首页> 外国专利> Compound having histone deacetylase-inhibiting activity, and pharmaceutical composition comprising the compound as an active ingredient

Compound having histone deacetylase-inhibiting activity, and pharmaceutical composition comprising the compound as an active ingredient

机译:具有组蛋白脱乙酰基酶抑制活性的化合物以及包含该化合物作为有效成分的药物组合物

摘要

A novel compound having histone deacetylase-inhibiting activity which is a cyclic tetrapeptide derivative represented by the general formula (1) given below and a pharmaceutical composition comprising such compound as an active ingredient. (In the formula, the cyclic tetrapeptide moiety has a known structure; R1 and R2 each independently represents an alkylene group containing 1 to 6 carbon atoms, which may be branched; X represents a group or bond selected from among —CO—, —O—, —S— or —SO—; Y represents a hydrogen or halogen atom, a phenyl group (including a substituted form), a pyridyl group (including a substituted form), an alkyl group (including a halogen-substituted form; hereinafter the same shall apply) containing 1 to 6 carbon atoms, an alkyloxy group containing 1 to 6 carbon atoms, an alkylcarbonyl group containing 1 to 6 carbon atoms, an alkyloxycarbonyl group containing 1 to 6 carbon atoms, an alkylthio group containing 1 to 6 carbon atoms, an alkylthiocarbonyl group containing 1 to 6 carbon atoms or a mono- or dialkylamino group containing 1 to 6 carbon atoms; when Y is a phenyl group (including a substituted form) or a pyridyl group (including a substituted form), it may form a further cyclic structure bound to R2.); embedded image
机译:一种具有组蛋白去乙酰化酶抑制活性的新型化合物,其是由下面给出的通式(1)表示的环状四肽衍生物,以及包含该化合物作为活性成分的药物组合物。 (在该式中,环状四肽部分具有已知的结构; R 1 和R 2 各自独立地表示含有1至6个碳原子的亚烷基,其可以是支链的; X代表选自-CO-,-O-,-S-或-SO-的基团或键; Y代表氢或卤素原子,苯基(包括取代形式),吡啶基(包括取代形式),含有1至6个碳原子的烷基(包括卤素取代形式;以下相同),含有1至6个碳原子的烷氧基,含有1至6个碳原子的烷基羰基,烷氧基羰基含1至6个碳原子的基团,含1至6个碳原子的烷硫基,含1至6个碳原子的烷硫基羰基或含1至6个碳原子的单或二烷基氨基;当Y为苯基时(包括取代形式)或吡啶基(包括取代形式),它可以进一步形成绑定到R 2 的环状结构。); “嵌入式图像”

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