Property Name |
Property Value |
Unit |
Raw Value |
Raw Unit |
Annotation |
Factor |
Reference |
Bioavailability |
91.0 |
% |
91 |
% |
PO, oral; |
|
DRUGBANK |
Bioavailability |
91.0 |
% |
91±6 |
% |
PO, oral; Drug form; |
|
The Pharmacological Basis of Therapeutics |
C Max |
275.0 |
ng/ml |
275±27 |
ng/ml |
IM,intramuscular injection; Drug form; |
|
The Pharmacological Basis of Therapeutics |
T Max |
0.72 |
h |
0.72±0.01 |
h |
IM,intramuscular injection; Drug form; |
|
The Pharmacological Basis of Therapeutics |
Clearance |
0.0102 |
L/h/kg |
0.17±0.02 |
ml/min/kg |
|
Elderly → ;Hepatitis, Hep ↓ ;Obesity ↓ ;Somking ↑ ; |
The Pharmacological Basis of Therapeutics |
Volume of Distribution |
1.2 |
L/kg |
1.24±0.09 |
L/kg |
|
Elderly → ;Obesity ↑ ;Hepatitis, Hep → ; |
The Pharmacological Basis of Therapeutics |
Half-life |
48.0 |
h |
~2 |
day |
elimination half-life; |
|
DRUGBANK |
Half-life |
45.0 |
h |
~40-50 |
h |
|
|
DRUGBANK |
Half-life |
93.0 |
h |
93±11 |
h |
intravenous injection, IV; |
Preg, pregnant ↑ ;Obesity ↑ ;Hepatic cirrhosis, cirr ↓ ;Hepatitis, Hep ↓ ;Age ↑ ;Somking ↓ ; |
The Pharmacological Basis of Therapeutics |
Toxicity LD50 |
1320.0 |
mg/kg |
1320.0 |
mg/kg |
PO, oral; Rattus, Rat; |
|
DRUGBANK |
Toxicity LD50 |
1600.0 |
mg/kg |
>1600 |
mg/kg |
PO, oral; monkey; |
|
DRUGBANK |
Toxicity LD50 |
1320.0 |
mg/kg |
1320.0 |
mg/kg |
PO, oral; Rattus, Rat; |
|
T3DB |
Toxicity LD50 |
1600.0 |
mg/kg |
>1600 |
mg/kg |
PO, oral; Rattus, Rat; |
|
T3DB |
Eliminate Route |
1.0 |
% |
<1 |
% |
Urinary excretion; Unchanged drug; |
|
The Pharmacological Basis of Therapeutics |
Protein Binding |
97.5 |
% |
97-98 |
% |
plasma proteins; |
|
DRUGBANK |
Protein Binding |
97.5 |
% |
97.5 |
% |
|
Elderly → ;RD, renal impairment, Renal disease,including uremia ↓ ;Obesity → ; |
The Pharmacological Basis of Therapeutics |