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卡拉烯——芳香双环倍半萜——来自印度柳珊瑚属 Subergorgia reticulata(埃利斯和索兰德,1786 年)。

Calamenenes--aromatic bicyclic sesquiterpenes--from the Indian gorgonian Subergorgia reticulata (Ellis and Solander, 1786).

机构信息

National Institute of Oceanography, Regional Centre, Council of Scientific and Industrial Research, Kochi 682 018, India.

出版信息

Nat Prod Res. 2011 Jan;25(2):169-74. doi: 10.1080/14786419.2010.495069.

Abstract

Three aromatic sesquiterpene derivatives, (+)-(7R, 10S)-2-methoxy calamenene (1), (+)-(7R, 10S)-2,5-dimethoxy calamenene (2) and (+)-(7R, 10S)-2-methoxy-5-acetoxy calamenene (3) were isolated from the methanol extract of the Indian gorgonian Subergorgia reticulata. Compound 2 has not been previously described in the literature. Compound 3 has not been isolated previously from a natural source. Compounds 1, 2 and 3 showed settlement inhibition activity against cyprids of Balanus amphitrite with EC(50) values of 4.4, 7.8 and 0.03 µg mL(-1), respectively. These compounds also exhibited considerable activity against Artemia nauplii at 50 µg mL(-1), indicative of their potential use as cytotoxic agents.

摘要

从印度柳珊瑚 Subergorgia reticulata 的甲醇提取物中分离得到三种芳香倍半萜衍生物:(+)-(7R,10S)-2-甲氧基菖蒲烯(1)、(+)-(7R,10S)-2,5-二甲氧基菖蒲烯(2)和(+)-(7R,10S)-2-甲氧基-5-乙氧基菖蒲烯(3)。化合物 2 在文献中尚未有过描述。化合物 3 以前从未从天然来源中分离得到。化合物 1、2 和 3 对藤壶幼体表现出抑制附着活性,EC50 值分别为 4.4、7.8 和 0.03 µg mL(-1)。这些化合物在 50 µg mL(-1)时对卤虫无节幼体也表现出相当的活性,表明它们具有作为细胞毒性剂的潜力。

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