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沙蚕毒素内酯 A,一种开环脱碳的海鞘烷内酯,以及沙蚕毒素内酯 B-I,八种具有抗血栓活性的多氧化海鞘烷内酯,来自南海软珊瑚 Sarcophyton cinereum。

Sarcocinerenolides A, an open-loop decarbonizing cembranolide, and sarcocinerenolides B-I, eight polyoxygenated cembranolides with anti-thrombotic activity from the South China Sea soft coral Sarcophyton cinereum.

机构信息

Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, PR China.

Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, PR China; College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao, 266100, PR China.

出版信息

Phytochemistry. 2024 Jul;223:114109. doi: 10.1016/j.phytochem.2024.114109. Epub 2024 Apr 30.

Abstract

A previously undescribed open-loop decarbonizing cembranolide, sarcocinerenolide A, and eight undescribed cembranolides, sarcocinerenolides B-I, characterized by poly-membered oxygen ring fragments were isolated from the soft coral Sarcophyton cinereum collected from the South China Sea. The structures and absolute configurations of these previously undescribed compounds were precisely determined by analysis of NMR data, DP4+ and ECD spectra. The bioactivities of the compounds were evaluated using zebrafish models and sarcocinerenolides C and H exhibited anti-thrombotic activity.

摘要

从南海采集的软珊瑚 Sarcophyton cinereum 中分离得到一种以前未描述的开环脱碳酸cembranolide,即 sarcocinerenolide A,以及八种以前未描述的cembranolide,即 sarcocinerenolides B-I,其特征是具有多成员含氧环片段。通过分析 NMR 数据、DP4+和 ECD 光谱,精确确定了这些以前未描述的化合物的结构和绝对构型。使用斑马鱼模型评估了化合物的生物活性,结果表明 sarcocinerenolide C 和 H 具有抗血栓活性。

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