| Property Name |
Property Value |
Unit |
Raw Value |
Raw Unit |
Annotation |
Factor |
Reference |
| Bioavailability |
70.0 |
% |
70 |
% |
PO, oral; |
|
DRUGBANK |
Bioavailability |
66.0 |
% |
66±28 |
% |
PO, oral; |
|
The Pharmacological Basis of Therapeutics |
Bioavailability |
103.0 |
% |
103±13 |
% |
IM,intramuscular injection; |
|
The Pharmacological Basis of Therapeutics |
| C Max |
10.0 |
ng/ml |
10.0 |
ng/ml |
PO, oral; schizophrenia; |
|
The Pharmacological Basis of Therapeutics |
C Max |
45.0 |
ng/ml |
45.0 |
ng/ml |
PO, oral; Active metabolite; schizophrenia; |
|
The Pharmacological Basis of Therapeutics |
| T Max |
1.0 |
h |
~1 |
h |
PO, oral; schizophrenia; |
|
The Pharmacological Basis of Therapeutics |
| Clearance |
2.2 |
L/h |
15-59 |
ml/min |
Renal clearance; Elderly; Renal metabolism; |
Age ↓ ; |
DRUGBANK |
Clearance |
0.32 |
L/h/kg |
5.4±1.4 |
ml/min/kg |
hydrolysis; |
Elderly ↓ ;RD, renal impairment, Renal disease,including uremia ↓ ; |
The Pharmacological Basis of Therapeutics |
Clearance |
0.32 |
L/h/kg |
5.4 |
ml/min/kg |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
| Volume of Distribution |
1.5 |
L/kg |
~1.0-2.0 |
L/kg |
|
|
DRUGBANK |
Volume of Distribution |
1.1 |
L/kg |
1.1±0.2 |
L/kg |
|
|
The Pharmacological Basis of Therapeutics |
Volume of Distribution |
1.1 |
L/kg |
1.1 |
L/kg |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
| Half-life |
3.0 |
h |
3 |
h |
extensive metabolizers, EM; |
|
DRUGBANK |
Half-life |
20.0 |
h |
20 |
h |
poor metabolizers, PM; |
|
DRUGBANK |
Half-life |
3.2 |
h |
3.2±0.8 |
h |
|
RD, renal impairment, Renal disease,including uremia ↑ ;Age ↑ ; |
The Pharmacological Basis of Therapeutics |
Half-life |
20.0 |
h |
20±3 |
h |
Active metabolite; |
RD, renal impairment, Renal disease,including uremia ↑ ;Age ↑ ; |
The Pharmacological Basis of Therapeutics |
Half-life |
3.2 |
h |
3.2 |
h |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
| Toxicity LD50 |
57.7 |
mg/kg |
57.7 |
mg/kg |
PO, oral; Rattus, Rat; |
|
DRUGBANK |
Toxicity LD50 |
34.0 |
mg/kg |
34.0 |
mg/kg |
intravenous injection, IV; Rattus, Rat; |
|
DRUGBANK |
Toxicity LD50 |
82.1 |
mg/kg |
82.1 |
mg/kg |
PO, oral; mouse; |
|
T3DB |
| Eliminate Route |
3.0 |
% |
3±2 |
% |
Urinary excretion; Unchanged drug; |
|
The Pharmacological Basis of Therapeutics |
| Protein Binding |
88.0 |
% |
88 |
% |
plasma proteins; human, homo sapiens; |
|
DRUGBANK |
Protein Binding |
89.0 |
% |
89 |
% |
|
Hepatic cirrhosis, cirr ↓ ; |
The Pharmacological Basis of Therapeutics |