JP2022507020A5 - - Google Patents

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Publication number
JP2022507020A5
JP2022507020A5 JP2021523948A JP2021523948A JP2022507020A5 JP 2022507020 A5 JP2022507020 A5 JP 2022507020A5 JP 2021523948 A JP2021523948 A JP 2021523948A JP 2021523948 A JP2021523948 A JP 2021523948A JP 2022507020 A5 JP2022507020 A5 JP 2022507020A5
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Japan
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substituted
unsubstituted
pharmaceutically acceptable
acceptable salt
compound according
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JP2021523948A
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English (en)
Japanese (ja)
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JP2022507020A (ja
JP7482861B2 (ja
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Priority claimed from PCT/US2019/060350 external-priority patent/WO2020097389A1/en
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Publication of JP2022507020A5 publication Critical patent/JP2022507020A5/ja
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JP2021523948A 2018-11-09 2019-11-07 二環式化合物 Active JP7482861B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201862758364P 2018-11-09 2018-11-09
US62/758,364 2018-11-09
US201962916739P 2019-10-17 2019-10-17
US62/916,739 2019-10-17
PCT/US2019/060350 WO2020097389A1 (en) 2018-11-09 2019-11-07 Bicyclic compounds

Publications (3)

Publication Number Publication Date
JP2022507020A JP2022507020A (ja) 2022-01-18
JP2022507020A5 true JP2022507020A5 (https=) 2022-11-07
JP7482861B2 JP7482861B2 (ja) 2024-05-14

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JP2021523948A Active JP7482861B2 (ja) 2018-11-09 2019-11-07 二環式化合物

Country Status (11)

Country Link
US (1) US11866431B2 (https=)
EP (1) EP3877356A4 (https=)
JP (1) JP7482861B2 (https=)
KR (1) KR20210108367A (https=)
CN (1) CN113302175A (https=)
AU (1) AU2019375983A1 (https=)
BR (1) BR112021008741A2 (https=)
CA (1) CA3118752A1 (https=)
IL (1) IL282984A (https=)
MX (1) MX2021005314A (https=)
WO (1) WO2020097389A1 (https=)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20210108367A (ko) 2018-11-09 2021-09-02 비바체 테라퓨틱스, 인크. 비시클릭 화합물
EP3917911A1 (en) * 2019-01-31 2021-12-08 Kyorin Pharmaceutical Co., Ltd. 15-pgdh inhibitors
MX2021012638A (es) 2019-04-16 2022-01-04 Vivace Therapeutics Inc Compuestos biciclicos.
JP2023524863A (ja) * 2020-05-08 2023-06-13 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング 三環式のヘテロ環
US11787775B2 (en) 2020-07-24 2023-10-17 Genentech, Inc. Therapeutic compounds and methods of use
IL301691A (en) 2020-09-30 2023-05-01 Univ Leuven Kath 1,2,3,4-tetrahydroquinoline derivatives as inhibitors of the yap/taz-tead activation for treating cancer
WO2022120355A1 (en) 2020-12-02 2022-06-09 Ikena Oncology, Inc. Tead degraders and uses thereof
CA3205726A1 (en) 2021-01-25 2022-07-28 Alfredo C. Castro Combination of a 3-(imidazol-4-yl)-4-(amino)-benzenesulfonamide tead inhibitor with an egfr inhibitor and/or mek inhibitor for use in the treatment of lung cancer
WO2022233442A1 (en) * 2021-02-10 2022-11-10 Merck Patent Gmbh 2,8-dihydropyrazolo[3,4-b]indole derivatives for use in the treatment of cancer
TW202304865A (zh) * 2021-03-23 2023-02-01 美商百愛及生物醫藥公司 Nlrp3發炎體之抑制劑
WO2022221866A1 (en) 2021-04-16 2022-10-20 Ikena Oncology, Inc. Mek inhibitors and uses thereof
JP7843780B2 (ja) * 2021-05-05 2026-04-10 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング 癌の処置に使用するための2,8-ジヒドロピラゾロ[3,4-b]インドール誘導体
CA3177022A1 (en) * 2021-05-11 2022-11-11 Opna Immuno-Oncology Sa Compounds and methods for yap/tead modulation and indications therefor
WO2022240966A1 (en) 2021-05-11 2022-11-17 Opna Immuno-Oncology Sa Compounds and methods for yap/tead modulation and indications therefor
JP2024519845A (ja) * 2021-05-19 2024-05-21 ジェネンテック, インコーポレイテッド 併用療法
TW202317104A (zh) * 2021-06-25 2023-05-01 美商賽迪拉治療股份有限公司 Tead抑制劑及其用途
KR20240046891A (ko) * 2021-08-12 2024-04-11 티와이케이 메디슨즈, 인코포레이티드 다환 화합물 및 그의 용도
KR20240055778A (ko) 2021-09-01 2024-04-29 노파르티스 아게 Tead 억제제를 포함하는 제약 조합물 및 암의 치료를 위한 이의 용도
WO2023057371A1 (en) 2021-10-04 2023-04-13 Basilea Pharmaceutica International Ag, Allschwil 1,2,4-oxadiazol-5-one derivatives for the treatment of cancer
WO2023060227A1 (en) 2021-10-07 2023-04-13 Ikena Oncology, Inc. Tead inhibitors and uses thereof
CN113861061A (zh) * 2021-10-25 2021-12-31 成都市科隆化学品有限公司 一种不含无机铵盐的氨基酸酰胺盐酸盐及其合成方法
CN114181039A (zh) * 2021-12-23 2022-03-15 凯美克(上海)医药科技有限公司 一种4,4-二苯基-3-丁烯-1-醇的合成方法
EP4452253A4 (en) 2021-12-23 2026-04-15 The Katholieke Univ Leuven 2-PYRAZOLE, ANILINES AND RELATED ANALOGUES TO INHIBIT YAP/TAZ-TEAD
CN119053602A (zh) 2022-01-28 2024-11-29 柏奥艾奇实验室公司 Nlrp3炎性体的n-氧化物抑制剂
AU2023225036A1 (en) * 2022-02-25 2024-07-11 Katholieke Universiteit Leuven Dihydroquinazolinones and related analogs for inhibiting yap/taz-tead
CN114539080A (zh) * 2022-03-02 2022-05-27 八叶草健康产业研究院(厦门)有限公司 一种2-(2-氨基-6-氯苯基)-乙酸钠的制备方法
WO2023173053A1 (en) 2022-03-10 2023-09-14 Ikena Oncology, Inc. Mek inhibitors and uses thereof
WO2023173057A1 (en) 2022-03-10 2023-09-14 Ikena Oncology, Inc. Mek inhibitors and uses thereof
KR20250029773A (ko) * 2022-03-22 2025-03-05 스포로스 바이오디스커버리, 인크. Tead 억제제 및 사용 방법
US11878958B2 (en) 2022-05-25 2024-01-23 Ikena Oncology, Inc. MEK inhibitors and uses thereof
KR20250034120A (ko) * 2022-07-06 2025-03-10 비비디온 테라퓨틱스, 인코포레이티드 Wrn 헬리케이스 억제제를 포함하는 약제학적 조성물
CN119968359A (zh) 2022-09-29 2025-05-09 英矽智能科技知识产权有限公司 Tead抑制剂及其使用方法
WO2024092116A1 (en) 2022-10-26 2024-05-02 Ikena Oncology, Inc. Combination of tead inhibitors and egfr inhibitors and uses thereof
US20240197715A1 (en) 2022-11-18 2024-06-20 Novartis Ag Pharmaceutical combinations and uses thereof
WO2024173761A1 (en) 2023-02-17 2024-08-22 Ikena Oncology, Inc. Combinations comprising mek inhibitors for use in the treatment of cancer
EP4669319A1 (en) 2023-02-23 2025-12-31 Novartis AG TEAD AND HER2 INHIBITOR COMBINATIONS FOR CANCER TREATMENT
WO2024176131A1 (en) 2023-02-23 2024-08-29 Novartis Ag Tead- and kras g12d-inhibitor combinations for treating cancer
KR20260029501A (ko) * 2023-05-24 2026-03-04 베액티카 테라퓨틱스 아베 Tead에 대한 결합제로서의 방향족 아미드 및 이의 접합체
WO2025054190A1 (en) * 2023-09-05 2025-03-13 Vivace Therapeutics, Inc. Pharmaceutical formulations and dosing schedules of a yap/taz-tead inhibitor
CN117327007B (zh) * 2023-09-26 2024-09-13 上海陶术生物科技有限公司 一种vt107的制备方法
WO2025101655A1 (en) * 2023-11-08 2025-05-15 Vivace Therapeutics, Inc. Compounds for modulating yap-tead/hippo pathway
WO2025141118A1 (en) 2023-12-27 2025-07-03 Institut National de la Santé et de la Recherche Médicale Arylalkyloxyindole compounds and derivatives and their use
US12509459B2 (en) 2024-03-26 2025-12-30 BioAge Labs, Inc. Inhibitors of NLRP3 inflammasome
WO2025215527A2 (en) 2024-04-10 2025-10-16 Novartis Ag Pharmaceutical combinations and uses thereof

Family Cites Families (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL135495A (en) 1995-09-28 2002-12-01 Hoechst Ag Intermediate compounds for the preparation of quinoline-converted amines - 2 - carboxylic acid
AU6279598A (en) 1997-02-18 1998-09-08 Neurocrine Biosciences, Inc. Biazacyclic CRF antagonists
PL341364A1 (en) 1997-12-22 2001-04-09 Upjohn Co 4-hydroxyqinoline-3-carboxamides and hydrazides as antiviral agents
IT1303123B1 (it) * 1998-10-13 2000-10-30 Rotta Research Lab Derivati basici di benz(e)isoindol-1-oni e pirrolo(3,4-c)chinolin-1-oni ad attivita' 5ht3 antagonista, loro preparazione ed
WO2000075145A1 (en) 1999-06-03 2000-12-14 Abbott Laboratories Cell adhesion-inhibiting antiinflammatory compounds
AUPQ841300A0 (en) 2000-06-27 2000-07-20 Fujisawa Pharmaceutical Co., Ltd. New aminoalcohol derivatives
US7067532B2 (en) 2000-11-02 2006-06-27 Astrazeneca Substituted quinolines as antitumor agents
FR2827599A1 (fr) * 2001-07-20 2003-01-24 Neuro3D Composes derives de quinoleine et quinoxaline,preparation et utilisations
US7544699B2 (en) 2003-08-08 2009-06-09 Transtech Pharma, Inc. Aryl and heteroaryl compounds, compositions, and methods of use
WO2005082865A1 (ja) 2004-02-27 2005-09-09 Astellas Pharma Inc. 縮合二環性ピリミジン誘導体
WO2006080477A1 (en) 2005-01-25 2006-08-03 Tanabe Seiyaku Co., Ltd. Norvaline derivative and method for preparation thereof
BRPI0707302B8 (pt) 2006-01-27 2021-05-25 Fibrogen Inc compostos de cianoisoquinolina que atuam no dano tecidual associado com isquemia, hipóxia e anemia, bem como composição farmacêutica que os compreende
WO2007097929A1 (en) 2006-02-16 2007-08-30 Fibrogen, Inc. Compounds and methods for treatment of stroke
UY30183A1 (es) 2006-03-02 2007-10-31 Astrazeneca Ab Derivados de quinolina
WO2008023157A1 (en) 2006-08-21 2008-02-28 Argenta Discovery Limited Nitrogen containing heterocyclic compounds useful as m3-receptor modulators
AR065093A1 (es) * 2007-02-05 2009-05-13 Merck Frosst Canada Ltd Compuestos farmacéuticos inhibidores de la biosintesis de leucotrienos
CN101679357A (zh) * 2007-05-09 2010-03-24 辉瑞大药厂 取代的杂环衍生物及其组合物和作为抗菌剂的药物用途
US20100254942A1 (en) * 2007-08-03 2010-10-07 Biotron Limited Hepatitis c antiviral compositions and methods
EA019869B1 (ru) 2007-11-28 2014-06-30 Дана Фарбер Кансер Инститьют, Инк. Низкомолекулярные миристатные ингибиторы тирозинкиназы bcr-abl и способы их применения
WO2009075826A1 (en) 2007-12-07 2009-06-18 Fibrogen, Inc. Methods for increasing white blood cells
KR20120006016A (ko) * 2009-04-06 2012-01-17 다이이찌 산쿄 가부시키가이샤 치환 페닐기를 갖는 고리형 화합물
JP2012524800A (ja) * 2009-04-22 2012-10-18 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ モノアシルグリセロールリパーゼ阻害剤としてのアゼチジニルジアミド
EP2588455B1 (en) * 2010-07-02 2018-04-04 Gilead Sciences, Inc. 2-quinolinyl-acetic acid derivatives as hiv antiviral compounds
BR112013009828A2 (pt) 2010-10-22 2016-07-26 Janssen Pharmaceutica Nv diamidas de amino-pirrolidina-azetidina como inibidores de monoacilglicerol lipase
CA2743391A1 (en) * 2011-05-27 2012-11-27 Queen's University At Kingston Compounds and methods for catalytic directed ortho substitution of aromatic amides and esters
IN2014CN03234A (https=) * 2011-11-03 2015-07-03 Merck Sharp & Dohme
US9012443B2 (en) 2011-12-07 2015-04-21 Amgen Inc. Bicyclic aryl and heteroaryl sodium channel inhibitors
EP2858635A1 (en) 2012-06-11 2015-04-15 The Regents of The University of California Inhibitors of hippo-yap signaling pathway
EP3219706A1 (en) 2012-07-16 2017-09-20 Fibrogen, Inc. Process for making isoquinoline compounds
CN105163727B (zh) * 2013-05-03 2018-08-17 豪夫迈·罗氏有限公司 刺激神经发生的异喹啉衍生物
US20140336182A1 (en) 2013-05-13 2014-11-13 Amgen Inc. Aurora Kinase Modulators and Method of Use
US9776995B2 (en) 2013-06-12 2017-10-03 Amgen Inc. Bicyclic sulfonamide compounds as sodium channel inhibitors
US9452986B2 (en) 2014-02-06 2016-09-27 Abbvie Inc. 6-heteroaryloxy- or 6-aryloxy-quinoline-2-carboxamides and method of use
SG11201607973XA (en) 2014-03-24 2016-11-29 Guangdong Zhongsheng Pharmaceutical Co Ltd Quinoline derivatives as smo inhibitors
CA2974078A1 (en) 2015-01-20 2016-07-28 Millennium Pharmaceuticals, Inc. Quinazoline and quinoline compounds and uses thereof
EP3156404A1 (en) 2015-10-15 2017-04-19 Inventiva New compounds inhibitors of the yap/taz-tead interaction and their use in the treatment of malignant mesothelioma
MA53943A (fr) 2015-11-20 2021-08-25 Vitae Pharmaceuticals Llc Modulateurs de ror-gamma
WO2018028591A1 (zh) 2016-08-09 2018-02-15 殷建明 一种喹啉衍生物及其用途
US11629220B2 (en) 2017-08-21 2023-04-18 Drexel Unversity Renewable furan based amine curing agents for epoxy thermoset
CN117402114A (zh) 2018-01-26 2024-01-16 埃克塞里艾克西斯公司 用于治疗激酶依赖性病症的化合物
EP3746135A4 (en) 2018-01-30 2022-03-09 Foghorn Therapeutics Inc. METHODS AND COMPOUNDS FOR TREATMENT OF DISEASE
KR20210108367A (ko) 2018-11-09 2021-09-02 비바체 테라퓨틱스, 인크. 비시클릭 화합물
MX2021012638A (es) 2019-04-16 2022-01-04 Vivace Therapeutics Inc Compuestos biciclicos.
WO2022087008A1 (en) 2020-10-21 2022-04-28 Vivace Therapeutics, Inc. Tertiary carboxamide compounds

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