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水苏碱型水溶性生物碱具有潜在的抗神经炎症活性,来源于苦参的种子。

Water-soluble matrine-type alkaloids with potential anti-neuroinflammatory activities from the seeds of Sophora alopecuroides.

机构信息

Institute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou 510632, People's Republic of China.

Guangdong Clinical Translational Center for Targeted Drug, Department of Pharmacology, School of Medicine, Jinan University, Guangzhou 510632, People's Republic of China.

出版信息

Bioorg Chem. 2021 Nov;116:105337. doi: 10.1016/j.bioorg.2021.105337. Epub 2021 Sep 11.

Abstract

A phytochemical investigation on the alkaloids from water-soluble part of Sophora alopecuroides led to obtain forty matrine-type alkaloids (1-40) including eighteen new ones (1-18), which covers almost all positions of the oxygen substitution in matrine-type structure. Notably, eight compounds (1-8) belong to rare bis-amide matrine-type alkaloid. The new structures were determined based on extensive spectroscopic data, electronic circular dichroism (ECD) calculations, and six instances, verified by X-ray crystallography. Most of isolates showed anti-neuroinflammatory activities based on the expression of tumor necrosis factor (TNF)-α and interleukin (IL)-6 in BV2 microglia cells. Especially, compound 39 can suppress those two mediator secretions in a dose-dependent manner with IC values of 21.6 ± 0.5 and 16.7 ± 0.8 μM, respectively. Further mechanistic study revealed that 39 suppressed the phosphorylation of IκBα and p65 subunit to regulate the NF-κB signaling pathway.

摘要

从苦参水溶性部分的生物碱进行植物化学研究,得到了四十个苦参碱型生物碱(1-40),包括十八个新化合物(1-18),几乎涵盖了苦参碱型结构中所有位置的氧取代。值得注意的是,有八个化合物(1-8)属于罕见的双酰胺苦参碱型生物碱。新结构是基于广泛的光谱数据、电子圆二色性(ECD)计算和六个实例,通过 X 射线晶体学验证确定的。大多数分离物基于 TNF-α和 IL-6 在 BV2 小胶质细胞中的表达,显示出抗神经炎症活性。特别是,化合物 39 可以以剂量依赖的方式抑制这两种介质的分泌,IC 值分别为 21.6±0.5 和 16.7±0.8 μM。进一步的机制研究表明,39 抑制 IκBα和 p65 亚基的磷酸化,以调节 NF-κB 信号通路。

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