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Pyrrolidine hydroxamic acid derivatives, useful as metalloprotease inhibitors in the treatment of cancers, rheumatic disorders or neuropathological degenerative disorders, e.g. cerebral ischemia or epilepsy

机译:吡咯烷异羟肟酸衍生物,可用作金属蛋白酶抑制剂,用于治疗癌症,风湿性疾病或神经病理性变性疾病,例如脑缺血或癫痫

摘要

Pyrrolidine hydroxamic acid derivatives (I), their optical isomers and salts with acids and bases are new. Pyrrolidine hydroxamic acid derivatives of formula (I), their optical isomers and salts with acids and bases are new. Ar = aryl or heteroaryl; R1 = A, 1-6C alkylene or AXR'1; A = 1-6C alkylene (optionally substituted by one or more OH, 1-6C alkoxy, or 1-6C acyloxy groups); X = O or S; R'1 = H, 1-6C alkyl, aryl 1-6C alkyl or heteroaryl 1-6C alkyl; and R2 , R3, and R4 = H, 1-6C alkyl, or 1-6C alkenyl. An Independent claim is included for the preparation of (I).
机译:吡咯烷异羟肟酸衍生物(I),它们的旋光异构体以及与酸和碱的盐是新的。式(I)的吡咯烷异羟肟酸衍生物,它们的旋光异构体以及与酸和碱的盐是新的。 Ar =芳基或杂芳基; R1 = A,1-6C亚烷基或AXR'1; A = 1-6C亚烷基(任选地被一个或多个OH,1-6C烷氧基或1-6C酰氧基取代); X = O或S; R'1 = H,1-6C烷基,芳基1-6C烷基或杂芳基1-6C烷基; R 2,R 3和R 4 = H,1-6C烷基或1-6C烯基。准备(I)包括独立权利要求。

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