Add time:08/18/2019         Source:sciencedirect.com

A series of new quinolone-3-carboxylic acids featuring a hydroxyl group at C-5 position were synthesized and evaluated for their in vitro activity against HIV in C8166 cell culture. All the compounds showed anti-HIV-1 activity with low micromolar to submicromolar EC50 values. The most active compound 2k exhibited activity against wild-type HIV-1 with an EC50 value of 0.13 μΜ. Preliminary structure–activity relationship of the newly synthesized quinolone analogues was also investigated. Further docking study revealed that the anti-HIV activity of these compounds might involve a two-metal chelating mechanism.

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