✦ LIBER ✦

Synthesis of N1′-([18F]fluoroethyl)naltrindole ([18F]FEtNTI): a radioligand for positron emission tomographic studies of delta opioid receptors

✍ Scribed by William B. Mathews; Chris M. Kinter; James Palma; Robert V. Daniels; Hayden T. Ravert; Robert F. Dannals; John R. Lever

Publisher: John Wiley and Sons
Year: 1999
Tongue: French
Weight: 736 KB
Volume: 42
Category: Article
ISSN: 0022-2135
DOI: 10.1002/(sici)1099-1344(199901)42:1<43::aid-jlcr165>3.0.co;2-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of [18F] SR144385: a selective

Synthesis of [18F] SR144385: a selective radioligand for positron emission tomographic studies of brain cannabinoid receptors

✍ William B. Mathews; Hayden T. Ravert; John L. Musachio; Richard A. Frank; Muriel 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 French ⚖ 290 KB 👁 1 views

Synthesis of N-(piperidin-1-yl)-5-(4-met

Synthesis of N-(piperidin-1-yl)-5-(4-methoxyphenyl)-1-(2-chlorophenyl)-4-[18F]fluoro-1H-pyrazole-3-carboxamide by nucleophilic [18F] fluorination: a PET radiotracer for studying CB1 cannabinoid receptors

✍ Reeti Katoch-Rouse; Andrew G. Horti 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 French ⚖ 91 KB

## Abstract The feasibility of nucleophilic displacement of bromide in the 4‐bromopyrazole ring with [^18^F]fluoride has been demonstrated by the synthesis of two radiolabeled compounds: __N__‐(piperidin‐1‐yl)‐5‐(4‐methoxyphenyl)‐1‐(2‐chlorophenyl)‐4‐[^18^F]fluoro‐1__H__‐pyrazole‐3‐carboxamide, ([^

Synthesis of 2-Amino-6-(2- [18F] fluoro-

Synthesis of 2-Amino-6-(2- [18F] fluoro-pyridine-4-ylmethoxy)-9-(octyl-β-D-glucosyl)-purine: A Novel Radioligand for Positron Emission Tomography Studies of the O6-Methylguanine-DNA Methyltransferase (MGMT) Status of Tumor Tissue.

✍ Ralf Schirrmacher; Ute Muehlhausen; Bjoern Waengler; Esther Schirrmacher; Jost R 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB

Synthesis and preliminary in vivo evalua

Synthesis and preliminary in vivo evaluation of 4-[18F]fluoro-N-{2-[4-(6-trifluoromethylpyridin-2-yl)piperazin-1-yl]ethyl}benzamide, a potential PET radioligand for the 5-HT1A receptor

✍ M. Vandecapelle; F. Dumont; F. De Vos; K. Strijckmans; D. Leysen; K. Audenaert; 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 French ⚖ 138 KB 👁 1 views

## Abstract 4‐Fluoro‐__N__‐{2‐[4‐(6‐trifluoromethylpyridin‐2‐yl)piperazin‐1‐yl]ethyl}benzamide is a full 5‐HT~1A~ agonist with high affinity (__pK__~__i__~=9.3), selectivity and a __c__ log __P__ of 3.045. The corresponding PET radioligand 4‐[^18^F]fluoro‐__N__‐{2‐[4‐(6‐trifluoromethylpyridin‐2‐yl)