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来自通风口的抗化合物通过脲酶抑制作用及研究。 (不过此英文表述似乎不太准确规范)

Anti Compounds from Vent. through Urease Inhibitory and Studies.

作者信息

Eftekhari Mahdieh, Shams Ardekani Mohammad Reza, Amin Mohsen, Mansourian Mahboubeh, Saeedi Mina, Akbarzadeh Tahmineh, Khanavi Mahnaz

机构信息

Pharmaceutical Sciences Research center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Department of Pharmacognosy and Pharmaceutical Biotechnology, Faculty of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

Iran J Pharm Res. 2021 Summer;20(3):476-489. doi: 10.22037/ijpr.2021.114485.14876.

Abstract

Vent. has been used by indigenous people of southwest Iran for treating peptic ulcers and gastrointestinal infections. This study aimed to investigate the antibacterial activity of extract and fractions and to analyze the bioactive components of the fractions. Total plant extract and different fractions of Vent. were prepared. Antibacterial activities were evaluated against the clinical strain of and standard strains of , , and using agar dilution and disc diffusion methods. Phytochemical analysis of the fractions was performed using silica gel chromatography and 1D and 2D NMR spectroscopy. Moreover, the urease inhibitory effects of the isolated compounds were assessed and . Three novel kaempferol derivatives and two thymol derivatives were isolated from aerial parts, and the structures were determined by comparison with published data. The -hexane fraction was found to exert the most significant anti activity with the minimum inhibitory concentration of 50 µg/mL. All fractions demonstrated antibacterial activity toward . urease inhibition assay showed that stigmasterol, tiliroside, and carvacrol were found to be the most potent enzyme inhibitors in the isolated compounds. Molecular interactions of the compounds with the active site of urease were supported by the molecular docking analysis. Novel bioactive compounds in were described in this study. The antibacterial effects suggested the potential use of the compounds in pharmaceutical formulations inconsistent with the traditional use of the plant in the treatment of gastrointestinal infections.

摘要

文特(Vent.)已被伊朗西南部的原住民用于治疗消化性溃疡和胃肠道感染。本研究旨在研究其提取物和馏分的抗菌活性,并分析馏分的生物活性成分。制备了文特的总植物提取物和不同馏分。采用琼脂稀释法和纸片扩散法,对临床分离株以及标准菌株[具体菌株名称未给出]进行抗菌活性评估。利用硅胶柱色谱法以及一维和二维核磁共振光谱对馏分进行植物化学分析。此外,还评估了分离得到的化合物对[具体评估对象未给出]的脲酶抑制作用。从文特地上部分分离出三种新的山奈酚衍生物和两种百里香酚衍生物,并通过与已发表数据对比确定了其结构。发现正己烷馏分具有最显著的抗菌活性,最低抑菌浓度为50μg/mL。所有馏分均对[具体对象未给出]表现出抗菌活性。脲酶抑制试验表明,在分离得到的化合物中,豆甾醇、椴树苷和香芹酚是最有效的酶抑制剂。分子对接分析支持了化合物与脲酶活性位点的分子相互作用。本研究描述了文特中的新型生物活性化合物。抗菌作用表明这些化合物在药物制剂中的潜在用途,这与该植物在治疗胃肠道感染方面的传统用途一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1128/8653682/9df1730ce1f1/ijpr-20-476-g001.jpg

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