JP2018526416A5 - - Google Patents

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Publication number
JP2018526416A5
JP2018526416A5 JP2018512944A JP2018512944A JP2018526416A5 JP 2018526416 A5 JP2018526416 A5 JP 2018526416A5 JP 2018512944 A JP2018512944 A JP 2018512944A JP 2018512944 A JP2018512944 A JP 2018512944A JP 2018526416 A5 JP2018526416 A5 JP 2018526416A5
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JP
Japan
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compound according
hydrogen
alkyl
aryl
haloalkyl
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JP2018512944A
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English (en)
Japanese (ja)
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JP6966425B2 (ja
JP2018526416A (ja
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Priority claimed from PCT/US2016/050685 external-priority patent/WO2017044567A1/en
Publication of JP2018526416A publication Critical patent/JP2018526416A/ja
Publication of JP2018526416A5 publication Critical patent/JP2018526416A5/ja
Application granted granted Critical
Publication of JP6966425B2 publication Critical patent/JP6966425B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2018512944A 2015-09-09 2016-09-08 抗がん剤としての複素環式の限定された三環系スルホンアミド Expired - Fee Related JP6966425B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562216168P 2015-09-09 2015-09-09
US62/216,168 2015-09-09
PCT/US2016/050685 WO2017044567A1 (en) 2015-09-09 2016-09-08 Heterocyclic constrained tricyclic sulfonamides as anti-cancer agents

Publications (3)

Publication Number Publication Date
JP2018526416A JP2018526416A (ja) 2018-09-13
JP2018526416A5 true JP2018526416A5 (enExample) 2019-11-07
JP6966425B2 JP6966425B2 (ja) 2021-11-17

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ID=56940436

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2018512944A Expired - Fee Related JP6966425B2 (ja) 2015-09-09 2016-09-08 抗がん剤としての複素環式の限定された三環系スルホンアミド

Country Status (6)

Country Link
US (1) US10221158B2 (enExample)
EP (1) EP3347350A1 (enExample)
JP (1) JP6966425B2 (enExample)
CN (1) CN108349943A (enExample)
CA (1) CA2997769A1 (enExample)
WO (1) WO2017044567A1 (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017507962A (ja) 2014-03-11 2017-03-23 アイカーン スクール オブ メディスン アット マウント サイナイIcahn School of Medicine at Mt. Sinai 限定された三環式スルホンアミド
WO2015138500A1 (en) 2014-03-11 2015-09-17 Icahn School Of Medicine At Mount Sinai Sulfonamides derived from tricyclyl-2-aminocycloalkanols as anticancer agents
EP3347355B1 (en) 2015-09-09 2022-07-13 Icahn School of Medicine at Mount Sinai Heterotricyclic sulfonamides as anti-cancer agents
WO2021150695A1 (en) * 2020-01-22 2021-07-29 Icahn School Of Medicine At Mount Sinai Constrained n-substituted tetrahydrobenzoazepine sulfonamides as anticancer and neuroprotective agents
WO2021170913A1 (en) * 2020-02-28 2021-09-02 Rappta Therapeutics Oy Tricyclic modulators of pp2a
US12398103B2 (en) * 2020-03-20 2025-08-26 Atux Iskay Llc 3-diarylmethylenes and uses thereof
CN114272378B (zh) * 2020-09-27 2023-06-23 四川大学华西医院 一种使cttnbp2nl功能缺失的试剂在制备治疗疾病的药物中的用途
CN116806217A (zh) * 2021-02-08 2023-09-26 拉帕塔疗法公司 蛋白磷酸酶2a(pp2a)的取代的环状调节剂及其使用方法
EP4288414A1 (en) * 2021-02-08 2023-12-13 Rappta Therapeutics Oy Substituted cyclic modulators of protein phosphatase 2a (pp2a) and methods using same
CN118119607A (zh) * 2021-08-18 2024-05-31 阿图什伊斯卡伊有限责任公司 作为抗癌、抗炎、抗纤维和神经保护剂的2-二芳基甲基-4-氨基四氢吡喃衍生物及相关化合物
AU2023318912A1 (en) * 2022-08-04 2025-03-06 Rappta Therapeutics Oy Aromatic compounds for use as protein phosphatase 2a (pp2a) modulators

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4634766A (en) 1983-10-31 1987-01-06 Merck Frosst Canada, Inc. 1,4-diaza-phenothiazines
GB8510680D0 (en) 1985-04-26 1985-06-05 Smith Kline French Lab Pyridine derivatives
US4882351A (en) 1987-10-14 1989-11-21 Roussel Uclaf Tricyclic compounds
ATE225334T1 (de) 1993-07-26 2002-10-15 Eisai Co Ltd Sulfonamide und sulfonsäure-ester mit je einem trizyclischen heteroring
WO1997030038A1 (en) 1996-02-15 1997-08-21 Mitsubishi Chemical Corporation Diarylsultam derivatives
US6333322B1 (en) 1996-03-13 2001-12-25 Eisai Co., Ltd. Nitrogen-containing tricyclic compounds and drugs containing the same
WO1999043683A1 (en) 1998-02-27 1999-09-02 Eisai Co., Ltd. Heterocycle-fused benzothiazine derivatives
WO2002024657A2 (en) 2000-09-20 2002-03-28 Schering Corporation Substituted imidazoles as dual histamine h1 and h3 agonists or antagonists
JP4428053B2 (ja) 2002-02-05 2010-03-10 味の素株式会社 ガバペンチン若しくはプレガバリンおよびn型カルシウムチャンネル拮抗剤を含有する医薬組成物
TW200400816A (en) 2002-06-26 2004-01-16 Lilly Co Eli Tricyclic steroid hormone nuclear receptor modulators
EP1838690A2 (en) 2004-12-21 2007-10-03 Devgen N.V. Compounds with kv4 ion channel activity
IT1362675B (it) 2005-03-15 2009-06-25 Menarini Internat Operations Luxembourg Sa N-idrossiammidi -sostituiti con gruppi triciclici come inibitori dell'istone deacelitasi,loro preparazione ed impiego in formulazioni farmaceutiche
KR20080000665A (ko) 2005-04-22 2008-01-02 알란토스 파마슈티컬즈 홀딩, 인코포레이티드 디펩티딜 펩티다아제-ⅳ 억제제
GB0508992D0 (en) 2005-05-03 2005-06-08 Novartis Ag Organic compounds
CL2007003244A1 (es) 2006-11-16 2008-04-04 Millennium Pharm Inc Compuestos derivados de pirimido[5,4-d][2]benzazepina; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento del cancer.
WO2008121859A1 (en) 2007-03-30 2008-10-09 Xenon Pharmaceuticals Inc. Methods of using tricyclic compounds in treating sodium channel-mediated diseases or conditions
BR112014003567A2 (pt) * 2011-08-16 2018-08-14 Mt Sinai School Of Medicine composto, uso de um composto, e, composição farmacêutica
CA2882826A1 (en) 2012-08-24 2014-02-27 Board Of Regents Of The University Of Texas System Pro-neurogenic compounds
CN102942562B (zh) 2012-12-05 2014-10-01 天津市斯芬克司药物研发有限公司 一种苯并咪唑衍生物及其制备方法和应用
US9796717B2 (en) 2013-02-19 2017-10-24 Icahn School Of Medicine At Mount Sinai Tricyclic heterocycles as anticancer agents
JP2017507962A (ja) 2014-03-11 2017-03-23 アイカーン スクール オブ メディスン アット マウント サイナイIcahn School of Medicine at Mt. Sinai 限定された三環式スルホンアミド
WO2015138500A1 (en) 2014-03-11 2015-09-17 Icahn School Of Medicine At Mount Sinai Sulfonamides derived from tricyclyl-2-aminocycloalkanols as anticancer agents
US10450282B2 (en) 2015-08-06 2019-10-22 Icahn School Of Medicine At Mount Sinai Stereospecific process for 3-heterocyclylcycloaliphatic-1,2-diols
WO2017044572A1 (en) 2015-09-09 2017-03-16 Icahn School Of Medicine At Mount Sinai Ring constrained diarylamino sulfonamides as anti-cancer agents
EP3347355B1 (en) 2015-09-09 2022-07-13 Icahn School of Medicine at Mount Sinai Heterotricyclic sulfonamides as anti-cancer agents
WO2017044575A1 (en) 2015-09-09 2017-03-16 Icahn School Of Medicine At Mount Sinai Constrained benzhydryl sulfonamides as anticancer and neuroprotective agents
WO2017044571A1 (en) 2015-09-09 2017-03-16 Icahn School Of Medicine At Mount Sinai Tricyclic sultam sulfonamides as anticancer and neuroprotective agents

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