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Volumn 18, Issue 23, 2008, Pages 6168-6170
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New synthesis and evaluation of enantiomers of 7-methyl-2-exo-(3′-iodo-5′-pyridinyl)-7-azabicyclo[2.2.1]heptane as stereoselective ligands for PET imaging of nicotinic acetylcholine receptors
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Author keywords
C 11; Enantiomers; nAChR; Positron emission tomography (PET)
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Indexed keywords
7 METHYL 2 EXO (3' IODO 5' PYRIDINYL) 7 AZABICYCLO[2.2.1]HEPTANE;
EPIBATIDINE;
NICOTINIC RECEPTOR;
NICOTINIC RECEPTOR BLOCKING AGENT;
RADIOLIGAND;
UNCLASSIFIED DRUG;
ANIMAL EXPERIMENT;
ARTICLE;
BABOON;
CAUDATE NUCLEUS;
CEREBELLUM;
CONTROLLED STUDY;
DRUG HALF LIFE;
DRUG RECEPTOR BINDING;
DRUG SYNTHESIS;
DRUG UPTAKE;
ENANTIOSELECTIVITY;
FRONTAL CORTEX;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
MOUSE;
NONHUMAN;
POSITRON EMISSION TOMOGRAPHY;
RADIOISOTOPE DISTRIBUTION;
THALAMUS;
ANIMALS;
BICYCLO COMPOUNDS, HETEROCYCLIC;
BRAIN;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
HEPTANES;
LIGANDS;
MICE;
MOLECULAR STRUCTURE;
PAPIO;
POSITRON-EMISSION TOMOGRAPHY;
RADIOPHARMACEUTICALS;
RECEPTORS, NICOTINIC;
STEREOISOMERISM;
PAPIO;
RODENTIA;
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EID: 55549115005
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmcl.2008.10.012 Document Type: Article |
Times cited : (8)
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References (18)
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