Property Name |
Property Value |
Unit |
Raw Value |
Raw Unit |
Annotation |
Reference |
Absorption |
95.0 |
% |
>95 |
% |
PO, oral; |
DRUGBANK |
Bioavailability |
56.0 |
% |
56 |
% |
PO, oral; |
DRUGBANK |
Bioavailability |
90.0 |
% |
90 |
% |
PO, oral; increasing doses; |
DRUGBANK |
T Max |
0.65 |
h |
0.3-1 |
h |
PO, oral; |
DRUGBANK |
Metabolic |
100.0 |
% |
~100 |
% |
Liver metabolism; |
DRUGBANK |
Clearance |
54.0 |
L/h |
30-78 |
L/h |
Urinary excretion; |
DRUGBANK |
Clearance |
0.60 |
L/h/kg |
10 |
ml/min/kg |
intravenous injection, IV; human, homo sapiens; |
Human Intravenous Pharmacokinetic Dataset |
Volume of Distribution |
1.3 |
L/kg |
1-1.5 |
L/kg |
|
DRUGBANK |
Volume of Distribution |
1.1 |
L/kg |
1.1 |
L/kg |
intravenous injection, IV; human, homo sapiens; |
Human Intravenous Pharmacokinetic Dataset |
Half-life |
1.5 |
h |
1-2 |
h |
|
DRUGBANK |
Half-life |
4.0 |
h |
4 |
h |
Hepatitis, Hep; |
DRUGBANK |
Half-life |
1.5 |
h |
1.5 |
h |
intravenous injection, IV; human, homo sapiens; |
Human Intravenous Pharmacokinetic Dataset |
Toxicity LD50 |
730.0 |
mg/kg |
730.0 |
mg/kg |
mouse; |
DRUGBANK |
Toxicity LD50 |
1300.0 |
mg/kg |
1300.0 |
mg/kg |
Rattus, Rat; |
DRUGBANK |
Toxicity LD50 |
730.0 |
mg/kg |
730.0 |
mg/kg |
mouse; |
T3DB |
Toxicity LD50 |
1300.0 |
mg/kg |
1300.0 |
mg/kg |
Rattus, Rat; |
T3DB |
Eliminate Route |
100.0 |
% |
~100 |
% |
Urinary excretion; |
DRUGBANK |
Protein Binding |
50.0 |
% |
~50 |
% |
|
DRUGBANK |