Three undescribed diterpenoids from Pini Lignum Nodi with hepatoprotective activities

Three new abietane-type diterpenes, named pinusins A-C (<b>1</b>-<b>3</b>) were isolated from Pini Lignum Nodi (the dried tuberculate or branched nodes of <i>Pinus massoniana</i> Lamb.), together with five known diterpenoids (<b>4</b>-<b>8</b>), a flavonoid (<b>9</b>) and a monoterpene (<b>10</b>). The structures of these compounds were elucidated based on detailed spectroscopic analyses (1D, 2D NMR, HRESIMS, IR, and UV), while ECD calculations determined their absolute configurations. All compounds were assayed <i>in vitro</i> for their protective activities against acetaminophen (APAP)-induced hepatotoxicity at 10 <i>μ</i>M. Compounds <b>1</b>-<b>4</b>, <b>9</b>, and <b>10</b> experimentally exerted protective effects against APAP-induced HepG2 cell damage.

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Journal
Journal of Asian Natural Products Research
Published
2025-04-04
DOI
https://doi.org/10.1080/10286020.2025.2481289
Primary Topic
Natural product bioactivities and synthesis
Type
article
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article

Three undescribed diterpenoids from Pini Lignum Nodi with hepatoprotective activities

Chuang-Jun Li, Jiaqi Chen, Jie Ma, Dongming Zhang et al.
Journal of Asian Natural Products Research
Natural product bioactivities and synthesis
article

Three undescribed diterpenoids from Pini Lignum Nodi with hepatoprotective activities

Chuang-Jun Li, Jiaqi Chen, Jie Ma, Dongming Zhang, Lingzhi Zhang, Yingda Zang, Hua Sun
article en

Abstract

Three new abietane-type diterpenes, named pinusins A-C (<b>1</b>-<b>3</b>) were isolated from Pini Lignum Nodi (the dried tuberculate or branched nodes of <i>Pinus massoniana</i> Lamb.), together with five known diterpenoids (<b>4</b>-<b>8</b>), a flavonoid (<b>9</b>) and a monoterpene (<b>10</b>). The structures of these compounds were elucidated based on detailed spectroscopic analyses (1D, 2D NMR, HRESIMS, IR, and UV), while ECD calculations determined their absolute configurations. All compounds were assayed <i>in vitro</i> for their protective activities against acetaminophen (APAP)-induced hepatotoxicity at 10 <i>μ</i>M. Compounds <b>1</b>-<b>4</b>, <b>9</b>, and <b>10</b> experimentally exerted protective effects against APAP-induced HepG2 cell damage.

Journal of Asian Natural Products ResearchVol. 27(6)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
Zero hunger
Openalex Percentile: Top 94%
Natural product bioactivities and synthesis
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Three undescribed diterpenoids from Pini Lignum Nodi with hepatoprotective activities — Chuang-Jun Li, Jiaqi Chen, et al. · Journal of Asian Natural Products Research (2025) | TGRS Research Map | TGRS