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Discovery of Metal Ions Chelator Quercetin Derivatives with Potent Anti-HCV Activities.


ABSTRACT: Analogues or isosteres of ?,?-diketoacid (DKA) 1a show potent inhibition of hepatitis C virus (HCV) NS5B polymerase through chelation of the two magnesium ions at the active site. The anti-HCV activity of the flavonoid quercetin (2) could partly be attributed to it being a structural mimic of DKAs. In order to delineate the structural features required for the inhibitory effect and improve the anti-HCV potency, two novel types of quercetin analogues, 7-O-arylmethylquercetins and quercetin-3-O-benzoic acid esters, were designed, synthesized and evaluated for their anti-HCV properties in cell-based assays. Among the 38 newly synthesized compounds, 7-O-substituted derivative 3i and 3-O-substituted derivative 4f were found to be the most active in the corresponding series (EC50 = 3.8 ?M and 9.0 ??, respectively). Docking studies suggested that the quercetin analogues are capable of establishing key coordination with the two magnesium ions as well as interactions with residues at the active site of HCV NS5B.

SUBMITTER: Zhong D 

PROVIDER: S-EPMC6272327 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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Discovery of Metal Ions Chelator Quercetin Derivatives with Potent Anti-HCV Activities.

Zhong Dongwei D   Liu Mingming M   Cao Yang Y   Zhu Yelin Y   Bian Shihui S   Zhou Jiayi J   Wu Fengjie F   Ryu Kum-Chol KC   Zhou Lu L   Ye Deyong D  

Molecules (Basel, Switzerland) 20150416 4


Analogues or isosteres of α,γ-diketoacid (DKA) 1a show potent inhibition of hepatitis C virus (HCV) NS5B polymerase through chelation of the two magnesium ions at the active site. The anti-HCV activity of the flavonoid quercetin (2) could partly be attributed to it being a structural mimic of DKAs. In order to delineate the structural features required for the inhibitory effect and improve the anti-HCV potency, two novel types of quercetin analogues, 7-O-arylmethylquercetins and quercetin-3-O-be  ...[more]

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