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ID: ALA3779870

Journal: Eur J Med Chem

Title: Differential metabolism of 3FDT and docetaxel in RLMs, rats, and HLMs.

Authors: Tang ML, Zhou L, Chang J, Hu ZH, Qin Y, Sun X.

Abstract: 3FDT, an analog of docetaxel with a blocked metabolism at its 3'-N-tert-butyloxyl group with three fluorine atoms, exhibits more potent cytotoxicity than docetaxel both with human cancer cell line SK-OV-3 in vitro and with human non-small cell lung cancer A549 xenografts in vivo. To further develop pharmacodynamically and pharmacokinetically favorable fluorinated docetaxel analogs as anticancer agents, we chose 3FDT as the model compound to identify the metabolites of 3FDT in RLMs, rats, and HLMs and the cytochrome P450 enzymes responsible for the metabolism of 3FDT. Our findings indicated that the major metabolic site switched from the C3' appendage for docetaxel to the taxane ring for 3FDT, and the main metabolizing P450 enzymes switched from CYP3A to CYP3A4 and CYP2E1.

CiteXplore: 26922231

DOI: 10.1016/j.ejmech.2016.02.007