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作为治疗 2 型糖尿病的胰岛素增敏剂的天然存在的 friedelane 三萜的研究。

Studies of naturally occurring friedelane triterpenoids as insulin sensitizers in the treatment type 2 diabetes mellitus.

机构信息

Instituto Universitario de Bio-Orgánica Antonio González and Departamento de Química Orgánica, Universidad de La Laguna, Avenida Astrofísico Francisco Sánchez 2, 38206 La Laguna, Tenerife, Spain.

出版信息

Phytochemistry. 2012 Dec;84:116-24. doi: 10.1016/j.phytochem.2012.07.025. Epub 2012 Aug 25.

Abstract

Type 2 diabetes mellitus (T2DM) is a rapidly expanding public epidemic and frequently results in severe vascular complications. In an attempt to find anti-diabetic agents, we report herein on the isolation, structural elucidation and bioactivity of nine friedelane-type triterpenes (1-9) and twenty two known ones (10-31) from the root barks of Celastrus vulcanicola and Maytenus jelskii. Their structures were elucidated on the basis of spectroscopic analysis, including 1D and 2D NMR techniques. Two compounds from this series (1 and 3) exhibited increased insulin-mediated signalling, which suggests these friedelane triterpenes have potential therapeutic use in insulin resistant states.

摘要

2 型糖尿病(T2DM)是一种迅速蔓延的公共流行病,常导致严重的血管并发症。为了寻找抗糖尿病药物,我们从 Celastrus vulcanicola 和 Maytenus jelskii 的根皮中分离、鉴定并研究了 9 种新的(1-9)和 22 种已知的(10-31)法呢烷型三萜的结构和生物活性。根据包括 1D 和 2D NMR 技术在内的光谱分析确定了它们的结构。该系列中的两种化合物(1 和 3)表现出增强的胰岛素介导的信号传导,这表明这些法呢烷三萜类化合物在胰岛素抵抗状态下具有潜在的治疗用途。

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