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一种新型双(14-硫杂柔红霉素)的DNA结合及生物活性

The DNA-association and biological activity of a new bis(14-thiadaunomycin).

作者信息

Skorobogaty A, Brownlee R T, Chandler C J, Kyratzis I, Phillips D R, Reiss J A, Trist H

机构信息

Department of Biochemistry, La Trobe University, Bundoora, Victoria, Australia.

出版信息

Anticancer Drug Des. 1988 Jun;3(1):41-56.

PMID:3382506
Abstract

A new bis-daunomycin has been synthesized and characterized by 13C-n.m.r. and reversed-phase h.p.l.c. The compound was found to be highly self-associated in aqueous solution and to bis-intercalate into DNA with a residence time about 200-fold greater than the parent compound daunomycin. Although the bis-daunomycin and its parent congener were taken up by V79 Chinese hamster ovarian leukaemia cells to similar extents, the cytotoxicity of the former was considerably lower. The possible in vivo relationship between DNA binding affinity and cytotoxicity is discussed.

摘要

一种新的双柔红霉素已被合成,并通过碳-13核磁共振和反相高效液相色谱进行了表征。该化合物在水溶液中高度自缔合,并以比母体化合物柔红霉素长约200倍的停留时间双插入DNA。尽管双柔红霉素及其母体同系物被V79中国仓鼠卵巢白血病细胞摄取的程度相似,但前者的细胞毒性要低得多。文中讨论了DNA结合亲和力与细胞毒性之间可能的体内关系。

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