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Unveiling the Anti-tubercular Properties of Biscoumarins, through Biological Evaluation and Docking Studies
Letters in Drug Design & Discovery ( IF 1 ) Pub Date : 2020-12-31 , DOI: 10.2174/1570180817999200724173656
Poornima Acharya 1 , M.M.V. Ramana 1 , Manish Upadhyay 2 , Ganesh Pavale 1
Affiliation  

Background: Biscoumarin scaffolds are known for their promising pharmacological properties. These compounds have not been studied for their activity against tuberculosis strains.

Objective: Unveil the antitubercular properties of biscoumarin scaffolds.

Methods: Biscoumarin derivatives (3a-3l) were synthesized using lemon juice as a catalyst and were investigated for their in-vitro anti-tubercular activity against the H37Rv strain of Mycobacterium tuberculosis using Microplate Alamar Blue Assay Method (MABA). Their binding interaction was investigated by Molecular Docking Studies using InhA with PDB-ID: 2NSD as target receptors in the Hsub>37



中文翻译:

通过生物学评估和对接研究揭示双香豆素的抗结核特性

背景:双香豆素支架因其有希望的药理特性而闻名。尚未研究这些化合物对结核菌株的活性。

目的:揭示双香豆素支架的抗结核特性。

方法:以柠檬汁为催化剂合成双香豆素衍生物(3a-3l),并使用微孔板阿拉法蓝测定法(MABA)研究其对结核分枝杆菌H 37 R v菌株的体外抗结核活性。通过分子对接研究,使用InhA和PDB-ID:2NSD作为Hsub> 37中的靶受体,研究了它们的结合相互作用。

更新日期:2021-02-26
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