A new nemoralisin-type diterpenoid from <i>Aglaia lawii</i>

A new nemoralisin-type diterpenoid, nemoralisin O (<b>1</b>), along with ten previously identified compounds, was obtained from <i>Aglaia lawii</i> bark. Structural characterisation was performed using various spectroscopic techniques, with a focus on 1D and 2D NMR, and HR-ESI-MS analysis. The absolute stereochemistry of compound <b>1</b> was established by comparing its experimental ECD spectrum with theoretical ECD spectra of all eight possible stereoisomers using TD-DFT calculations, and by evaluating compatibility of calculated <sup>1</sup>H chemical shifts with experimental values using DP4 probability method. The cytotoxic effects of some isolated compounds on HepG2 human liver cancer cells and the inhibition of α-glucosidase were evaluated. Compounds <b>4</b>, <b>5</b>, and <b>6</b> exhibited weak cytotoxicity against HepG2 cells, and showed no inhibitory activity against α-glucosidase (IC<sub>50</sub> &gt; 256 µg/ml).

Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28558512.v1
Primary Topic
Phytochemical compounds biological activities
Type
article
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article

A new nemoralisin-type diterpenoid from Aglaia lawii

Figshare
Phytochemical compounds biological activities
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A new nemoralisin-type diterpenoid from Aglaia lawii

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Abstract

A new nemoralisin-type diterpenoid, nemoralisin O (<b>1</b>), along with ten previously identified compounds, was obtained from <i>Aglaia lawii</i> bark. Structural characterisation was performed using various spectroscopic techniques, with a focus on 1D and 2D NMR, and HR-ESI-MS analysis. The absolute stereochemistry of compound <b>1</b> was established by comparing its experimental ECD spectrum with theoretical ECD spectra of all eight possible stereoisomers using TD-DFT calculations, and by evaluating compatibility of calculated <sup>1</sup>H chemical shifts with experimental values using DP4 probability method. The cytotoxic effects of some isolated compounds on HepG2 human liver cancer cells and the inhibition of α-glucosidase were evaluated. Compounds <b>4</b>, <b>5</b>, and <b>6</b> exhibited weak cytotoxicity against HepG2 cells, and showed no inhibitory activity against α-glucosidase (IC<sub>50</sub> &gt; 256 µg/ml).

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Phytochemical compounds biological activities
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