TRENDS IN DRUG DEVELOPMENT FOR THE TREATMENT OF AIDS - COMPOUNDS INTERFERING WITH THE INITIAL-STAGES OF THE HIV REPLICATIVE CYCLE

被引：6

作者：

DECLERCQ, E

机构：

[1] Rega Institute for Medical Research, Katholieke Universiteit Leuven

来源：

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES | 1994年 / 2卷 / 1-2期

关键词：

D O I：

10.1016/0928-0987(94)90049-3

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

[No abstract available]

引用

页码：4 / 6

页数：3

共 20 条

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[3] DIFFERENTIAL ANTIHERPESVIRUS AND ANTIRETROVIRUS EFFECTS OF THE (S) AND (R) ENANTIOMERS OF ACYCLIC NUCLEOSIDE PHOSPHONATES - POTENT AND SELECTIVE INVITRO AND INVIVO ANTIRETROVIRUS ACTIVITIES OF (R)-9-(2-PHOSPHONOMETHOXYPROPYL)-2,6-DIAMINOPURINE [J].

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[4] HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) STRAINS SELECTED FOR RESISTANCE AGAINST THE HIV-1-SPECIFIC [2',5'-BIS-O-(TERT-BUTYLDIMETHYLSILYL)-3'-SPIRO-5''-(4''-AMINO-1'',2''-OXATHIOLE-2'',2''-DIOXIDE)]-BETA-D-PENTOFURANOSYL (TSAO) NUCLEOSIDE ANALOGS RETAIN SENSITIVITY TO HIV-1-SPECIFIC NONNUCLEOSIDE INHIBITORS [J].

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[5] HIV-1-SPECIFIC REVERSE-TRANSCRIPTASE INHIBITORS SHOW DIFFERENTIAL ACTIVITY AGAINST HIV-1 MUTANT STRAINS CONTAINING DIFFERENT AMINO-ACID SUBSTITUTIONS IN THE REVERSE-TRANSCRIPTASE [J].

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[7] STRUCTURAL INVESTIGATION AND ANTI-HIV ACTIVITIES OF HIGH-MOLECULAR-WEIGHT ATA POLYMERS [J].

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[8] HIGHLY POTENT AND SELECTIVE-INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS BY THE BICYCLAM DERIVATIVE JM3100 [J].

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[9] POTENT AND SELECTIVE-INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS (HIV)-1 AND HIV-2 REPLICATION BY A CLASS OF BICYCLAMS INTERACTING WITH A VIRAL UNCOATING EVENT [J].

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[10] BROAD-SPECTRUM ANTI-DNA VIRUS AND ANTIRETROVIRUS ACTIVITY OF PHOSPHONYLMETHOXYALKYLPURINES AND PHOSPHONYLMETHOXYALKYLPYRIMIDINES [J].

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