Property Name |
Property Value |
Unit |
Raw Value |
Raw Unit |
Annotation |
Reference |
AUC |
4.8 |
ng.h/ml |
4.78 |
ng.h/ml |
ophthalmic administration; |
DRUGBANK |
AUC |
6.5 |
ng.h/ml |
6.46 |
ng.h/ml |
intravenous injection, IV; |
DRUGBANK |
Bioavailability |
78.0 |
% |
78.0±24.5 |
% |
ophthalmic administration; different study; |
DRUGBANK |
Bioavailability |
60.0 |
% |
60.0 |
% |
ophthalmic administration; different study; |
DRUGBANK |
Bioavailability |
61.0 |
% |
61±6 |
% |
PO, oral; |
The Pharmacological Basis of Therapeutics |
C Max |
1.1 |
ng/ml |
1.14 |
ng/ml |
ophthalmic administration; |
DRUGBANK |
C Max |
61.0 |
ng/ml |
61±39 |
ng/ml |
PO, oral; extensive metabolizers, EM; |
The Pharmacological Basis of Therapeutics |
C Max |
114.0 |
ng/ml |
114±21 |
ng/ml |
PO, oral; poor metabolizers, PM; |
The Pharmacological Basis of Therapeutics |
T Max |
0.25 |
h |
0.25 |
h |
ophthalmic administration; |
DRUGBANK |
T Max |
1.2 |
h |
1.2±0.4 |
h |
PO, oral; extensive metabolizers, EM; |
The Pharmacological Basis of Therapeutics |
T Max |
1.8 |
h |
1.8±0.8 |
h |
PO, oral; poor metabolizers, PM; |
The Pharmacological Basis of Therapeutics |
Metabolic |
90.0 |
% |
90 |
% |
Liver metabolism; |
DRUGBANK |
Clearance |
33.4 |
L/h |
557±61 |
ml/min |
Plasma clearance; normal,healthy; |
DRUGBANK |
Clearance |
45.1 |
L/h |
751.5±90.6 |
ml/min |
Total clearance; normal,healthy; |
DRUGBANK |
Clearance |
5.8 |
L/h |
97.2±10.1 |
ml/min |
Renal clearance; normal,healthy; |
DRUGBANK |
Clearance |
0.46 |
L/h/kg |
7.7±1.2 |
ml/min/kg |
hydrolysis; |
The Pharmacological Basis of Therapeutics |
Clearance |
0.51 |
L/h/kg |
8.5 |
ml/min/kg |
intravenous injection, IV; human, homo sapiens; |
Human Intravenous Pharmacokinetic Dataset |
Volume of Distribution |
1.5 |
L/kg |
1.3-1.7 |
L/kg |
|
DRUGBANK |
Volume of Distribution |
1.7 |
L/kg |
1.7±0.2 |
L/kg |
hydrolysis; |
The Pharmacological Basis of Therapeutics |
Volume of Distribution |
1.5 |
L/kg |
1.5 |
L/kg |
intravenous injection, IV; human, homo sapiens; |
Human Intravenous Pharmacokinetic Dataset |
Half-life |
2.9 |
h |
2.9±0.3 |
h |
normal,healthy; |
DRUGBANK |
Half-life |
2.7 |
h |
2.7±0.5 |
h |
CYP2D6 genetic polymorphisms; |
The Pharmacological Basis of Therapeutics |
Half-life |
7.5 |
h |
7.5±3.0 |
h |
poor metabolizers, PM; hydrolysis; PO, oral; |
The Pharmacological Basis of Therapeutics |
Half-life |
3.7 |
h |
3.7±1.7 |
h |
extensive metabolizers, EM; PO, oral; |
The Pharmacological Basis of Therapeutics |
Half-life |
2.2 |
h |
2.2 |
h |
intravenous injection, IV; human, homo sapiens; |
Human Intravenous Pharmacokinetic Dataset |
Toxicity LD50 |
1028.0 |
mg/kg |
1028.0 |
mg/kg |
PO, oral; Rattus, Rat; |
DRUGBANK |
Toxicity LD50 |
1137.0 |
mg/kg |
1137.0 |
mg/kg |
PO, oral; mouse; |
DRUGBANK |
Eliminate Route |
8.0 |
% |
8±4 |
% |
Urinary excretion; PO, oral; Unchanged drug; |
The Pharmacological Basis of Therapeutics |
Protein Binding |
10.0 |
% |
~10 |
% |
plasma proteins; |
DRUGBANK |
Protein Binding |
10.0 |
% |
<10 |
% |
|
The Pharmacological Basis of Therapeutics |