Abstract

Nine tannins, including gallo- and ellagitannins, were evaluated as potential inhibitors of HIV replication. 1,3,4-Tri-O-galloylquinic acid [1], 3,5-di-O-galloyl-shikimic acid [2], 3,4,5-tri-O-galloylshikimic acid [3], punicalin [6], and punicalagin [7] inhibited HIV replication in infected H9 lymphocytes with little cytotoxicity. Two compounds, punicalin and punicacortein C [8], inhibited purified HIV reverse transcriptase with ID50 of 8 and 5 microM, respectively. Further studies with H9 lymphocytes indicated that chebulagic acid [5] and punicalin did not inactivate virus directly. However, 1,3,4-tri-O-galloylquinic acid and 3,5-di-O-galloylshikimic acid were more effective inhibitors under those conditions. All tannins appear to inhibit virus-cell interactions. Thus, inspite of their anti-RT activity, the mechanism by which tannins inhibit HIV may not be associated with this enzyme.

Keywords

Reverse transcriptaseReplication (statistics)VirologyHuman immunodeficiency virus (HIV)Viral replicationBiologyLymphocyteLentivirusViral diseaseVirusImmunologyBiochemistryRNAGene

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Year
1990
Type
article
Volume
53
Issue
3
Pages
587-595
Citations
169
Access
Closed

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Gen-ichiro Nonaka, Itsuo Nishioka, Makoto Nishizawa et al. (1990). Anti-Aids Agents, 2: Inhibitory Effect of Tannins on HIV Reverse Transcriptase and HIV Replication in H9 Lymphocyte Cells. Journal of Natural Products , 53 (3) , 587-595. https://doi.org/10.1021/np50069a008

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DOI
10.1021/np50069a008