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一系列含恶唑大环化合物的合成及其G-四链体稳定性能

Synthesis and G-quadruplex stabilizing properties of a series of oxazole-containing macrocycles.

作者信息

Minhas Gurpreet Singh, Pilch Daniel S, Kerrigan John E, LaVoie Edmond J, Rice Joseph E

机构信息

Department of Pharmaceutical Chemistry, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854-8020, USA.

出版信息

Bioorg Med Chem Lett. 2006 Aug 1;16(15):3891-5. doi: 10.1016/j.bmcl.2006.05.038. Epub 2006 Jun 2.

Abstract

The synthesis of 24-membered macrocycles containing four, six, and seven oxazole moieties is described. Selected compounds were evaluated for their ability to specifically bind and stabilize G-quadruplex DNA and for cytotoxic activity. An unexpected oxidative cleavage reaction afforded a macrocyclic imide that was also evaluated for G-quadruplex stabilizing and cytotoxic activity.

摘要

描述了含有四个、六个和七个恶唑部分的24元大环化合物的合成。对选定的化合物进行了评估,以确定它们特异性结合并稳定G-四链体DNA的能力以及细胞毒性活性。一个意外的氧化裂解反应生成了一种大环酰亚胺,也对其进行了G-四链体稳定和细胞毒性活性的评估。

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