Basic Information
Experimental Physicochemical Property
Not Available
Pharmacokinetic/ Toxicokinetic Property
| Property Name | Property Value | Unit | Raw Value | Raw Unit | Annotation | Factor | Reference |
|---|---|---|---|---|---|---|---|
| Bioavailability | 70.0 | % | >70 | % | PO, oral; | DRUGBANK | |
| T Max | 1.5 | h | 1-2 | h | PO, oral; | DRUGBANK | |
| Clearance | 24.0 | L/h | 24.0 | L/h | apparent clearance; at steady state; | DRUGBANK | |
| Volume of Distribution | 164.0 | L | 164.0 | L | Apparent volume of distribution; at steady state; | DRUGBANK | |
| Half-life | 6.5 | h | 6.5 | h | elimination half-life; | DRUGBANK | |
| Eliminate Route | 78.0 | % | ~78 | % | Faeces excretion; PO, oral; | DRUGBANK | Eliminate Route | 22.0 | % | ~22 | % | Urinary excretion; PO, oral; | DRUGBANK | Eliminate Route | 32.8 | % | ~32.76 | % | Faeces excretion; PO, oral; Unchanged drug; | DRUGBANK |
| Protein Binding | 96.0 | % | ~96 | % | plasma proteins; | Plasma Concentration → ; | DRUGBANK |
Maximum Dosage
Not Available
Drug Property Radar Chart
Note: Center: Q1-1.5*IQR, Edge: Q3+1.5*IQR; Q1: Quantile 1, Q3: Quantile 3, IQR: Q3-Q1