JP2016508521A5 - - Google Patents

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Publication number
JP2016508521A5
JP2016508521A5 JP2015558219A JP2015558219A JP2016508521A5 JP 2016508521 A5 JP2016508521 A5 JP 2016508521A5 JP 2015558219 A JP2015558219 A JP 2015558219A JP 2015558219 A JP2015558219 A JP 2015558219A JP 2016508521 A5 JP2016508521 A5 JP 2016508521A5
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JP
Japan
Prior art keywords
group
compound
substituted
formula
represented
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
JP2015558219A
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English (en)
Japanese (ja)
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JP2016508521A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2014/017127 external-priority patent/WO2014130534A1/en
Publication of JP2016508521A publication Critical patent/JP2016508521A/ja
Publication of JP2016508521A5 publication Critical patent/JP2016508521A5/ja
Pending legal-status Critical Current

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JP2015558219A 2013-02-19 2014-02-19 抗腫瘍剤としての三環式複素環 Pending JP2016508521A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361766387P 2013-02-19 2013-02-19
US61/766,387 2013-02-19
PCT/US2014/017127 WO2014130534A1 (en) 2013-02-19 2014-02-19 Tricyclic heterocycles as anticancer agents

Publications (2)

Publication Number Publication Date
JP2016508521A JP2016508521A (ja) 2016-03-22
JP2016508521A5 true JP2016508521A5 (enExample) 2017-03-23

Family

ID=51391756

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015558219A Pending JP2016508521A (ja) 2013-02-19 2014-02-19 抗腫瘍剤としての三環式複素環

Country Status (13)

Country Link
US (2) US9796717B2 (enExample)
EP (1) EP2958565A4 (enExample)
JP (1) JP2016508521A (enExample)
KR (1) KR20150119390A (enExample)
CN (1) CN105073117A (enExample)
AU (1) AU2014219042A1 (enExample)
BR (1) BR112015019818A2 (enExample)
CA (1) CA2901493A1 (enExample)
IL (1) IL240612A0 (enExample)
MX (1) MX2015010407A (enExample)
RU (1) RU2015139700A (enExample)
SG (1) SG11201506450RA (enExample)
WO (1) WO2014130534A1 (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015138496A1 (en) 2014-03-11 2015-09-17 Icahn School Of Medicine At Mount Sinai Constrained tricyclic sulfonamides
US9937186B2 (en) 2014-03-11 2018-04-10 Icahn School Of Medicine At Mount Sinai Sulfonamides derived from tricyclyl-2-aminocycloalkanols as anticancer agents
WO2017044567A1 (en) 2015-09-09 2017-03-16 Icahn School Of Medicine At Mount Sinai Heterocyclic constrained tricyclic sulfonamides as anti-cancer agents
CA2997784A1 (en) 2015-09-09 2017-03-16 Icahn School Of Medicine At Mount Sinai Heterocyclic constrained tricyclic 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
WO2023164940A1 (zh) * 2022-03-04 2023-09-07 中国福利会国际和平妇幼保健院 氮杂吩噻嗪类化合物及其在制备治疗子宫内膜癌的药物中的应用

Family Cites Families (18)

* 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
JP2002507192A (ja) * 1997-06-17 2002-03-05 シェーリング コーポレイション ファルネシルタンパク質トランスフェラーゼの新規三環式スルホンアミドインヒビター
WO1999043683A1 (en) * 1998-02-27 1999-09-02 Eisai Co., Ltd. Heterocycle-fused benzothiazine derivatives
AR031612A1 (es) * 2000-09-20 2003-09-24 Schering Corp Imidazoles sustituidos, composiciones farmaceuticas, metodo para su preparacion y el uso de los mismos para preparar un medicamento como agonistas o antagonistas h1 y h3 de histamina
TW200400816A (en) 2002-06-26 2004-01-16 Lilly Co Eli Tricyclic steroid hormone nuclear receptor modulators
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
BRPI0608469A2 (pt) 2005-04-22 2010-01-05 Alantos Pharmaceuticals Holding Inc inibidores de dipeptidil peptidase-iv
GB0508992D0 (en) 2005-05-03 2005-06-08 Novartis Ag Organic compounds
HK1198384A1 (en) 2011-08-16 2015-04-17 Mt. Sinai School Of Medicine Tricyclic compounds as anticancer agents
WO2014031986A1 (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
WO2015138496A1 (en) 2014-03-11 2015-09-17 Icahn School Of Medicine At Mount Sinai Constrained tricyclic sulfonamides
US9937186B2 (en) 2014-03-11 2018-04-10 Icahn School Of Medicine At Mount Sinai Sulfonamides derived from tricyclyl-2-aminocycloalkanols as anticancer agents

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