Journal of Medicinal Chemistry · 2008 · 164 citations · 10 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryStructure-activity RelationshipsVirologyAntiretroviral TherapyAntiviral AgentsAntiviral PharmacologyEnzyme InhibitionLigand BindingMolecular DockingAntiviral Drug DesignAntiviral Structure-activity RelationshipsAntiviral TherapeuticsChemical SubstituentsIntegrase ProteinsIntegrase Strand Transfer InhibitorsMolecular Docking Of InhibitorsStructural Virology
A set of 4-quinolone-3-carboxylic acids bearing different substituents on the condensed benzene ring was designed and synthesized as potential HIV-1 integrase inhibitors structurally related to elvitegravir. Some of the new compounds proved to be able to inhibit the strand transfer step of the virus integration process in the micromolar range. Docking studies and quantum mechanics calculations were used to rationalize these data.
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