Monoamine oxidase inhibition by selected anilide derivatives

L Legoabe, J Kruger, A Petzer, JJ Bergh…

文献索引：Legoabe, Lesetja; Kruger, Johann; Petzer, Anel; Bergh, Jacobus J.; Petzer, Jacobus P. European Journal of Medicinal Chemistry, 2011 , vol. 46, # 10 p. 5162 - 5174

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被引用次数: 19

摘要

A series of anilide derivatives were synthesized and evaluated as inhibitors of recombinant human monoamine oxidase (MAO) A and B. The most potent inhibitors among the derivatives that were initially evaluated were (2E)-N-(3-chlorophenyl)-3-phenylprop-2- enamide (2c) and (2E)-N-(3-bromophenyl)-3-phenylprop-2-enamide (2d) with IC50 values of 0.53 μM and 0.45 μM, respectively. These derivatives exhibited reversible and selective ...