Mitomycin |
Mitomycin-C; Mutamycin |
Article: Mitomycin
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| Mitomycin | |
| Systematic (IUPAC) name | |
| 6-Amino-1,1a,2,8,8a,8b-hexahydro-8- (hydroxymethyl)- 8a-methoxy-5-methyl-azirino[2', 3':3,4] pyrrolo[1,2-a]indole-4,7-dione carbamate (ester) | |
| Identifiers | |
| CAS number | 50-07-7 |
| ATC code | L01DC03 |
| PubChem | 5746 |
| DrugBank | APRD00284 |
| Chemical data | |
| Formula | C15H18N4O5 |
| Mol. weight | 334.327 g/mol |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | Hepatic |
| Half life | 8-48 min |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. | D (Au, U.S.) |
| Legal status | ℞-only (U.S.), POM (UK) |
| Routes | Exclusively intravenous |
The mitomycins are a family of aziridine-containing natural products isolated from Streptomyces lavendulae. One of these compounds, mitomycin C, finds use as a chemotherapeutic agent by virtue of its antitumour antibiotic activity. It is given intravenously to treat upper gastro-intestinal (e.g. esophageal carcinoma) and breast cancers, as well as by bladder instillation for superficial bladder tumours. It causes delayed bone marrow toxicity and therefore it is usually administered at 6-weekly intervals. Prolonged use may result in permanent bone-marrow damage. It may also cause lung fibrosis and renal damage.

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