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A spiroketal-enol ether derivative from Tanacetum vulgare selectively inhibits HSV-1 and HSV-2 glycoprotein accumulation in Vero cells

A spiroketal-enol ether derivative from Tanacetum vulgare selectively inhibits HSV-1 and HSV-2 glycoprotein accumulation in Vero cells

Álvarez, Ángel L., Habtemariam, Solomon, Moneim, Ahmed, Melón, Santiago, Dalton, Kevin and Parra, Francisco (2015) A spiroketal-enol ether derivative from Tanacetum vulgare selectively inhibits HSV-1 and HSV-2 glycoprotein accumulation in Vero cells. Antiviral Research, 119. pp. 8-18. ISSN 0166-3542 (Print), 1872-9096 (Online) (doi:https://doi.org/10.1016/j.antiviral.2015.04.004)

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Abstract

The inhibitory effects of Tanacetum vulgare rhizome extracts on HSV-1 and HSV-2 in vitro replication were assessed. Unlike extracts obtained from the aerial parts, adsorption inhibition and virucidal activities seemed not to be relevant for the observed antiviral action of tansy rhizome extracts. Instead, the most significant effects were the inhibition of virus penetration and a novel mechanism consisting of the specific arrest of viral gene expression and consequently the decrease of viral protein accumulation within infected cells. Through a bioactivity-guided fractionation protocol we isolated and identified the spiroketal-enol ether derivative (E)-2-(2,4-hexadiynyliden)-1,6-dioxaspiro[4.5]dec-3-ene as the active compound responsible for this inhibitory effect.

Item Type: Article
Uncontrolled Keywords: Antiviral, HSV, Tanacetum, Tansy, Rhizome, Spiroketals
Faculty / School / Research Centre / Research Group: Faculty of Engineering & Science
Faculty of Engineering & Science > School of Science (SCI)
Last Modified: 15 Jul 2020 02:30
URI: http://gala.gre.ac.uk/id/eprint/13404

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