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DNA的磷酸基团作为硝基咪唑-氮丙啶放射增敏剂RSU-1069的潜在作用靶点。

The phosphate-group of DNA as a potential target for RSU-1069, a nitroimidazole-aziridine radiosensitizer.

作者信息

Silver A R, O'Neill P, Jenkins T C, McNeil S S

出版信息

Int J Radiat Oncol Biol Phys. 1986 Jul;12(7):1203-6. doi: 10.1016/0360-3016(86)90258-0.

Abstract

Strand breakage of plasmid DNA by parent and radiation-reduced RSU-1069 (2.0-8.0 mmol dm-3) has been measured in air over 4 hr at 310K. Reduced RSU-1069 was shown to be approximately 4 times as efficient as the parent compound at causing strand breakage. The aziridine moiety of both parent and reduced RSU-1069 is required for strand break production and, furthermore, is capable of alkylating inorganic phosphate (k = 1.0 X 10(-3) dm3 mol-1 s-1) and a series of nucleotides (k = 0.8 - 2.1 X 10(-3) dm3 mol-1 s-1) at pH 7.0. From the determined rate constants and the nature of the adducts observed, it was shown that phosphate is a target on nucleotides, although additional sites probably exist particularly, on dGMP and dAMP. The mechanism of action of RSU-1069 is discussed in terms of its ability to act as a cytotoxic agent, radiosensitizer and bioreductive drug.

摘要

在310K的空气中,已对母体化合物和辐射降解后的RSU - 1069(2.0 - 8.0 mmol dm⁻³)使质粒DNA链断裂的情况进行了4小时的测定。结果表明,辐射降解后的RSU - 1069在导致链断裂方面的效率约为母体化合物的4倍。母体化合物和辐射降解后的RSU - 1069的氮丙啶部分都是产生链断裂所必需的,此外,在pH 7.0时,它们能够使无机磷酸盐(k = 1.0×10⁻³ dm³ mol⁻¹ s⁻¹)和一系列核苷酸(k = 0.8 - 2.1×10⁻³ dm³ mol⁻¹ s⁻¹)烷基化。根据所测定的速率常数和观察到的加合物的性质表明,磷酸盐是核苷酸上的一个靶点,不过可能还存在其他位点,特别是在dGMP和dAMP上。从RSU - 1069作为细胞毒性剂、放射增敏剂和生物还原药物的作用能力方面对其作用机制进行了讨论。

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