Suppr超能文献

齐墩果酸及其衍生物:具有细胞活性的新型蛋白酪氨酸磷酸酶1B抑制剂。

Oleanolic acid and its derivatives: new inhibitor of protein tyrosine phosphatase 1B with cellular activities.

作者信息

Zhang Yi-Nan, Zhang Wei, Hong Di, Shi Lei, Shen Qiang, Li Jing-Ya, Li Jia, Hu Li-Hong

机构信息

Shanghai Research Center for Modernization of Traditional Chinese Medicine, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Science, Chinese Academy of Sciences, 199 Guo Shou Jing Road, Shanghai 201203, China.

出版信息

Bioorg Med Chem. 2008 Sep 15;16(18):8697-705. doi: 10.1016/j.bmc.2008.07.080. Epub 2008 Aug 3.

Abstract

Protein tyrosine phosphatase 1B is a key factor in the negative regulation of insulin pathway and a promising target for treatment of diabetes and obesity. Herein, a series of competitive inhibitors were optimized from oleanolic acid, a natural triterpenoid identified against PTP1B by screening libraries of traditional Chinese medicinal herbs. Modifying at 3 and 28 positions, we obtained compound 13 with a K(i) of 130 nM, which exhibited good selectivity between other phosphatases involved in insulin pathway except T-cell protein tyrosine phosphatase. Further evaluation in cell models illustrated that the derivatives enhanced insulin receptor phosphorylation in CHO/hIR cells and also stimulated glucose uptake in L6 myotubes with or addition of without insulin.

摘要

蛋白酪氨酸磷酸酶1B是胰岛素信号通路负调控的关键因子,也是治疗糖尿病和肥胖症的一个有前景的靶点。在此,从齐墩果酸出发优化得到了一系列竞争性抑制剂,齐墩果酸是一种天然三萜类化合物,通过筛选中草药文库鉴定出其对蛋白酪氨酸磷酸酶1B具有活性。通过在3位和28位进行修饰,我们得到了K(i)为130 nM的化合物13,该化合物对胰岛素信号通路中除T细胞蛋白酪氨酸磷酸酶外的其他磷酸酶表现出良好的选择性。在细胞模型中的进一步评估表明,这些衍生物增强了CHO/hIR细胞中胰岛素受体的磷酸化,并且在有或无胰岛素添加的情况下均刺激了L6肌管中的葡萄糖摄取。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验