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Journal of Medicinal Chemistry|April 1, 1985
Stereoselective metabolism of conformational analogues of warfarin by beta-naphthoflavone-inducible cytochrome P-450L D Heimark, W F TragerJournal of Medicinal Chemistry|August 1, 1984
The preferred solution conformation of warfarin at the active site of cytochrome P-450 based on the CD spectra in octanol/water model systemL D Heimark, W F TragerBiochemistry|September 28, 1998
Mechanism-based inactivation of cytochrome P450 2B1 by 8-methoxypsoralen and several other furanocoumarinsL L Koenigs, W F TragerJournal of Medicinal Chemistry|August 1, 1985
Substrate probes for the mechanism of aromatic hydroxylation catalyzed by cytochrome P-450: selectively deuterated analogues of warfarinE D Bush, W F TragerBiomedical Mass Spectrometry|February 1, 1985
A stable isotope assay for phenprocoumon and its metabolitesL D Heimark, W F TragerDrug Metabolism and Disposition: the Biological Fate of Chemicals|June 1, 1995
Inhibition of (S)-warfarin metabolism by sulfinpyrazone and its metabolitesM He, K L Kunze, W F TragerResearch Communications in Chemical Pathology and Pharmacology|October 1, 1976
Warfarin: stereochemical aspects of its metabolism in vivo in the ratL R Pohl, R Bales, W F TragerBiomedical & Environmental Mass Spectrometry|April 1, 1990
The use of Brauman's least squares approach for the quantification of deuterated chlorophenolsK Korzekwa, W N Howald, W F TragerJournal of Medicinal Chemistry|May 1, 1975
Biotransformation of phenprocoumon in the ratL R Pohl, R E Haddock, W F TragerBiochemistry|November 14, 1989
Isotopically labeled chlorobenzenes as probes for the mechanism of cytochrome P-450 catalyzed aromatic hydroxylationK R Korzekwa, D C Swinney, W F TragerPageof 11