Property Name |
Property Value |
Unit |
Raw Value |
Raw Unit |
Annotation |
Factor |
Reference |
AUC |
2.9 |
ng.h/ml |
172±96 |
ng.min/ml |
Tablet, PO, oral; |
|
DRUGBANK |
AUC |
25.1 |
ng.h/ml |
1508±1360 |
ng.min/ml |
Tablet, PO, oral; |
|
DRUGBANK |
AUC |
1.3 |
ng.h/ml |
1.25±0.67 |
ng.h/ml |
sublingual; |
|
DRUGBANK |
AUC |
10.4 |
ng.h/ml |
10.38±3.70 |
ng.h/ml |
sublingual; increasing doses; |
increasing doses ↓ ; |
DRUGBANK |
AUC |
0.42 |
ng.h/ml |
0.42±0.35 |
ng.h/ml |
Transdermal preparations; |
|
DRUGBANK |
AUC |
3.8 |
ng.h/ml |
3772.0 |
pg.h/ml |
nasal spray; |
|
DRUGBANK |
AUC |
3.8 |
ng.h/ml |
3772.0 |
pg.h/ml |
|
|
DRUGBANK |
Bioavailability |
54.0 |
% |
54 |
% |
sublingual; |
|
DRUGBANK |
Bioavailability |
50.0 |
% |
50 |
% |
Tablet, PO, oral; |
|
DRUGBANK |
Bioavailability |
65.0 |
% |
65 |
% |
buccal; |
|
DRUGBANK |
Bioavailability |
76.0 |
% |
76 |
% |
sublingual; |
|
DRUGBANK |
Bioavailability |
82.0 |
% |
82 |
% |
nasal spray; |
|
DRUGBANK |
Bioavailability |
50.0 |
% |
~50 |
% |
buccal; |
|
The Pharmacological Basis of Therapeutics |
C Max |
0.40 |
ng/ml |
0.4±0.1 |
ng/ml |
Tablet, PO, oral; |
|
DRUGBANK |
C Max |
0.20 |
ng/ml |
0.20±0.06 |
ng/ml |
sublingual; |
|
DRUGBANK |
C Max |
1.6 |
ng/ml |
1.61±0.60 |
ng/ml |
sublingual; increasing doses; |
increasing doses ↓ ; |
DRUGBANK |
C Max |
0.24 |
ng/ml |
0.24±0.20 |
ng/ml |
Transdermal preparations; |
|
DRUGBANK |
C Max |
0.82 |
ng/ml |
815±301 |
pg/ml |
nasal spray; |
|
DRUGBANK |
C Max |
0.82 |
ng/ml |
815±301 |
pg/ml |
|
|
DRUGBANK |
C Max |
0.80 |
ng/ml |
0.8±0.3 |
ng/ml |
buccal; |
|
The Pharmacological Basis of Therapeutics |
C Max |
1.4 |
ng/ml |
1.4±0.5 |
ng/ml |
Transdermal preparations; |
|
The Pharmacological Basis of Therapeutics |
T Max |
0.50 |
h |
20-40 |
min |
Tablet, PO, oral; |
|
DRUGBANK |
T Max |
0.97 |
h |
0.69-1.25 |
h |
sublingual; increasing doses; |
increasing doses ↓ ; |
DRUGBANK |
T Max |
3.6 |
h |
3.6±1.3 |
h |
Transdermal preparations; |
|
DRUGBANK |
T Max |
1.0 |
h |
<1 |
h |
nasal spray; |
|
DRUGBANK |
T Max |
1.0 |
h |
<1 |
h |
|
|
DRUGBANK |
T Max |
0.40 |
h |
0.4(0.3-6) |
h |
buccal; |
|
The Pharmacological Basis of Therapeutics |
T Max |
35.0 |
h |
35±15 |
h |
Transdermal preparations; |
|
The Pharmacological Basis of Therapeutics |
Clearance |
0.50 |
L/h/kg |
0.5(0.3-0.7) |
L/h/kg |
Plasma clearance; |
|
DRUGBANK |
Clearance |
51.0 |
L/h |
27-75 |
L/h |
intravenous injection, IV; patients; |
|
DRUGBANK |
Clearance |
41.5 |
L/h |
3-80 |
L/h |
hepatopathy,LD; |
|
DRUGBANK |
Clearance |
54.0 |
L/h |
30-78 |
L/h |
RD, renal impairment, Renal disease,including uremia; |
|
DRUGBANK |
Clearance |
0.78 |
L/h/kg |
13±2 |
ml/min/kg |
hydrolysis; |
Neonates ↓ ;Children ↓ ;Elderly ↓ ;Prem, premature ↓ ; |
The Pharmacological Basis of Therapeutics |
Clearance |
0.28 |
L/h/kg |
4.7 |
ml/min/kg |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Volume of Distribution |
5.5 |
L/kg |
3.0-8 |
L/kg |
intravenous injection, IV; |
|
DRUGBANK |
Volume of Distribution |
25.4 |
L/kg |
25.4 |
L/kg |
PO, oral; |
|
DRUGBANK |
Volume of Distribution |
4.4 |
L/kg |
0.8-8 |
L/kg |
intravenous injection, IV; hepatopathy,LD; patients; |
|
DRUGBANK |
Volume of Distribution |
4.0 |
L/kg |
4.0±0.4 |
L/kg |
|
|
The Pharmacological Basis of Therapeutics |
Volume of Distribution |
0.89 |
L/kg |
0.89 |
L/kg |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Half-life |
7.0 |
h |
7 |
h |
|
|
DRUGBANK |
Half-life |
8.5 |
h |
5-12 |
h |
sublingual; |
|
DRUGBANK |
Half-life |
3.7 |
h |
3.7±0.4 |
h |
|
Prem, premature ↑ ;Children → ;CPBS ↑ ;Age ↑ ; |
The Pharmacological Basis of Therapeutics |
Half-life |
3.0 |
h |
3 |
h |
intravenous injection, IV; human, homo sapiens; |
|
Human Intravenous Pharmacokinetic Dataset |
Toxicity LD50 |
2.9 |
mg/kg |
2.91 |
mg/kg |
intravenous injection, IV; Rattus, Rat; |
|
DRUGBANK |
Toxicity LD50 |
18.0 |
mg/kg |
18.0 |
mg/kg |
PO, oral; Rattus, Rat; |
|
DRUGBANK |
Toxicity LD50 |
368.0 |
mg/kg |
368.0 |
mg/kg |
PO, oral; mouse; |
|
DRUGBANK |
Toxicity LD50 |
3.1 |
mg/kg |
3.1 |
mg/kg |
Rattus, Rat; |
|
T3DB |
Toxicity LD50 |
0.0300 |
mg/kg |
0.03 |
mg/kg |
monkey; |
|
T3DB |
Eliminate Route |
75.0 |
% |
75 |
% |
Urinary excretion; |
|
DRUGBANK |
Eliminate Route |
9.0 |
% |
9 |
% |
Faeces excretion; |
|
DRUGBANK |
Eliminate Route |
5.3 |
% |
<5.3 |
% |
Urinary excretion; Unchanged drug; |
|
DRUGBANK |
Eliminate Route |
0.0900 |
% |
0.09 |
% |
Faeces excretion; Unchanged drug; |
|
DRUGBANK |
Eliminate Route |
8.0 |
% |
8 |
% |
Urinary excretion; Unchanged drug; |
|
The Pharmacological Basis of Therapeutics |
Protein Binding |
82.5 |
% |
80-85 |
% |
plasma proteins; |
|
DRUGBANK |
Protein Binding |
77.9 |
% |
77.9±1.1 |
% |
human, homo sapiens; |
|
DRUGBANK |
Protein Binding |
12.0 |
% |
12±5.4 |
% |
human, homo sapiens; |
|
DRUGBANK |
Protein Binding |
84.0 |
% |
84±2 |
% |
|
|
The Pharmacological Basis of Therapeutics |