Additional Bioactive Silvestrol Analogs from the Rootsof <i>Aglaia perviridis</i> Collected in Vietnam

The tropical plant <i>Aglaia perviridis</i> is known to produce cyclopenta[<i>b</i>]benzofuran and other types of rocaglate derivatives including silvestrol (<b>3</b>) and 5‴-episilvestrol (<b>4</b>) that are of current pharmacological interest. In the present work, further investigation of <i>A. perviridis</i> roots collected in Vietnam has yielded two new rocaglate acetonide derivatives (<b>1</b> and <b>2</b>) and a known pentanor-3,4-<i>seco</i>-dammarane triterpenoid (<b>7</b>) found for the first time as a natural product, in addition to four known rocaglates (<b>3</b>–<b>6</b>). The structures of compounds <b>1</b> and <b>2</b> were confirmed by partial synthesis experiments, and their potential occurrence as extraction artifacts was investigated by targeted selective ion monitoring using UHPLC-MS. All compounds obtained were evaluated against a panel of four human cancer cell lines, in which the six rocaglate derivatives (<b>1</b>–<b>6</b>) tested all showed submicromolar potencies.

Publication Details

Journal
Figshare
Published
2025-03-05
DOI
https://doi.org/10.1021/acs.jnatprod.4c01247.s001
Primary Topic
Phytochemical compounds biological activities
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article
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article

Additional Bioactive Silvestrol Analogs from the Rootsof Aglaia perviridis Collected in Vietnam

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Phytochemical compounds biological activities
article

Additional Bioactive Silvestrol Analogs from the Rootsof Aglaia perviridis Collected in Vietnam

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Abstract

The tropical plant <i>Aglaia perviridis</i> is known to produce cyclopenta[<i>b</i>]benzofuran and other types of rocaglate derivatives including silvestrol (<b>3</b>) and 5‴-episilvestrol (<b>4</b>) that are of current pharmacological interest. In the present work, further investigation of <i>A. perviridis</i> roots collected in Vietnam has yielded two new rocaglate acetonide derivatives (<b>1</b> and <b>2</b>) and a known pentanor-3,4-<i>seco</i>-dammarane triterpenoid (<b>7</b>) found for the first time as a natural product, in addition to four known rocaglates (<b>3</b>–<b>6</b>). The structures of compounds <b>1</b> and <b>2</b> were confirmed by partial synthesis experiments, and their potential occurrence as extraction artifacts was investigated by targeted selective ion monitoring using UHPLC-MS. All compounds obtained were evaluated against a panel of four human cancer cell lines, in which the six rocaglate derivatives (<b>1</b>–<b>6</b>) tested all showed submicromolar potencies.

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Phytochemical compounds biological activities
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