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一种原型生物还原DNA沟槽结合配体。

A prototype bioreductive DNA groove binding ligand.

作者信息

Haworth I S, Burt C, Gago F, Reynolds C A, Richards W G

机构信息

Physical Chemistry Laboratory, Oxford, UK.

出版信息

Anticancer Drug Des. 1991 Feb;6(1):59-70.

PMID:1707627
Abstract

Molecular mechanics calculations have been used to evaluate the potential bioreductive behaviour of several DNA minor groove binding ligands containing quinone/hydroquinone redox systems. The proposed structures are analogues of the Hoechst 33258 molecule with modifications of the benzimidazole rings. Binding energies of simple analogues indicate the reduced forms bind more strongly to the DNA minor groove. N-methylation of the imidazole ring(s) produces structures which can form extended quinone methides. These also show stronger binding in the reduced form and it is speculated that such structures might provide a basis for the design of groove binding ligands which will act as bioreductive alkylating agents.

摘要

分子力学计算已被用于评估几种含有醌/对苯二酚氧化还原系统的DNA小沟结合配体的潜在生物还原行为。所提出的结构是Hoechst 33258分子的类似物,其中苯并咪唑环有所修饰。简单类似物的结合能表明还原形式与DNA小沟的结合更强。咪唑环的N-甲基化产生了可以形成扩展醌甲基化物的结构。这些结构在还原形式下也表现出更强的结合,据推测,此类结构可能为设计作为生物还原烷基化剂的小沟结合配体提供基础。

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