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来自泽漆根和茎的瑞香烷二萜类化合物及其抗炎活性。

Lathyrane Diterpenoids From the Roots and Stems of Euphorbia prolifera and Their Anti-inflammatory Activity.

作者信息

Liu Kexin, Xu Yang, Wang Yali, Zhang Zhiqi, Sun Dejuan, Li Hua, Chen Lixia

机构信息

Wuya College of Innovation, Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, China.

Institute of Structural Pharmacology & TCM Chemical Biology, Fujian Key Laboratory of Chinese Materia Medica, College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, China.

出版信息

Chem Biodivers. 2025 Aug;22(8):e202500495. doi: 10.1002/cbdv.202500495. Epub 2025 Apr 26.

Abstract

Euphorbia prolifera, classified under the genus Euphorbia within the Euphorbiaceae family, is a perennial herbaceous plant. This plant exhibits a distinct biogeographical preference, with its natural populations predominantly located in the eastern and southeastern territories of the Asian continent. The roots and stems of E. prolifera have been investigated as a rich source of diterpenoids, and 12 lathyrane diterpenoids, including three previously undescribed ones, were isolated. Their structures were determined by analysing spectroscopic data (one- and two-dimensional nuclear magnetic resonance), and high-resolution electrospray ionization mass spectrometry, and by comparing them with previously published data. Meanwhile, all the compounds were evaluated for in vitro anti-inflammatory bioactivities. The findings indicated that compound 8 exhibited superior inhibitory effects compared with the positive control drug (dexamethasone) on nitric oxide production in lipopolysaccharide-induced RAW264.7 cells with a minimum inhibitory concentration value of 3.95 ± 0.49 µM. Using target screening and molecular docking technology, it is hypothesized that compound 8 may play an anti-inflammatory role by combining with human Filamin-B.

摘要

泽漆隶属于大戟科大戟属,是一种多年生草本植物。这种植物表现出明显的生物地理偏好,其天然种群主要分布在亚洲大陆的东部和东南部地区。泽漆的根和茎已被研究作为二萜类化合物的丰富来源,从中分离出了12种赖百当二萜类化合物,其中包括3种先前未描述的化合物。通过分析光谱数据(一维和二维核磁共振)、高分辨率电喷雾电离质谱,并与先前发表的数据进行比较,确定了它们的结构。同时,对所有化合物进行了体外抗炎生物活性评估。研究结果表明,化合物8在脂多糖诱导的RAW264.7细胞中对一氧化氮产生的抑制作用优于阳性对照药物(地塞米松),最低抑制浓度值为3.95±0.49µM。利用靶点筛选和分子对接技术,推测化合物8可能通过与人细丝蛋白B结合发挥抗炎作用。

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