Suppr超能文献

卷柏素和双黄酮类化合物作为来自卷柏的蛋白酪氨酸磷酸酶1B抑制剂及其对葡萄糖摄取的刺激作用。

Selaginellin and biflavonoids as protein tyrosine phosphatase 1B inhibitors from Selaginella tamariscina and their glucose uptake stimulatory effects.

作者信息

Nguyen Phi-Hung, Ji Da-Jung, Han Yu-Ran, Choi Jae-Sue, Rhyu Dong-Young, Min Byung-Sun, Woo Mi-Hee

机构信息

College of Pharmacy, Drug Research and Development Center, Catholic University of Daegu, Gyeongsan 712-702, Republic of Korea; Institute of Natural Products Chemistry, Vietnam Academy of Science and Technology, 18-Hoang Quoc Viet, Hanoi, Viet Nam.

College of Pharmacy, Drug Research and Development Center, Catholic University of Daegu, Gyeongsan 712-702, Republic of Korea.

出版信息

Bioorg Med Chem. 2015 Jul 1;23(13):3730-7. doi: 10.1016/j.bmc.2015.04.007. Epub 2015 Apr 10.

Abstract

As part of an ongoing search for new antidiabetic agents from medicinal plants, the methanol extract of the aerial parts of Selaginella tamariscina was found to possess stimulatory effect on glucose uptake in 3T3-L1 adipocyte cells. Thus, bioassay-guided isolation of this active extract yielded two new compounds (1 and 2) along with five known biflavonoids (3-7). Their structures were elucidated by extensive analysis of spectroscopic and physicochemical data. The absolute configuration of compound 2 was determined by specific rotation and CD data analysis. All isolates exhibited potent inhibitory effects on PTP1B enzyme with IC50 values ranging from 4.5±0.1 to 13.2±0.8μM. Furthermore, the isolates (1-7) showed significant stimulatory effects on 2-NBDG uptake in 3T3-L1 adipocyte cells. Of these, compounds (1, 6, and 7) which exhibited mixed-competitive inhibition modes against PTP1B, showed potent stimulatory effects on 2-NBDG uptake. This result indicated the potential of these biflavonoids as lead molecules for development of antidiabetic agents and the beneficial use of S. tamariscina against hyperglycemia.

摘要

作为从药用植物中寻找新型抗糖尿病药物的一项正在进行的研究的一部分,发现卷柏地上部分的甲醇提取物对3T3-L1脂肪细胞的葡萄糖摄取具有刺激作用。因此,通过生物测定法对该活性提取物进行分离,得到了两种新化合物(1和2)以及五种已知的双黄酮类化合物(3-7)。通过对光谱和物理化学数据的广泛分析阐明了它们的结构。通过旋光和圆二色性数据分析确定了化合物2的绝对构型。所有分离物对PTP1B酶均表现出强效抑制作用,IC50值范围为4.5±0.1至13.2±0.8μM。此外,分离物(1-7)对3T3-L1脂肪细胞中的2-NBDG摄取显示出显著的刺激作用。其中,对PTP1B表现出混合竞争性抑制模式的化合物(1、6和7)对2-NBDG摄取显示出强效刺激作用。这一结果表明这些双黄酮类化合物作为抗糖尿病药物开发的先导分子的潜力,以及卷柏对高血糖的有益作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验