Abstract:
:CBD-2115 was selected from a library of 148 compounds based on a pyridinyl-indole scaffold as a first-in-class 4R-tau radiotracer. In vitro binding assays showed [3H]CBD-2115 had a KD value of 6.9 nM and a nominal Bmax of 500 nM in 4R-tau expressing P301L transgenic mouse tissue. In binding assays with human brain tissue homogenates, [3H]CBD-2115 has a higher affinity (4.9 nM) for progressive supranuclear palsy specific 4R-tau deposits than [3H]flortaucipir (45 nM) or [3H]MK-6240 (>50 nM). [18F]CBD-2115 was reliably synthesized (3-11% radiochemical yield with molar activity of 27-111 GBq/μmol and >97% radiochemical purity). Dynamic PET imaging was conducted in mice, rats, and nonhuman primates, and all species showed initial brain uptake of 0.5-0.65 standardized uptake value with fast clearance from normal tissues. [3H]CBD-2115 could be a useful lead radioligand for further research in 4R-tauopathies, and PET radiotracer development will focus on improving brain uptake and binding affinity.
journal_name
ACS Chem Neuroscijournal_title
ACS chemical neuroscienceauthors
Lindberg A,Knight AC,Sohn D,Rakos L,Tong J,Radelet A,Mason NS,Stehouwer JS,Lopresti BJ,Klunk WE,Sandell J,Sandberg A,Hammarström P,Svensson S,Mathis CA,Vasdev Ndoi
10.1021/acschemneuro.0c00801subject
Has Abstractpub_date
2021-01-26 00:00:00issn
1948-7193pub_type
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