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紫珠中二萜类新化合物及其抗炎活性。

New diterpenoids from Callicarpa dichotoma and their anti-inflammatory activity.

作者信息

Fang Qiaomiao, Zhang Xueer, Feng Minhua, Yang Weiqun, Peng Guangtian, Zhao Zhongxiang, Lin Chaozhan, Zhu Chenchen, Wu Aizhi

机构信息

School of Pharmaceutical Sciences, GuangZhou University of Chinese Medicine, GuangZhou 510006, China.

School of Pharmaceutical Sciences, GuangZhou University of Chinese Medicine, GuangZhou 510006, China.

出版信息

Fitoterapia. 2025 Jul;184:106666. doi: 10.1016/j.fitote.2025.106666. Epub 2025 Jun 7.

DOI:10.1016/j.fitote.2025.106666
PMID:40490086
Abstract

Callicarpa dichotoma is a distinctive herbal plant of the genus Callicarpa. However, research on the phytochemical and pharmacological properties of C. dichotoma is very limited. Presently, three new diterpenoids, named dichotomapene A - C(1-3), along with fourteen known analogues (4-17), were isolated from C. dichotoma. Their structures were elucidated by spectroscopy, quantum chemical electronic circular dichroism (ECD) calculations, and single-crystal X-ray diffraction analysis. Compound 1 was an unusual abietane-type diterpenoid with a five-membered lactone ring formed between C-6 and C-18. The undescribed crystal structures of compounds 4, 6, and 13 were obtained for the first time. The anti-inflammatory activity of six diterpenoids on RAW 264.7 murine macrophages induced by LPS was further investigated by measuring the secretion of nitric oxide (NO). Cytotoxic experiments manifested that compound 14 had significant toxicity on RAW 264.7 cells. Griess assay results indicated that compound 7 displayed the best anti-inflammatory activity among five diterpenoids. Furthermore, molecular docking analysis was conducted to interpret the anti-inflammatory mechanism of 7 interacted with inducible nitric oxide synthase(iNOS). This study is the first investigation of diterpenoids within C. dichotoma.

摘要

紫珠是紫珠属一种独特的草本植物。然而,对紫珠的植物化学和药理特性的研究非常有限。目前,从紫珠中分离出了三种新的二萜类化合物,命名为二歧紫珠素A - C(1 - 3),以及十四种已知类似物(4 - 17)。通过光谱学、量子化学电子圆二色性(ECD)计算和单晶X射线衍射分析对它们的结构进行了阐明。化合物1是一种不寻常的枞烷型二萜类化合物,在C - 6和C - 18之间形成了一个五元内酯环。首次获得了化合物4、6和13未描述的晶体结构。通过测量一氧化氮(NO)的分泌,进一步研究了六种二萜类化合物对脂多糖诱导的RAW 264.7小鼠巨噬细胞的抗炎活性。细胞毒性实验表明化合物14对RAW 264.7细胞具有显著毒性。Griess分析结果表明,化合物7在五种二萜类化合物中表现出最佳的抗炎活性。此外,进行了分子对接分析以解释化合物7与诱导型一氧化氮合酶(iNOS)相互作用的抗炎机制。本研究是对紫珠中二萜类化合物的首次研究。

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