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纺锤菌素和偏端霉素的合成类似物——吡咯甲酰胺类抗肿瘤抗生素新的吡啶和碳环类似物的合成

Synthetic analogues of netropsin and distamycin--synthesis of a new pyridine and carbocyclic analogues of the pyrrolecarboxamide antitumour antibiotics.

作者信息

Bartulewicz D, Bielawski K, Markowska A, Zwierz K, Pućkowska A, Rózański A

机构信息

Department of Organic Chemistry, Medical Academy, Białystok, Poland.

出版信息

Acta Biochim Pol. 1998;45(1):41-57.

PMID:9701495
Abstract

A new series of pyridine-containing analogues III-XXII of distamycin A and netrop sin was investigated by the molecular mechanics technique and molecular modelling. A pyridine analogue of netropsin (VII) is described, the first compound based on molecular studies, and two carbocyclic analogues of distamycin A with an N-terminal chloro- or bromoacetyl group (VIa, VIIa) were synthesized, as well as carbocyclic analogues of netropsin (VIIIb, Xb), potential carriers of alkylating elements. The potential use of VIa, VII, VIIa, VIIIb and Xb as carriers to place into the minor groove of DNA chemical groups capable of modifying DNA, is discussed.

摘要

通过分子力学技术和分子建模研究了一系列新的含吡啶的放线菌素A和纺锤菌素类似物III - XXII。描述了一种纺锤菌素的吡啶类似物(VII),这是基于分子研究的首个化合物,还合成了两种具有N - 末端氯乙酰基或溴乙酰基的放线菌素A碳环类似物(VIa,VIIa),以及纺锤菌素的碳环类似物(VIIIb,Xb),它们是潜在的烷基化元素载体。讨论了VIa、VII、VIIa、VIIIb和Xb作为载体将能够修饰DNA的化学基团置于DNA小沟中的潜在用途。

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