Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:3383472rdf:typepubmed:Citationlld:pubmed
pubmed-article:3383472lifeskim:mentionsumls-concept:C0030705lld:lifeskim
pubmed-article:3383472lifeskim:mentionsumls-concept:C0018802lld:lifeskim
pubmed-article:3383472lifeskim:mentionsumls-concept:C0007209lld:lifeskim
pubmed-article:3383472lifeskim:mentionsumls-concept:C1883254lld:lifeskim
pubmed-article:3383472lifeskim:mentionsumls-concept:C2603343lld:lifeskim
pubmed-article:3383472lifeskim:mentionsumls-concept:C0144413lld:lifeskim
pubmed-article:3383472pubmed:issue5lld:pubmed
pubmed-article:3383472pubmed:dateCreated1988-7-29lld:pubmed
pubmed-article:3383472pubmed:abstractTextIn animal experiments, a new inotropic agent, (-)-(R)-1-(p-hydroxyphenyl)-2-[(3,4-dimethoxyphenetyl)amino] ethanol, designated TA-064 was found to possess a more positive inotropic than chronotropic action. Its effectiveness and lack of significant toxicity make it beneficial for clinical use as a cardiotonic in human heart failure. The effects of TA-064 were investigated in patients with various types of heart disease (n = 29). Cardiac output increased, left ventricular end-systolic dimension decreased, and left ventricular fractional shortening increased for 15 minutes after a single intravenous dose (1 mg). The plasma level of TA-064 at the cessation of infusion was 61.1 +/- 49.6 ng/ml and thereafter declined biexponentially. After a single oral dose (10 mg), TA-064 appeared in the plasma at 30 minutes and reached its peak levels of 13.7 +/- 5.6 ng/ml at 60 minutes. Seven hours later, the plasma level was 5.9 +/- 3.1 ng/ml which was considered to be within the effective range according to the results after intravenous administration. In conclusion, minimal effective plasma levels of TA-064 are obtained by oral administration of 10 mg three times a day.lld:pubmed
pubmed-article:3383472pubmed:languageenglld:pubmed
pubmed-article:3383472pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3383472pubmed:citationSubsetIMlld:pubmed
pubmed-article:3383472pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3383472pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3383472pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3383472pubmed:statusMEDLINElld:pubmed
pubmed-article:3383472pubmed:monthMaylld:pubmed
pubmed-article:3383472pubmed:issn0160-9289lld:pubmed
pubmed-article:3383472pubmed:authorpubmed-author:KawakitaSSlld:pubmed
pubmed-article:3383472pubmed:authorpubmed-author:KinoshitaMMlld:pubmed
pubmed-article:3383472pubmed:authorpubmed-author:FukuharaTTlld:pubmed
pubmed-article:3383472pubmed:authorpubmed-author:MotomuraMMlld:pubmed
pubmed-article:3383472pubmed:authorpubmed-author:BitoKKlld:pubmed
pubmed-article:3383472pubmed:authorpubmed-author:MashiroIIlld:pubmed
pubmed-article:3383472pubmed:authorpubmed-author:OzakiNNlld:pubmed
pubmed-article:3383472pubmed:authorpubmed-author:MitsunamiKKlld:pubmed
pubmed-article:3383472pubmed:authorpubmed-author:SakodaSSlld:pubmed
pubmed-article:3383472pubmed:authorpubmed-author:TsutamotoTTlld:pubmed
pubmed-article:3383472pubmed:issnTypePrintlld:pubmed
pubmed-article:3383472pubmed:volume11lld:pubmed
pubmed-article:3383472pubmed:ownerNLMlld:pubmed
pubmed-article:3383472pubmed:authorsCompleteYlld:pubmed
pubmed-article:3383472pubmed:pagination334-9lld:pubmed
pubmed-article:3383472pubmed:dateRevised2007-11-15lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:meshHeadingpubmed-meshheading:3383472-...lld:pubmed
pubmed-article:3383472pubmed:year1988lld:pubmed
pubmed-article:3383472pubmed:articleTitleClinicopharmacological studies of a newly synthesized cardiotonic agent (TA-064) in patients with congestive heart failure.lld:pubmed
pubmed-article:3383472pubmed:affiliationFirst Department of Internal Medicine, Shiga University of Medical Science, Otsu, Japan.lld:pubmed
pubmed-article:3383472pubmed:publicationTypeJournal Articlelld:pubmed