
Japan
Prior art keywords
optionally substituted
alkyl
compound according
cycloalkyl
heterocyclyl
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.)
Pending
Application number
JP2017551647A
Other languages
English (en)
Japanese (ja)
Other versions
JP2018516238A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2016/025554 external-priority patent/WO2016161286A1/en
Publication of JP2018516238A publication Critical patent/JP2018516238A/ja
Publication of JP2018516238A5 publication Critical patent/JP2018516238A5/ja
Pending legal-status Critical Current

Links

JP2017551647A 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 Pending JP2018516238A (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/US2016/025554 WO2016161286A1 (en) 2015-04-03 2016-04-01 Inhibitors of indoleamine 2,3-dioxygenase for the treatment of cancer

Publications (2)

Publication Number Publication Date
JP2018516238A JP2018516238A (ja) 2018-06-21
JP2018516238A5 true JP2018516238A5 (enExample) 2019-05-09

Family

ID=55702190

Family Applications (3)

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JP2017551629A Withdrawn JP2018515438A (ja) 2015-04-03 2016-04-01 癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法
JP2017551628A Withdrawn JP2018519245A (ja) 2015-04-03 2016-04-01 癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法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

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JP2017551629A Withdrawn JP2018515438A (ja) 2015-04-03 2016-04-01 癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法
JP2017551628A Withdrawn JP2018519245A (ja) 2015-04-03 2016-04-01 癌の治療のためのインドールアミン−2,3−ジオキシゲナーゼの阻害剤およびそれらの使用方法

Country Status (20)

Country Link
US (4) US10399932B2 (enExample)
EP (3) EP3277671A1 (enExample)
JP (3) JP2018516238A (enExample)
KR (3) KR20170134981A (enExample)
CN (3) CN108093636A (enExample)
AR (1) AR104176A1 (enExample)
AU (3) AU2016243937A1 (enExample)
BR (3) BR112017020895A2 (enExample)
CA (3) CA2981660A1 (enExample)
CL (1) CL2017002494A1 (enExample)
CO (1) CO2017011183A2 (enExample)
EA (3) EA033395B1 (enExample)
HK (1) HK1247922A1 (enExample)
IL (3) IL254720A0 (enExample)
MX (3) MX2017012729A (enExample)
PE (1) PE20180117A1 (enExample)
SG (3) SG11201807980QA (enExample)
TW (1) TW201700453A (enExample)
UY (1) UY36601A (enExample)
WO (3) WO2016161279A1 (enExample)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9527835B2 (en) 2014-02-13 2016-12-27 Incyte Corporation Cyclopropylamines as LSD1 inhibitors
NZ723203A (en) 2014-02-13 2020-08-28 Incyte Corp Cyclopropylamines as lsd1 inhibitors
PH12020552066A1 (en) 2014-02-13 2022-05-11 Incyte Corp Cyclopropylamines as lsd1 inhibitors
US9695180B2 (en) 2014-07-10 2017-07-04 Incyte Corporation Substituted imidazo[1,2-a]pyrazines as LSD1 inhibitors
US9695167B2 (en) 2014-07-10 2017-07-04 Incyte Corporation Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors
TWI687419B (zh) 2014-07-10 2020-03-11 美商英塞特公司 作為lsd1抑制劑之咪唑并吡啶及咪唑并吡嗪
TW201700453A (zh) * 2015-04-03 2017-01-01 必治妥美雅史谷比公司 Ido抑制劑
TWI714567B (zh) 2015-04-03 2021-01-01 美商英塞特公司 作為lsd1抑制劑之雜環化合物
LT3334709T (lt) 2015-08-12 2025-03-10 Incyte Holdings Corporation Lsd1 inhibitoriaus druskos
BR112018005870A2 (pt) * 2015-09-24 2018-10-16 Glaxosmithkline Ip No 2 Ltd composto, e, método de prevenção e/ou tratamento do hiv.
JP2020502189A (ja) * 2016-12-20 2020-01-23 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited インドールアミン2,3−ジオキシゲナーゼのモジュレーター
EP3558966A1 (en) * 2016-12-20 2019-10-30 GlaxoSmithKline Intellectual Property Development Limited Modulators of indoleamine 2,3-dioxygenase
AU2017382405B2 (en) 2016-12-22 2021-12-16 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
US20200188482A1 (en) * 2017-04-28 2020-06-18 The Brigham And Women`S Hospital, Inc. Targeting gamma-delta t cells in obesity and cachexia
EP3618818A4 (en) 2017-05-03 2020-12-09 Vivace Therapeutics, Inc. NON-CONDENSED TRICYCLIC COMPOUNDS
EP3632893A4 (en) * 2017-06-02 2020-12-09 Shenyang Research Institute of Chemical Industry Co., Ltd. VINYLARENE DERIVATIVE AND ITS USE
JP2020525486A (ja) * 2017-06-28 2020-08-27 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited インドールアミン2,3−ジオキシゲナーゼのモジュレーター
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
EP3691623B1 (en) 2017-08-21 2022-10-05 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
WO2019113236A1 (en) 2017-12-06 2019-06-13 Vivace Therapeutics, Inc. Benzocarbonyl compounds
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
WO2019222431A1 (en) 2018-05-16 2019-11-21 Vivace Therapeutics, Inc. Oxadiazole compounds
CA3104398A1 (en) * 2018-07-06 2020-01-09 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
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
WO2020023355A1 (en) * 2018-07-23 2020-01-30 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
US10968200B2 (en) 2018-08-31 2021-04-06 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
CA3128064A1 (en) * 2019-02-01 2020-08-06 Glaxosmithkline Intellectual Property Development Limited Combination treatments for cancer comprising belantamab mafodotin and an anti ox40 antibody and uses and methods thereof
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
JP2024510949A (ja) 2021-03-05 2024-03-12 ウニヴェルシタット・バーゼル Ebv関連疾患又は状態の治療用組成物

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
US7312214B2 (en) 2002-05-10 2007-12-25 Bristol-Myers Squibb Company 1, 1-disubstituted cycloalkyl derivatives as factor Xa inhibitors
WO2005030705A1 (en) * 2003-09-24 2005-04-07 Methylgene, Inc. Inhibitors of histone deacetylase
CN1882529A (zh) * 2003-09-24 2006-12-20 梅特希尔基因公司 组蛋白脱乙酰基酶抑制剂
TWI309240B (en) 2004-09-17 2009-05-01 Hoffmann La Roche Anti-ox40l antibodies
WO2006105021A2 (en) 2005-03-25 2006-10-05 Tolerrx, Inc. Gitr binding molecules and uses therefor
SG10201809390QA (en) 2005-05-10 2018-11-29 Incyte Holdings Corp Modulators of indoleamine 2,3-dioxygenase and methods of using the same
AU2006265108C1 (en) 2005-07-01 2013-01-17 E. R. Squibb & Sons, L.L.C. Human monoclonal antibodies to programmed death ligand 1 (PD-L1)
EP1971583B1 (en) 2005-12-20 2015-03-25 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
CA2649043C (en) * 2006-04-19 2013-09-17 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.
JP5319532B2 (ja) 2006-09-19 2013-10-16 インサイト・コーポレイション インドールアミン2,3−ジオキシゲナーゼのモジュレーターとしてのn−ヒドロキシアミジノヘテロサイクル
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
WO2009009116A2 (en) 2007-07-12 2009-01-15 Tolerx, Inc. Combination therapies employing gitr binding molecules
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
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
KR20190069615A (ko) 2008-12-09 2019-06-19 제넨테크, 인크. 항-pd-l1 항체 및 t 세포 기능을 향상시키기 위한 그의 용도
CN102574924A (zh) 2009-09-03 2012-07-11 先灵公司 抗-gitr抗体
EP2493862B1 (en) 2009-10-28 2016-10-05 Newlink Genetics Corporation Imidazole derivatives as ido inhibitors
KR101434070B1 (ko) 2009-12-10 2014-08-25 에프. 호프만-라 로슈 아게 인간 csf-1r 세포외 도메인 4에 우선적으로 결합하는 항체 및 그의 용도
US9150656B2 (en) 2010-03-04 2015-10-06 Macrogenics, Inc. Antibodies reactive with B7-H3, immunologically active fragments thereof and uses thereof
WO2011107553A1 (en) 2010-03-05 2011-09-09 F. Hoffmann-La Roche Ag Antibodies against human csf-1r and uses thereof
KR101647871B1 (ko) 2010-03-05 2016-08-11 에프. 호프만-라 로슈 아게 인간 csf-1r에 대한 항체 및 이의 용도
EP3357510B1 (en) 2010-05-04 2020-08-05 Five Prime Therapeutics, Inc. Antibodies that bind csf1r
SG10201506906VA (en) 2010-09-09 2015-10-29 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
WO2013079174A1 (en) 2011-11-28 2013-06-06 Merck Patent Gmbh Anti-pd-l1 antibodies and uses thereof
CN104159921B (zh) 2011-12-15 2018-05-04 霍夫曼-拉罗奇有限公司 针对人csf-1r的抗体及其用途
WO2013119716A1 (en) 2012-02-06 2013-08-15 Genentech, Inc. Compositions and methods for using csf1r inhibitors
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
CA2871445C (en) 2012-05-11 2020-07-07 Five Prime Therapeutics, Inc. Methods of treating conditions with antibodies that bind colony stimulating factor 1 receptor (csf1r)
UY34887A (es) 2012-07-02 2013-12-31 Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware Optimización de anticuerpos que se fijan al gen de activación de linfocitos 3 (lag-3) y sus usos
HK1212214A1 (en) 2012-08-31 2016-06-10 戊瑞治疗有限公司 Methods of treating conditions with antibodies that bind colony stimulating factor 1 receptor (csf1r)
SI2970155T1 (en) * 2013-03-15 2018-06-29 Bristol-Myers Squibb Company INHIBITORS INDOLEAMIN 2,3-DIOXYGENESIS (IDO)
MX2015012056A (es) 2013-03-15 2015-12-16 Squibb Bristol Myers Co Inhibidores de indolamina-2,3-dioxigenasa (ido).
WO2015031295A1 (en) * 2013-08-27 2015-03-05 Bristol-Myers Squibb Company Ido inhibitors
TW201700453A (zh) * 2015-04-03 2017-01-01 必治妥美雅史谷比公司 Ido抑制劑

Similar Documents

Publication Publication Date Title
JP2018516238A5 (enExample)
JP2018519245A5 (enExample)
JP2018515438A5 (enExample)
JP2016528197A5 (enExample)
JP2020517616A5 (enExample)
JP2016519653A5 (enExample)
JP2019529484A5 (enExample)
JP2016518324A5 (enExample)
JP2017537080A5 (enExample)
JP2013056930A5 (enExample)
JP2014508804A5 (enExample)
JP2014525438A5 (enExample)
JP2016503799A5 (enExample)
JP2014518544A5 (enExample)
JP2017509689A5 (enExample)
JP2016536286A5 (enExample)
JP2017528498A5 (enExample)
JP2015503625A5 (enExample)
JP2017502940A5 (enExample)
JP2017526726A5 (enExample)
JP2014521688A5 (enExample)
RU2017111200A (ru) Циклогексилэтилзамещенные диаза- и триаза-трициклические соединения в качестве антагонистов индоламин-2,3-диоксигеназы для лечения рака
JP2016537366A5 (enExample)
JP2011524422A5 (enExample)
JP2016513660A5 (enExample)