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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Reactive intermediates and bioactivation pathways characterization of avitinib by LC-MS/MS: In vitro metabolic investigation
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Reactive intermediates and bioactivation pathways characterization of avitinib by LC-MS/MS: In vitro metabolic investigation

机译:LC-MS / MS的反应性中间体和生物活化途径表征Avitinib:体外代谢调查

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Avitinib (AC0010) is a third generation inhibitor of the EGFR (epidermal growth factor receptor) that was permitted parallel phase I clinical trials in the US and in 2014. It is estimated to enter in market within two years. In the current study, eight in vitro metabolites were detected and their chemical structures were postulated. The main in vitro phase-I metabolic reaction was N-oxidation in piperazine moiety. The generation of reactive metabolites in avitinib metabolism was investigated using rat liver microsomes while adding capturing agents, viz potassium cyanide for reactive iminium intermediates, GSH for iminoquinones and methoxylamine for aldehyde forming stable adducts which are identifiable by LC-MS/MS. Ten reactive intermediates (four iminoquinones, three iminium and three aldehydes) were characterized. The three capturing agents used resulted in proposing four different bioactivation pathways. Upon literature examination, no former articles were found for avitinib metabolism including the produced reactive metabolites. (C) 2018 Elsevier B.V. All rights reserved.
机译:Avitinib(AC0010)是EGFR(表皮生长因子受体)的第三代抑制剂,其在美国和2014年允许并行临床试验。估计在两年内进入市场。在目前的研究中,检测到八个体外代谢物,并假设其化学结构。主要的体外相 - I代谢反应是哌嗪部分的N-氧化。使用大鼠肝微粒体研究阿维替尼代谢的反应性代谢物的产生,同时添加捕获剂,用于反应性亚胺中间体的Viz钾氰化物,用于醛基醌和甲氧基胺的GSH形成稳定的加合物,其通过LC-MS / MS识别。表征了十种反应性中间体(四种IMINIINONE,三种亚氨基和三只醛)。使用的三种捕获剂导致提出四种不同的生物活化途径。在文学检查后,没有发现禽素代谢的前一篇文章,包括产生的反应性代谢物。 (c)2018年elestvier b.v.保留所有权利。

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