5-Alkyl-2-[(aryl and alkyloxylcarbonylmethyl)thiol-6(1-naphthylmethyl) pyrimidin-4(3H)-ones as an unique HIV reverse transcriptase inhibitors of S-DABO series

被引:46
作者
He, YP
Chen, FN [1 ]
Sun, GF
Wang, YP
De Clercq, E
Balzarini, J
Pannecouque, C
机构
[1] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
[2] Katholieke Univ Leuven, Med Res Inst, B-3000 Louvain, Belgium
关键词
D O I
10.1016/j.bmcl.2004.04.008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The introduction of a beta-carbonyl group to the C-2 side chain of S-DABO led to the finding of a series of novel potent anti-HIV agent. Some derivatives proved to be highly effective in inhibiting HIV-1 replication at nanomolar concentrations. Furthermore, the novel S-DABOs differ from the classical NNRTIs in that some compounds are active against both HIV-1 and HIV-2. They might interfere with another target or at least act on RT in a different way as compared to typical NNRTIs. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3173 / 3176
页数:4
相关论文
共 25 条
[1]   Efavirenz [J].
Adkins, JC ;
Noble, S .
DRUGS, 1998, 56 (06) :1055-1064
[2]   3,4-DIHYDRO-2-ALKOXY-6-BENZYL-4-OXOPYRIMIDINES (DABOS) - A NEW CLASS OF SPECIFIC INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 [J].
ARTICO, M ;
MASSA, S ;
MAI, A ;
MARONGIU, ME ;
PIRAS, G ;
TRAMONTANO, E ;
LACOLLA, P .
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 1993, 4 (06) :361-368
[3]   Selected non-nucleoside reverse transcriptase inhibitors (NNRTIs): the DABOs family [J].
Artico, M .
DRUGS OF THE FUTURE, 2002, 27 (02) :159-175
[4]   HIGHLY SPECIFIC-INHIBITION OF HUMAN IMMUNODEFICIENCY VIRUS TYPE-1 BY A NOVEL 6-SUBSTITUTED ACYCLOURIDINE DERIVATIVE [J].
BABA, M ;
TANAKA, H ;
DECLERCQ, E ;
PAUWELS, R ;
BALZARINI, J ;
SCHOLS, D ;
NAKASHIMA, H ;
PERNO, CF ;
WALKER, RT ;
MIYASAKA, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (03) :1375-1381
[5]   Nevirapine: A review of its use in the prevention and treatment of paediatric HIV infection [J].
Bardsley-Elliot A. ;
Perry C.M. .
Paediatric Drugs, 2000, 2 (5) :373-407
[6]   SJ-3366, a unique and highly potent nonnucleoside reverse transcriptase inhibitor of human immunodeficiency virus type 1 (HIV-1) that also inhibits HIV-2 [J].
Buckheit, RW ;
Watson, K ;
Fliakas-Boltz, V ;
Russell, J ;
Loftus, TL ;
Osterling, MC ;
Turpin, JA ;
Pallansch, LA ;
White, EL ;
Lee, JW ;
Lee, SH ;
Oh, JW ;
Kwon, HS ;
Chung, SG ;
Cho, EH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (02) :393-400
[7]  
De Clercq E, 2000, REV MED VIROL, V10, P255, DOI 10.1002/1099-1654(200007/08)10:4&lt
[8]  
255::AID-RMV282&gt
[9]  
3.0.CO
[10]  
2-6