Suppr超能文献

宝兴玉兰花蕾中的花椒毒酚具有抑制蛋白质糖基化、醛糖还原酶和白内障形成的作用。

Scopoletin from the flower buds of Magnolia fargesii inhibits protein glycation, aldose reductase, and cataractogenesis ex vivo.

机构信息

Diabetic Complications Research Center, Division of Traditional Korean Medicine Integrated Research, Korea Institute of Oriental Medicine, Daejeon, 305-811, Korea.

出版信息

Arch Pharm Res. 2010 Sep;33(9):1317-23. doi: 10.1007/s12272-010-0904-z. Epub 2010 Oct 9.

Abstract

Five compounds previously known structures, scopoletin (1), northalifoline (2), stigmast-4-en-3-one (3), tiliroside (4), and oplopanone (5) were obtained from the flower buds of Magnolia fargesii using chromatographic separation methods. The structures of 1-5 were identified by the interpretation of their spectroscopic data including 1D- and 2D-NMR as well as by comparison with reported values. Three compounds 1-3 were found from M. fargesii for the first time in this study. All the isolates (1-5) were subjected to in vitro bioassays to evaluate the inhibitory activity on advanced glycation end products formation and rat lens aldose reductase (RLAR). Compound 1 showed a remarkable inhibitory activity on advanced glycation end products formation with IC(50) value of 2.93 μM (aminoguanidine: 961 μM), and showed a significant RLAR inhibitory activity with IC(50) value of 22.5 μM (3.3-tetramethyleneglutaric acid: 28.7 μM). Compound 4 exhibited potent inhibitory activity against RLAR (IC(50) = 14.9 μM). In the further experiment ex vivo, cataractogenesis of rat lenses induced with xylose was significantly inhibited by compound 1 treatment.

摘要

从 Magnolia fargesii 的花蕾中,采用色谱分离方法得到了 5 种已知结构的化合物:东莨菪内酯(1)、北美黄连碱(2)、豆甾-4-烯-3-酮(3)、芫花素(4)和吴茱萸碱(5)。通过解析其光谱数据(包括 1D-和 2D-NMR)以及与文献值进行比较,确定了 1-5 的结构。在本研究中,化合物 1-3 首次从 M. fargesii 中分离得到。所有分离得到的化合物(1-5)均进行了体外生物活性测定,以评估其对晚期糖基化终产物形成和大鼠晶状体醛糖还原酶(RLAR)的抑制活性。化合物 1 对晚期糖基化终产物形成具有显著的抑制活性,IC50 值为 2.93 μM(氨基胍:961 μM),对 RLAR 具有显著的抑制活性,IC50 值为 22.5 μM(3.3-四亚甲基戊二酸:28.7 μM)。化合物 4 对 RLAR 具有很强的抑制活性(IC50 = 14.9 μM)。在进一步的动物实验中,用木糖诱导的大鼠晶状体白内障形成明显受到化合物 1 处理的抑制。

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