Pharmacology, Toxicology and Pharmaceutical Science
Intrinsic Clearance
100%
Drug-Drug Interaction
83%
Cytochrome P450
68%
CYP3A4
56%
Pharmacokinetics
52%
Repaglinide
28%
Experimental Therapeutic
21%
Elimination
20%
Midazolam
19%
CYP3A
18%
Benzodiazepine
18%
Rosuvastatin
18%
Drug Metabolism
18%
Tolbutamide
18%
Diazepam
16%
Saquinavir
14%
Pitavastatin
14%
Clarithromycin
13%
Drug Interaction
12%
Epileptic Absence
12%
Alprazolam
12%
Macaca fascicularis
12%
Effusion
11%
Fexofenadine
10%
Dextromethorphan
10%
CYP2C9
10%
Plasma Protein Binding
10%
Polypeptide
10%
Drug Concentration
9%
Valsartan
9%
CYP2D6
9%
Phenytoin
9%
Atorvastatin
9%
Erythromycin
9%
Telmisartan
8%
First Pass Effect
8%
Quinidine
8%
Triazolam
8%
Enzyme Kinetics
8%
Serotonin 3 Antagonist
8%
Lipophilicity
8%
Ethoxycoumarin
8%
Cytochrome P450 Inhibitor
8%
Alosetron
8%
Rifampicin
8%
Zofran
8%
Cytochrome
7%
Cytochrome P450 3A5
7%
CYP2C8
7%
Phospholipid
7%
Medicine and Dentistry
In Vitro
36%
Drug Interaction
26%
Hepatocyte
17%
Cytochrome P450
13%
CYP3A4
11%
Intrinsic Clearance
8%
First Pass Effect
8%
Incubation
6%
Drug Clearance
6%
Metabolic Clearance
5%
Gut
5%
Membrane Permeability
5%
Intestinal Availability
5%
Biochemistry, Genetics and Molecular Biology
CYP3A4
13%
Glucuronidation
12%
Glucuronosyltransferase
12%
Hepatocyte
7%
CYP3A
5%
Substrate Concentration
5%