Cytochrome P450 (P450) reaction phenotyping is a key process toward accurately determining the contribution of different P450s to the metabolism of new chemical entities. The significance of P450s to drug disposition has led to the identification of selective chemical and antibody inhibitors for individual P450 enzymes. De-spite these advances, the maximal inhibition attainable is limited by the use of inhibitor concentrations that maintain selectivity for the individual P450s. Thus, most commercially available inhibitors produce a maximal inhibition of 80%. Herein, the combination of chemical plus antibody inhibitors is explored to find whether P450 3A could be selectively and completely (>99%) inhibited by using both inhibitors simulta...
Discovery of the new drug or evaluation of chemical moiety which possesses drug like properties are ...
Human cytochrome P450 (CYP) 3A4 is the most abundant hepatic and intestinal phase I enzyme that meta...
A novel in vitro model was recently developed in our laboratories for the prediction of magnitude of...
Cytochrome P450 (CYP) constitutes a superfamily of heme- containing enzymes that catalyze the oxidat...
The cytochrome P450s (CYPs) play a central role in the metabolism of various endogenous and exogenou...
Three-dimensional homology models of cytochromes P450 (P450) 2B1 and P450 3A4 have been utilized alo...
Cytochromes P450 (CYP) are a superfamily of enzymes, involved in metabolism of xenobiotic compounds....
The inhibition of human cytochrome P450s (CYPs) is one of the most common mechanisms which can lead ...
The cytochrome P450 (CYP) gene family strongly influences drug development. We determined potency va...
Identifying selective inhibitors of cytochrome P450 isoforms is a useful tool in defining the role o...
Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmacology and Toxicology S...
The 2012 EMA drug interaction guidance and the FDA draft drug interaction guidance proposed that hu...
Introduction: Direct and time-dependent inhibition (TDI) of cytochrome P450 enzymes (CYP) raises dru...
To gain insight into the specificity of cytochrome P-450 2D6 toward inhibitors, a preliminary pharma...
The selectivity of inhibition for four dopamine receptor agonists (pramipexole, ropinirole, pergolid...
Discovery of the new drug or evaluation of chemical moiety which possesses drug like properties are ...
Human cytochrome P450 (CYP) 3A4 is the most abundant hepatic and intestinal phase I enzyme that meta...
A novel in vitro model was recently developed in our laboratories for the prediction of magnitude of...
Cytochrome P450 (CYP) constitutes a superfamily of heme- containing enzymes that catalyze the oxidat...
The cytochrome P450s (CYPs) play a central role in the metabolism of various endogenous and exogenou...
Three-dimensional homology models of cytochromes P450 (P450) 2B1 and P450 3A4 have been utilized alo...
Cytochromes P450 (CYP) are a superfamily of enzymes, involved in metabolism of xenobiotic compounds....
The inhibition of human cytochrome P450s (CYPs) is one of the most common mechanisms which can lead ...
The cytochrome P450 (CYP) gene family strongly influences drug development. We determined potency va...
Identifying selective inhibitors of cytochrome P450 isoforms is a useful tool in defining the role o...
Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmacology and Toxicology S...
The 2012 EMA drug interaction guidance and the FDA draft drug interaction guidance proposed that hu...
Introduction: Direct and time-dependent inhibition (TDI) of cytochrome P450 enzymes (CYP) raises dru...
To gain insight into the specificity of cytochrome P-450 2D6 toward inhibitors, a preliminary pharma...
The selectivity of inhibition for four dopamine receptor agonists (pramipexole, ropinirole, pergolid...
Discovery of the new drug or evaluation of chemical moiety which possesses drug like properties are ...
Human cytochrome P450 (CYP) 3A4 is the most abundant hepatic and intestinal phase I enzyme that meta...
A novel in vitro model was recently developed in our laboratories for the prediction of magnitude of...