Property Name |
Property Value |
Unit |
Raw Value |
Raw Unit |
Annotation |
Factor |
Reference |
AUC |
2000.0 |
ng.h/ml |
2.0 |
mcg.h/ml |
PO, oral; |
|
DRUGBANK |
Bioavailability |
63.0 |
% |
63.0 |
% |
PO, oral; |
|
DRUGBANK |
Bioavailability |
94.0 |
% |
94.0 |
% |
PO, oral; high-fat meal; |
high-fat meal ↑ ; |
DRUGBANK |
Bioavailability |
63.0 |
% |
63.0 |
% |
PO, oral; extensive metabolizers, EM; |
|
The Pharmacological Basis of Therapeutics |
Bioavailability |
94.0 |
% |
94.0 |
% |
PO, oral; poor metabolizers, PM; |
|
The Pharmacological Basis of Therapeutics |
C Max |
350.0 |
ng/ml |
350.0 |
ng/ml |
PO, oral; |
|
DRUGBANK |
C Max |
160.0 |
ng/ml |
160.0 |
ng/ml |
PO, oral; extensive metabolizers, EM; |
|
The Pharmacological Basis of Therapeutics |
C Max |
915.0 |
ng/ml |
915.0 |
ng/ml |
PO, oral; poor metabolizers, PM; |
|
The Pharmacological Basis of Therapeutics |
T Max |
1.5 |
h |
1-2 |
h |
PO, oral; |
|
DRUGBANK |
T Max |
2.0 |
h |
2.0 |
h |
PO, oral; poor metabolizers, PM; extensive metabolizers, EM; |
|
The Pharmacological Basis of Therapeutics |
Clearance |
0.47 |
L/h/kg |
0.27-0.67 |
L/h/kg |
|
|
DRUGBANK |
Clearance |
0.37 |
L/h/kg |
6.2 |
ml/min/kg |
apparent clearance; at steady state; hydrolysis; extensive metabolizers, EM; |
hepatopathy,LD ↓ ; |
The Pharmacological Basis of Therapeutics |
Clearance |
0.0360 |
L/h/kg |
0.6 |
ml/min/kg |
apparent clearance; at steady state; hydrolysis; poor metabolizers, PM; |
|
The Pharmacological Basis of Therapeutics |
Clearance |
0.56 |
L/h/kg |
9.3 |
ml/min/kg |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Volume of Distribution |
2.1 |
L/kg |
1.6-2.6 |
L/kg |
PO, oral; |
|
DRUGBANK |
Volume of Distribution |
0.85 |
L/kg |
~0.85 |
L/kg |
Steady state volume of distribution; intravenous injection, IV; |
|
DRUGBANK |
Volume of Distribution |
2.3 |
L/kg |
2.3 |
L/kg |
Apparent volume of distribution; at steady state; hydrolysis; extensive metabolizers, EM; |
|
The Pharmacological Basis of Therapeutics |
Volume of Distribution |
1.1 |
L/kg |
1.1 |
L/kg |
Apparent volume of distribution; at steady state; hydrolysis; poor metabolizers, PM; |
|
The Pharmacological Basis of Therapeutics |
Volume of Distribution |
0.85 |
L/kg |
0.85 |
L/kg |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Half-life |
4.3 |
h |
3-5.6 |
h |
CYP2D6 genetic polymorphisms; |
|
DRUGBANK |
Half-life |
5.3 |
h |
5.3 |
h |
extensive metabolizers, EM; at steady state; |
|
The Pharmacological Basis of Therapeutics |
Half-life |
20.0 |
h |
20.0 |
h |
poor metabolizers, PM; at steady state; |
|
The Pharmacological Basis of Therapeutics |
Half-life |
5.2 |
h |
5.2 |
h |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Eliminate Route |
80.0 |
% |
>80 |
% |
Urinary excretion; |
|
DRUGBANK |
Eliminate Route |
17.0 |
% |
<17 |
% |
Faeces excretion; |
|
DRUGBANK |
Eliminate Route |
3.0 |
% |
<3 |
% |
Unchanged drug; |
|
DRUGBANK |
Eliminate Route |
1.5 |
% |
1-2 |
% |
Urinary excretion; Unchanged drug; |
|
The Pharmacological Basis of Therapeutics |
Protein Binding |
98.7 |
% |
98.7 |
% |
plasma proteins; |
|
DRUGBANK |
Protein Binding |
96.2 |
% |
~96.2 |
% |
|
|
DRUGBANK |
Protein Binding |
98.7 |
% |
98.7±0.3 |
% |
|
|
The Pharmacological Basis of Therapeutics |