𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of d-[11C]oxyphenonium iodide, a potential radioligand for in vivo visualization of human cholinergic muscarinic receptor-sites by positron emission tomography

✍ Scribed by Jurgen W. Vlek; Karla G. Feitsma; Thom W. van der Mark; Ben F.H. Drenth; Anne M.J. Paans; Willem Vaalburg


Publisher
Elsevier Science
Year
1990
Weight
340 KB
Volume
41
Category
Article
ISSN
0883-2889

No coin nor oath required. For personal study only.

✦ Synopsis


Carbon-11 labeled d-oxyphenonium iodide, a cholinergic antagonist is synthesized for in vivo visualization of muscarinic receptor-sites on airway tissue by positron emission tomography (PET). Methylation with [11C]CH3I of d-demethyloxyphenonium, followed by HPLC purification affords the desired radiopharmaceutical with a radiochemical yield of 66% (based on [11C]CH3I, and corrected for decay) and with a specific activity of 110-300 Ci/mmol. The biologically active labeled d-enantiomer is prepared within 40 min after EOB. Optical and chemical purity proved to be better than 99.9%. Radiochemical purity was determined to be higher than 99%.


πŸ“œ SIMILAR VOLUMES


Synthesis of radiotracers for studying m
✍ Robert F. Dannals; Bengt LΓ₯ngstrΓΆm; Hayden T. Ravert; Alan A. Wilson; Henry N. W πŸ“‚ Article πŸ“… 1988 πŸ› Elsevier Science βš– 298 KB

Dexetimide (Fig. la), a potent muscarinic cholinergic receptor antagonist, and levetimide (Fig. lb), its pharmacologically inactive enantiomer, were labeled with "C for non-invasive in vivo studies of muscarinic cholinergic receptors in the human brain using positron emission tomography. The synthes

Synthesis and biological evaluation of S
✍ Raquel Garcia; Catarina Xavier; AntΓ³nio Paulo; Isabel Santos; Torsten Kniess; R. πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 French βš– 157 KB

The novel 2-mercaptoimidazole derivatives, 1-[4-((2-methoxyphenyl)-1-piperazinyl)butyl]-2-mercaptoimidazole (3) and methyl[4-((2-methoxyphenyl)-1-piperazinyl))butyl] (2-mercapto-1-methylimidazol-5-yl)methanamide ( 8), were efficiently labelled with 11 C through methylation of the thioketone function