Property Name |
Property Value |
Unit |
Raw Value |
Raw Unit |
Annotation |
Reference |
Absorption |
64.0 |
% |
28-100 |
% |
|
DRUGBANK |
Bioavailability |
28.0 |
% |
28(0-80) |
% |
PO, oral; |
The Pharmacological Basis of Therapeutics |
C Max |
1456864.6 |
ng/ml |
11.2 |
mM |
intravenous infusion, IV in drop; tumor; |
The Pharmacological Basis of Therapeutics |
Clearance |
0.96 |
L/h/kg |
16±7 |
ml/min/kg |
|
The Pharmacological Basis of Therapeutics |
Clearance |
1.6 |
L/h/kg |
26 |
ml/min/kg |
intravenous injection, IV; human, homo sapiens; |
Human Intravenous Pharmacokinetic Dataset |
Volume of Distribution |
0.25 |
L/kg |
0.25±0.12 |
L/kg |
|
The Pharmacological Basis of Therapeutics |
Volume of Distribution |
0.23 |
L/kg |
0.23 |
L/kg |
intravenous injection, IV; human, homo sapiens; |
Human Intravenous Pharmacokinetic Dataset |
Half-life |
0.25 |
h |
10-20 |
min |
|
DRUGBANK |
Half-life |
0.18 |
h |
11±4 |
min |
|
The Pharmacological Basis of Therapeutics |
Half-life |
20.0 |
h |
~20 |
h |
terminal half-life; |
The Pharmacological Basis of Therapeutics |
Half-life |
0.12 |
h |
0.12 |
h |
intravenous injection, IV; human, homo sapiens; |
Human Intravenous Pharmacokinetic Dataset |
Toxicity LD50 |
230.0 |
mg/kg |
230.0 |
mg/kg |
PO, oral; mouse; |
DRUGBANK |
Toxicity LD50 |
230.0 |
mg/kg |
230.0 |
mg/kg |
PO, oral; mouse; |
T3DB |
Eliminate Route |
13.5 |
% |
7-20 |
% |
Urinary excretion; Unchanged drug; |
DRUGBANK |
Eliminate Route |
10.0 |
% |
<10 |
% |
Urinary excretion; Unchanged drug; |
The Pharmacological Basis of Therapeutics |
Protein Binding |
10.0 |
% |
8-12 |
% |
|
DRUGBANK |
Protein Binding |
10.0 |
% |
8-12 |
% |
|
The Pharmacological Basis of Therapeutics |