Anti-HIV pronucleotides:: Sate versus phenyl as a protecting grow of AZT phosphoramidate derivatives

被引:12
作者
Beltran, T
Egron, D
Lefebvre, I
Périgaud, C
Pompon, A
Gosselin, G
Aubertin, AM
Imbach, JL
机构
[1] Univ Montpellier 2, Chim Bioorgan Lab, UMR CNRS USTL 5625, F-34095 Montpellier 5, France
[2] Univ Strasbourg 1, Inst Virol, INSERM U74, F-67000 Strasbourg, France
来源
NUCLEOSIDES & NUCLEOTIDES | 1999年 / 18卷 / 4-5期
关键词
D O I
10.1080/15257779908041617
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
We comparatively studied the decomposition pathways in CEM cell extract of several PHENYL phosphoramidate diesters of AZT. A correlation between anti-MIN activities in TK- cell lines and pharmacokinetic data has been observed. This study would help to design corresponding SATE phosphoramidate diesters which revealed potent anti-HIV properties.
引用
收藏
页码:973 / 975
页数:3
相关论文
共 3 条
[1]   Anti-HIV pronucleotides:: Decomposition pathways and correlation with biological activities [J].
Egron, D ;
Lefebvre, I ;
Périgaud, C ;
Beltran, T ;
Pompon, A ;
Gosselin, G ;
Aubertin, AM ;
Imbach, JL .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1998, 8 (09) :1045-1050
[2]  
LEFEBVRE I, 1997, LC GC EUR, V10, P602
[3]   INTRACELLULAR DELIVERY OF BIOACTIVE AZT NUCLEOTIDES BY ARYL PHOSPHATE DERIVATIVES OF AZT [J].
MCGUIGAN, C ;
PATHIRANA, RN ;
BALZARINI, J ;
DECLERCQ, E .
JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (08) :1048-1052