Egyszerű nézet

dc.contributor.author Erdélyi-Tóth, V
dc.contributor.author Csetényi, J
dc.contributor.author Kanyár, B
dc.contributor.author Kerpel-Fronius, Sándor
dc.contributor.author Eckhardt, S
dc.date.accessioned 2022-09-01T06:49:15Z
dc.date.available 2022-09-01T06:49:15Z
dc.date.issued 1981
dc.identifier 0019378116
dc.identifier.citation journalVolume=17;journalIssueNumber=3;journalTitle=EUROPEAN JOURNAL OF CANCER;pagerange=329-335;journalAbbreviatedTitle=EUR J CANCER;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/8082
dc.description.abstract N-Formyl-leurosine labeled with 14C in the formyl group was administered to six patients with malignant disease, and the pharmacokinetic behavior of the drug was determined. Chromatographic studies on plasma showed the presence of unchanged drug and 7 metabolites. No metabolites were found in the urine. The plasma decay curve of the unchanged drug was biphasic with half-life values of t1 2α = 18.6 min and t1 2β = 4.28 hr. Within 72 hr only 30-40% of the radioactivity could be recovered in urine and feces in 5 patients. One patient consumed laxatives during the treatment. In this case 95% of the 14C-dose was recovered. The contribution made by fecal elimination was 80%. © 1981.
dc.format.extent 329-335
dc.relation.ispartof urn:issn:0959-8049
dc.title THE PHARMACOKINETICS OF N-[C-14-FORMYL]-LEUROSINE IN HUMANS
dc.type Journal Article
dc.date.updated 2019-12-05T12:27:14Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 2226498
dc.identifier.wos A1981LC62200008
dc.identifier.pubmed 7262170
dc.contributor.institution Országos Onkológiai Intézet
dc.contributor.institution Farmakológiai és Farmakoterápiás Intézet


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