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Merck

Catechins containing a galloyl moiety as potential anti-HIV-1 compounds.

Drug discovery today (2012-03-15)
Yali Zhao, Fan Jiang, Ping Liu, Wei Chen, Kejia Yi
RESUMEN

Catechins containing galloyl moieties are important natural antioxidant compounds. In this paper, we review the multiple mechanisms whereby catechins containing a galloyl moiety can target key proteins to inhibit sexual transmission of HIV-1, as well as HIV-1 fusion, HIV-1 reverse transcriptase, HIV-1 integrase and HIV-1 protease. Furthermore, catechins with a galloyl moiety can mediate host cell factors such as nitric oxide synthase, nuclear factor-κB and casein kinase II to inhibit HIV-1 infection. The most significant inhibitory effect is blocking gp120 binding to isolated human CD4+ T cells. The multiple mechanisms underlying the anti-HIV activity of galloyl-containing catechins predict that these catechins could be used as alternative therapies in the treatment of HIV infection.

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Sigma-Aldrich
(−)-Epicatechin gallate, ≥98% (HPLC), from green tea
Epicatechin gallate, primary reference standard