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Structure-Affinity-Pharmacokinetics Relationships of Novel 18 F-Labeled 1,4-Diazepane Derivatives for Orexin 1 Receptor Imaging.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2024 Nov 14; Vol. 67 (21), pp. 18781-18793. Date of Electronic Publication: 2024 Oct 21. - Publication Year :
- 2024
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Abstract
- The orexin 1 receptor (OX1R) has been suggested to be involved in the reward and autonomic nervous systems. Positron emission tomography (PET) of OX1R contributes to elucidating its role and developing new drugs. However, there are no useful PET probes for in vivo imaging of OX1R. Here, we newly designed and synthesized <superscript>18</superscript> F-labeled 1,4-diazepane derivatives and evaluated their utilities as OX1R PET probes. In particular, BTF showed high and selective binding affinity for OX1R. In a biodistribution study using normal mice, [ <superscript>18</superscript> F]BTF exhibited brain uptake, and radioactivity in the brain was significantly decreased by preinjection of unlabeled BTF. In a PET/CT study, it was suggested that [ <superscript>18</superscript> F]BTF has the potential to visualize high-expression regions of OX1R in the normal mouse brain. Collectively, [ <superscript>18</superscript> F]BTF has the fundamental features of an OX1R PET probe, and further studies may lead to the development of more useful probes.
- Subjects :
- Animals
Mice
Tissue Distribution
Structure-Activity Relationship
Radiopharmaceuticals pharmacokinetics
Radiopharmaceuticals chemistry
Radiopharmaceuticals chemical synthesis
Humans
Male
Positron-Emission Tomography methods
Positron Emission Tomography Computed Tomography
Orexin Receptors metabolism
Fluorine Radioisotopes chemistry
Brain metabolism
Brain diagnostic imaging
Azepines chemistry
Azepines pharmacokinetics
Azepines chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 67
- Issue :
- 21
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 39431857
- Full Text :
- https://doi.org/10.1021/acs.jmedchem.4c01090