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Validation of Model of Cytochrome P450 2D6: An in Silico Tool for Predicting Metabolism and Inhibition
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Update: Clinically Significant Cytochrome P‐450 Drug Interactions
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Impact of incorporating the 2C5 crystal structure into comparative models of cytochrome P450 2D6
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Comparative Protein Modelling by Satisfaction of Spatial Restraints
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Lead discovery using molecular docking
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Chemically modified heparins as inhibitors of heparan sulfate specific endo-.beta.-glucuronidase (heparanase) of metastatic melanoma cells
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Diversity in the Oxidation of Substrates by Cytochrome P450 2D6: Lack of an Obligatory Role of Aspartate 301−Substrate Electrostatic Bonding
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Use of Robust Classification Techniques for the Prediction of Human Cytochrome P450 2D6 Inhibition
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Development of a pharmacophore for inhibition of human liver cytochrome P-450 2D6: molecular modeling and inhibition studies
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Phe120 contributes to the regiospecificity of cytochrome P450 2D6: mutation leads to the formation of a novel dextromethorphan metabolite
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Crystal structures of ligand complexes of P450eryF exhibiting homotropic cooperativity
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Crystal Structure of Hemoprotein Domain of P450BM-3, a Prototype for Microsomal P450's
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Recent Advances: the Cytochrome P450 Enzymes
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Binding of bufuralol, dextromethorphan, and 3,4-methylenedioxymethylamphetamine to wild-type and F120A mutant cytochrome P450 2D6 studied by resonance Raman spectroscopy
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