| Identification | |
|---|---|
| Name | Sulfoxone |
| Accession Number | DB01145 (APRD00704) |
| Type | small molecule |
| Description | Sulfoxone is a water-soluble sulfone used as an antileprosy drug. It has been used with limited success in the treatment of dermatitis herpetiformis. |
| Structure |
|
| Categories (*) | |
| Molecular Weight | 404.482 |
| Groups | approved |
| Monoisotopic Weight | 404.017048324 |
| Pharmacology | |
| Indication | For the treatment of leprosy and dermatitis herpetiformis |
| Mechanism of action | Sulfoxone is a competitive inhibitor of bacterial enzyme dihydropteroate synthetase. The normal substrate for the enzyme, para-aminobenzoic acid (PABA) cannot bind as usual. The inhibited reaction is necessary in these organisms for the synthesis of folic acid. |
| Absorption | Rapidly absorbed. |
| Protein binding | 69% |
| Biotransformation | Hepatic. |
| Route of elimination | Not Available |
| Toxicity | Oral, rat LD50: 7000 mg/kg |
| Affected organisms |
|
| Interactions | |
| Drug Interactions | Not Available |
| Food Interactions | Not Available |
| Dihydropteroate synthetase | |
|---|---|
| Name | Dihydropteroate synthetase |
| Gene Name | Not Available |
| Pharmacological action | yes |
| Actions | inhibitor |
| References |
|
| DTHybrid score | 1.0586 |
| Id | Partner name | Gene Name | Score |
|---|---|---|---|
| 620 | Bifunctional dihydrofolate reductase-thymidylate synthase | Not Available | 0.1176 |
| 3811 | Cytochrome P450 19A1 | CYP19A1 | 0.064 |
| 4757 | Cytochrome P450 2C9 | CYP2C9 | 0.0616 |
| 6013 | Cytochrome P450 2E1 | CYP2E1 | 0.0205 |
| 4924 | Cytochrome P450 2C8 | CYP2C8 | 0.019 |
| 4512 | Cytochrome P450 3A4 | CYP3A4 | 0.0153 |