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首页> 外文期刊>Natural product communications >LC-MS-based Screening of East Indian Sandalwood Oil for Mycobacterium tuberculosis Shikimate Kinase and Plasmodium falciparum Thioredoxin Reductase Inhibitory Activities
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LC-MS-based Screening of East Indian Sandalwood Oil for Mycobacterium tuberculosis Shikimate Kinase and Plasmodium falciparum Thioredoxin Reductase Inhibitory Activities

机译:基于LC-MS的东印度檀香油筛选分枝杆菌结核病Shikimate激酶和疟原虫疟原虫氧化酶还原酶抑制作用

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摘要

M tuberculosis shikimate kinase (MtSK) and P. falciparum thioredoxin reductase (PfTrxR) represent promising drug targets in tuberculosis and malaria therapy respectively. East Indian Sandalwood oil (EISO) has many reported therapeutic benefits including antibacterial and antiplasmodial effects. The aim of this study was to screen EISO for MtSK and PfTrxR inhibition as potential mechanisms of antimycobacterial and antiplasmodial activities. Liquid chromatography-mass spectrometry (LC-MS) functional assays were used to assess MtSK and PfTrxR inhibition. In this study, EISO displayed antitubercular activity against M tuberculosis H37Rv at MIC value of 0.002% v/v. Subsequently preliminary screening of the MtSK inhibition by EISO showed an IC50 value of 0.015% v/v. Additionally, EISO presented 90% inhibition of PffrxR at 0.01% v/v suggesting a potential mechanism of action for reported antimalarial activity.
机译:M结核病Shikiming激酶(MTSK)和P. falciparum硫蛋白还原酶(pftrxr)分别代表结核病和疟疾治疗的有前途的药物靶标。 东印度檀香油(EISO)有许多报告的治疗益处,包括抗菌和抗癌效应。 本研究的目的是筛查eiso用于MTSK和PFTRXR的抑制作用作为抗细微细菌和抗癌症活性的潜在机制。 液相色谱 - 质谱(LC-MS)功能测定用于评估MTSK和PFTRXR抑制。 在本研究中,EISO在MIC值为0.002%V / v的MIC值下显示抗胆管活性H37RV。 随后通过EISO初步筛选MTSK抑制显示IC50值为0.015%v / v。 此外,EISO呈现90%的PFFRXR抑制0.01%V / V,表明报告的抗疟活动的潜在作用机制。

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