Property Name | Property Value | Unit | Raw Value | Raw Unit | Reference |
---|---|---|---|---|---|
Melting Point | 234.0 | ℃ | 231-237 | ℃ | FDA Label/Product monograph |
Water Solubility | 0.2 | % | 0.2 | % | FDA Label/Product monograph |
Property Name | Property Value | Unit | Raw Value | Raw Unit | Annotation | Reference |
---|---|---|---|---|---|---|
Absorption | 95.0 | % | 95 | % | PO, oral; | DRUGBANK |
Bioavailability | 4.0 | % | 4 | % | PO, oral; | DRUGBANK |
T Max | 0.75 | h | 0.5-1 | h | PO, oral; | DRUGBANK |
Volume of Distribution | 100.0 | L | ~100 | L | DRUGBANK | |
Half-life | 11.5 | h | 11.5 | h | terminal half-life; Single dose; | DRUGBANK | Half-life | 17.0 | h | 17 | h | at steady state; | DRUGBANK |
Toxicity LD50 | 300.0 | mg/kg | 300.0 | mg/kg | PO, oral; mouse; | DRUGBANK | Toxicity LD50 | 980.0 | mg/kg | 980.0 | mg/kg | PO, oral; Rattus, Rat; | DRUGBANK | Toxicity LD50 | 3200.0 | mg/kg | 3200.0 | mg/kg | PO, oral; rabbit; | DRUGBANK |
Eliminate Route | 50.0 | % | 50 | % | Urinary excretion; | DRUGBANK |
Protein Binding | 90.0 | % | ~90 | % | plasma proteins; | DRUGBANK |
Not Available