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Org Biomol Chem ; 22(22): 4550-4558, 2024 06 05.
Article in English | MEDLINE | ID: mdl-38768281

ABSTRACT

Nuclear imaging of aggregated α-synuclein pathology is an urgent clinical need for Parkinson's disease, yet promising tracers for brain α-synuclein aggregates are still rare. In this work, a class of compact benzothiazole derivatives was synthesized and evaluated for α-synuclein aggregates. Among them, azobenzothiazoles exhibited specific and selective detection of α-synuclein aggregates under physiological conditions. Fluoro-pegylated azobenzothiazole NN-F further demonstrated high-affinity binding to α-synuclein aggregates and efficient 18F-radiolabeling via nucleophilic displacement of a tosyl precursor. [18F]NN-F was stable in plasma in vitro and showed efficient brain uptake with little defluorination in vivo.


Subject(s)
Benzothiazoles , Brain , Fluorine Radioisotopes , Protein Aggregates , alpha-Synuclein , alpha-Synuclein/metabolism , alpha-Synuclein/chemistry , Fluorine Radioisotopes/chemistry , Benzothiazoles/chemistry , Benzothiazoles/chemical synthesis , Brain/metabolism , Brain/diagnostic imaging , Animals , Humans , Mice , Molecular Structure , Positron-Emission Tomography
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