Basic Information
Experimental Physicochemical Property
| Property Name | Property Value | Unit | Raw Value | Raw Unit | Reference |
|---|---|---|---|---|---|
| Boiling Point | 2642.0 | ℃ | 2642 | ℃ | MSDS |
| Melting Point | 1900.0 | ℃ | 1900 | ℃ | MSDS |
Pharmacokinetic/ Toxicokinetic Property
| Property Name | Property Value | Unit | Raw Value | Raw Unit | Annotation | Reference |
|---|---|---|---|---|---|---|
| Absorption | 5.3 | % | 0.5-10 | % | PO, oral; Drug form; | DRUGBANK |
| Half-life | 28.0 | h | 15-41 | h | elimination half-life; | DRUGBANK |
| Toxicity LD50 | 155.0 | mg/kg | 135-175 | mg/kg | PO, oral; mouse; | DRUGBANK | Toxicity LD50 | 79.5 | mg/kg | 46-113 | mg/kg | PO, oral; Rattus, Rat; | DRUGBANK | Toxicity LD50 | 2000.0 | mg/kg | >2000 | mg/kg | PO, oral; Rattus, Rat; | DRUGBANK | Toxicity LD50 | 5000.0 | mg/kg | >5 | g/kg | Rattus, Rat; | DRUGBANK | Toxicity LD50 | 3500.0 | mg/kg | 3.5 | g/kg | Rattus, Rat; | DRUGBANK | Toxicity LD50 | 11300.0 | mg/kg | 11.3 | g/kg | Rattus, Rat; | DRUGBANK | Toxicity LD50 | 3300.0 | mg/kg | 3.3 | g/kg | Rattus, Rat; | DRUGBANK | Toxicity LD50 | 1500.0 | mg/kg | 1.5 | g/kg | Rattus, Rat; | DRUGBANK |
| Eliminate Route | 80.0 | % | 80 | % | 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