Design, synthesis, radiolabeling and in vivo evaluation of potential positron emission tomography (PET) radioligands for brain imaging of the 5-HT7 receptor

作者：Lacivita Enza; Niso Mauro; Hansen Hanne D; Di Pilato Pantaleo; Herth Matthias M; Lehel Szabolcs; Ettrup Anders; Montenegro Lisa; Perrone Roberto; Berardi Francesco; Colabufo Nicola A; Leopoldo Marcello^*; Knudsen Gitte M

来源：Bioorganic & Medicinal Chemistry, 2014, 22(5): 1736-1750.

DOI：10.1016/j.bmc.2014.01.016

• 5-HT7 receptor
• PET
• Radioligand
• Arylpiperazine

Here we describe the design, synthesis, and pharmacological evaluation of a set of compounds structurally related to the high affinity serotonin 5-HT7 receptor agonist N-(4-cyanophenylmethyl)-4-(2-diphenyl)-1-piperazinehexanamide (6, LP-211). Specific structural modifications were performed in order to maintain affinity for the target receptor and to improve the selectivity over 5-HT1A and adrenergic alpha(1) receptors. The synthesized compounds have chemical features that could enable labeling with a positron emitter radioisotope (carbon-11 or fluorine-18) and lipophilicity within the range considered optimal for brain penetration and low non-specific binding. 4-[2-(4-Methoxyphenyl) phenyl]-N-(pyridin-4ylmethyl) piperazinehexanamide (23a) and N-pyridin-4-ylmethyl-3-[4-[2-(4-methoxyphenyl) phenyl] piperazin-1-yl]ethoxy]propanamide (26a) were radiolabeled on the methoxy group with carbon-11. Positron emission tomography (PET) analysis revealed that [C-11]-23a and [C-11]-26a were P-glycoprotein (P-gp) substrates and rapidly metabolized, resulting in poor brain uptake. These features were not predicted by in vitro tests.

• 出版日期2014-3-1