COMPARISON OF ANTIVIRAL EFFECTS OF ZIDOVUDINE PHOSPHORAMIDATE AND PHOSPHORODIAMIDATE DERIVATIVES AGAINST HIV AND ULV INVITRO

被引:7
作者
KINCHINGTON, D
HARVEY, JJ
OCONNOR, TJ
JONES, BCNM
DEVINE, KG
TAYLORROBINSON, D
JEFFRIES, DJ
MCGUIGAN, C
机构
[1] MRC, CLIN RES CTR, DIV SEXUALLY TRANSMITTED DIS, HARROW HA1 3UJ, MIDDX, ENGLAND
[2] UNIV SOUTHAMPTON, DEPT CHEM, SOUTHAMPTON SO9 5NH, HANTS, ENGLAND
[3] UNIV LONDON UNIV COLL, DEPT CHEM, LONDON WC1H 0AJ, ENGLAND
[4] MED COLL ST BARTHOLOMEWS HOSP, DEPT VIROL, LONDON EC1A 7BE, ENGLAND
关键词
D O I
10.1177/095632029200300205
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
A number of zidovudine phosphoramidate and phosphorodiamidate derivatives were prepared, including some previously unreported benzyl esterified amino acyl compounds. These were found to be active in vitro against the human immunodeficiency virus (HIV-1), and were tested subsequently in the S+L-tissue culture assay against urethane leukaemia virus (ULV), a murine leukaemia virus (MuLV). The fifteen compounds tested showed a similar range of activity against the two viruses. No active compounds were missed in the MuLV system which was usually more sensitive to antiviral effects. Five compounds showed some toxicity to the mouse cells only. We are using this system in parallel with HIV assays to identify those derivatives which will be tested subsequently against a murine retrovirus in vivo.
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页码:107 / 112
页数:6
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