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Synthesis and Docking Study of Novel Pyranocoumarin Derivatives

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Abstract

A new series of fused tricyclic coumarin derivatives were designed, synthesized by a simple and convenient method, starting from 4-hydroxycoumarin and virtually screened by molecular docking on the target protein 3FRZ (PDB ID: 3FRZ), a HCV RNA-dependent RNA polymerase, for potency against hepatitis C virus (HCV). Efficient binding to the target protein was found for most of the synthesized compounds.

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ACKNOWLEDGMENTS

The authors are grateful to Koneru Lakshmaiah Education Foundation, Green Fields, Vaddeswaram, Guntur (Dist.), Andhra Pradesh, India for providing all the required facilities and the financial support.

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Correspondence to M. V. Basaveswara Rao.

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Karteek, S.D., Reddy, A.G., Tej, M.B. et al. Synthesis and Docking Study of Novel Pyranocoumarin Derivatives. Russ J Org Chem 57, 272–282 (2021). https://doi.org/10.1134/S1070428021020196

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