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J Med Chem ; 49(11): 3172-84, 2006 Jun 01.
Article in English | MEDLINE | ID: mdl-16722636

ABSTRACT

Molecular modeling studies and an updated highly predictive 3-D QSAR model led to the discovery of exceptionally potent indolyl aryl sulfones (IASs) characterized by the presence of either a pyrrolidyn-2-one nucleus at the indole-2-carboxamide or some substituents at the indole-2-carbohydrazide. Compounds 7 and 9 were found active in the sub-nanomolar range of concentration in both MT-4 and C8166 cell-based anti-HIV assays. These compounds, and in particular compound 9, also showed excellent inhibitory activity against both HIV-112 and HIV-AB1 primary isolates in lymphocytes and against HIV WT in macrophages.


Subject(s)
Anti-HIV Agents/chemical synthesis , HIV-1/drug effects , Indoles/chemical synthesis , Models, Molecular , Sulfones/chemical synthesis , Anti-HIV Agents/chemistry , Anti-HIV Agents/pharmacology , Cells, Cultured , Drug Design , Drug Resistance, Viral , HIV-1/genetics , HIV-1/isolation & purification , Humans , Indoles/chemistry , Indoles/pharmacology , Lymphocytes/drug effects , Lymphocytes/virology , Macrophages/drug effects , Macrophages/virology , Pyrrolidinones/chemistry , Quantitative Structure-Activity Relationship , Solubility , Sulfones/chemistry , Sulfones/pharmacology
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