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柳珊瑚 Lobophytum crassum 的细胞毒性和抗炎萜类化合物。

Cytotoxic and anti-inflammatory cembranoids from the soft coral Lobophytum crassum.

机构信息

Department of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung 804, Taiwan, Republic of China.

出版信息

J Nat Prod. 2008 Nov;71(11):1819-24. doi: 10.1021/np8004584. Epub 2008 Oct 30.

Abstract

Five new cembranoids, namely, crassumolides A and B and D-F (1 and 2 and 4-6), along with four known metabolites, 7-10, were isolated from the soft coral Lobophytum crassum. Crassumolide C (3) was isolated for the first time from a natural source. The structures of these compounds were elucidated by extensive spectroscopic analysis and comparison of the NMR data with those of known analogues. The absolute stereochemistry of 1 was determined using the modified Mosher's method. Chemical transformation of 7 into the corresponding methyl ester 3 revealed the absolute stereochemistry of 3. Compounds 1, 3, and 7 were cytotoxic toward Ca9-22 cancer cells, and 10 was broadly cytotoxic toward all six test cancer cell lines used. Compounds 1, 3, 7, and 10 were found to inhibit the accumulation of the pro-inflammatory proteins iNOS and COX-2 at 10 μM.

摘要

从软珊瑚 Lobophytum crassum 中分离得到了 5 种新的海鞘素,分别为 crassumolide A 和 B 以及 D-F(1 和 2 和 4-6),以及 4 种已知代谢产物 7-10。Crassumolide C(3)是首次从天然来源中分离得到的。通过广泛的光谱分析和与已知类似物的 NMR 数据比较,确定了这些化合物的结构。使用改进的 Mosher 法确定了 1 的绝对立体化学。7 转化为相应甲酯 3 的化学转化揭示了 3 的绝对立体化学。化合物 1、3 和 7 对 Ca9-22 癌细胞具有细胞毒性,而化合物 10 对所有 6 种测试的癌细胞系均具有广泛的细胞毒性。发现化合物 1、3、7 和 10 在 10 μM 时可抑制促炎蛋白 iNOS 和 COX-2 的积累。

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