Basic Information
Experimental Physicochemical Property
| Property Name | Property Value | Unit | Raw Value | Raw Unit | Reference |
|---|---|---|---|---|---|
| Melting Point | 400.0 | ℃ | 400 | ℃ | MSDS |
| Water Solubility | 17000.0 | mg/L | 17 | g/L | MSDS |
Pharmacokinetic/ Toxicokinetic Property
| Property Name | Property Value | Unit | Raw Value | Raw Unit | Annotation | Reference |
|---|---|---|---|---|---|---|
| T Max | 3.0 | h | 3 | h | PO, oral; | DRUGBANK |
| Metabolic | 0 | % | 0 | % | DRUGBANK | |
| Half-life | 7.0 | h | ~6-8 | h | human, homo sapiens; | DRUGBANK |
| Toxicity LD50 | 3621.0 | mg/kg | 3621.0 | mg/kg | PO, oral; mouse; | DRUGBANK |
| Eliminate Route | 95.0 | % | ~95 | % | Urinary excretion; | 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