化学
吡唑
选择性
立体化学
酶
抑制性突触后电位
分子模型
基因亚型
组合化学
生物化学
基因
心理学
神经科学
催化作用
作者
Franco Chimenti,Rossella Fioravanti,Adriana Bolasco,Fedele Manna,Paola Chimenti,Daniela Secci,Francesca Rossi,Paola Turini,Francesco Ortuso,Stefano Alcaro,Maria Cristina Cardia
标识
DOI:10.1016/j.ejmech.2007.12.026
摘要
A series of N1-propanoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives were synthesized and assayed as inhibitors of MAO-A and MAO-B isoforms. Most of the tested compounds showed inhibitory activity with micromolar values and MAO-A selectivity. In addition a computational work was carried out on the most selective compound 3b to highlight the most relevant interactions in the mechanism of recognition within both the MAO-A and the MAO-B enzyme active sites.
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