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从车前草种子中生物导向分离血管紧张素转换酶抑制剂

Bioguided isolation of angiotensin-converting enzyme inhibitors from the seeds of Plantago asiatica L.

机构信息

The MOE Key Laboratory for Standardization of Chinese Medicines, Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Zhangjiang Hi-Tech Park, Shanghai 201210, PR China.

出版信息

Phytother Res. 2010 Jul;24(7):1088-94. doi: 10.1002/ptr.3071.

Abstract

Ethanolic extract of the seeds of Plantago asiatica L. showed significant inhibitory activity of angiotensin-converting enzyme (ACE) determined by monitoring the transformation from a substrate hippuryl-histidyl-leucine (HHL) to the product hippuric acid (HA) in vitro using an UPLC-MS method. The bioguided fractionation of the extract resulted in the isolation of four ACE inhibitory active phenylpropanoid glycosides acteoside, isoacteoside, plantainoside D, and plantamajoside with IC(50) values of 2.69 mM, 2.46 mM, 2.17 mM, and 2.47 mM, respectively. Their structures were elucidated through the analysis of NMR, UV, IR and MS data. Our study is the first demonstration that Plantago asiatica L. and its major constituents have ACE inhibitory activity in vitro. It is assumed that the identified compounds contribute to the angiotensin-converting enzyme-inhibitory activity of the extract.

摘要

车前子乙醇提取物在体外通过监测从底物 hippuryl-histidyl-leucine (HHL) 到产物 hippuric acid (HA) 的转化,用 UPLC-MS 方法测定,显示出显著的血管紧张素转化酶 (ACE) 抑制活性。提取物的生物导向分离导致分离出四个 ACE 抑制活性的苯丙素糖苷,即毛蕊花糖苷、异毛蕊花糖苷、车前苷 D 和车前苷,其 IC(50) 值分别为 2.69 mM、2.46 mM、2.17 mM 和 2.47 mM。通过分析 NMR、UV、IR 和 MS 数据,阐明了它们的结构。我们的研究首次证明,车前子及其主要成分在体外具有 ACE 抑制活性。据推测,鉴定出的化合物对提取物的血管紧张素转化酶抑制活性有贡献。

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