Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10916021 | Nuclear Medicine and Biology | 2014 | 7 Pages |
Abstract
'Click chemistry' was successfully applied to the synthesis of [18 F]FPTC resulting in high radiochemical yields. [18 F]FPTC showed specific binding in vitro, but not in vivo. Based on the logP value and its ability to block [125I]ICYP binding to C6 cells, FPTC may be a lead to suitable cerebral β-AR ligands.
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Authors
Leila Mirfeizi, Anna A. Rybczynska, Aren van Waarde, Lachlan Campbell-Verduyn, Ben L. Feringa, Rudi A.J.O. Dierckx, Philip H. Elsinga,