We isolated a new ellagitannin, davicratinic acid A (), together with four known ellagitannins, davidiin (), granatin A (), pedunculagin (), and 3--galloylgranatin A (), from an aqueous acetone extract of dried leaves. The known ellagitannins were identified based on spectroscopic data. The structure of davicratinic acid A (), a monomeric ellagitannin possessing a unique, skew-boat glucopyranose core, was established based on spectroscopic data. Additionally, we examined the effects of several tannins with good yields from this plant on drug-resistant bacteria and human oral squamous cell carcinomas, and found that davidiin () exhibited the most potent antibacterial and antitumor properties among the tannins examined.
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http://dx.doi.org/10.3390/molecules22030470 | DOI Listing |
Molecules
January 2021
Department of Natural Product Chemistry, Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852-8521, Japan.
The aim of this study was to characterize hydrolyzable tannins in Polygonaceous plants, as only a few plants have previously been reported to contain ellagitannins. From , a new hydrolyzable tannin called persicarianin was isolated and characterized to be 3--galloyl-4,6-()-dehydrohexahydroxydiphenoyl-d-glucose. Interestingly, acid hydrolysis of this compound afforded ellagic acid, despite the absence of a hexahydroxydiphenoyl group.
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March 2017
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama 700-8530, Japan.
We isolated a new ellagitannin, davicratinic acid A (), together with four known ellagitannins, davidiin (), granatin A (), pedunculagin (), and 3--galloylgranatin A (), from an aqueous acetone extract of dried leaves. The known ellagitannins were identified based on spectroscopic data. The structure of davicratinic acid A (), a monomeric ellagitannin possessing a unique, skew-boat glucopyranose core, was established based on spectroscopic data.
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