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
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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 (https=) 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 (https=)
EP (1) EP2958565A4 (https=)
JP (1) JP2016508521A (https=)
KR (1) KR20150119390A (https=)
CN (1) CN105073117A (https=)
AU (1) AU2014219042A1 (https=)
BR (1) BR112015019818A2 (https=)
CA (1) CA2901493A1 (https=)
IL (1) IL240612A0 (https=)
MX (1) MX2015010407A (https=)
RU (1) RU2015139700A (https=)
SG (1) SG11201506450RA (https=)
WO (1) WO2014130534A1 (https=)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015138500A1 (en) 2014-03-11 2015-09-17 Icahn School Of Medicine At Mount Sinai Sulfonamides derived from tricyclyl-2-aminocycloalkanols as anticancer agents
WO2015138496A1 (en) 2014-03-11 2015-09-17 Icahn School Of Medicine At Mount Sinai Constrained tricyclic sulfonamides
WO2017044575A1 (en) * 2015-09-09 2017-03-16 Icahn School Of Medicine At Mount Sinai Constrained benzhydryl sulfonamides as anticancer and neuroprotective agents
CA2997784A1 (en) * 2015-09-09 2017-03-16 Icahn School Of Medicine At Mount Sinai Heterocyclic constrained tricyclic sulfonamides as anti-cancer agents
CA2997769A1 (en) 2015-09-09 2017-03-16 Icahn School Of Medicine At Mount Sinai Heterocyclic constrained tricyclic sulfonamides as anti-cancer 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
US5834462A (en) 1993-07-26 1998-11-10 Eisai Co., Ltd. Tricyclic heterocyclic sulfonamide and sulfonic ester derivatives
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
PE86199A1 (es) * 1997-06-17 1999-09-24 Schering Corp Sulfonamida inhibidor de la enzima farnesilo transferasa
AU2641899A (en) 1998-02-27 1999-09-15 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
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
AU2006239929B2 (en) 2005-04-22 2011-11-03 Alantos Pharmaceuticals Holding, Inc. Dipeptidyl peptidase-IV inhibitors
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
AU2013305591B2 (en) 2012-08-24 2017-04-13 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
WO2015138500A1 (en) 2014-03-11 2015-09-17 Icahn School Of Medicine At Mount Sinai Sulfonamides derived from tricyclyl-2-aminocycloalkanols as anticancer agents
WO2015138496A1 (en) 2014-03-11 2015-09-17 Icahn School Of Medicine At Mount Sinai Constrained tricyclic sulfonamides

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