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α-异头型同嘧啶寡聚脱氧核苷酸硫代磷酸酯的合成及其物理化学和生物化学性质

Synthesis of alpha-anomeric homopyrimidine oligo DNA phosphorothioates and their physicochemical and biochemical properties.

作者信息

Shinozuka K, Yamada N, Sawai H

出版信息

Nucleic Acids Symp Ser. 1995(34):121-2.

PMID:8841582
Abstract

alpha-Anomeric 2'-deoxycytidine and thymidine were synthesized in a stereospecific manner. With these nucleosides, pyrimidine homooligomers having either exclusively phosphodiester or phosphorothioate linkages were prepared using phosphoramidite method. All tested alpha-DNA.RNA complex was found to be inert toward the action of RNase H, even when phosphorothioate analogs were used as the DNA component. Among the alpha-anomeric homooligomers, alpha-oligocytidilate phosphorothioate exhibited potent inhibitory effect towards the action of RNase H on a DNA.RNA complex.

摘要

以立体专一的方式合成了α-异头2'-脱氧胞苷和胸苷。利用亚磷酰胺法,用这些核苷制备了仅具有磷酸二酯或硫代磷酸酯键的嘧啶同聚物。所有测试的α-DNA.RNA复合物即使在使用硫代磷酸酯类似物作为DNA组分时,也被发现对RNase H的作用呈惰性。在α-异头同聚物中,α-硫代磷酸化寡聚胞苷酸对RNase H作用于DNA.RNA复合物表现出强烈的抑制作用。

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