Source:http://linkedlifedata.com/resource/pubmed/id/15464398
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
7
|
| pubmed:dateCreated |
2004-10-6
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| pubmed:abstractText |
A series of 11C-labeled analogs of the acetylcholinesterase (AChE) inhibitor pyridostigmine have been synthesized for evaluation as new potential positron emission tomography (PET) imaging agents for heart AChE. The appropriate precursors for radiolabeling were slightly modified from commercial reagents. The new tracers [11C]pyridostigmine (1), [11C]para-pyridostigmine (2) and [11C]ortho-pyridostigmine (3) were prepared by N-[11C]methylation of the precursors using [11C]methyl triflate. Pure target compounds were isolated by a solid-phase extraction (SPE) purification procedure with 60-85% radiochemical yields (decay corrected to end of bombardment), and a synthesis time of 10-15 min. The initial PET dynamic studies of compounds (1-3) in rat heart showed rapid heart uptake and blood pool clearance to give high quality heart images. These results suggest the new tracers delineate the heart very clearly and could be potential heart AChE imaging agents.
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| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acetylcholinesterase,
http://linkedlifedata.com/resource/pubmed/chemical/Carbon Radioisotopes,
http://linkedlifedata.com/resource/pubmed/chemical/Cholinesterase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Pyridostigmine Bromide,
http://linkedlifedata.com/resource/pubmed/chemical/Radiopharmaceuticals
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| pubmed:status |
MEDLINE
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| pubmed:month |
Oct
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| pubmed:issn |
0969-8051
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
31
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
957-64
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| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:15464398-Acetylcholinesterase,
pubmed-meshheading:15464398-Animals,
pubmed-meshheading:15464398-Carbon Radioisotopes,
pubmed-meshheading:15464398-Cholinesterase Inhibitors,
pubmed-meshheading:15464398-Feasibility Studies,
pubmed-meshheading:15464398-Female,
pubmed-meshheading:15464398-Heart,
pubmed-meshheading:15464398-Humans,
pubmed-meshheading:15464398-Male,
pubmed-meshheading:15464398-Metabolic Clearance Rate,
pubmed-meshheading:15464398-Myocardium,
pubmed-meshheading:15464398-Organ Specificity,
pubmed-meshheading:15464398-Positron-Emission Tomography,
pubmed-meshheading:15464398-Pyridostigmine Bromide,
pubmed-meshheading:15464398-Radiopharmaceuticals,
pubmed-meshheading:15464398-Rats,
pubmed-meshheading:15464398-Rats, Sprague-Dawley,
pubmed-meshheading:15464398-Tissue Distribution
|
| pubmed:year |
2004
|
| pubmed:articleTitle |
Facile synthesis and initial PET imaging of novel potential heart acetylcholinesterase imaging agents [11C]pyridostigmine and its analogs.
|
| pubmed:affiliation |
Department of Radiology, Krannert Institute of Cardiology2, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
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| pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't,
Evaluation Studies
|