Abstract
Compounds 1-14 were synthesized in a search for high-affinity CRF1 receptor ligands that could be radiolabeled with (11)C or (18)F for use as positron emission tomography (PET) radiotracers. Derivatives of 2 were developed which contained amide N-fluoroalkyl substituents. Compounds [(18)F]24 and [(18)F]25 were found to have appropriate lipophilicities of logP7.4=2.2 but microPET imaging with [(18)F]25 demonstrated limited brain uptake.
Keywords:
CRF-1 receptor; Corticotropin-releasing factor; Fluorine-18; PET imaging; Positron emission tomography.
Copyright © 2015 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Aminopyridines / chemical synthesis
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Aminopyridines / metabolism
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Aminopyridines / pharmacology*
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Animals
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Brain / metabolism*
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Cell Line
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Fluorine Radioisotopes
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Heterocyclic Compounds, 2-Ring / chemical synthesis
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Heterocyclic Compounds, 2-Ring / metabolism
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Heterocyclic Compounds, 2-Ring / pharmacology*
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Humans
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Ligands
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Macaca fascicularis
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Male
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Peptide Fragments / chemistry
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Positron-Emission Tomography
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Pyrazines / chemical synthesis
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Pyrazines / metabolism
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Pyrazines / pharmacology*
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Radiopharmaceuticals / chemical synthesis
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Radiopharmaceuticals / metabolism
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Radiopharmaceuticals / pharmacology*
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Receptors, Corticotropin-Releasing Hormone / metabolism*
Substances
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Aminopyridines
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CRF receptor type 2
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Fluorine Radioisotopes
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Heterocyclic Compounds, 2-Ring
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Ligands
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Peptide Fragments
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Pyrazines
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Radiopharmaceuticals
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Receptors, Corticotropin-Releasing Hormone
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antisauvagine 30
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CRF receptor type 1