Molecular orbital-generated QSARs in a homologous series of alkoxyresorufins and studies of their interactive docking with P450s
Author:
Publisher
Informa UK Limited
Subject
Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/00498259509061923
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1. Alkoxyresorufin-O-deethylase Activities and Polychlorinated Biphenyl Patterns in Shrews as Biomarkers in Environmental Risk Assessments: Sensitivity and Specificity;Environmental Science & Technology;2005-08-18
2. Quantitative structure-activity relationships within a homologous series of 7-alkoxyresorufins exhibiting activity towards CYP1A and CYP2B enzymes: molecular modelling studies on key members of the resorufin series with CYP2C5-derived models of human CYP1A1, CYP1A2, CYP2B6 and CYP3A4;Xenobiotica;2004-06
3. Comparative molecular field analysis and QSAR on substrates binding to cytochrome P450 2D6;Bioorganic & Medicinal Chemistry;2003-12
4. Quantitative structure–activity relationships (QSARs) within the cytochrome P450 system: QSARs describing substrate binding, inhibition and induction of P450s;InflammoPharmacology;2003-02
5. Quantitative structure-activity relationship (QSAR) and three-dimensional QSAR analysis of a series of xanthates as inhibitors and inactivators of cytochrome P450 2B1;Xenobiotica;2002-01
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