Basic Information
Experimental Physicochemical Property
| Property Name | Property Value | Unit | Raw Value | Raw Unit | Reference |
|---|---|---|---|---|---|
| Log P | 0.49 | - | 0.49 | - | ChemSpider |
Pharmacokinetic/ Toxicokinetic Property
| Property Name | Property Value | Unit | Raw Value | Raw Unit | Annotation | Reference |
|---|---|---|---|---|---|---|
| Bioavailability | 25.0 | % | 25 | % | DRUGBANK | |
| T Max | 0.75 | h | 0.75 | h | DRUGBANK | |
| Clearance | 159.0 | L/h | 159.0 | L/h | apparent clearance; PO, oral; | DRUGBANK |
| Volume of Distribution | 34.0 | L | 34.0 | L | Steady state volume of distribution; | DRUGBANK |
| Half-life | 0.90 | h | 0.9(0.6-2.8) | h | elimination half-life; Oral single dose; | DRUGBANK |
| Eliminate Route | 84.0 | % | 84 | % | Faeces excretion; Single dose; normal,healthy; human, homo sapiens; | DRUGBANK | Eliminate Route | 12.0 | % | 12 | % | Urinary excretion; Single dose; normal,healthy; human, homo sapiens; | DRUGBANK |
| Protein Binding | 97.5 | % | ~97.5 | % | plasma proteins; human, homo sapiens; | DRUGBANK | Protein Binding | 93.7 | % | 93.7 | % | human, homo sapiens; | DRUGBANK | Protein Binding | 41.1 | % | 41.1 | % | human, homo sapiens; | 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