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醌结构在抗肿瘤蒽环类药物诱导的线粒体损伤中的作用。阿霉素与5-亚氨基柔红霉素的比较。

Role of the quinone structure in the mitochondrial damage induced by antitumor anthracyclines. Comparison of adriamycin and 5-iminodaunorubicin.

作者信息

Pollakis G, Goormaghtigh E, Ruysschaert J M

出版信息

FEBS Lett. 1983 May 8;155(2):267-72. doi: 10.1016/0014-5793(82)80618-2.

Abstract

Adriamycin cardiotoxicity has been correlated with a disturbance of heart mitochondrial functions. Here, 5-iminodaunorubicin was compared with adriamycin for its capability to interfere in the mitochondrial electron transport with subsequent membrane damaging. The results suggest that minor chemical modifications of the anthraquinone moiety of anthracycline glycoside drugs should be a promising way to decrease mitochondrial membrane damage induced by this class of antitumor drugs.

摘要

阿霉素的心脏毒性与心脏线粒体功能紊乱有关。在此,将5-亚氨基柔红霉素与阿霉素在干扰线粒体电子传递及随后的膜损伤能力方面进行了比较。结果表明,对蒽环类糖苷药物蒽醌部分进行微小的化学修饰应该是减少这类抗肿瘤药物引起的线粒体膜损伤的一种有前景的方法。

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