DISCOVERY OF H5N1 ENTRY INHIBITORS AND THE SAR STUDY

Yingxia Li Dingding Gao
Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai

We first found that chlorogenin 3-O-b-chacotrioside (1) and its acetate2showed potent inhibitory activity against H5N1 entry. The subsequent search for simplified molecules, ursolate saponin (3) with monosaccharide residue was found to show improved activity.








 




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