Add time:08/28/2019         Source:sciencedirect.com

Metabolism of tamoxifen N-oxide by phenobarbitone-induced rat liver microsomes gave a major metabolite which was identified as E-1-[4-(2-dimethylaminoethoxy)phenyl]-1,2-diphenyl-1-buten-3-ol N-oxide (α-hydroxytamoxifen N-oxide) by comparison of mass spectral properties with synthetic material. This new metabolite was also formed from tamoxifen. Tamoxifen epoxide was synthesised; its microsomal metabolism gave the corresponding N-oxide. Neither tamoxifen epoxide nor its N-oxide was detected as a product of tamoxifen metabolism.

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