Author: Jo, Seri; Kim, Hyojin; Kim, Suwon; Shin, Dong Hae; Kim, Miâ€Sun
Title: Characteristics of flavonoids as potent MERSâ€CoV 3Câ€like protease inhibitors Cord-id: fzcuu4ma Document date: 2019_9_12
ID: fzcuu4ma
Snippet: Middle East respiratory syndromeâ€coronavirus (MERSâ€CoV) is a zoonotic virus transmitted between animals and human beings. It causes MERS with high mortality rate. However, no vaccine or specific treatment is currently available. Since antiviral activity of some flavonoids is known, we applied a flavonoid library to probe inhibitory compounds against MERSâ€CoV 3Câ€like protease (3CLpro). Herbacetin, isobavachalcone, quercetin 3â€Î²â€dâ€glucoside and helichrysetin were found to block the
Document: Middle East respiratory syndromeâ€coronavirus (MERSâ€CoV) is a zoonotic virus transmitted between animals and human beings. It causes MERS with high mortality rate. However, no vaccine or specific treatment is currently available. Since antiviral activity of some flavonoids is known, we applied a flavonoid library to probe inhibitory compounds against MERSâ€CoV 3Câ€like protease (3CLpro). Herbacetin, isobavachalcone, quercetin 3â€Î²â€dâ€glucoside and helichrysetin were found to block the enzymatic activity of MERSâ€CoV 3CLpro. The binding of the four flavonoids was also confirmed independently using a tryptophanâ€based fluorescence method. The systematic comparison of the binding affinity of flavonoids made it possible to infer their scaffolds and functional groups required to bind with MERSâ€CoV 3CLpro. An inducedâ€fit docking analysis revealed that S1 and S2 sites play a role in interaction with flavonoids. The experimental and computational study showed that flavonol and chalcone are favourite scaffolds to bind with the catalytic site of MERSâ€CoV 3CLpro. It was also deduced that some flavonoid derivatives with hydrophobic or carbohydrate attached to their core structures have a good inhibitory effect. Therefore, we suggest that flavonoids with these characteristics can be used as templates to develop potent MERSâ€CoV 3CLpro inhibitors.
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