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[18F]p-MPPF: A Radiolabeled Antagonist for the Study of 5-HT1A Receptors with PET

✍ Scribed by A Plenevaux; C Lemaire; J Aerts; G Lacan; D Rubins; W.P Melega; C Brihaye; C Degueldre; S Fuchs; E Salmon; P Maquet; S Laureys; P Damhaut; D Weissmann; D Le Bars; J.-F Pujol; A Luxen


Book ID
117687611
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
763 KB
Volume
27
Category
Article
ISSN
0969-8051

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πŸ“œ SIMILAR VOLUMES


p-[18F]-MPPF: A potential radioligand fo
✍ Chyng-Yann Shiue; Grace G. Shiue; P. David Mozley; Mei-Ping Kung; Zhi-Ping Zhuan πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 154 KB πŸ‘ 2 views

The purpose of this study was to develop a radiopharmaceutical that could be used to selectively image 5-HT 1A receptors with positron emission tomography (PET). No-carrier-added 4-(28-methoxyphenyl)-1-[28-(N-29-pyridinyl)-p-[ 18 F]fluorobenzamido]ethylpiperazine ( p-[ 18 F]-MPPF, 2) was synthesized

In vivo characterization of p-[18F]MPPF,
✍ Nathalie Ginovart; Wadad Hassoun; Didier Le Bars; Dinah Weissmann; Vincent Levie πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 574 KB

The in vivo and ex vivo distributions and the pharmacological profile of the fluorinated phenylpiperazine derivative p-[ 18 F]MPPF (4-(2Ј-methoxyphenyl)-1-[2Ј-(N-2Π‰-pyridinyl)-p-fluorobenzamido]-ethylpiperazine) were evaluated in the cat brain as a potential selective antagonist for 5-HT 1A receptor