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A combined pharmacokinetic model for the hypoxia-targeted prodrug PR-104A in humans, dogs, rats and mice predicts species differences in clearance and toxicity

机译:针对人,狗,大鼠和小鼠进行低氧靶向的前药PR-104A的组合药代动力学模型可预测清除和毒性的物种差异

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摘要

Background PR-104 is a phosphate ester that is systemically converted to the corresponding alcohol PR-104A. The latter is activated by nitroreduction in tumours to cytotoxic DNA cross-linking metabolites. Here, we report a population pharmacokinetic (PK) model for PR-104 and PR-104A in non-human species and in humans.
机译:背景技术PR-104是一种磷酸酯,可被系统转化为相应的醇PR-104A。后者在肿瘤中被硝基还原为细胞毒性DNA交联代谢物而被激活。在这里,我们报告了P​​R-104和PR-104A在非人类物种和人类中的群体药代动力学(PK)模型。

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