Basic Information
Experimental Physicochemical Property
| Property Name | Property Value | Unit | Raw Value | Raw Unit | Reference |
|---|---|---|---|---|---|
| Log P | 2.17 | - | 2.17 | - | Dahiya S, Kaushik A, and Pathak K, 2015 |
| Melting Point | 151.0 | ℃ | 149-153 | ℃ | MSDS |
Pharmacokinetic/ Toxicokinetic Property
| Property Name | Property Value | Unit | Raw Value | Raw Unit | Annotation | Reference |
|---|---|---|---|---|---|---|
| T Max | 2.1 | h | 1.25-3 | h | PO, oral; | DRUGBANK |
| Clearance | 5.0 | L/h | ~5 | L/h | Average clearance; | DRUGBANK |
| Volume of Distribution | 25.0 | L | ~25 | L | DRUGBANK | |
| Half-life | 4.0 | h | ~4 | h | DRUGBANK | |
| Eliminate Route | 75.0 | % | 70-80 | % | Urinary excretion; | DRUGBANK | Eliminate Route | 20.0 | % | ~20 | % | Faeces excretion; | DRUGBANK |
| Protein Binding | 99.0 | % | >99 | % | 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