抗菌活性
珊瑚
立体化学
化学
假交替单胞菌
绿脓素
最小抑制浓度
微生物学
细菌
生物
体外
生物化学
生态学
遗传学
群体感应
16S核糖体RNA
毒力
基因
作者
Shaobo Zhu,Yuan-Min Chang,Ming‐Zhi Su,Li‐Gong Yao,Song‐Wei Li,Hong Wang,Yue‐Wei Guo
出处
期刊:Marine Drugs
[MDPI AG]
日期:2024-01-20
卷期号:22 (1): 50-50
被引量:3
摘要
Five new cembrane-type diterpenes, lobocalines A–E (1–5), and four new steroids, lobocaloids A–D (9–12), along with six known related compounds (6–8 and 13–15) were isolated from the Yalong Bay soft coral Lobophytum catalai Tixier-Durivault. The structures of the new compounds were elucidated by extensive spectroscopic analysis, NMR calculation with DP4+ analysis, time-dependent density functional theory–electronic circular dichroism (TDDFT-ECD) calculations, X-ray diffraction analyses and comparison with the reported spectroscopic data of known compounds. Further, with the aid of X-ray diffraction analysis, the structure of lobocrasol B (15) was firmly revised as 15a. In in vitro bioassays, compound 2 showed moderate antibacterial activities against fish pathogenic bacteria Streptococcus parauberis KSP28 and Phoyobacterium damselae FP2244 with minimum inhibitory concentration (MIC) values of 8.7 and 17.3 µg/mL, respectively. All the steroids exhibited antibacterial activities against the S. parauberis KSP28 with MIC values ranging from 12.3 to 53.6 µg/mL. Compounds 2, 7 and 14 have remarkable inhibitory effects on the hemolysin production of Staphylococcus aureus, while compounds 8–12 have medium inhibitory effects on the pyocyanin production in Pseudomonas aeruginosa.
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