JP2017510660A5 - - Google Patents

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Publication number
JP2017510660A5
JP2017510660A5 JP2017504608A JP2017504608A JP2017510660A5 JP 2017510660 A5 JP2017510660 A5 JP 2017510660A5 JP 2017504608 A JP2017504608 A JP 2017504608A JP 2017504608 A JP2017504608 A JP 2017504608A JP 2017510660 A5 JP2017510660 A5 JP 2017510660A5
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JP
Japan
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alkenyl
alkyl
compound according
compound
aryl
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JP2017504608A
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English (en)
Japanese (ja)
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JP2017510660A (ja
JP6726658B2 (ja
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Priority claimed from PCT/US2015/025084 external-priority patent/WO2015157504A1/en
Publication of JP2017510660A publication Critical patent/JP2017510660A/ja
Publication of JP2017510660A5 publication Critical patent/JP2017510660A5/ja
Application granted granted Critical
Publication of JP6726658B2 publication Critical patent/JP6726658B2/ja
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JP2017504608A 2014-04-11 2015-04-09 ヒストン脱アセチル化酵素阻害剤 Active JP6726658B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201461978606P 2014-04-11 2014-04-11
US61/978,606 2014-04-11
PCT/US2015/025084 WO2015157504A1 (en) 2014-04-11 2015-04-09 Histone deacetylase inhibitors

Publications (3)

Publication Number Publication Date
JP2017510660A JP2017510660A (ja) 2017-04-13
JP2017510660A5 true JP2017510660A5 (cg-RX-API-DMAC10.html) 2018-05-31
JP6726658B2 JP6726658B2 (ja) 2020-07-22

Family

ID=54288395

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017504608A Active JP6726658B2 (ja) 2014-04-11 2015-04-09 ヒストン脱アセチル化酵素阻害剤

Country Status (6)

Country Link
US (1) US10246455B2 (cg-RX-API-DMAC10.html)
EP (1) EP3129373B1 (cg-RX-API-DMAC10.html)
JP (1) JP6726658B2 (cg-RX-API-DMAC10.html)
CN (1) CN107001354B (cg-RX-API-DMAC10.html)
TW (1) TWI573787B (cg-RX-API-DMAC10.html)
WO (1) WO2015157504A1 (cg-RX-API-DMAC10.html)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3268358A1 (en) 2015-03-13 2018-01-17 Forma Therapeutics, Inc. Alpha-cinnamide compounds and compositions as hdac8 inhibitors
WO2017004274A2 (en) * 2015-06-29 2017-01-05 Nantbioscience, Inc. Compositions and methods of rit1 inhibition
MA44334A (fr) 2015-10-29 2018-09-05 Novartis Ag Conjugués d'anticorps comprenant un agoniste du récepteur de type toll
CN105622605B (zh) * 2016-03-01 2017-10-13 苏州艾缇克药物化学有限公司 一种5‑溴‑7‑氮杂吲哚的合成方法
TWI659949B (zh) * 2016-05-16 2019-05-21 臺北醫學大學 組蛋白去乙醯酶6抑制劑及其用途
CN107011238B (zh) * 2017-03-14 2020-05-01 北京化工大学 一类组蛋白去乙酰化酶抑制剂及其制备方法和用途
EP3615025A4 (en) * 2017-04-26 2020-11-25 The Board of Trustees of the University of Illionis NRF AND HIF ACTIVATORS / HDAC INHIBITORS AND THERAPEUTIC METHODS USING THEM
CN109705015B (zh) * 2017-10-25 2022-05-24 成都先导药物开发股份有限公司 组蛋白去乙酰化酶抑制剂及其制备方法与用途
CN108794469A (zh) * 2018-04-28 2018-11-13 通化师范学院 一种吡咯化合物的合成新工艺及抗肿瘤作用的用途
CN115636774B (zh) * 2022-12-01 2023-12-22 南开大学 一种贝利司他的合成方法

Family Cites Families (17)

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US4288595A (en) * 1980-04-24 1981-09-08 American Home Products Corporation 7-(Substituted)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamines
GB0305142D0 (en) * 2003-03-06 2003-04-09 Eisai London Res Lab Ltd Synthesis
GB0318254D0 (en) * 2003-08-04 2003-09-10 Northwick Park Inst For Medica Therapeutic delivery of carbon monoxide
WO2005013691A1 (en) 2003-08-04 2005-02-17 Hemocorm Limited Use of boranocarbonates for the therapeutic delivery of carbon monoxide
WO2006050076A1 (en) * 2004-10-29 2006-05-11 Janssen Pharmaceutica, N.V. Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders
CA2615105A1 (en) 2005-07-14 2007-01-25 Takeda San Diego, Inc. Histone deacetylase inhibitors
US20110288070A1 (en) * 2008-05-05 2011-11-24 ROGERS Kathryn Methods for treating cognitive disorders using inhibitors of histone deacetylase
EP2456757B1 (en) * 2009-07-22 2019-05-01 The Board of Trustees of the University of Illionis Hdac inhibitors and therapeutic methods using the same
WO2011019634A2 (en) * 2009-08-10 2011-02-17 Taipei Medical University Aryl substituted sulfonamide compounds and their use as anticancer agents
DK2506716T3 (en) * 2009-12-01 2017-09-04 Abbvie Inc HIS UNKNOWN TRICYCLIC RELATIONS
CA2787784A1 (en) 2010-01-29 2011-08-04 Dana-Farber Cancer Institute, Inc. Small molecules for the modulation of mcl-1 and methods of modulating cell death, cell division, cell differentiation and methods of treating disorders
TWI429628B (zh) * 2010-03-29 2014-03-11 Univ Taipei Medical 吲哚基或吲哚啉基羥肟酸化合物
US9273028B2 (en) * 2010-10-29 2016-03-01 Biogen Ma Inc. Heterocyclic tyrosine kinase inhibitors
CA2825599C (en) * 2011-02-01 2021-07-13 The Board Of Trustees Of The University Of Illinois 4-methyl-n-hydroxybenzamide compounds as histone deacetylase (hdac) inhibitors
EP2771321A4 (en) 2011-10-28 2015-04-08 Chong Kun Dang Pharm Corp HYDROXAMATE DERIVATIVES FOR HDAC INHIBITORS AND PHARMACEUTICAL COMPOSITIONS THEREWITH
WO2013097052A1 (en) * 2011-12-30 2013-07-04 Abbott Laboratories Bromodomain inhibitors
ES2704704T3 (es) * 2013-12-12 2019-03-19 Chong Kun Dang Pharmaceutical Corp Nuevos derivados de azaindol como inhibidores selectivos de la histona desacetilasa (HDAC) y composiciones farmacéuticas que los comprenden

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