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Antimicrobial Activity of Quinazolin Derivatives of 1,2-Di(quinazolin-4-yl)diselane against Mycobacteria

机译:1,2-二(喹唑啉-4-基)二硒烷喹唑啉衍生物对分枝杆菌的抗菌活性

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摘要

Mycobacterium tuberculosis (M. tuberculosis) is one of the leading causes of morbidity and mortality. Currently, the emergence of drug resistance has an urgent need for new drugs. In previous study, we found that 1,2-di(quinazolin-4-yl)diselane (DQYD), a quinazoline derivative, has anticancer activities against many cancers. However, whether DQYD has the activity of antimycobacterium is still little known. Here our results show that DQYD has a similar value of the minimum inhibitory concentration with clinical drugs against mycobacteria and also has the ability of bacteriostatic activity with dose-dependent and time-dependent manner. Furthermore, the activities of DQYD against M. tuberculosis are associated with intracellular ATP homeostasis. Meanwhile, mycobacterium DNA damage level was increased after DQYD treatment. But there was no correlation between survival of mycobacteria in the presence of DQYD and intercellular reactive oxygen species. This study enlightens the possible benefits of quinazoline derivatives as potential antimycobacterium compounds and furtherly suggests a new strategy to develop new methods for searching antituberculosis drugs.
机译:结核分枝杆菌(M. tuberculosis)是发病率和死亡率的主要原因之一。当前,耐药性的出现迫切需要新药。在先前的研究中,我们发现1,2-二(喹唑啉-4-基)二甲醚(DQYD)是一种喹唑啉衍生物,具有抗多种癌症的抗癌活性。然而,DQYD是否具有抗分枝杆菌的活性仍然鲜为人知。在这里,我们的结果表明,DQYD具有与临床药物对抗分枝杆菌的最小抑菌浓度相似的值,并且具有剂量依赖性和时间依赖性的抑菌活性。此外,DQYD对抗结核分枝杆菌的活性与细胞内ATP稳态有关。同时,DQYD处理后分枝杆菌DNA损伤水平增加。但是,在存在DQYD的情况下,分枝杆菌的存活与细胞间活性氧之间没有相关性。这项研究启发了喹唑啉衍生物作为潜在的抗分枝杆菌化合物的可能益处,并进一步提出了开发寻找抗结核药物新方法的新策略。

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