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Biochemistry
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September 28, 1998
Mechanism-based inactivation of cytochrome P450 2B1 by 8-methoxypsoralen and several other furanocoumarins
L L Koenigs, W F Trager
Journal of Medicinal Chemistry
|
August 1, 1985
Substrate probes for the mechanism of aromatic hydroxylation catalyzed by cytochrome P-450: selectively deuterated analogues of warfarin
E D Bush, W F Trager
Biomedical Mass Spectrometry
|
February 1, 1985
A stable isotope assay for phenprocoumon and its metabolites
L D Heimark, W F Trager
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
June 1, 1995
Inhibition of (S)-warfarin metabolism by sulfinpyrazone and its metabolites
M He, K L Kunze, W F Trager
Research Communications in Chemical Pathology and Pharmacology
|
October 1, 1976
Warfarin: stereochemical aspects of its metabolism in vivo in the rat
L R Pohl, R Bales, W F Trager
Biomedical & Environmental Mass Spectrometry
|
April 1, 1990
The use of Brauman's least squares approach for the quantification of deuterated chlorophenols
K Korzekwa, W N Howald, W F Trager
Journal of Medicinal Chemistry
|
May 1, 1975
Biotransformation of phenprocoumon in the rat
L R Pohl, R E Haddock, W F Trager
Biochemistry
|
November 14, 1989
Isotopically labeled chlorobenzenes as probes for the mechanism of cytochrome P-450 catalyzed aromatic hydroxylation
K R Korzekwa, D C Swinney, W F Trager
Drug Metabolism Reviews
|
January 1, 1995
Isotope effect studies on the cytochrome P450 enzymes
K R Korzekwa, J R Gillette, W F Trager
Journal of Medicinal Chemistry
|
February 1, 1978
Conformations of selected 3-substituted 4-hydroxycoumarins in solution by nuclear magnetic resonance. Warfarin and phenprocoumon
E J Valente, W R Porter, W F Trager
Page
of 9
Search research articles
Search
Showing results (11-20 of 85) with videos related to
Sort By:
Page
of 9
Biochemistry
|
September 28, 1998
Mechanism-based inactivation of cytochrome P450 2B1 by 8-methoxypsoralen and several other furanocoumarins
L L Koenigs, W F Trager
Journal of Medicinal Chemistry
|
August 1, 1985
Substrate probes for the mechanism of aromatic hydroxylation catalyzed by cytochrome P-450: selectively deuterated analogues of warfarin
E D Bush, W F Trager
Biomedical Mass Spectrometry
|
February 1, 1985
A stable isotope assay for phenprocoumon and its metabolites
L D Heimark, W F Trager
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
June 1, 1995
Inhibition of (S)-warfarin metabolism by sulfinpyrazone and its metabolites
M He, K L Kunze, W F Trager
Research Communications in Chemical Pathology and Pharmacology
|
October 1, 1976
Warfarin: stereochemical aspects of its metabolism in vivo in the rat
L R Pohl, R Bales, W F Trager
Biomedical & Environmental Mass Spectrometry
|
April 1, 1990
The use of Brauman's least squares approach for the quantification of deuterated chlorophenols
K Korzekwa, W N Howald, W F Trager
Journal of Medicinal Chemistry
|
May 1, 1975
Biotransformation of phenprocoumon in the rat
L R Pohl, R E Haddock, W F Trager
Biochemistry
|
November 14, 1989
Isotopically labeled chlorobenzenes as probes for the mechanism of cytochrome P-450 catalyzed aromatic hydroxylation
K R Korzekwa, D C Swinney, W F Trager
Drug Metabolism Reviews
|
January 1, 1995
Isotope effect studies on the cytochrome P450 enzymes
K R Korzekwa, J R Gillette, W F Trager
Journal of Medicinal Chemistry
|
February 1, 1978
Conformations of selected 3-substituted 4-hydroxycoumarins in solution by nuclear magnetic resonance. Warfarin and phenprocoumon
E J Valente, W R Porter, W F Trager
Page
of 9