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首页> 外文期刊>Journal of Medicinal Chemistry >Novel nonsubstrate inhibitors of human thymidine phosphorylase, a potential target for tumor-dependent angiogenesis.
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Novel nonsubstrate inhibitors of human thymidine phosphorylase, a potential target for tumor-dependent angiogenesis.

机译:人胸苷磷酸化酶的新型非底物抑制剂,其为肿瘤依赖性血管生成的潜在靶标。

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摘要

Thymidine phosphorylase/platelet-derived endothelial cell growth factor (TP/PD-ECGF) is an enzyme involved in thymidine metabolism and homeostasis, and its catalytic activity appears to play an important role in angiogenesis. Here we describe the cloning and expression of a His-tagged human TP/PD-ECGF and its assay with uracil and thymine analogues. We present the design, synthesis, and biological evaluation of novel 6-(phenylalkylamino)uracil derivatives which, at micromolar concentrations, inhibit both catabolic and anabolic reactions of human TP in vitro. These base analogues are not converted by the enzyme into the nucleoside form, thus representing pure nonsubstrate inhibitors of the enzyme.
机译:胸苷磷酸化酶/血小板源性内皮细胞生长因子(TP / PD-ECGF)是一种参与胸苷代谢和体内稳态的酶,其催化活性似乎在血管生成中起重要作用。在这里,我们描述了带有组氨酸标签的人TP / PD-ECGF的克隆和表达及其尿嘧啶和胸腺嘧啶类似物的测定。我们目前的设计,合成和新型的6-(苯基烷基氨基)尿嘧啶衍生物的生物评估,在微摩尔浓度,抑制人TP的分解代谢和合成代谢反应。这些碱基类似物不会被酶转化为核苷形式,因此代表了该酶的纯非底物抑制剂。

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