Mechanism of anti-HIV action of masked alaninyl d4T-MP derivatives

被引:111
作者
Balzarini, J
Karlsson, A
Aquaro, S
Perno, CF
Cahard, D
Naesens, L
DeClercq, E
McGuigan, C
机构
[1] UNIV ROMA TOR VERGATA,DEPT EXPTL MED,I-00173 ROME,ITALY
[2] UNIV WALES COLL CARDIFF,WELSH SCH PHARM,CARDIFF CF1 3XF,S GLAM,WALES
[3] KAROLINSKA INST,S-17177 STOCKHOLM,SWEDEN
关键词
D O I
10.1073/pnas.93.14.7295
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
So324 is a 2',3'-dideoxy-2',3'-didehydrothymidine-5'-monophosphate (d4T-MP) prodrug containing at the phosphate moiety a phenyl group and the methylester of alanine linked to the phosphate through a phosphoramidate linkage. So324 has anti-HIV activity in human GEM, MT4, and monocyte/macrophage cells that is superior to that of d4T. In contrast to d4T, So324 is also able to inhibit HIV replication in thymidine kinase-deficient CEM cells, After uptake of So324 by intact human lymphocytes, d4T-MP is released and subsequently converted intracellularly to d4T-TP. In addition, accumulation of substantial amounts of a novel d4T derivative has been found. This d4T metabolite has been characterized as alaninyl d4T-MP. The latter metabolite accumulates at approximate to 13- to 200-fold higher levels than d4T-TP depending the experimental conditions. Alaninyl d4T-MP should be considered as an intra- and/or extracellular depot form of d4T and/or d4T-MP. These findings may explain the superior anti-retroviral activity of So324 over d4T in cell culture.
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页码:7295 / 7299
页数:5
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