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潜在的抗癌剂——柔红霉素的硝酰基衍生物。

Potential anticancer agents--nitroxyl derivatives of Rubomycin.

作者信息

Emanuel N M, Konovalova N P, Diatchkovskaya R F

出版信息

Neoplasma. 1985;32(3):285-92.

PMID:4022191
Abstract

Two new of the spin-labeled analogues of Rubomycin were studied. It was shown that spin-labeled derivatives were less toxic than the parent compound and had a broad-spectrum antitumor activity. Spin-labeled derivative was clearly less cardiotoxic in the rat model than Rubomycin (Daunorubomycin).

摘要

对柔红霉素的两种新的自旋标记类似物进行了研究。结果表明,自旋标记衍生物的毒性低于母体化合物,且具有广谱抗肿瘤活性。在大鼠模型中,自旋标记衍生物的心脏毒性明显低于柔红霉素(道诺霉素)。

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