Drug intelligence / Profile preview

(-)-[18F]fluorobenzovesamicol

Development stage
Preclinical
Lead developer
Université d'Orléans
Modality
Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Positron Emitters → Radiopharmaceuticals, Small Molecules
Administration
Intravenous
01

Overview

(-)-[18F]fluorobenzovesamicol (also known as (-)-[18F]FBVM) is a radiolabeled vesamicol derivative developed as a positron emission tomography (PET) imaging tracer targeting the vesicular acetylcholine transporter (VAChT). It is designed to visualize and quantify cholinergic terminal density in vivo, which is a key biomarker for assessing cholinergic dysfunction in neurodegenerative disorders such as Alzheimer's disease, Parkinson's disease, and dementia with Lewy bodies. Preclinical studies in rodents have demonstrated that (-)-[18F]fluorobenzovesamicol has a high binding affinity (Ki = 0.9 nM) and selectivity for VAChT, showing a significantly higher striatum-to-cerebellum uptake ratio and superior signal-to-noise ratio compared to other tracers like (-)-[18F]FEOBV.

Other names
(-)-(R,R)-5-[18F]fluorobenzovesamicol(-)-5-[18F]fluorobenzovesamicol(-)-5-FBVM(-)-[18F]FBVM(-)[18F]FBVM5-FBVM[18F]FBVMfluorobenzovesamicol
02

Targets

SLC18A3 (Vesicular acetylcholine transporter)

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