化学
立体化学
结构-活动关系
化学合成
氨基苯甲酸
生物活性
体外
生物化学
药物化学
作者
José G. Trujillo‐Ferrara,Leticia Montoya Cano,L. Michel Espinoza-Fonseca
标识
DOI:10.1016/s0960-894x(03)00198-7
摘要
The synthesis, acetylcholinesterase inhibitory capacity and structure-activity relationships of simple-structured m-Aminobenzoic acid derivatives are reported. Compound 1b was found to be more potent than galanthamine and tacrine in inhibiting acetylcholinesterase.
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