Identification of pyrazole derivative as an antiviral agent against chikungunya through HTVS

Surender Singh Jadav, Barij Nayan Sinha, Boris Pastorino, Xavier De Lamballerie, Rolf Hilgenfeld, Venkatesan Jayaprakash*

*Korrespondierende/r Autor/-in für diese Arbeit
14 Zitate (Scopus)

Abstract

Structure based High-throughput Virtual Screening (HTVS) of ChikV nsP2 protease (PDB: 3TRK) with two publicly available database ZINC12 and BindingDB has been carried out to identify suitable inhibitors for the treatment of chikungunya infection. HTVS protocol implemented in GLIDE 5.0 (Schrodinger LLC) has been employed to screen the drug-like subset of ZINC12 (10,090,210) and protease inhibitors in BindingDB (83,000). One of the chemical scaffolds from the list of different chemical classes was selected for the synthesis of (ZINC04725220, compound 11). Few more schiff's bases (13-21) were also synthesized with the intermediate 1,3-diphenyl-1H-pyrazole-4-carbaldehyde (4-6) and tested for anti-ChikV (strain OPY1, Reunion Island 2006) activity using Cytopathic effect reduction (CPE) assay. Surprisingly, only compound 11(IC50: 5..g/ml ie 14.15 ..M) has shown inhibitory activity against ChikV. Further precise docking of compound 11 with target protein was carried out to understand the molecular interactions important for activity.

OriginalspracheEnglisch
ZeitschriftLetters in Drug Design and Discovery
Jahrgang12
Ausgabenummer4
Seiten (von - bis)292-301
Seitenumfang10
ISSN1570-1808
DOIs
PublikationsstatusVeröffentlicht - 2015

Strategische Forschungsbereiche und Zentren

  • Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)

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