L 741051;
L 754394;
PROTEINASE INHIBITOR;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
AREA UNDER THE CURVE;
ARTICLE;
DOG;
DRUG BLOOD LEVEL;
DRUG METABOLISM;
DRUG STRUCTURE;
ENZYME INACTIVATION;
HUMAN IMMUNODEFICIENCY VIRUS;
MALE;
NONHUMAN;
PRIORITY JOURNAL;
PROTEINASE INHIBITION;
RAT;
Interspecies variation in liver weight, hepatic blood flow and antipyrine intrinsic clearance in extrapolation of data to benzodiazepines and phenytoin
Buxenbaum H (1980) Interspecies variation in liver weight, hepatic blood flow and antipyrine intrinsic clearance in extrapolation of data to benzodiazepines and phenytoin. J Pharmacokinet Biopharm 8:165-176.
Potent and selective inactivation of human liver microsomal cytochrome P450 isoforms hy L-754,394, an investigational human immune deficiency virus protease inhibitor
Chiba M, Nishime JA and Lin JH (1995) Potent and selective inactivation of human liver microsomal cytochrome P450 isoforms hy L-754,394, an investigational human immune deficiency virus protease inhibitor. J Pharmacol Exp Ther 275:1527-1534.
Alteration of plasma sex hormone levels associated with old age and its effect on hepatic drug metabolism in rats
Fujita S, Chiba M, Ohta M, Kitani K and Suzuki T (1940) Alteration of plasma sex hormone levels associated with old age and its effect on hepatic drug metabolism in rats. J Pharmacoi Exp Ther 253:369-374.
Prediction of pharmacokinetic alterations caused by drug-drug interactions: Metabolic interaction in the liver
Ito K, Iwatsubo T, Kanamitsu S, Ueda K, Suzuki H and Sugiyama Y (1998) Prediction of pharmacokinetic alterations caused by drug-drug interactions: Metabolic interaction in the liver. Pharmacol Rev 50:387-411.
Time and dose-dependent pharmacokinetics of L-754,394, an HIV protease inhibitor, in rats, dogs and monkeys
Lin JH, Chiba M, Chen IW, Vastag KJ, Nishime JA, Dorsey BD, Michelson SR and McDaniel SL (1995) Time and dose-dependent pharmacokinetics of L-754,394, an HIV protease inhibitor, in rats, dogs and monkeys. J Pharmacol Exp Ther 274:264-269.
Competing pathways in drug metabolism 1: Effect of varying input concentrations on gentisamide conjugation in the once-through in situ perfused rat liver
Morris ME, Yuen V, Tang BK and Pang KS (1988) Competing pathways in drug metabolism 1: Effect of varying input concentrations on gentisamide conjugation in the once-through in situ perfused rat liver. J Pharmacol Exp Ther 245:614-624.
In vitro studies on the metabolic activation of the furanopyridine L-754,394, a highly potent and selective mechanism-based inhibitor of cytochrome 3A4
Sahali-Sahly Y, Balani SK, Lin JH and Baillie TA (1996) In vitro studies on the metabolic activation of the furanopyridine L-754,394, a highly potent and selective mechanism-based inhibitor of cytochrome 3A4. Chem Res Toxicol 9:1007-1012.