Cephradine
Anspor, Velosef (cephradine) is a small molecule pharmaceutical. Cephradine was first approved as Velosef on 1982-01-01. It is used to treat bacterial infections, bacterial skin diseases, escherichia coli infections, klebsiella infections, and proteus infections amongst others in the USA.
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Commercial
Therapeutic Areas
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New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Clinical
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3 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Cystitis | D003556 | EFO_1000025 | N30 | — | — | — | 1 | — | 1 |
Indications Phases 3
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Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Pneumonia | D011014 | EFO_0003106 | J18 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Cephradine |
| INN | cefradine |
| Description | Cephradine is a first-generation cephalosporin antibiotic with a methyl substituent at position 3, and a (2R)-2-amino-2-cyclohexa-1,4-dien-1-ylacetamido substituent at position 7, of the cephem skeleton. It has a role as an antibacterial drug. It is a cephalosporin and a beta-lactam antibiotic allergen. |
| Classification | Small molecule |
| Drug class | — |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | CC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)[C@H](N)C3=CCC=CC3)[C@H]2SC1 |
Identifiers
| PDB | — |
| CAS-ID | 38821-53-3 |
| RxCUI | — |
| ChEMBL ID | CHEMBL1604 |
| ChEBI ID | 3547 |
| PubChem CID | 38103 |
| DrugBank | DB01333 |
| UNII ID | 9YA6SX5S4D (ChemIDplus, GSRS) |
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Estimated US medical usage
Cephradine
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Additional graphs summarizing 2,012 documents
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Safety
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1,253 adverse events reported
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