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• W2969343304 startingPage "111635" @default.
• W2969343304 abstract "The discovery of novel potent neuraminidase (NA) inhibitors remains an attractive approach for treating infectious diseases caused by influenza. In this study, we describe the design and synthesis of novel N-substituted oseltamivir derivatives for probing the 150-cavity which is nascent to the activity site of NA. NA inhibitory studies showed that new derivatives demonstrated the inhibitory activity with IC50 values at nM level against NA of a clinical influenza virus strain. Moreover, the in silico ADME predictions showed that the selected compounds had comparable properties with oseltamivir carboxylate, which demonstrated the druggablity of these derivatives. Furthermore, molecular docking studies showed that the most potent compound 6f and 10i could adopt different modes of binding interaction with NA, which may provide novel solutions for treating oseltamivir-resistant influenza. Based on the research results, we consider that compounds 6f and 10i have the potential for further studies as novel antiviral agents." @default.
• W2969343304 created "2019-08-29" @default.
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• W2969343304 date "2019-11-01" @default.
• W2969343304 modified "2023-09-27" @default.
• W2969343304 title "Novel N-Substituted oseltamivir derivatives as potent influenza neuraminidase inhibitors: Design, synthesis, biological evaluation, ADME prediction and molecular docking studies" @default.
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• W2969343304 doi "https://doi.org/10.1016/j.ejmech.2019.111635" @default.
• W2969343304 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31493744" @default.
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