Journal of Medicinal Chemistry · 2006 · 182 citations · 23 references
PharmacyMedicinal ChemistryDrug DesignDrug DiscoveryPharmacophore ModelingAntifungal AgentsMolecular DockingPotency OptimizationProtein-ligand DockingQuantitative Structure-activity RelationshipsStructure-activity Relationship AnalysisFlexible DockingHydrogen BondingHydrogen Bonding EffectsNew Antifungal AgentsNovel Antifungal Drug DevelopmentPharmacophore Model ConstructionReceptor-based Pharmacophore GenerationReceptor-based Pharmacophore Screening
In a continuing effort to develop highly potent azole antifungal agents, the three-dimensional quantitative structure-activity relationship methods, CoMFA and CoMSIA, were applied using a set of novel azole antifungal compounds. The binding mode of the compounds at the active site of lanosterol 14alpha-demethylase was further explored using the flexible docking method. Various hydrophobic, van der Waals, pi-pi stacking, and hydrogen bonding interactions were observed between the azoles and the enzyme. Based on results from the molecular modeling, a receptor-based pharmacophore model was established to guide the rational optimization of the azole antifungal agents. Thus, a total of 57 novel azoles were designed and synthesized by a three-step optimization process. In vitro antifungal assay revealed that the antifungal activities of these novel azoles were greatly improved, which confirmed the reliability of the model from molecular modeling.
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High-resolution crystal structure of cytochrome P450cam
T.L. Poulos, B.C. Finzel, Andrew Howard · Journal of Molecular Biology · 1987 · 1.4K citations
Larissa M. Podust, T.L. Poulos, Michael R. Waterman · Proceedings of the National Academy of Sciences · 2001 · 523 citations · Full text