Antipoliovirus Flavonoids from Psiadia Dentata

Author:

Robin Valérie1,Irurzun Alicia2,Amoros Maryvonne1,Boustie Joël1,Carrasco Luis2

Affiliation:

1. UPRES, Pharmacochimie de Molécules de Synthèse et de Substances Naturelles, Faculté de Pharmacie, Rennes, France

2. Centro de Biología Molecular, Facultad de Ciencias, Universidad Autónoma de Madrid-CSIC, Madrid, Spain

Abstract

The search for antiviral agents against vesicular stomatitis virus, herpes simplex virus type 1 and poliovirus type 2 in plants extracts, led to the isolation of two antipoliovirus flavonoids from the medicinal plant Psiadia dentata (Cass.) DC, Asteraceae: 3-methylkaempferol and 3,4′-dimethylkaempferol. The antipoliovirus activity of both compounds was estimated by comparison with 3-methylquercetin, guanidine and Ro-090179. The most potent inhibitor of poliovirus replication was 3-methylkaempferol, and therefore we investigated its mechanism of action. We showed, using the inhibition of [3H]uridine incorporation in viral RNA and performing a dot-blot with one RNA probe specific for the poliovirus genomic strand RNA, that 3-methylkaempferol inhibits the genomic RNA synthesis of poliovirus.

Publisher

SAGE Publications

Reference31 articles.

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4. 3-methylquercetin is a potent and selective inhibitor of poliovirus RNA synthesis

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