SYNTHESIS OF PYRRYL ARYL SULFONES TARGETED AT THE HIV-1 REVERSE-TRANSCRIPTASE

被引:35
作者
ARTICO, M
SILVESTRI, R
STEFANCICH, G
MASSA, S
SCINTU, F
PAGNOZZI, E
MASU, D
PINNA, E
TINTI, E
LACOLLA, P
机构
[1] UNIV TRIESTE,DIPARTIMENTO SCI FARMACEUT,I-34127 TRIESTE,ITALY
[2] UNIV CAGLIARI,DIPARTIMENTO BIOL SPERIMENTALE,I-09124 CAGLIARI,ITALY
关键词
D O I
10.1002/ardp.19953280304
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Various aryl 1-pyrryl sulfones were synthesized and tested as inhibitors of HIV-1, 2-Nitrophenyl-2-ethoxycarbonyl-1-pyrryl sulfone, the most active among test derivatives, was selected as lead compound of the aryl pyrryl sulfone series. The in vitro anti-HIV-1 activity and cytotoxicity of 41 compounds is reported. Some structure-activity relationships are discussed also in comparison with the known NPPS (2-nitorphenyl phenyl sulfone).
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页码:223 / 229
页数:7
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