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带有咪唑鎓或吡啶鎓环的5-硝基咪唑衍生物对DNA半保留复制的抑制作用及对DNA非预定合成的增强作用

Inhibition of the semiconservative DNA synthesis and potentiation of the unscheduled DNA synthesis by 5-nitroimidazole derivatives with an imidazolium or pyridinium ring.

作者信息

Santos L, Cornago P, Lopez Zumel M C, Pintado M

机构信息

Instituto de Química Fisica Rocasolano, Madrid, Spain.

出版信息

Biomed Biochim Acta. 1989;48(10):757-64.

PMID:2561390
Abstract

The effects of four pyridinium and one imidazolium derivatives of 5-nitroimidazole have been tested for their action on the kinetics of DNA semiconservative synthesis and of the unscheduled DNA synthesis carried out by TC-SV40 cells. Unscheduled synthesis was induced by 25 Gy X-rays, and the kinetics were evaluated through the measurement of the newly synthetized DNA labelled with [3H-methyl]thymidine. All derivatives inhibit the DNA semiconservative synthesis and increase the unscheduled DNA synthesis to different degrees, but not in the suitable way to reveal the mechanism of interaction with DNA as responsible of the product's radiosensitizing actions on the same mammalian tumor cells.

摘要

已对5-硝基咪唑的四种吡啶鎓衍生物和一种咪唑鎓衍生物对DNA半保留合成动力学以及TC-SV40细胞进行的DNA修复合成动力学的作用进行了测试。用25 Gy X射线诱导DNA修复合成,通过测量用[3H-甲基]胸腺嘧啶标记的新合成DNA来评估其动力学。所有衍生物均抑制DNA半保留合成,并不同程度地增加DNA修复合成,但方式并不合适,无法揭示与DNA相互作用的机制,而这种机制被认为是该产物对相同哺乳动物肿瘤细胞产生放射增敏作用的原因。

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