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pubmed-article:3426756pubmed:abstractTextTrideuterated 5-hydroxymethtryptoline was found in the urine of rats treated with trideuterated ethanol. The combined treatment with disulfiram lead to a more than 10-fold increase in the excretion rate. The chiral analysis revealed unequal abundance of enantiomers suggesting the involvement of a stereoselective (enzymatic) mechanism in the formation 5-hydroxymethtryptoline during ethanol intoxication.lld:pubmed
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pubmed-article:3426756pubmed:articleTitleSerotonin condensation product 5-hydroxymethtryptoline: evidence for in vivo formation from acetaldehyde during intoxication using deuterium labelled ethanol.lld:pubmed
pubmed-article:3426756pubmed:affiliationPasarow Analytical Neurochemical Facility, Nancy Pritzker Laboratory of Behavioral Neurochemistry, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, California 94305.lld:pubmed
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