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Lobosteroids A–F: Six New Highly Oxidized Steroids from the Chinese Soft Coral Lobophytum sp.

Authors :
Xia, Zi-Yi
Sun, Man-Man
Jin, Yang
Yao, Li-Gong
Su, Ming-Zhi
Liang, Lin-Fu
Wang, Hong
Guo, Yue-Wei
Source :
Marine Drugs; Aug2023, Vol. 21 Issue 8, p457, 14p
Publication Year :
2023

Abstract

To explore the steroidal constituents of the soft coral Lobophytum sp. at the coast of Xuwen County, Guangdong Province, China, a chemical investigation of the above-mentioned soft coral was carried out. After repeated column chromatography over silica gel, Sephadex LH-20, and reversed-phase HPLC, six new steroids, namely lobosteroids A–F (1–6), along with four known compounds 7–10, were obtained. Their structures were determined by extensive spectroscopic analysis and comparison with the spectral data reported in the literature. Among them, the absolute configuration of 1 was determined by X-ray diffraction analysis using Cu Kα radiation. These steroids were characterized by either the presence of an α,β-α′,β′-unsaturated carbonyl, or an α,β-unsaturated carbonyl moiety in ring A, or the existence of a 5α,8α-epidioxy system in ring B, as well as diverse oxidation of side chains. The antibacterial bioassays showed that all isolated steroids exhibited significant inhibitory activities against the fish pathogenic bacteria Streptococcus parauberis FP KSP28, Phoyobacterium damselae FP2244, and Streptococcus parauberis SPOF3K, with IC<subscript>90</subscript> values ranging from 0.1 to 11.0 µM. Meanwhile, compounds 2 and 6–10 displayed potent inhibitory effects against the vancomycin-resistant Enterococcus faecium bacterium G7 with IC<subscript>90</subscript> values ranging from 4.4 to 18.3 µM. Therefore, ten highly oxidized steroids with strong antibacterial activities were isolated from the Chinese soft coral Lobophytum sp., which could be developed as new chemotypes of antibacterial drug leads. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16603397
Volume :
21
Issue :
8
Database :
Complementary Index
Journal :
Marine Drugs
Publication Type :
Academic Journal
Accession number :
170736889
Full Text :
https://doi.org/10.3390/md21080457