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NEW SUBSTITUTED HYDROXAMIC ACID DERIVATIVE WITH HDAC (HISTONE DEACETYLASE) INHIBITING ACTIVITY

机译:具有HDAC(组氨酸硬脂酸)抑制活性的新的取代羟基乙酸衍生物

摘要

PROBLEM TO BE SOLVED: To provide a new carcinostatic and therapeutic agent for immunological disease having HDAC (Histone Deacetylase) inhibiting activity.;SOLUTION: The invention relates to the substituted hydroxamic acid derivative represented by general formula (1) and its pharmaceutically permissible salt and its hydrate [in the formula, A is a nitrogen or carbon atom, B and D are each the same or different carbonyl group or methylene group, E is a CH=CH group, a CH2-CH2 group or O-CH2 group, F is a (substituted)phenyl group, a phenethyl group, a 3-phenylpropyl group, a cyclohexyl group, a naphthyl group, etc.].;COPYRIGHT: (C)2007,JPO&INPIT
机译:解决的问题:提供一种具有HDAC(组蛋白脱乙酰基酶)抑制活性的新的用于免疫疾病的抗癌和治疗剂。解决方案:本发明涉及由通式(1)表示的取代的异羟肟酸衍生物及其药学上允许的盐和其水合物[式中,A为氮或碳原子,B和D分别为相同或不同的羰基或亚甲基,E为CH = CH基,CH 2 -CH 2 基团或O-CH 2 基团,F为(取代)苯基,苯乙基,3-苯丙基,环己基,萘基,等等];版权:(C)2007,日本特许厅&INPIT

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