General Information of Drug (ID: )

Drug Name
Synonyms
#Ro5 Violations (Lipinski): 1 Molecular Weight (mw)
Logarithm of the Partition Coefficient (xlogp)
Rotatable Bond Count (rotbonds)
Hydrogen Bond Donor Count (hbonddonor)
Hydrogen Bond Acceptor Count (hbondacc)
ADMET Property
Absorption AUC
The area under the plot of plasma concentration (AUC) of drug is 200 mcgh/L [1]
Absorption Cmax
The maximum plasma concentration (Cmax) of drug is 28 mcg/L [1]
Bioavailability
The bioavailability of drug is 14% [1]
Clearance
The total plasma clearance of drug is 625 mL/min [2]
Elimination
Atorvastatin and its metabolites are mainly eliminated in the bile without enterohepatic recirculation []
Half-life
The concentration or amount of drug in body reduced by one-half in 14 hours (atorvastatin), and 30 hours (its metabolites) []
Metabolism
The drug is metabolized via the cytochrome P450 3A4 in the intestine and liver []
Vd
The volume of distribution (Vd) of drug is 380 L []
Cross-matching ID

References

1 Ray SK, Rege NN: Atorvastatin: in the management of hyperlipidaemia. J Postgrad Med. 2000 Jul-Sep;46(3):242-3.
2 Lennernas H: Clinical pharmacokinetics of atorvastatin. Clin Pharmacokinet. 2003;42(13):1141-60.