Three new diterpenoids from the aerial parts of <i>Callicarpa macrophylla</i>

Three previously unreported diterpenoids, <i>iso</i>-gaultheric acid (<b>1</b>), 7<i>α</i>-hydroxy-karamatsuic acid (<b>2</b>) and <i>iso</i>-bodinieric acid J (<b>3</b>), along with seven known diterpenoids (<b>4-10</b>), were yielded from the 95% ethanol extract of the aerial parts of <i>Callicarpa macrophylla</i> Vahl. The elucidation of their structure was accomplished through integrated interpretation of physicochemical characteristics combined with multi-spectral investigations, including 1D/2D NMR, ECD and HR-ESI-MS. Anti-inflammatory activity tests were conducted on the compounds <b>3</b>-<b>9</b>, revealing that <b>6</b> inhibited LDH release with an IC<sub>50</sub> value of 14.79 ± 2.69 µM.

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Publication Details

Journal
Natural Product Research
Published
2025-05-22
DOI
https://doi.org/10.1080/14786419.2025.2505602
Primary Topic
Biological Activity of Diterpenoids and Biflavonoids
Type
article
Field-Weighted Citation Impact
0.00

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article

Three new diterpenoids from the aerial parts of Callicarpa macrophylla

Chao Peng, Rong-Shuai Li, Wei‐Lie Xiao, Xingjie Zhang et al.
Natural Product Research
Biological Activity of Diterpenoids and Biflavonoids
article

Three new diterpenoids from the aerial parts of Callicarpa macrophylla

Chao Peng, Rong-Shuai Li, Wei‐Lie Xiao, Xingjie Zhang, Jian-Lin Lai, Xiong Qiu, Xiaoli Li, Liang Gou, Yan-Mei Ning, X. L. Ji
article en

Abstract

Three previously unreported diterpenoids, <i>iso</i>-gaultheric acid (<b>1</b>), 7<i>α</i>-hydroxy-karamatsuic acid (<b>2</b>) and <i>iso</i>-bodinieric acid J (<b>3</b>), along with seven known diterpenoids (<b>4-10</b>), were yielded from the 95% ethanol extract of the aerial parts of <i>Callicarpa macrophylla</i> Vahl. The elucidation of their structure was accomplished through integrated interpretation of physicochemical characteristics combined with multi-spectral investigations, including 1D/2D NMR, ECD and HR-ESI-MS. Anti-inflammatory activity tests were conducted on the compounds <b>3</b>-<b>9</b>, revealing that <b>6</b> inhibited LDH release with an IC<sub>50</sub> value of 14.79 ± 2.69 µM.

Natural Product Research
Yunnan University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 90%
Biological Activity of Diterpenoids and Biflavonoids
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Three new diterpenoids from the aerial parts of <i>Callicarpa macrophylla</i> — Chao Peng, Rong-Shuai Li, et al. · Natural Product Research (2025) | TGRS Research Map | TGRS