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印度尼西亚软珊瑚 Sinularia sp. 的多羟基甾醇及其对法尼醇 X 激活受体的作用。

Polyhydroxylated sterols from the Indonesian soft coral Sinularia sp. and their effect on farnesoid X-activated receptor.

机构信息

Dipartimento di Chimica delle Sostanze Naturali, Università di Napoli Federico II, Via D. Montesano 49, 80131 Napoli, Italy.

出版信息

Steroids. 2012 Apr;77(5):433-40. doi: 10.1016/j.steroids.2011.12.026. Epub 2012 Jan 10.

Abstract

Chemical investigation of the Indonesian soft coral Sinularia sp. resulted in the isolation of three known (1, 2 and 7) and five new (3-6 and 8) sterols, characterized by either 24-methylcholestane or gorgostane skeletons. The stereostructures of the new compounds have been elucidated by application of HR-MS and 2D NMR techniques. The isolated steroids have been evaluated for their interaction with the farnesoid X-activated receptor (FXR) and some of them, including the new compound 3 and gorgosterol (7), showed a consistent antagonistic activity, potentially useful for the treatment of cholestasis. The FXR antagonistic activity of gorgosterol (7) was also supported by gene expression experiments. Our results represent the first evaluation of soft coral steroids for interaction with nuclear receptors and qualify gorgosterol (7) as a new chemotype of FXR antagonist.

摘要

从印度尼西亚软珊瑚 Sinularia sp. 中提取的化学成分研究,分离得到三种已知(1、2 和 7)和五种新的(3-6 和 8)甾醇,其特征为 24-甲基胆甾烷或高利甾烷骨架。通过高分辨质谱和二维 NMR 技术,解析了新化合物的立体结构。对分离得到的甾体化合物进行了法尼醇 X 受体(FXR)相互作用的评估,其中包括新化合物 3 和高利甾醇(7)在内的一些化合物表现出一致的拮抗活性,可能对治疗胆汁淤积症有用。高利甾醇(7)的 FXR 拮抗活性也得到了基因表达实验的支持。我们的研究结果首次评估了软珊瑚甾体化合物与核受体的相互作用,并将高利甾醇(7)确定为 FXR 拮抗剂的一种新化学型。

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