Design, synthesis and anti-HIV integrase evaluation of N-(5-chloro-8- hydroxy-2-styrylquinolin-7-yl)benzenesulfonamide derivatives

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Abstract

Styrylquinoline derivatives are demonstrated to be HIV-1 integrase inhibitors. On the basis of our previous CoMFA analysis of a series of styrylquinoline derivatives, N-[(2-substituted-styryl)-5-chloro-8- hydroxyquinolin-7-yl]-benzenesulfonamide derivatives were designed and synthesized,and their possible HIV IN inhibitory activity was evaluated. © 2010 by the authors.

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Jiao, Z. G., He, H. Q., Zeng, C. C., Tan, J. J., Hu, L. M., & Wang, C. X. (2010). Design, synthesis and anti-HIV integrase evaluation of N-(5-chloro-8- hydroxy-2-styrylquinolin-7-yl)benzenesulfonamide derivatives. Molecules, 15(3), 1903–1917. https://doi.org/10.3390/molecules15031903

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