Published August 2017 | Version v1
Journal article

Synthesis, radiolabeling and preclinical evaluation of a [11C]GMOM derivative as PET radiotracer for the ion channel of the N-methyl-D-aspartate receptor

  • 1. Department of Radiology & Nuclear Medicine, Neuroscience Campus Amsterdam, VU University Medical Center, P.O. Box 7057, Amsterdam, 1007 MB (Netherlands)

Description

Presently available PET ligands for the NMDAr ion channel generally suffer from fast metabolism. The purpose of this study was to develop a metabolically more stable ligand for the NMDAr ion channel, taking [11C]GMOM ([11C]1) as the lead compound.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.nucmedbio.2017.05.003

Additional details

Identifiers

DOI
10.1016/j.nucmedbio.2017.05.003;
PII
S0969805117300148;

Publishing Information

Journal Title
Nuclear Medicine and Biology
Journal Volume
51
Journal Page Range
p. 25-32
ISSN
0969-8051
CODEN
NMBIEO

Optional Information

Copyright
Copyright (c) 2017 The Authors. Published by Elsevier Inc.