Synthesis of 3-[18F]fluoromethyl-BTCP and evaluation as a potential PET radioligand for the dopamine transporter in baboons
✍ Scribed by Ponchant, M.; Varastet, M.; Hantraye, P.; Chicheportiche, R.; Kamenka, J.M.; Crouzel, C.
- Book ID
- 124133782
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 611 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0969-8051
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract This study evaluated the utility of __(S)‐N__‐[(1‐ethyl‐2‐pyrrolidinyl)methyl]‐5‐(3‐[^18^F]fluoropropyl)‐2,3‐dimethoxybenzamide ([^18^F]fluoropropylepidepride), [^18^F]5‐FPrEpid, as a ligar d for PET studies of cerebral dopamine D2 receptors. The in vitro affinity for the rat striatal d
## Abstract In an attempt to visualize the NMDA glutamatergic receptors and after checking the biological activity of the cold 3‐fluoromethyl‐TCP 3, 3‐[^18^F]‐fluoro‐methyl‐TCP 4 was synthesized by a nucleophilic substitution of 3‐bromomethyl‐TCP 5 with [^18^F^−^].