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Drug Metabolism and Disposition: the Biological Fate of Chemicals|April 2, 2014
Common drugs inhibit human organic cation transporter 1 (OCT1)-mediated neurotransmitter uptakeKelli H Boxberger, Bruno Hagenbuch, Jed N Lampe
Chemical Research in Toxicology|September 28, 2023
Consideration of Nevirapine Analogs To Reduce Metabolically Linked Hepatotoxicity: A Cautionary Tale of the Deuteration ApproachSylvie E Kandel, Emily G Gracey, Jed N Lampe
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 1, 2026
A CYP3A7 metabolically competent human induced pluripotent stem cell-derived hepatocyte-like cell (hHLC<sub>3A7</sub>) model for drug safety assessment in the newbornEmily G Gracey, Sylvie E Kandel, Jed N Lampe
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 24, 2024
HCV Antiviral Drugs Have the Potential to Adversely Perturb the Fetal-Maternal Communication Axis through Inhibition of CYP3A7 DHEA-S OxidationHannah M Work, John C Hackett, Jed N Lampe
The Journal of Biological Chemistry|July 20, 2024
Drug metabolism of ciprofloxacin, ivacaftor, and raloxifene by Pseudomonas aeruginosa cytochrome P450 CYP107S1Sylvie E Kandel, Brian C Tooker, Jed N Lampe
Bioorganic & Medicinal Chemistry Letters|April 15, 2022
Identification of Aloe-derived natural products as prospective lead scaffolds for SARS-CoV-2 main protease (M<sup>pro</sup>) inhibitorsEmily G Hicks, Sylvie E Kandel, Jed N Lampe
Annual Reports in Medicinal Chemistry|March 24, 2015
Cytochrome P450 Enzyme Metabolites in Lead Discovery and DevelopmentSylvie E Kandel, Larry C Wienkers, Jed N Lampe
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 3, 2024
Comparison of the CYP3A Selective Inhibitors CYP3cide, Clobetasol, and Azamulin for Their Potential to Distinguish CYP3A7 Activity in the Presence of CYP3A4/5Hannah M Work, Sylvie E Kandel, Jed N Lampe
Biochemistry|December 21, 2007
Nile Red is a fluorescent allosteric substrate of cytochrome P450 3A4Jed N Lampe, Cristina Fernandez, Abhinav Nath, et al.
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