Substituted tetrahydroquinolines as potent allosteric inhibitors of reverse transcriptase and its key mutants.
Bioorg Med Chem Lett
; 19(17): 5119-23, 2009 Sep 01.
Article
em En
| MEDLINE
| ID: mdl-19631528
ABSTRACT
Non-nucleoside reverse transcriptase inhibitors (NNRTIs) are key elements of multidrug regimens, called HAART (Highly Active Antiretroviral Therapy), that are used to treat HIV-1 infections. Elucidation of the structure-activity relationships of the thiocarbamate moiety of the previous published lead compound 2 provided a series of novel tetrahydroquinoline derivatives as potent inhibitors of HIV-1 RT with nanomolar intrinsic activity on the WT and key mutant enzymes and potent antiviral activity in infected cells. The SAR optimization, mutation profiles, preparation of compounds, and pharmacokinetic profile of compounds are described.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Quinolinas
/
Inibidores da Transcriptase Reversa
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Fármacos Anti-HIV
/
Transcriptase Reversa do HIV
Idioma:
En
Ano de publicação:
2009
Tipo de documento:
Article