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Chalcones as novel influenza A (H1N1) neuraminidase inhibitors from Glycyrrhiza inflata

tetano

Editor, Senior Moderator
Bioorg Med Chem Lett. 2010 Nov 5. [Epub ahead of print]
Chalcones as novel influenza A (H1N1) neuraminidase inhibitors from Glycyrrhiza inflata.

Dao TT, Nguyen PH, Lee HS, Kim E, Park J, Lim SI, Oh WK.

BK21 Project Team, College of Pharmacy, Chosun University, 375 Seosuk-dong, Dong-gu, Gwangju 501-759, Republic of Korea.
Abstract

The emergence of highly pathogenic influenza A virus strains, such as the new H1N1 swine influenza (novel influenza), represents a serious threat to global human health. During our course of an anti-influenza screening program on natural products, one new licochalcone G (1) and seven known (2-8) chalcones were isolated as active principles from the acetone extract of Glycyrrhiza inflata. Compounds 3 and 6 without prenyl group showed strong inhibitory effects on various neuraminidases from influenza viral strains, H1N1, H9N2, novel H1N1 (WT), and oseltamivir-resistant novel H1N1 (H274Y) expressed in 293T cells. In addition, the efficacy of oseltamivir with the presence of compound 3 (5μM) was increased against H274Y neuraminidase. This evidence of synergistic effect makes this inhibitor to have a potential possibility for control of pandemic infection by oseltamivir-resistant influenza virus.
Copyright ? 2010 Elsevier Ltd. All rights reserved.

PMID: 21123068 [PubMed - as supplied by publisher]

http://www.ncbi.nlm.nih.gov/pubmed/21123068
 
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