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HIV-1 integrase inhibition of biscoumarin analogues
Authors:Su Chang-Xiao  Mouscadet Jean-Francois  Chiang Chih-Chia  Tsai Hou-Jen  Hsu Ling-Yih
Affiliation:School of Pharmacy, National Defense Medical Center, Taipei 114, Taiwan, ROC.
Abstract:Nineteen biscoumarins bearing free and modified hydroxyl substituents at benzoyloxyphenyl linker have been synthesized by multiple step synthesis. Among these biscoumarins, thirteen were found to be active molecules against HIV-1 integrase (HIV-1 IN). The structure-activity relationship of the nineteen compounds on HIV IN may be useful for the design of potent therapeutic agents.
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