Pyridine N-oxide derivatives: unusual anti-HIV compounds with multiple mechanisms of antiviral action
Author(s) -
Jan Balzarini,
Miguel Stevens,
Erik De Clercq,
Dominique Schols,
Christophe Pannecouque
Publication year - 2005
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkh530
Subject(s) - reverse transcriptase , mechanism of action , virology , nucleoside , human immunodeficiency virus (hiv) , chemistry , nucleoside reverse transcriptase inhibitor , reverse transcriptase inhibitor , pharmacology , biology , in vitro , stereochemistry , gene , rna , biochemistry
Pyridine N-oxide derivatives represent a new class of anti-HIV compounds, for which some members exclusively act through inhibition of HIV-1 reverse transcriptase and thus characteristically behave as non-nucleoside reverse transcriptase inhibitors. Other members act, additionally or alternatively, at a post-integrational event in the replication cycle of HIV, that is, at the level of HIV gene expression. Repeated administration of one of the prototype compounds (JPL-32) to DBA/2 and hu-PBMC-SCID mice demonstrated, in the absence of any acute toxicity, protective activity against HIV-induced destruction of CD4 human T lymphocytes.
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