Aminimides as Potential CNS Acting Agents. II* Design, Synthesis, and Receptor Binding of 4′-Arylalkyl Aminimide Analogues of Clozapine as Prospective Novel Antipsychotics
Ben Capuano A , Ian T. Crosby A D , Edward J. Lloyd A , Juliette E. Neve A B and David A. Taylor CA Department of Medicinal Chemistry, Victorian College of Pharmacy, Monash University, 381 Royal Parade, Parkville VIC 3052, Australia.
B Current address: Natural Product Discovery, Eskitis Institute for Cell and Molecular Therapies, Griffith University, Nathan QLD 4111, Australia.
C Department of Pharmaceutical Biology, Victorian College of Pharmacy, Monash University, 381 Royal Parade, Parkville VIC 3052, Australia.
D Corresponding author. Email: ian.crosby@vcp.monash.edu.au
Australian Journal of Chemistry 61(1) 5-10 https://doi.org/10.1071/CH07275
Submitted: 3 August 2007 Accepted: 30 October 2007 Published: 18 January 2008
Abstract
We report the synthesis of a series of second generation aminimide-based analogues of clozapine, investigating the length of the linker between the aminimide functional group and the introduced aryl moiety. The chemistry and structural characterization of this series of 4′-arylalkyl aminimide analogues of clozapine are described. Preliminary findings on the biochemical effects of linker length and type of aryl moiety on affinity for dopamine D4 and serotonin 5-HT2A receptors are discussed. All of the compounds showed a marked reduction in binding at the two receptors when compared with clozapine, thus showing a reduced potential for atypical antipsychotic activity.
Acknowledgement
The receipt of a Monash Graduate Scholarship (JEN) for support of the present research is gratefully acknowledged.
[1]
P. Seeman,
H. H. M. Van Tol,
Trends Pharmacol. Sci. 1994, 15, 264.
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CAS |
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CAS |
| Crossref | GoogleScholarGoogle Scholar |
CAS |
| Crossref | GoogleScholarGoogle Scholar |
CAS |
| Crossref | GoogleScholarGoogle Scholar |
CAS |
| Crossref | GoogleScholarGoogle Scholar |
CAS |
| Crossref | GoogleScholarGoogle Scholar |
CAS |
| Crossref | GoogleScholarGoogle Scholar |
CAS |
| Crossref | GoogleScholarGoogle Scholar |
CAS |
[12]
[13]
* Part I, Aust. J. Chem. 2007, 60, 673.