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来自海南海绵 Septosa 皮海绵的倍半萜。

Sesquiterpenes from the Hainan Sponge Dysidea septosa.

作者信息

Huang Xiao-Chun, Li Jia, Li Zhen-Yu, Shi Lei, Guo Yue-Wei

机构信息

State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, People's Republic of China.

出版信息

J Nat Prod. 2008 Aug;71(8):1399-403. doi: 10.1021/np8002035. Epub 2008 Jul 16.

Abstract

Five new sesquiterpenes, named lingshuiolides A (1) and B (2), lingshuiperoxide (6), isodysetherin (10), and spirolingshuiolide (12), along with several known related analogues (7- 9, 11, and 13- 15), were isolated from the Hainan marine sponge Dysidea septosa. The structures of new compounds 1, 2, 6, 10, and 12 were determined by detailed analysis of 1D and 2D NMR spectra and by comparison with related model compounds. The absolute configuration of lingshuiolide B (2) was established by using the modified Mosher's method. Spirolingshuiolide (12) represents the first example of a sesquiterpene with a rearranged drimane skeleton. Compounds 7- 9 and 15 exhibited significant inhibitory activity against human protein tyrosine phosphatase 1B (hPTP1B), an enzyme involved in the regulation of insulin signaling. In particular, 15 showed the most potent effect, with an IC 50 value of 1.9 microg/mL.

摘要

从海南海洋海绵隔指海绵(Dysidea septosa)中分离出了5种新的倍半萜,分别命名为陵水内酯A(1)和B(2)、陵水过氧化物(6)、异去醚萜(10)和螺旋陵水内酯(12),以及几种已知的相关类似物(7 - 9、11和13 - 15)。通过对一维和二维核磁共振谱的详细分析并与相关模型化合物进行比较,确定了新化合物1、2、6、10和12的结构。采用改良的莫舍尔法确定了陵水内酯B(2)的绝对构型。螺旋陵水内酯(12)是具有重排杜松烷骨架的倍半萜的首个实例。化合物7 - 9和15对人蛋白酪氨酸磷酸酶1B(hPTP1B)表现出显著的抑制活性,hPTP1B是一种参与胰岛素信号调节的酶。特别是,15表现出最强的效果,IC50值为1.9微克/毫升。

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