| Literature DB >> 16458504 |
Jaya Prabhakaran1, Ramin V Parsey, Vattoly J Majo, Shu-Chi Hsiung, Matthew S Milak, Hadassah Tamir, Norman R Simpson, Ronald L Van Heertum, J John Mann, J S Dileep Kumar.
Abstract
Synthesis and in vivo evaluation of 2-{4-[4-(3-methoxyphenyl)piperazin-1-yl]-butyl}-4-methyl-2H-[1,2,4]triazine-3,5-dione (5 or MMT), a high affinity and selective serotonin 5-HT1AR agonist PET tracer, are described. GTPgammaS assay shows that MMT is an agonist with an EC50 comparable to 5-HT. Radiolabeling of 5 was achieved in 30% yield (EOS) from desmethyl-MMT (4) with >99% chemical and radiochemical purities and a specific activity >1000 Ci/mmol. PET studies in baboon show that [11C]5 penetrates the blood-brain barrier but, because of low specific binding and fast clearance of radioactivity it is not a suitable PET tracer for the in vivo quantification of 5-HT1AR.Entities:
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Year: 2006 PMID: 16458504 DOI: 10.1016/j.bmcl.2006.01.052
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823