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首页> 外文期刊>Journal of Labelled Compounds and Radiopharmaceuticals >Design, synthesis and biological evaluation of deuterated nintedanib for improving pharmacokinetic properties
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Design, synthesis and biological evaluation of deuterated nintedanib for improving pharmacokinetic properties

机译:氘代nintedanib改善药代动力学特性的设计,合成和生物学评估

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摘要

Nintedanib is a novel triple angiokinase inhibitor that inhibits three growth factors simultaneously. Deuterated derivatives of nintedanib at certain metabolically active sites were prepared and evaluated in vitro and in vivo. In particular, deuterated compound SKLB-C2202 had significantly improved pharmacokinetic properties compared with nintedanib. These efforts lay the foundation for further investigating the druggability of SKLB-C2202.
机译:Nintedanib是一种新型的三联血管激酶抑制剂,可同时抑制三种生长因子。制备了在某些代谢活性位点的nintedanib氘代衍生物,并在体外和体内进行了评估。特别是,氘代化合物SKLB-C2202与nintedanib相比具有显着改善的药代动力学特性。这些努力为进一步研究SKLB-C2202的可药用性奠定了基础。

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