Epirubicin
From Wikipedia, the free encyclopedia
Epirubicin
|
|
Systematic (IUPAC) name | |
10-(4-amino-5-hydroxy-6-methyl-oxan-2-yl) oxy-6,8,11-trihydroxy-8-(2-hydroxyacetyl)- 1-methoxy-9,10-dihydro-7H-tetracene-5,12-dione | |
Identifiers | |
CAS number | |
ATC code | L01 |
PubChem | |
DrugBank | |
Chemical data | |
Formula | C27H29NO11 |
Mol. mass | 543.519 g/mol |
Pharmacokinetic data | |
Bioavailability | NA |
Protein binding | 77% |
Metabolism | Hepatic glucuronidation and oxidation |
Half life | ? |
Excretion | Biliary and renal |
Therapeutic considerations | |
Pregnancy cat. | |
Legal status | |
Routes | Intravenous |
Epirubicin (marketed by Pfizer under the trade name Ellence®) is an anthracycline drug used for chemotherapy. Similarly to other anthracyclines, it acts by intercalating DNA strands.
Intercalation results in complex formation which inhibits DNA and RNA synthesis. It also triggers DNA cleavage by topoisomerase II, resulting in mechanisms that lead to cell death. Binding to cell membranes and plasma proteins may be involved in the compound's cytotoxic effects. Epirubicin also generates free radicals that cause cell and DNA damage.
Epirubicin is favoured over doxorubicin, the most popular anthracycline, in some chemotherapy regimens as it appears to cause less side-effects. Epirubicin has a different spatial orientation of the hydroxyl group at the 4' carbon of the sugar, which may account for its faster elimination and reduced toxicity. Epirubicin is primarily used against breast and ovarian cancer, gastric cancer, lung cancer, and lymphomas.