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首页> 外文期刊>Journal of Medicinal Chemistry >In Vitro Activation of Cytochrome P450 46A1 (CYP46A1) by Efavirenz-Related Compounds
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In Vitro Activation of Cytochrome P450 46A1 (CYP46A1) by Efavirenz-Related Compounds

机译:通过EFAVIREVEN相关的化合物体外激活细胞色素P450 46A1(CYP46A1)

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摘要

Cytochrome P450 46A1 (CYP46A1) is a central nervous system-specific enzyme, which catalyzes cholesterol 24-hydroxylation. Currently CYP46A1 is being evaluated in a clinical trial for activation by small doses of the anti-HIV drug efavirenz. Eight efavirenz-related compounds were investigated for CYP46A1 activation in vitro, induction of a CYP46A1 spectral response, spectral Kd values, interaction with the P450 allosteric sites, and a model of binding to the enzyme active site. We gained insight into structure-activity relationships of efavirenz for CYP46A1 activation and found that the investigated efavirenz primary metabolites are stronger and better activators of CYP46A1 than efavirenz. We also established that CYP46A1 is activated by racemates and that a conformational-selection mechanism is operative in CYP46A1. The results suggest structural modifications of efavirenz to further increase CYP46A1 activation without inhibition at high compound concentrations. It is possible that not only efavirenz but its metabolites activate CYP46A1 in vivo.
机译:细胞色素P450 46A1(CYP46A1)是一种中枢神经系统特异性酶,其催化胆固醇24-羟基化。目前,CYP46A1正在通过小剂量的抗HIV药物EFAVIRENZ激活的临床试验中进行评估。研究了八种相关的化合物,用于体外CYP46A1活化,诱导CYP46A1光谱响应,光谱KD值,与P450变构位点的相互作用以及与酶活性位点的结合模型。我们获得了CYP46A1活化的efaviraenz结构 - 活动关系的洞察力,发现研究的EFAVIRENZ原发性代谢物比Efaviraz更强,更好的CYP46A1激活剂。我们还建立了CYP46A1由外向物激活,并且构象选择机制在CYP46A1中可操作。结果表明EFAVIRENZ的结构修饰进一步增加CYP46A1活化而不在高化合物浓度下抑制。不仅可以efaviraz,但它的代谢物激活体内CYP46A1。

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