Rational Design, Pharmacomodulation, and Synthesis of Dual 5‑Hydroxytryptamine 7 (5-HT7)/5-Hydroxytryptamine 2A (5-HT2A) Receptor Antagonists and Evaluation by [18F]-PET Imaging in a Primate Brain

We report the synthesis of 46 tertiary amine-bearing N-alkylated benzo­[d]­imidazol-2­(3H)-ones, imidazo­[4,5-b]­pyridin-2­(3H)-ones, imidazo­[4,5-c]­pyridin-2­(3H)-ones, benzo­[d]­oxazol-2­(3H)-ones, oxazolo­[4,5-b]­pyridin-2­(3H)-ones and N,N′-dialkylated benzo­[d]­imidazol-2­(3H)-ones. These comp...

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Published in:Journal of medicinal chemistry 2015-10, Vol.58 (20), p.8066-8096
Main Authors: Deau, Emmanuel, Robin, Elodie, Voinea, Raluca, Percina, Nathalie, Satała, Grzegorz, Finaru, Adriana-Luminita, Chartier, Agnès, Tamagnan, Gilles, Alagille, David, Bojarski, Andrzej J, Morisset-Lopez, Séverine, Suzenet, Franck, Guillaumet, Gérald
Format: Article
Language:English
Subjects:
Animals
Blood-Brain Barrier
Brain - diagnostic imaging
Chemical Sciences
Drug Design
Image Processing, Computer-Assisted
Isotope Labeling
Ligands
Macaca mulatta
Positron-Emission Tomography
Radiopharmaceuticals - chemical synthesis
Radiopharmaceuticals - pharmacology
Receptor, Serotonin, 5-HT2A - drug effects
Receptors, Serotonin - drug effects
Serotonin Antagonists - chemical synthesis
Serotonin Antagonists - pharmacology
Structure-Activity Relationship
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Summary:We report the synthesis of 46 tertiary amine-bearing N-alkylated benzo­[d]­imidazol-2­(3H)-ones, imidazo­[4,5-b]­pyridin-2­(3H)-ones, imidazo­[4,5-c]­pyridin-2­(3H)-ones, benzo­[d]­oxazol-2­(3H)-ones, oxazolo­[4,5-b]­pyridin-2­(3H)-ones and N,N′-dialkylated benzo­[d]­imidazol-2­(3H)-ones. These compounds were evaluated against 5-HT7R, 5-HT2AR, 5-HT1AR, and 5-HT6R as potent dual 5-HT7/5-HT2A serotonin receptors ligands. A thorough study of the structure–activity relationship of the aromatic rings and their substituents, the alkyl chain length and the tertiary amine was conducted. 1-(4-(4-(4-Fluorobenzoyl)­piperidin-1-yl)­butyl)-1H-benzo­[d]­imidazol-2­(3H)-one (79) and 1-(6-(4-(4-fluorobenzoyl)­piperidin-1-yl)­hexyl)-1H-benzo­[d]­imidazol-2­(3H)-one (81) were identified as full antagonist ligands on cyclic adenosine monophosphate (cAMP, K B = 4.9 and 5.9 nM, respectively) and inositol monophosphate (IP1, K B = 0.6 and 16 nM, respectively) signaling pathways of 5-HT7R and 5-HT2AR. Both antagonists crossed the blood–brain barrier as evaluated with [18F] radiolabeled compounds [ 18 F]­79 and [ 18 F]­81 in a primate’s central nervous system using positron emission tomography. Both radioligands showed standard uptake values ranging from 0.8 to 1.1, a good plasmatic stability, and a distribution consistent with 5-HT7R and 5-HT2AR in the CNS.
ISSN:0022-2623
1520-4804
DOI:10.1021/acs.jmedchem.5b00874