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[洋红霉素嗪(洋红嗪)的合成、毒性及抗肿瘤作用]

[Synthesis, toxicity and antitumor action of carminomycin azine (carminazine)].

作者信息

Povarov L S, Gol'dberg L E, Bazhanov V S, Shepelevtseva N G, Vertogradova T P

出版信息

Antibiotiki. 1981 Aug;26(8):620-3.

PMID:6895293
Abstract

Carminomycin azine designated as carminazine was prepared by condensation of carminomycin with hydrazine hydrate. It was shown in the experiments on mice that the toxicity of carminazine was 2 and 7 times lower than that of carminomycin on its intravenous and oral administration respectively. The effect of both drugs on hemopoiesis of the mice was similar. As regards the selectivity of the antitumor effect on lymphosarcoma, strain L10-1, carminazine was inferior to carminomycin.

摘要

将柔红霉素嗪命名为卡敏嗪,它是通过柔红霉素与水合肼缩合制备而成。在小鼠实验中表明,卡敏嗪静脉注射和口服时的毒性分别比柔红霉素低2倍和7倍。两种药物对小鼠造血功能的影响相似。就对L10 - 1株淋巴肉瘤的抗肿瘤作用选择性而言,卡敏嗪不如柔红霉素。

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