Basic Information
Experimental Physicochemical Property
Not Available
Pharmacokinetic/ Toxicokinetic Property
| Property Name | Property Value | Unit | Raw Value | Raw Unit | Annotation | Reference |
|---|---|---|---|---|---|---|
| Bioavailability | 10.0 | % | <10 | % | DRUGBANK | |
| C Max | 3.7 | ng/ml | 1.6-5.7 | ug/L | Oral single dose; normal,healthy; adults; | DRUGBANK |
| T Max | 1.5 | h | 0.5-2.5 | h | PO, oral; | DRUGBANK |
| Half-life | 16.0 | h | 13-19 | h | terminal half-life; at steady state; | DRUGBANK |
| Toxicity LD50 | 300.0 | mg/kg | 300.0 | mg/kg | PO, oral; mouse; | DRUGBANK | Toxicity LD50 | 3200.0 | mg/kg | 3200.0 | mg/kg | PO, oral; rabbit; | DRUGBANK | Toxicity LD50 | 980.0 | mg/kg | 980.0 | mg/kg | PO, oral; Rattus, Rat; | DRUGBANK |
| Eliminate Route | 70.0 | % | ~70 | % | Faeces excretion; | DRUGBANK | Eliminate Route | 30.0 | % | ~30 | % | Urinary excretion; | DRUGBANK |
| Protein Binding | 95.0 | % | >95 | % | 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