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The synthesis and evaluation of N1-(4-(2-[18F]-fluoroethyl)phenyl)-N8-hydroxyoctanediamide ([18F]-FESAHA), A PET radiotracer designed for the delineation of histone deacetylase expression in cancer

✍ Scribed by Brian M. Zeglis; NagaVaraKishore Pillarsetty; Vadim Divilov; Ronald A. Blasberg; Jason S. Lewis

Book ID
116799711
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
910 KB
Volume
38
Category
Article
ISSN
0969-8051

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## Abstract 4‐Fluoro‐__N__‐{2‐[4‐(6‐trifluoromethylpyridin‐2‐yl)piperazin‐1‐yl]ethyl}benzamide is a full 5‐HT~1A~ agonist with high affinity (__pK__~__i__~=9.3), selectivity and a __c__ log __P__ of 3.045. The corresponding PET radioligand 4‐[^18^F]fluoro‐__N__‐{2‐[4‐(6‐trifluoromethylpyridin‐2‐yl)