| Synonyms: | |
| Status: | Approved (1973) |
| Entry Type: | Small molecule |
| Molecule Category: | UNKNOWN |
| UNII: | W46JY43EJR |
Structure
| InChI Key | UEJSSZHHYBHCEL-UHFFFAOYSA-N |
|---|---|
| Smile | |
| InChI |
|
Physicochemical Descriptors
| Property Name | Value |
|---|---|
| Molecular Formula | C10H9AgN4O2S |
| Molecular Weight | 357.14 |
| AlogP | 0.86 |
| Hydrogen Bond Acceptor | 5.0 |
| Hydrogen Bond Donor | 2.0 |
| Number of Rotational Bond | 3.0 |
| Polar Surface Area | 97.97 |
| Molecular species | NEUTRAL |
| Aromatic Rings | 2.0 |
| Heavy Atoms | 17.0 |
Pharmacology
| Action | Mechanism of Action | Reference |
|---|---|---|
| INHIBITOR | Bacterial dihydropteroate synthase inhibitor |
| Targets | EC50(nM) | IC50(nM) | Kd(nM) | Ki(nM) | Inhibition(%) | |
|---|---|---|---|---|---|---|
|
Enzyme
Transferase
|
- | 750 | - | - | 100.1 | |
|
Epigenetic regulator
Eraser
Histone deacetylase
HDAC class IIb
|
- | - | - | - | -0.91-61.84 |
Indications
| Mesh Heading | Maximum Phase | Mesh ID | Reference |
|---|---|---|---|
| Burns | 3 | D002056 | ClinicalTrials |
| Infections | 1 | D007239 | ClinicalTrials |
| Osteomyelitis | 1 | D010019 | ClinicalTrials |
Related Entries
Scaffolds
Cross References
| Resources | Reference |
|---|---|
| ChEBI | 9142 |
| ChEMBL | CHEMBL1382627 |
| DrugBank | DB05245 |
| EPA CompTox | DTXSID4048646 |
| FDA SRS | W46JY43EJR |
| Human Metabolome Database | HMDB15610 |
| PharmGKB | PA164744951 |
| PubChem | 441244 |
| SureChEMBL | SCHEMBL16043898 |
CONTENTS