Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
1994-6-14
pubmed:abstractText
Methods have been developed for the preparation of radioiodinated N-substituted 2 beta-carbomethoxy-3 beta-(4-chlorophenyl)tropanes. The syntheses, physical properties, radiolabeling, and characterization of the pharmacological properties of N-(3(Z)-iodopropen-1-yl)-2 beta-carbomethoxy-3 beta-(4-chlorophenyl)tropane (12) and N-(3(E)-iodopropen-1-yl)-2 beta-carbomethoxy-3 beta-(4-chlorophenyl)tropane (13) are described. 2 beta-Carbomethoxy-3 beta-(p-substituted-phenyl)tropanes are potent ligands for the dopamine transporter. The radioiodinated derivatives are of interest because of the high uptake and prolonged striatal retention that may result from specific binding to low-capacity, high-affinity, dopamine reuptake sites. Radioiodine was introduced into the 3Z and 3E-position of N-(3-iodopropen-1-yl)-2 beta-carbomethoxy-3 beta-(4-chlorophenyl)tropane by iododemetalation of the corresponding 3-(tri-n-butylstannyl) derivatives. Competition binding data of various dopamine reuptake ligands with rat striatal tissue preparation for either [125I]-12 or [125I]-13 exhibited the following order of potency: E-13 > Z-12 > GBR 12909 >> mazindol >>> (-)-cocaine. Tissue distribution studies in rats showed that the E-13 was the best analogue. E-13 showed high striatal uptake (60 min, 1.23% dose/g; 120 min, 0.61% dose/g) and high striatal to cerebellum ratios (60 min, 15.9/1; 120 min, 16.5/1). These studies indicate that iodine-123-labeled E-13 is a potentially useful agent for imaging the dopamine reuptake sites by single-photon-emission computerized tomography.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0022-2623
pubmed:author
pubmed:issnType
Print
pubmed:day
13
pubmed:volume
37
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1535-42
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:8182712-Animals, pubmed-meshheading:8182712-Binding, Competitive, pubmed-meshheading:8182712-Carrier Proteins, pubmed-meshheading:8182712-Cocaine, pubmed-meshheading:8182712-Corpus Striatum, pubmed-meshheading:8182712-Dopamine, pubmed-meshheading:8182712-Dopamine Plasma Membrane Transport Proteins, pubmed-meshheading:8182712-Iodine Radioisotopes, pubmed-meshheading:8182712-Isotope Labeling, pubmed-meshheading:8182712-Male, pubmed-meshheading:8182712-Membrane Glycoproteins, pubmed-meshheading:8182712-Membrane Transport Proteins, pubmed-meshheading:8182712-Nerve Tissue Proteins, pubmed-meshheading:8182712-Protein Binding, pubmed-meshheading:8182712-Rats, pubmed-meshheading:8182712-Rats, Sprague-Dawley, pubmed-meshheading:8182712-Stereoisomerism, pubmed-meshheading:8182712-Tissue Distribution, pubmed-meshheading:8182712-Tomography, Emission-Computed, Single-Photon, pubmed-meshheading:8182712-Tropanes
pubmed:year
1994
pubmed:articleTitle
Synthesis and characterization of radioiodinated N-(3-iodopropen-1-yl)-2 beta-carbomethoxy-3 beta-(4-chlorophenyl)tropanes: potential dopamine reuptake site imaging agents.
pubmed:affiliation
Department of Radiology, University of Tennessee Medical Center at Knoxville 37920.
pubmed:publicationType
Journal Article, In Vitro