针对端粒g -悬垂的g -四联体相互作用剂不仅仅是简单的端粒酶抑制剂。

Jean-Fraņois Riou
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引用次数: 60

摘要

染色体的末端以富含g的单链悬垂端粒结束,可能采用特殊的结构,如t环和g四重体。g -四plex是端粒酶活性较差的底物,通过筛选或定向化学合成的不同类型的小分子配体选择性地稳定该结构并抑制端粒酶活性。这些配体与端粒酶的催化抑制剂有几点不同,在本综述中进行了讨论,特别强调了它们作为潜在抗肿瘤药物的生物活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
G-quadruplex interacting agents targeting the telomeric G-overhang are more than simple telomerase inhibitors.

The extremities of chromosomes end at telomeres in a G-rich single stranded overhang that may adopt peculiar structures such as T-loop and G-quadruplex. G-quadruplex is a poor substrate for telomerase activity and different classes of small molecule ligands that selectively stabilize this structure and inhibit telomerase activity have been selected by screening or synthesized by oriented chemistry. These ligands differ from catalytic inhibitors of telomerase by several points that were discussed in the present review, with a special emphasis on their biological activity as potential antitumor agents.

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