蛹虫草甾醇a - c,抗炎C30麦角甾醇与6/6/6/5/6-融合环系统。

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL
Zhi-Ang Chen, Hong-Fei Li, Shan-Shan Huang, Tian Jin, Wen-Zhe Xie, Juan He, Tao Feng
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引用次数: 0

摘要

蛹虫草是一种珍贵的食药用菌。其化学成分和生物活性已成为人们关注的焦点。在本研究中,从这种真菌中分离出三种不同寻常的C30麦角甾醇,虫草甾醇A-C(1-3)。它们的结构已经根据广泛的光谱方法以及计算量子化学来确定。它们具有不寻常的6/6/6/5/6-融合五环体系,这可能是由正常麦角甾醇主链通过添加两个骨架碳而得到的。化合物1 ~ 3对一氧化氮的生成具有显著的抑制活性,最大抑制浓度分别为3.0 μM、0.9 μM和2.3 μM。在5 μM浓度下可显著抑制肿瘤坏死因子-α和白细胞介素-6的分泌,提示蛹虫草及其虫草甾醇a - c具有潜在的抗炎应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cordycepsterols A-C, Anti-Inflammatory C30 Ergosterols with a 6/6/6/5/6-Fused Ring System from Cordyceps militaris.

Cordyceps militaris is a valuable edible and medicinal fungus. Its chemical composition and biological activity have become the focus of attention. In this study, three unusual C30 ergosterols, cordycepsterols A-C (1-3), have been isolated from this fungus. Their structures have been identified according to extensive spectroscopic methods as well as computational quantum chemistry. They possess an unusual 6/6/6/5/6-fused pentacyclic system which might be derived from a normal ergosterol backbone by adding two skeletal carbons. Compounds 1-3 exhibit significant inhibitory activity against nitric oxide production with half maximal inhibitory concentration values of 3.0, 0.9, and 2.3 μM, respectively. They could significantly suppress the secretion of tumor necrosis factor-α and interleukin-6 at the concentration of 5 μM, which indicated that C. militaris and its cordycepsterols A-C have a potential anti-inflammatory application prospect.

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来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
期刊介绍: The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin. When new compounds are reported, manuscripts describing their biological activity are much preferred. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
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