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ECSP17064695A - Compuestos y composiciones de alfa-cinamida como inhibidores de hdac8 - Google Patents

Compuestos y composiciones de alfa-cinamida como inhibidores de hdac8

Info

Publication number
ECSP17064695A
ECSP17064695A ECIEPI201764695A ECPI201764695A ECSP17064695A EC SP17064695 A ECSP17064695 A EC SP17064695A EC IEPI201764695 A ECIEPI201764695 A EC IEPI201764695A EC PI201764695 A ECPI201764695 A EC PI201764695A EC SP17064695 A ECSP17064695 A EC SP17064695A
Authority
EC
Ecuador
Prior art keywords
compositions
cinamide
alpha
inhibitors
hdac8 inhibitors
Prior art date
Application number
ECIEPI201764695A
Other languages
English (en)
Inventor
Pui Yee Ng
Cuixian Liu
Aleksandra Rudnitskaya
Mary-Margaret Zablocki
Kenneth W Bair
Matthew W Martin
Jennifer R Thomason
David R Lancia
Bingsong Han
Nicholas Barczak
Xiaozhang Zheng
Original Assignee
Forma Therapeutics Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Forma Therapeutics Inc filed Critical Forma Therapeutics Inc
Publication of ECSP17064695A publication Critical patent/ECSP17064695A/es

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
    • C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
    • C07C259/06—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/14—Radicals substituted by nitrogen atoms
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    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
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    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
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Abstract

La presente invención se refiere a inhibidores de histona deacetilasas, en particular HDAC8, que son útiles para el tratamiento de cáncer y otras enfermedades y trastornos, así como la síntesis y aplicaciones de dichos inhibidores.
ECIEPI201764695A 2015-03-13 2017-10-02 Compuestos y composiciones de alfa-cinamida como inhibidores de hdac8 ECSP17064695A (es)

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BR112017019453A2 (pt) 2015-03-13 2018-05-15 Forma Therapeutics Inc compostos e composições de alfa-cinamida como inibidores de hdac8
WO2017030892A1 (en) 2015-08-14 2017-02-23 Reaction Biology Corp. Histone deacetylase inhibitors and methods for use thereof
TW201711999A (zh) 2015-09-03 2017-04-01 佛瑪治療公司 ﹝６，６﹞稠合雙環組蛋白脫乙醯基酶８（ｈｄａｃ８）抑制劑
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
US20180127386A1 (en) 2016-10-20 2018-05-10 Forma Therapeutics, Inc. Methods using hdac11 inhibitors
CN107056631A (zh) * 2017-04-14 2017-08-18 六盘水师范学院 一种基于Heck反应的2‑烯基苯胺类化合物制备方法
US11230524B2 (en) * 2017-08-17 2022-01-25 Standard Llc Myocyte enhancer factor 2 (MEF2) modulators
US11535607B2 (en) 2018-04-20 2022-12-27 Valo Health, Inc. Isoindolines as HDAC inhibitors
JP2021522324A (ja) * 2018-04-20 2021-08-30 ヴァロ アーリー ディスカバリー， インコーポレイテッド Ｈｄａｃ阻害剤としてのイソインドリン
KR102055369B1 (ko) * 2018-08-09 2019-12-12 충북대학교 산학협력단 신규한 3/4-((치환된 벤즈아미도페녹시)메틸)-n-히드록시 벤즈아미드/프로펜아미드 화합물 및 이의 용도
CN113015735B (zh) * 2018-12-06 2024-06-21 诺华股份有限公司 用于诱导软骨发生以治疗关节损害的5-羟基-7-氧杂双环[2.2.1]庚烷-2-甲酰胺衍生物
CN113493407B (zh) * 2020-04-03 2025-01-28 中国医学科学院药物研究所 一种吡啶类化合物及其制法和药物用途
CN111728961B (zh) * 2020-08-05 2021-06-15 牡丹江医学院 一种用于治疗老年痴呆的药物组合物及其用途
CN114605304A (zh) * 2020-12-04 2022-06-10 杭州中美华东制药有限公司 一种(±)-2-(4-(1-氧代异吲哚-2-基)苯基)丁酸乙酯的合成方法
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