A ureidopenicillin with a broad spectrum of activity, but inactivated by β-lactamase.
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| Systematic (IUPAC) name | |
|---|---|
| (2S,5R,6R)-3,3-dimethyl-7-oxo-6-{[(2R)-2-{[(2-oxoimidazolidin-1-yl)carbonyl]amino}-2-phenylacetyl]amino}-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid | |
| Clinical data | |
| AHFS/Drugs.com | International Drug Names |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 37091-66-0 |
| ATC code | J01CA09 |
| PubChem | CID 6479523 |
| DrugBank | DB01061 |
| ChemSpider | 4980416 |
| UNII | HUM6H389W0 |
| KEGG | D02339 |
| ChEBI | CHEBI:2956 |
| ChEMBL | CHEMBL1537 |
| Chemical data | |
| Formula | C20H23N5O6S |
| Mol. mass | 461.491 g/mol |
| SMILES | eMolecules & PubChem |
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Azlocillin is an acylampicillin antibiotic with an extended spectrum of activity and greater in vitro potency than the carboxy penicillins. Azlocillin is similar to mezlocillin and piperacillin. It demonstrates antibacterial activity against a broad spectrum of bacteria, including Pseudomonas aeruginosa and, in contrast to most cephalosporins, exhibits activity against enterococci.
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