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• W2093623643 abstract "A series of twenty 2-aryl-4H-chromen-4-one (flavones) derivatives (3a–3s) were synthesized and tested for hMAO inhibitory activity. Fifteen compounds (3a, 3c, 3e–3h, 3j–3p, 3r, 3s) were found to be selective towards MAO-B, while 3d was selective towards MAO-A, and 3b, 3i and 3q were non-selective. Experimental Selectivity Index for MAO-B ranges from 2.0 (3g, 3p) to 30.0 (3j). Compound 3j, which is carrying 3,4-di-OMeC6H3 groups at R position on the molecule, was found to be potent MAO-B inhibitor amongst the fifteen with Ki value for MAO-B of 0.16 ± 0.01 μM comparable to that of standard drug, Selegiline (Ki for MAO-B is 0.16 ± 0.01 μM). Compound 3j also appeared as the most selective MAO-B inhibitor according to its best selectivity index (30.0), which is comparable to that of Selegiline (SIMAO-B = 35.0). Molecular docking and molecular dynamics simulation studies were carried out using Autodock-4.0 and Amber12 to understand the molecular level interaction and energy relation of MAO isoforms with selective inhibitors (3d and 3j). Simulation results are in good agreement with the experimental results. Leads identified may further be explored to develop potent isoform specific inhibitors of MAO." @default.
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• W2093623643 date "2015-02-01" @default.
• W2093623643 modified "2023-09-28" @default.
• W2093623643 title "Monoamine oxidase inhibitory activity of 2-aryl-4H-chromen-4-ones" @default.
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• W2093623643 doi "https://doi.org/10.1016/j.bioorg.2014.11.008" @default.
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