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箭叶淫羊藿叶中的类黄酮和prenylhydroquinones 及其对磷酸二酯酶 5A 的抑制作用。

Flavonoids and prenylhydroquinones from the prepared folium of Epimedium sagittatum Maxim. and their inhibition against phosphodiesterase5A.

机构信息

Engineering Research Center of Modern Preparation Technology of Traditional Chinese Medicine, Ministry of Education, Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.

Hubei Provincial Key Laboratory of Quality and Safety of Traditional Chinese Medicine Health Food, Jing Brand Research Institute, Jing Brand Co., Ltd., Daye 435100, Hubei, China.

出版信息

Fitoterapia. 2023 Jul;168:105465. doi: 10.1016/j.fitote.2023.105465. Epub 2023 Feb 28.

Abstract

An effort to identify novel active substances of the prepared folium of Epimedium sagittatum Maxim. (PFES) that was an important herb for male erectile dysfunction (ED) was taken. At present, phosphodiesterase-5A (PDE5A) is the most important target of new drugs for the treatment of ED. Therefore, the inhibition ingredients in PFES were systematically screened for the first time in this study. Eleven compounds, including eight new flavonoids and three prenylhydroquinones were isolated: sagittatosides DN (1-11), and their structures were elucidated by spectra and chemical analyses. Among them, a novel prenylflavonoid with oxyethyl group (1) was obtained and three prenylhydroquinones (9-11) were firstly isolated from Epimedium. All compounds were analyzed for the inhibition against PDE5A by molecular docking, and they all showed significant binding affinity as same as sildenafil. Their inhibitory activities were verified, and the results showed compound 6 had significant inhibition against PDE5A1. The isolation of new flavonoids and prenylhydroquinones with inhibitory activities of PDE5A from PFES implied that this herb might be a good source for the treatment of ED agents finding.

摘要

本研究首次对淫羊藿叶(PFES)中的具有新颖活性的物质进行了鉴定,淫羊藿叶是治疗男性勃起功能障碍(ED)的重要草药。目前,磷酸二酯酶 5A(PDE5A)是治疗 ED 的新药的最重要靶点。因此,本研究系统地筛选了 PFES 中的抑制成分。分离得到 11 种化合物,包括 8 种新的黄酮类化合物和 3 种异戊烯基对苯二酚: sagittatosides DN(1-11),并通过光谱和化学分析阐明了它们的结构。其中,获得了一种具有乙氧基的新型prenylflavonoid(1),并且首次从淫羊藿中分离出 3 种异戊烯基对苯二酚(9-11)。通过分子对接分析所有化合物对 PDE5A 的抑制作用,它们都表现出与西地那非相当的显著结合亲和力。验证了它们的抑制活性,结果表明化合物 6 对 PDE5A1 具有显著的抑制作用。从 PFES 中分离出具有 PDE5A 抑制活性的新黄酮类化合物和异戊烯基对苯二酚,表明该草药可能是寻找治疗 ED 药物的良好来源。

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