| Literature DB >> 25462237 |
Surender Singh Jadav1, Barij Nayan Sinha1, Rolf Hilgenfeld2, Boris Pastorino3, Xavier de Lamballerie4, Venkatesan Jayaprakash5.
Abstract
A series of arylalkylidene derivatives of 1,3-thiazolidin-4-one (1-20) were synthesized and tested for their antiviral activity against chikungunya virus (LR2006_OPY1) in Vero cell culture by CPE reduction assay. Five compounds (7-9, 16 and 19) were identified to have anti-ChikV activity at lower micro molar concentration. The compounds 7, 8, 9, 16 and 19 inhibited the virus at 0.42, 4.2, 3.6, 40.1 and 6.8 μM concentrations respectively. Molecular docking simulation has been carried out using the available X-ray crystal structure of the ChikV nsp2 protease, in order to elucidate the possible mechanism of action. Interaction of ligands with ChikV nsp2 protease (PDB Code: 3TRK) suggested the possible mechanism of protease inhibition to act as potent anti-ChikV agents.Entities:
Keywords: Antiviral; Chikungunya virus; Molecular docking; Thiazolidinone; nsp2 protease
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Year: 2014 PMID: 25462237 DOI: 10.1016/j.ejmech.2014.10.042
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514