Synthesis and Characterization of AαC Metabolites
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Corresponding Organization :
Other organizations : Institut de Recherche en Santé, Environnement et Travail, Structure Fédérative de Recherche en Biologie et Santé de Rennes, Inserm, Université de Rennes, Centre Hospitalier de Fougères, University of Minnesota
Variable analysis
- Preparation of [4b,5,6,7,8,8a-^13C6]AαC as a gift from Dr. Daniel Doerge, National Center for Toxicological Research (Jefferson, AR)
- Preparation of N-(deoxyguanosin-8-yl)-2-amino-9H-pyrido[2,3-b]indole (dG-C8-AαC) and [^13C10]-dG-C8-AαC as previously described
- Not explicitly mentioned
- Human liver microsomes obtained from the Tennessee Donor Services, Nashville, TN, and kindly provided by Prof. F. P. Guengerich, Vanderbilt University
- DMSO, ethoxyresorufin, methoxyresorufin, methanol, acetonitrile, ascorbic acid, hydrochloric acid, ammonium acetate, sulfatase from Helix pomatia (≥10,000 units/g solid) and β-Glucuronidase from Helix pomatia (≥30,000 units/g solid) purchased from Sigma Aldrich (St. Louis, MO, USA)
- AαC-3-OH and AαC-6-OH prepared with human liver microsomes or rat liver microsomes and spectroscopically characterized as previously reported
- Not explicitly mentioned
- Not explicitly mentioned
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