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拉乌因类 A-X:来自毛蕊木巴豆的具有抗炎活性的贝壳杉烷型二萜。

Lauinoids A-X: Labdane-type diterpenoids with anti-inflammatory activity from Croton laui.

机构信息

State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai, 201203, People's Republic of China; University of Chinese Academy of Sciences, No. 19A Yuquan Road, Beijing 100049, People's Republic of China.

Shandong Laboratory of Yantai Drug Discovery, Bohai Rim Advanced Research Institute for Drug Discovery, 198 East Binhai Road, Yantai, Shandong, 264117, People's Republic of China.

出版信息

Phytochemistry. 2024 Jul;223:114138. doi: 10.1016/j.phytochem.2024.114138. Epub 2024 May 16.

DOI:10.1016/j.phytochem.2024.114138
PMID:38762154
Abstract

Croton laui (Euphorbiaceae) is a traditional medicinal plant used by the Li ethnic group in China to treat headaches, stomachaches, and diphtheria. To understand the pharmacological basis of its medicinal use, an extensive investigation of the ethanolic extract of the bark of C. laui was performed. After repeated chromatography, twenty-four undescribed labdane-type diterpenoids, lauinoids A-X (1-24), and five known analogs (25-29) were isolated. Their structures and absolute configurations were established using a combination of spectroscopic analyses, electronic circular dichroism, nuclear magnetic resonance calculations, and single-crystal X-ray diffraction. Among them, compounds 1-3 exhibited an 11(12 → 13)-abeo-16-nor-labdane skeleton, which originated putatively from 9 through a plausible pathway that involves a semipinacol rearrangement process. Compounds 11 and 12 belong to the rare class of 14,15-dinor-labdane diterpenoids. Compounds 18 and 28 exhibited substantial inhibitory effects by suppressing lipopolysaccharide-induced NO production in RAW 264.7 macrophages, with IC values of 3.37 ± 0.23 and 5.82 ± 0.28 μM, respectively. This study has greatly expanded the chemical diversity of labdane diterpenoids from C. laui and will guide future research on this ethnomedicinal plant.

摘要

拉瑞木(大戟科)是中国黎族的传统药用植物,用于治疗头痛、胃痛和白喉。为了了解其药用的药理学基础,对拉瑞木树皮的乙醇提取物进行了广泛的研究。经过反复的色谱分离,从该植物中共分离得到 24 个未描述的贝壳杉烷型二萜类化合物,即 lauinoids A-X(1-24),和 5 个已知的类似物(25-29)。通过光谱分析、电子圆二色性、核磁共振计算和单晶 X 射线衍射的组合,确定了它们的结构和绝对构型。其中,化合物 1-3 表现出 11(12 → 13)-abeo-16-nor-labdane 骨架,推测来源于 9,通过一个可能涉及半频哪醇重排过程的途径。化合物 11 和 12 属于 14,15-二降贝壳杉烷二萜类化合物这一罕见类别。化合物 18 和 28 通过抑制 RAW 264.7 巨噬细胞中脂多糖诱导的 NO 产生,表现出显著的抑制作用,IC 值分别为 3.37 ± 0.23 和 5.82 ± 0.28 μM。本研究极大地扩展了拉瑞木中二萜类化合物的化学多样性,将指导对这种民族药用植物的进一步研究。

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