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ESI-MS 基方法评价及荷叶中原儿茶酸作为一种潜在的脲酶抑制剂的分子对接研究

Biological Evaluation and Molecular Docking of Protocatechuic Acid from Hibiscus sabdariffa L. as a Potent Urease Inhibitor by an ESI-MS Based Method.

机构信息

Department of Natural Drugs, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences Brno, Palackého tř. 1946/1, 612 42 Brno, Czech Republic.

Department of Applied Ecology, Faculty of Environmental Sciences, Czech University of Life Sciences Prague, Kamýcká 129, 165 21 Praha 6-Suchdol, Czech Republic.

出版信息

Molecules. 2017 Oct 11;22(10):1696. doi: 10.3390/molecules22101696.

Abstract

Studies on enzyme inhibition remain a crucial area in drug discovery since these studies have led to the discoveries of new lead compounds useful in the treatment of several diseases. In this study, protocatechuic acid (PCA), an active compound from L. has been evaluated for its inhibitory properties against jack bean urease (JBU) as well as its possible toxic effect on human gastric epithelial cells (GES-1). Anti-urease activity was evaluated by an Electrospray Ionization-Mass Spectrometry (ESI-MS) based method, while cytotoxicity was assayed by the MTT method. PCA exerted notable anti-JBU activity compared with that of acetohydroxamic acid (AHA), with IC values of 1.7 and 3.2 µM, respectively. PCA did not show any significant cytotoxic effect on (GES-1) cells at concentrations ranging from 1.12 to 3.12 µM. Molecular docking study revealed high spontaneous binding ability of PCA to the active site of urease. Additionally, the anti-urease activity was found to be related to the presence of hydroxyl moieties of PCA. This study presents PCA as a natural urease inhibitor, which could be used safely in the treatment of diseases caused by urease-producing bacteria.

摘要

研究酶抑制仍然是药物发现中的一个关键领域,因为这些研究导致了新的先导化合物的发现,这些化合物在治疗多种疾病方面具有重要作用。在这项研究中,我们评估了来自 L. 的原儿茶酸 (PCA) 对豆类脲酶 (JBU) 的抑制特性及其对人胃上皮细胞 (GES-1) 的可能毒性作用。通过基于电喷雾电离-质谱 (ESI-MS) 的方法评估抗脲酶活性,通过 MTT 法测定细胞毒性。与乙酰羟肟酸 (AHA) 相比,PCA 对 JBU 表现出显著的抗活性,IC 值分别为 1.7 和 3.2 µM。PCA 在 1.12 至 3.12 µM 的浓度范围内对 (GES-1) 细胞没有表现出任何显著的细胞毒性作用。分子对接研究表明 PCA 与脲酶的活性部位具有很高的自发结合能力。此外,抗脲酶活性与 PCA 中羟基的存在有关。本研究表明 PCA 是一种天然的脲酶抑制剂,可安全用于治疗由产脲酶细菌引起的疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8540/6151788/03688184aadb/molecules-22-01696-g001.jpg

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