pubmed-article:3426756 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C0036751 | lld:lifeskim |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C0000966 | lld:lifeskim |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C0001962 | lld:lifeskim |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C0011744 | lld:lifeskim |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C0728899 | lld:lifeskim |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C1514468 | lld:lifeskim |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C0598405 | lld:lifeskim |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C1522492 | lld:lifeskim |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C0332120 | lld:lifeskim |
pubmed-article:3426756 | lifeskim:mentions | umls-concept:C0233656 | lld:lifeskim |
pubmed-article:3426756 | pubmed:dateCreated | 1988-3-23 | lld:pubmed |
pubmed-article:3426756 | pubmed:abstractText | Trideuterated 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 |
pubmed-article:3426756 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3426756 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3426756 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3426756 | pubmed:language | eng | lld:pubmed |
pubmed-article:3426756 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3426756 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:3426756 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3426756 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3426756 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3426756 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3426756 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3426756 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:3426756 | pubmed:issn | 1358-6173 | lld:pubmed |
pubmed-article:3426756 | pubmed:author | pubmed-author:FaullKK | lld:pubmed |
pubmed-article:3426756 | pubmed:author | pubmed-author:TylerAA | lld:pubmed |
pubmed-article:3426756 | pubmed:author | pubmed-author:BeckOO | lld:pubmed |
pubmed-article:3426756 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:3426756 | pubmed:volume | 1 | lld:pubmed |
pubmed-article:3426756 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:3426756 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:3426756 | pubmed:pagination | 743-7 | lld:pubmed |
pubmed-article:3426756 | pubmed:dateRevised | 2008-2-26 | lld:pubmed |
pubmed-article:3426756 | pubmed:meshHeading | pubmed-meshheading:3426756-... | lld:pubmed |
pubmed-article:3426756 | pubmed:meshHeading | pubmed-meshheading:3426756-... | lld:pubmed |
pubmed-article:3426756 | pubmed:meshHeading | pubmed-meshheading:3426756-... | lld:pubmed |
pubmed-article:3426756 | pubmed:meshHeading | pubmed-meshheading:3426756-... | lld:pubmed |
pubmed-article:3426756 | pubmed:meshHeading | pubmed-meshheading:3426756-... | lld:pubmed |
pubmed-article:3426756 | pubmed:meshHeading | pubmed-meshheading:3426756-... | lld:pubmed |
pubmed-article:3426756 | pubmed:meshHeading | pubmed-meshheading:3426756-... | lld:pubmed |
pubmed-article:3426756 | pubmed:meshHeading | pubmed-meshheading:3426756-... | lld:pubmed |
pubmed-article:3426756 | pubmed:meshHeading | pubmed-meshheading:3426756-... | lld:pubmed |
pubmed-article:3426756 | pubmed:meshHeading | pubmed-meshheading:3426756-... | lld:pubmed |
pubmed-article:3426756 | pubmed:year | 1987 | lld:pubmed |
pubmed-article:3426756 | pubmed:articleTitle | Serotonin condensation product 5-hydroxymethtryptoline: evidence for in vivo formation from acetaldehyde during intoxication using deuterium labelled ethanol. | lld:pubmed |
pubmed-article:3426756 | pubmed:affiliation | Pasarow Analytical Neurochemical Facility, Nancy Pritzker Laboratory of Behavioral Neurochemistry, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, California 94305. | lld:pubmed |
pubmed-article:3426756 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:3426756 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:3426756 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |