南海软珊瑚和海绵中具有结构多样性的生物活性甾体。

IF 4.9 2区 医学 Q1 CHEMISTRY, MEDICINAL
Marine Drugs Pub Date : 2025-01-13 DOI:10.3390/md23010036
Lin-Mao Ke, Zi-Ru Zhang, Song-Wei Li, Yan-Bo Zeng, Ming-Zhi Su, Yue-Wei Guo
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引用次数: 0

摘要

从南海软珊瑚Lobophytum sp.和海绵Xestospongia sp.中分离到5个甾体化合物,包括2个新化合物(1和4)和1个已知天然产物(3)。化合物1-3来源于软珊瑚Lobophytum sp.,化合物4和5来源于海绵Xestospongia sp.。采用时变密度泛函理论-电子圆二色性(TDDFT-ECD)计算方法,并与文献中报道的光谱数据进行比较。对分离得到的化合物进行体外抗菌和抗炎活性评价。化合物1 ~ 3、4、5对耐万古霉素的屎肠球菌G1、副金黄色链球菌KSP28、豆selae光杆菌FP2244、garvieae乳球菌FP5245和铜绿假单胞菌ZJ028表现出较弱的抑菌活性。此外,化合物3通过抑制脂多糖(LPS)诱导的RAW 264.7细胞NO生成,显示出显著的抗炎活性,IC50值为13.48 μM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bioactive Steroids with Structural Diversity from the South China Sea Soft Coral Lobophytum sp. and Sponge Xestospongia sp.

A chemical investigation of the soft coral Lobophytum sp. and the sponge Xestospongia sp. from the South China Sea led to the isolation of five steroids, including two new compounds (1 and 4) and one known natural product (3). Compounds 1-3 were derived from the soft coral Lobophytum sp., while 4 and 5 were obtained from the sponge Xestospongia sp. The structures of these compounds were determined by extensive spectroscopic analysis, the time-dependent density functional theory-electronic circular dichroism (TDDFT-ECD) calculation method, and comparison with the spectral data previously reported in the literature. The antibacterial and anti-inflammatory activities of isolated compounds were evaluated in vitro. Compounds 1-3, 4, and 5 exhibited weak antibacterial activity against vancomycin-resistant Enterococcus faecium G1, Streptococcus parauberis KSP28, Photobacterium damselae FP2244, Lactococcus garvieae FP5245, and Pseudomonas aeruginosa ZJ028. Moreover, compound 3 showed significant anti-inflammatory activity by inhibiting lipopolysaccharide (LPS)-induced NO production in RAW 264.7 cells, with an IC50 value of 13.48 μM.

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来源期刊
Marine Drugs
Marine Drugs 医学-医药化学
CiteScore
9.60
自引率
14.80%
发文量
671
审稿时长
1 months
期刊介绍: Marine Drugs (ISSN 1660-3397) publishes reviews, regular research papers and short notes on the research, development and production of drugs from the sea. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible, particularly synthetic procedures and characterization information for bioactive compounds. There is no restriction on the length of the experimental section.
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