Synthesis and biological evaluation of some 5-nitro- and 5-amino derivatives of 2′-deoxycytidine, 2′,3′-dideoxyuridine, and 2′,3′-dideoxycytidine

被引:5
作者
Colacino, E
Sindona, G
Gosselin, G
Mathé, C
机构
[1] Univ Montpellier 2, Lab Chim Organ Biomol Synth, UMR 5625, CNRS, F-34095 Montpellier 5, France
[2] Univ Montpellier 2, Lab Cooperatif Idenix, UMR 5625, CNRS, F-34095 Montpellier 5, France
[3] Univ Calabria, Dipartimento Chim, I-87036 Cosenza, Italy
关键词
5-substituted pyrimidine nucleoside analogues; HIV; HBV;
D O I
10.1081/NCN-120026403
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this article, we describe the synthesis of 5-nitro-1-(2-deoxy-alpha-D-erythro-pentofuranosyl)cytosine (4alpha), 5-nitro-1-(2-deoxy-beta-D-erythro-pentofuranosyl)cytosine (4beta), 5-amino-1-(2-deoxy-a-D-erythro-pentofuranosyl)cytosine (5alpha), 5-nitro-1(2-deoxy-beta-D-erythro-pentofuranosyl)cytosine (5beta), 5-nitro-1-(2,3-dideoxy-beta-D-ribofuranosyl)uracil (6beta), 5-amino-1-(2,3-dideoxy-alpha,beta-D-ribofuranosyl)uracil (7), 5-nitro-1-(2,3-dideoxy-alpha,beta-D-ribofuranosyl)cytosine (8) and 5-amino-1-(2,3-dideoxy-beta-D-ribofuranosyl)cytosine (9beta). The prepared compounds were tested for their activity against HIV and HBV viruses, but they did not show significant activity.
引用
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页码:2013 / 2026
页数:14
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