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- W1992536259 abstract "The metabolism of doxorubicin (A) 4′-epidoxorubicin (E) and 4′-deoxydoxorubicin (D) was studied in vitro by incubating the analogs with rat liver subcellular fractions and in vivo by chromatographic analysis of human urine. Metabolites were identified by high-pressure liquid chromatography, fluorescence spectroscopy and enzymatic conversion. Human urine contained unchanged drug as well as the corresponding alcohol metabolites in all cases; however, urine of patients who received E also contained two glucuronides which could not be detected in the urine of patients who received A or D. We have identified these glucuronides as 4′-epidoxorubicin glucuronide (E-Glu) and 4′-epidoxorubicinol glucuronide (Eol-Glu). It was concluded that the glucuronide moiety is linked to the daunosamine sugar at the C4′-OH position. A hypothesis is proposed that this glucuronidation pathway may explain the differences in pharmacokinetics and toxicity between E and A. Rat liver microsomes were found to convert all three drugs to the 7-deoxyaglycones at the same rate. Rat liver 100,000 g supernatant was found to be capable of converting these drugs to their respective alcohol metabolites, doxorubicinol (Aol) being formed somewhat slower than 4′-epidoxorubicinol (Eol) and 4′-deoxydoxorubicinol (Dol)." @default.
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- W1992536259 date "1984-07-01" @default.
- W1992536259 modified "2023-10-03" @default.
- W1992536259 title "Metabolism of 4′-modified analogs of doxorubicin. Unique glucuronidation pathway for 4′-epidoxorubicin" @default.
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- W1992536259 doi "https://doi.org/10.1016/0277-5379(84)90165-2" @default.
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