Drug ID | DDPD00730 |
|
Drug Name | Thiabendazole | |
Molecular Weight | 201.248 | |
Molecular Formula | C10H7N3S | |
CAS Number | 148-79-8 | |
SMILES | N1C2=CC=CC=C2N=C1C1=CSC=N1 | |
External Links | ||
DRUGBANK | DB00730 | |
T3DB | T3D3931 | |
PubChem Compound | 5430 | |
Drugs.com | Drugs.com Drug Page |
Property Name | Property Value | Unit | Raw Value | Raw Unit | Reference |
---|---|---|---|---|---|
Log P | 2.47 | - | 2.47 | - | NIELSEN,LS ET AL. (1992) |
Melting Point | 300.0 | ℃ | 300 | ℃ | PhysProp |
Water Solubility | 50.0 | mg/L | 50 | mg/L | WAUCHOPE,RD ET AL. 1991A) |
pKa | 4.64 | - | 4.64 | - | CHAMBERLAIN,K ET AL. (1996) |
Property Name | Property Value | Unit | Raw Value | Raw Unit | Annotation | Reference |
---|---|---|---|---|---|---|
T Max | 1.5 | h | 1-2 | h | PO, oral; | DRUGBANK |
Metabolic | 100.0 | % | ~100 | % | Liver metabolism; | DRUGBANK |
Half-life | 1.2 | h | 1.2(0.9-2) | h | normal,healthy; | DRUGBANK | Half-life | 1.2 | h | 1.2(0.9-2) | h | anephric; | DRUGBANK | Half-life | 1.7 | h | 1.7(1.4-2) | h | normal,healthy; | DRUGBANK | Half-life | 1.7 | h | 1.7(1.4-2) | h | anephric; | DRUGBANK |
Toxicity LD50 | 3600.0 | mg/kg | 3.6 | g/kg | PO, oral; mouse; | DRUGBANK | Toxicity LD50 | 3100.0 | mg/kg | 3.1 | g/kg | PO, oral; Rattus, Rat; | DRUGBANK | Toxicity LD50 | 3800.0 | mg/kg | 3.8 | g/kg | PO, oral; rabbit; | DRUGBANK | Toxicity LD50 | 3600.0 | mg/kg | 3.6 | g/kg | PO, oral; mouse; | T3DB | Toxicity LD50 | 3100.0 | mg/kg | 3.1 | g/kg | PO, oral; Rattus, Rat; | T3DB | Toxicity LD50 | 3800.0 | mg/kg | 3.8 | g/kg | PO, oral; rabbit; | T3DB |
Not Available