| Trade Names: | |
| Synonyms: | |
| Status: | Approved (1959) |
| Entry Type: | Small molecule |
| Molecule Category: | Salt Prodrug |
| UNII: | 872109HX6B |
| Parent Compound: | CHLORAMPHENICOL |
| InChI Key | RPLOPBHEZLFENN-HTMVYDOJSA-M |
|---|---|
| Smile | |
| InChI |
|
| Property Name | Value |
|---|---|
| Molecular Formula | C15H15Cl2N2NaO8 |
| Molecular Weight | 445.19 |
| AlogP | 1.32 |
| Hydrogen Bond Acceptor | 7.0 |
| Hydrogen Bond Donor | 3.0 |
| Number of Rotational Bond | 10.0 |
| Polar Surface Area | 156.07 |
| Molecular species | ACID |
| Aromatic Rings | 1.0 |
| Heavy Atoms | 27.0 |
| Action | Mechanism of Action | Reference |
|---|---|---|
| INHIBITOR | Bacterial 70S ribosome inhibitor |
| Targets | EC50(nM) | IC50(nM) | Kd(nM) | Ki(nM) | Inhibition(%) | |
|---|---|---|---|---|---|---|
|
Enzyme
Transferase
|
- | - | - | - | 20.14 | |
|
Epigenetic regulator
Eraser
Histone deacetylase
HDAC class IIb
|
- | - | - | - | -19.87--2.74 |
| Mesh Heading | Maximum Phase | Mesh ID | Reference |
|---|---|---|---|
| Osteomyelitis | 1 | D010019 | ClinicalTrials |
| Resources | Reference |
|---|---|
| ChEMBL | CHEMBL1200729 |
| EPA CompTox | DTXSID2024747 |
| FDA SRS | 872109HX6B |
| KEGG | C13962 |
| PubChem | 656833 |
| SureChEMBL | SCHEMBL193134 |