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Comparative bioactivation of the novel anti-tuberculosis agent PA-824 in Mycobacteria and a subcellular fraction of human liver

机译:新型抗结核药PA-824在分枝杆菌和人类肝脏亚细胞部分中的比较生物激活

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摘要

BACKGROUND AND PURPOSEPA-824 is a 2-nitroimidazooxazine prodrug currently in Phase II clinical trial for tuberculosis therapy. It is bioactivated by a deazaflavin (F420)-dependent nitroreductase (Ddn) isolated from Mycobacterium tuberculosis to form a des-nitro metabolite. This releases toxic reactive nitrogen species which may be responsible for its anti-mycobacterial activity. There are no published reports of mammalian enzymes bioactivating this prodrug. We have investigated the metabolism of PA-824 following incubation with a subcellular fraction of human liver, in comparison with purified Ddn, M. tuberculosis and Mycobacterium smegmatis.
机译:背景和PURPOSEPA-824是一种2-硝基咪唑并恶嗪前药,目前正处于结核治疗的II期临床试验中。它通过从结核分枝杆菌中分离出来的依赖于脱氮黄素(F420)的硝基还原酶(Ddn)进行生物激活,形成脱硝基代谢产物。释放出有毒的活性氮,可能导致其抗分枝杆菌活性。尚未有哺乳动物生物激活这种前药的报道。与纯化的Ddn,结核分枝杆菌和耻垢分枝杆菌相比,我们已经研究了与人肝的亚细胞部分孵育后PA-824的代谢。

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