original ) (raw )Production of fluorine-18 labeled (3-N-methyl)benperidol for PET investigation of cerebral dopaminergic receptor binding
S. Moerlein
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 1992
View PDFchevron_right
Comparison of two fluorine-18 labeled benzamide derivatives that bind reversibly to dopamine D2 receptors: In vitro binding studies and positron emission tomography
Thomas Morton
Synapse, 1996
View PDFchevron_right
Biodistribution of N-alkyl and N-fluoroalkyl derivatives of spiroperidol; radiopharmaceuticals for PET studies of dopamine receptors
Dae Yoon Chi
International Journal of …, 1986
View PDFchevron_right
The use of [18F]4-fluorobenzyl iodide (FBI) in PET radiotracer synthesis: Model alkylation studies and its application in the design of dopamine D1 and D2 receptor-based imaging agents
Thomas Morton
Nuclear Medicine and Biology, 1993
View PDFchevron_right
Synthesis, Biodistribution, and Primate Imaging of Fluorine-18 Labeled 2β-Carbo-1‘-fluoro-2-propoxy-3β-(4-chlorophenyl)tropanes. Ligands for the Imaging of Dopamine Transporters by Positron Emission Tomography
Vernon Camp
Journal of Medicinal Chemistry, 2000
View PDFchevron_right
N-(3-[18F]fluoropropyl)-spiperone: The preferred 18F labeled spiperone analog for positron emission tomographic studies of the dopamine receptor
C. Dence
International Journal of Radiation Applications and Instrumentation. Part B. Nuclear Medicine and Biology, 1988
View PDFchevron_right
Fluorine-18 labelled substituted benzazepines as potential radiotracers for imaging dopamine D1 receptors by positron emission tomography
Jogeshwar Mukherjee
European Journal of Pharmacology, 1993
View PDFchevron_right
Cyclopropyl-FLB 457: A PET Radioligand for Low Densities of Dopamine D2 Receptors
Sangram Nag
Bioorganic & medicinal …, 2008
View PDFchevron_right
11C]Cyclopropyl-FLB 457: A PET radioligand for low densities of dopamine D 2 receptors
Jogeshwar Mukherjee , sankha chattopadhyay
Bioorganic & Medicinal Chemistry, 2008
View PDFchevron_right
Synthesis and evaluation of an 18F-labeled dopa prodrug as a PET tracer for studying brain dopamine metabolism
Tadashi Nozaki
Nuclear Medicine and Biology, 1996
View PDFchevron_right
Substituted benzamides as ligands for visualization of dopamine receptor binding in the human brain by positron emission tomography
Lars Farde
Proceedings of the National Academy of Sciences, 1985
View PDFchevron_right
A Comparative PET-study of five carbon-11 or fluorine-18 labelled salicylamides. Preparation and in vitro dopamine D-2 receptor binding
Lars Farde
International Journal of Radiation Applications and Instrumentation. Part B. Nuclear Medicine and Biology, 1991
View PDFchevron_right
The use of [18F] 4-fluorobenzyl iodide (FBI) in PET radiotracer synthesis: model alkylation studies and its application in the design of dopamine D1 and D2 receptor- …
Theresa Filtz
Nuclear medicine and …, 1993
View PDFchevron_right
Radiodefluorination of 3-Fluoro-5-(2-(2- 18F -thiazol-4-yl)ethynyl)benzonitrile ([18F]SP203), a Radioligand for Imaging Brain Metabotropic Glutamate Subtype-5 Receptors with Positron Emission Tomography, Occurs by Glutathionylation in Rat Brain
Amira Brown
Journal of Pharmacology and Experimental Therapeutics, 2008
View PDFchevron_right
(−)-N-[11C]propyl-norapomorphine: a positron-labeled dopamine agonist for PET imaging of D2 receptors
Lawrence Kegeles
Nuclear Medicine and Biology, 2000
View PDFchevron_right
Tissue Distribution, Autoradiography, and Metabolism of 4‐(2′‐Methoxyphenyl)‐1‐[2′‐[N‐2 ″‐Pyridinyl)‐p‐[18F] Fluorobenzamido] ethyl] piperazine (p‐[18F] MPPF), a New Serotonin 5‐HT1A Antagonist for Positron Emission Tomography
Alain Plenevaux
View PDFchevron_right
Radiosynthesis and Preclinical Evaluation of 18F-F13714 as a Fluorinated 5-HT1A Receptor Agonist Radioligand for PET Neuroimaging
Simon Ametamey , Yves Auberson , Adrian Newman-Tancredi
Journal of Nuclear Medicine, 2012
View PDFchevron_right
Synthesis of ω-[18F]fluoroalkyl analogs of YM-09151-2 for the measurement of D2-dopamine receptors with PET
Masatoshi Itoh
International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes, 1990
View PDFchevron_right
Fluorinated benzamide neuroleptics—2. Synthesis and radiosynthesis of (S)-N-[(1-ethyl-2-pyrrolidinyl)methyl]-5-(3-[18F]fluoropropyl)-3-substituted-2-methoxybenzamides
Jogeshwar Mukherjee
International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes, 1991
View PDFchevron_right
Binding of 5-(2′-[18F]fluoroenthyl)flumazenil to central benzodiazepine receptors measured in living baboon by positron emission tomography
S. Moerlein
European Journal of Pharmacology, 1992
View PDFchevron_right
Positron labeled muscarinic acetylcholine receptor antagonist: 2- and 4-[18F]fluorodexetimide. Syntheses and biodistribution
Carmen S Dence
International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology, 1991
View PDFchevron_right
Evaluation of fluorinated m-Tyrosine analogs as PET imaging agents of dopamine nerve terminals: comparison with 6-FluoroDOPA
Jerry Nickles
Journal of Nuclear Medicine
View PDFchevron_right
N-.omega.-Fluoroalkyl Analogs of (1R)-2.beta.-Carbomethoxy-3.beta.-(4-iodophenyl)tropane (.beta.-CIT): Radiotracers for Positron Emission Tomography and Single Photon Emission Computed Tomography Imaging of Dopamine Transporters
Ross Baldessarini
Journal of Medicinal Chemistry, 1994
View PDFchevron_right
Iodine-125 and fluorine-18 labeled aryl-1,4-dialkylpiperazines: potential radiopharmaceuticals for in vivo study of the dopamine uptake system
Marcian Van Dort
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 1992
View PDFchevron_right
A Comparison of 11C-Labeled L-DOPA and L-Fluorodopa as Positron Emission Tomography Tracers for the Presynaptic Dopaminergic System
Joakim Tedroff
Journal of Cerebral Blood Flow & Metabolism, 1999
View PDFchevron_right