Property Name |
Property Value |
Unit |
Raw Value |
Raw Unit |
Annotation |
Factor |
Reference |
Bioavailability |
50.0 |
% |
50±7 |
% |
PO, oral; intravenous injection, IV; |
|
The Pharmacological Basis of Therapeutics |
C Max |
149.0 |
ng/ml |
149±60 |
ng/ml |
PO, oral; Male, men; adults; normal,healthy; |
|
The Pharmacological Basis of Therapeutics |
C Max |
3.8 |
ng/ml |
3.8±2.4 |
ng/ml |
PO, oral; Active metabolite; Male, men; adults; normal,healthy; |
|
The Pharmacological Basis of Therapeutics |
T Max |
1.0 |
h |
1 |
h |
PO, oral; |
|
DRUGBANK |
T Max |
1.0 |
h |
1.0±0.5 |
h |
PO, oral; Male, men; adults; normal,healthy; |
|
The Pharmacological Basis of Therapeutics |
T Max |
1.0 |
h |
1.0±0.4 |
h |
PO, oral; Active metabolite; Male, men; adults; normal,healthy; |
|
The Pharmacological Basis of Therapeutics |
Tss |
120.0 |
h |
5.0 |
day |
|
|
DRUGBANK |
Metabolic |
75.0 |
% |
70-80 |
% |
Liver metabolism; |
|
DRUGBANK |
Clearance |
11.0 |
L/h |
183±59 |
ml/min |
|
RD, renal impairment, Renal disease,including uremia ↓ ; |
DRUGBANK |
Clearance |
0.66 |
L/h/kg |
11±2 |
ml/min/kg |
apparent clearance; hydrolysis; |
|
The Pharmacological Basis of Therapeutics |
Clearance |
0.90 |
L/h/kg |
15 |
ml/min/kg |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Volume of Distribution |
4.5 |
L/kg |
~3-6.0 |
L/kg |
Apparent volume of distribution; |
|
DRUGBANK |
Volume of Distribution |
2.6 |
L/kg |
2.6±0.3 |
L/kg |
Apparent volume of distribution; hydrolysis; |
|
The Pharmacological Basis of Therapeutics |
Volume of Distribution |
3.5 |
L/kg |
3.5 |
L/kg |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Half-life |
3.0 |
h |
~3 |
h |
elimination half-life; |
|
DRUGBANK |
Half-life |
3.0 |
h |
~3 |
h |
elimination half-life; Metabolite; |
|
DRUGBANK |
Half-life |
2.9 |
h |
2.9±0.7 |
h |
|
|
The Pharmacological Basis of Therapeutics |
Half-life |
4.0 |
h |
4 |
h |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Toxicity LD50 |
427.0 |
mg/kg |
427.0 |
mg/kg |
PO, oral; Rattus, Rat; |
|
DRUGBANK |
Eliminate Route |
90.0 |
% |
~90 |
% |
Urinary excretion; |
|
DRUGBANK |
Eliminate Route |
10.0 |
% |
~10 |
% |
Urinary excretion; Unchanged drug; |
|
DRUGBANK |
Eliminate Route |
0 |
% |
~0 |
% |
Urinary excretion; Unchanged drug; |
|
The Pharmacological Basis of Therapeutics |
Protein Binding |
16.0 |
% |
7-25 |
% |
plasma proteins; |
|
DRUGBANK |
Protein Binding |
7.0 |
% |
7 |
% |
|
|
The Pharmacological Basis of Therapeutics |