MersV1, Main, Merge, bibRecord, 000670

Characteristics of flavonoids as potent MERS‐CoV 3C‐like protease inhibitors

Identifieur interne : 000670 ( Main/Merge ); précédent : 000669; suivant : 000671

Characteristics of flavonoids as potent MERS‐CoV 3C‐like protease inhibitors

Auteurs : Seri Jo ; Hyojin Kim ; Suwon Kim ; Dong Hae Shin ; Mi-Sun Kim

Source :

Chemical Biology & Drug Design [ 1747-0277 ] ; 2019.

RBID : PMC:7162010

Abstract

Middle East respiratory syndrome‐coronavirus (MERS‐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 MERS‐CoV 3C‐like protease (3CLpro). Herbacetin, isobavachalcone, quercetin 3‐β‐d‐glucoside and helichrysetin were found to block the enzymatic activity of MERS‐CoV 3CLpro. The binding of the four flavonoids was also confirmed independently using a tryptophan‐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 MERS‐CoV 3CLpro. An induced‐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 MERS‐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 MERS‐CoV 3CLpro inhibitors.

Url:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162010

DOI: 10.1111/cbdd.13604
PubMed: 31436895
PubMed Central: 7162010

Links to Exploration step

PMC:7162010

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<p>Middle East respiratory syndrome‐coronavirus (MERS‐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 MERS‐CoV 3C‐like protease (3CLpro). Herbacetin, isobavachalcone, quercetin 3‐β‐<sc>d</sc>
‐glucoside and helichrysetin were found to block the enzymatic activity of MERS‐CoV 3CLpro. The binding of the four flavonoids was also confirmed independently using a tryptophan‐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 MERS‐CoV 3CLpro. An induced‐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 MERS‐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 MERS‐CoV 3CLpro inhibitors.</p>
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Serveur d'exploration MERS

Characteristics of flavonoids as potent MERS‐CoV 3C‐like protease inhibitors

Characteristics of flavonoids as potent MERS‐CoV 3C‐like protease inhibitors

Source :

Abstract

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Le document en format XML

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