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Synthesis of a Cholesteryl-HEG Phosphoramidite Derivative and Its Application to Lipid-conjugates of the Anti-HIV 5'TGGGAG3' Hotoda’s Sequence

机译:胆固醇-HEG亚磷酰胺衍生物的合成及其在抗HIV 5' TGGGAG 3' Hotoda序列的脂质缀合物中的应用

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摘要

A novel phosphoramidite derivative of cholesterol, with an ether-linked hexaethylene glycol (HEG) spacer arm, has been obtained through simple and reproducible solid phase modified oligonucleotide synthesis manipulations. This building block and the known phosphoramidite derivative of 3β-(2-hydroxyethoxy)cholesterol have been exploited in standard oligonucleotide synthesis protocols for the preparation of 5'- conjugates of the G-quadruplex-forming 5'TGGGAG3' oligomer, known as the Hotoda’s sequence, to produce new potential anti-HIV agents.
机译:通过简单且可重现的固相修饰寡核苷酸合成操作,已经获得了一种具有醚连接六甘醇(HEG)间隔臂的新型胆固醇胆固醇亚磷酰胺衍生物。在标准的寡核苷酸合成方案中已利用该结构单元和已知的3β-(2-羟基乙氧基)胆固醇的亚磷酰胺衍生物,用于制备形成G-四链体的 5 ' TGGGAG 3 '低聚物,称为Hotoda序列,可产生新的潜在抗HIV药物。

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