PubMed · 106901
Metabolism of diethylstilbestrol: identification of a catechol derived from dienestrol.
Abstract
The enzymatic oxidation of E-3,4-bis-(p-hydroxyphenyl)-hex-3-ene (diethylstilbestrol) by either mushroom tyrosinase or rat liver microsomes in the presence of NADPH and air yields a catechol. Upon further oxidation of both compounds with periodate and condensation of the resulting o-quinones with o-phenylenediamine, phenazines are produced. The phenazines derived from the products of both the plant and animal enzyme systems are identical to the product obtained by oxidation of diethylstilbestrol with potassium nitrosodisulfonate and condensation of the o-quinone produced with o-phenylenediamine. High and low resolution mass spectra of the phenazine are consistent with its derivation from a catechol having two fewer hydrogens than diethylstilbestrol.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
J Weidenfeld, P Carter, V N Reinhold, S B Tanner, L L Engel. 1978. Metabolism of diethylstilbestrol: identification of a catechol derived from dienestrol.. https://doi.org/10.1002/bms.1200051008
Cite the original work for its findings. Save a collection to share your selection of sources.