Property Name |
Property Value |
Unit |
Raw Value |
Raw Unit |
Annotation |
Factor |
Reference |
Bioavailability |
72.0 |
% |
72±7 |
% |
PO, oral; |
|
The Pharmacological Basis of Therapeutics |
C Max |
59.0 |
ng/ml |
59.0 |
ng/ml |
|
|
DRUGBANK |
C Max |
121.0 |
ng/ml |
121.0 |
ng/ml |
|
|
DRUGBANK |
C Max |
107.5 |
ng/ml |
76-139 |
ng/ml |
Oral single dose; adults; young; |
|
The Pharmacological Basis of Therapeutics |
T Max |
1.6 |
h |
1.6 |
h |
|
|
DRUGBANK |
T Max |
1.6 |
h |
1.6 |
h |
|
|
DRUGBANK |
T Max |
1.8 |
h |
1.0-2.6 |
h |
Oral single dose; adults; young; |
|
The Pharmacological Basis of Therapeutics |
Clearance |
0.0153 |
L/h/kg |
0.24-0.27 |
ml/min/kg |
Total clearance; |
|
DRUGBANK |
Clearance |
0.27 |
L/h/kg |
4.5±0.7 |
ml/min/kg |
hydrolysis; |
Children ↑ ;Elderly ↓ ;Hepatic cirrhosis, cirr ↓ ;RD, renal impairment, Renal disease,including uremia → ; |
The Pharmacological Basis of Therapeutics |
Clearance |
0.26 |
L/h/kg |
4.3 |
ml/min/kg |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Volume of Distribution |
0.61 |
L/kg |
0.54-0.68 |
L/kg |
human, homo sapiens; |
RD, renal impairment, Renal disease,including uremia ↑ ; |
DRUGBANK |
Volume of Distribution |
0.68 |
L/kg |
0.68±0.06 |
L/kg |
|
RD, renal impairment, Renal disease,including uremia ↑ ; |
The Pharmacological Basis of Therapeutics |
Volume of Distribution |
0.54 |
L/kg |
0.54 |
L/kg |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Half-life |
2.6 |
h |
2.6 |
h |
elimination half-life; |
|
DRUGBANK |
Half-life |
2.5 |
h |
2.5 |
h |
elimination half-life; |
|
DRUGBANK |
Half-life |
1.9 |
h |
1.9±0.2 |
h |
|
Children ↓ ;Hepatic cirrhosis, cirr ↑ ;RD, renal impairment, Renal disease,including uremia → ;Age ↑ ; |
The Pharmacological Basis of Therapeutics |
Half-life |
1.7 |
h |
1.7 |
h |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Toxicity LD50 |
695.0 |
mg/kg |
695.0 |
mg/kg |
PO, oral; male rat; |
|
DRUGBANK |
Toxicity LD50 |
695.0 |
mg/kg |
695.0 |
mg/kg |
PO, oral; Rattus, Rat; |
|
T3DB |
Eliminate Route |
1.0 |
% |
<1 |
% |
Urinary excretion; Unchanged drug; |
|
The Pharmacological Basis of Therapeutics |
Protein Binding |
92.5 |
% |
92.5±0.1 |
% |
|
|
DRUGBANK |
Protein Binding |
92.0 |
% |
92 |
% |
|
RD, renal impairment, Renal disease,including uremia ↓ ;Hepatic cirrhosis, cirr ↓ ; |
The Pharmacological Basis of Therapeutics |