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首页> 外文期刊>South African Journal of Botany >New perspective of drug discovery from herbal medicinal plants: Andrographis paniculata and Bacopa monnieri (terpenoids) and novel target identification against Staphylococcus aureus
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New perspective of drug discovery from herbal medicinal plants: Andrographis paniculata and Bacopa monnieri (terpenoids) and novel target identification against Staphylococcus aureus

机译:来自草药药用植物的药物发现的新视角:Andrographis Paniculata和Bacopa Monnieri(Terpenoids)和对葡萄球菌的新靶标鉴定

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Drug discovery process includes screening of potential compounds to propose as drug and identification of potential targets to be inhibited in order to combat disease prognosis. A combined approach of phytochemistry and bioinformatics is used to deal with drug discovery against antimicrobial resistance by identifying potential targets and candidate drugs. The work includes evaluation of antimicrobial activity of terpenoid-based plant extracts against antibiotic resistant microorganisms. The study was conducted to explain possible new perspective of drug discovery. Phytocompounds from herbal medicinal plants Bacopa monnieri and Andrographis paniculata were employed. Phytochemical tests were performed for both the plants to screen the presence of phytocompounds. Antimicrobial activities of the crude extracts of two medicinal plants (Bacopa monnieri and Andrographis paniculata) were screened. Best reported zone of inhibition observed with Andrographis paniculata was 1.5 cm in Pseudomonas aeruginosa and 1.0 cm in Bacillus subtilis. The least inhibition was shown by Bacopa monnieri, i.e. 0.7 cm in Pseudomonas aeruginosa and 0.6 cmin Bacillus subtilis. In silico analysis of phytochemicals is studied against multidrug resistant (MDR) strains of methicillin resistant Staphylococcus aureus using computer- aided drug discovery. Identification of target proteins was performed using database mining. Subsequently, molecular docking was done to depict the interaction of chosen terpenoid (Bacoside, Bacopa saponin, andrographin and beta-sitosterol) against the identified target proteins (PDB entry 2X4K & 2IHY) of MRSA. Andrographin and bacoside has more specificity towards the target protein identified for Staphylococcus aureus. This justifies them as potential compound with antimicrobial property. This study concludes the antimicrobial property of medicinal extracts of Bacopa monnieri and Andrographis paniculata against methicillin resistance Staphylococcus aureus and establishes the interaction of current phytochemicals involved in antimicrobial activity through an in-silico approach to reduce the cost incurred in experimental efforts. (C) 2019 SAAB. Published by Elsevier B.V. All rights reserved.
机译:药物发现过程包括筛选潜在的化合物,以提出抑制疾病预后的潜在目标的药物和鉴定潜在的目标。通过鉴定潜在的靶标和候选药物,使用植物化学和生物信息学的组合方法来处理针对抗微生物抗性的药物发现。该工作包括评估萜类植物植物提取物对抗抗生素抗性微生物的抗菌活性的评估。进行该研究以解释药物发现可能的新视角。采用来自草药药用植物的植物化合物和Andrographis Paniculata。对植物进行植物化学测试以筛选植物植物的存在。筛选了两种药用植物的粗提取物(Bacopa Monnieri和Andrographis Paniculata)的抗菌活性。用Andrographis Paniculata观察到的最佳报告的抑制区是铜绿假单胞菌的1.5厘米,在枯草芽孢杆菌中1.0厘米。 Bacopa Monnieri,即在假单胞菌铜绿假单胞菌和0.6cmin枯草芽孢杆菌中的0.7cm表示最少的抑制。在使用计算机辅助药物发现的植物抗性(MDR)耐甲氧西林金黄色葡萄球菌的多药抗性(MDR)菌株的植物化学分析中的植物化学分析。使用数据库挖掘进行靶蛋白的鉴定。随后,进行分子对接以描述所选择的萜类化(BacoSide,Bacobaa,Andrographin和Beta-sitosterol)对MRSA的鉴定的靶蛋白(PDB入口2x4K& 2Hy)的相互作用。 Andrographin和BacoSide对鉴定的金黄色葡萄球菌鉴定的靶蛋白质具有更多特异性。这使其证明它们是具有抗微生物性质的潜在化合物。本研究结论了Bacopa Monnieri和Andrographis Paniculata对甲氧西林抗性金黄色葡萄球菌的抗微生物性能,并建立了通​​过In-Silico方法在实验努力中降低了抗微生物活性中涉及抗菌活性的当前植物化学物质的相互作用。 (c)2019 Saab。 elsevier b.v出版。保留所有权利。

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