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秦岭海桐中进一步的倍半萜及其抗炎活性。

Further sesquiterpenoids from Pittosporum qinlingense and their anti-inflammatory activity.

机构信息

Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, Yangling 712100, Shaanxi, PR China.

Xi'an Modern Chemistry Research Institute, Xi'an 710065, Shaanxi, PR China.

出版信息

Fitoterapia. 2022 Oct;162:105292. doi: 10.1016/j.fitote.2022.105292. Epub 2022 Sep 5.

DOI:10.1016/j.fitote.2022.105292
PMID:36064153
Abstract

Four new sesquiterpenoid glycoside esters, Pitqinlingoside N-Q (1-4), together with eleven known metabolites (5-15), were isolated from 95% EtOH extract of the twigs, fruits and leaves of P. qinlingense. The structures of new compounds were elucidated on the basis of extensive spectroscopic analyses, including IR, UV, HRMS, NMR and electronic circular dichroism spectra. Unusal glycoside esters are characterized by the presence of polyacylated β-D-fucopyranosyl and β-d-glucopyranosyl units. Pitqinlingoside N (1), O (2), P (3), boscialin (5) and arvoside C (6) showed significant nitric oxide production inhibition in lipopolysaccharide (LPS)-induced BV-2 microglial cells with IC values ranging from 1.58 to 28.74 μM. Structure-activity relationships of the isolated compounds are discussed.

摘要

从秦岭白皮松的嫩枝、果实和叶片的 95%乙醇提取物中分离得到了四个新的倍半萜糖苷酯,即 Pitqinlingoside N-Q(1-4),以及十一个已知的代谢产物(5-15)。新化合物的结构是基于广泛的光谱分析确定的,包括 IR、UV、HRMS、NMR 和电子圆二色谱。不常见的糖苷酯的特点是存在多酰化的β-D-岩藻吡喃糖基和β-d-吡喃葡萄糖基单元。Pitqinlingoside N(1)、O(2)、P(3)、boscialin(5)和 arvoside C(6)在脂多糖(LPS)诱导的 BV-2 小胶质细胞中显示出显著的一氧化氮生成抑制作用,IC 值范围为 1.58 至 28.74 μM。讨论了分离化合物的结构-活性关系。

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