Synthesis of [18F]FETO, a novel potential 11‐β hydroxylase inhibitor
- 25 February 2003
- journal article
- research article
- Published by Wiley in Journal of Labelled Compounds and Radiopharmaceuticals
- Vol. 46 (4) , 379-388
- https://doi.org/10.1002/jlcr.680
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Long-term impairment of the lacrimal glands after radioiodine therapy: a cross-sectional studyEuropean Journal of Nuclear Medicine and Molecular Imaging, 2002
- Synthesis and preliminary evaluation of [18F]FEtP4A, a promising PET tracer for mapping acetylcholinesterase in vivoNuclear Medicine and Biology, 2002
- Development of an automated system for synthesizing 18F-labeled compounds using [18F]fluoroethyl bromide as a synthetic precursorApplied Radiation and Isotopes, 2002
- Efficient synthesis of 2-bromo-1-[18F]fluoroethane and its application in the automated preparation of 18F-fluoroethylated compoundsApplied Radiation and Isotopes, 2001
- Metabolic and pharmacokinetic considerations in the design of 2-phenyl substituted metyrapone derivatives: 2-methoxyphenylmetyrapone as a radioligand for functional diagnosis of adrenal pathologyNuclear Medicine and Biology, 1995
- Synthesis of two radiofluorinated cocaine analogues using distilled 2-[18F]fluoroethyl bromideApplied Radiation and Isotopes, 1995
- Significance of steroidogenic enzymes in the pathogenesis of hyperfunctioning and non-hyperfunctioning adrenal tumorSteroids, 1995
- 3-(2′-[18F]fluoroethyl)spiperone, a potent dopamine antagonist: Synthesis, structural analysis and in-vivo utilization in humansInternational Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes, 1990
- A rapid and efficient method for the fluoroalkylation of amines and amides. Development of a method suitable for incorporation of the short-lived positron emitting radionuclide fluorine-18The Journal of Organic Chemistry, 1987