Current Topics in Medicinal Chemistry

Allen B. Reitz
Fox Chase Chemical Diversity Center, Inc.
Doylestown, PA
USA

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Ketanserin and Spiperone as Templates for Novel Serotonin 5-HT2A Antagonists

Author(s): Richard A. Glennon, Kamel Metwally, Malgorzata Dukat, Abd M. Ismaiel, Joseph De. Los Angeles, Jeffery Herndon, Milt Teitler and Nantaka Khorana

Affiliation: Department ofMedicinal Chemistry, School of Pharmacy, Virginia CommonwealthUniversity, Richmond, VA 23298 USA

Abstract:

The structures of ketanserin (1) and spiperone (2) were examined in detail to determine the role of various substituent groups on 5-HT2A receptor affinity and selectivity. It was found that the presence of the quinazoline ring of ketanserin detracts from selectivity and that various ring-opened analogs displayed ketanserin-like affinity and up to 30-fold enhanced selectivity. The triazaspirodecanone portion of spiperone is a major determinant of its 5-HT2A affinity and selectivity. The conformational rigidity imposed by the ring, as well as the nature of the N1-substituent, are important factors in controlling binding at 5-HT2A, 5-HT2C, 5-HT1A, and dopamine D2 receptors. Replacement of the N1-phenyl ring of spiperone with a methyl group (KML-010 48) resulted in a compound that binds at 5-HT2A receptors with slightly lower affinity than spiperone, but that lacked affinity (Ki > 10,000 nM) for 5-HT2C and 5-HT1A receptors and binds with 400-fold reduced affinity at D2 receptors.

Keywords: Ketanserin and Spiperone, Serotonin 5-HT2A, KETANSERIN ANALOGS, Quinazoline-Abbreviated Analogs, Benzoylpiperidine

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Article Details

VOLUME: 2
ISSUE: 6
Page: [539 - 558]
Pages: 20
DOI: 10.2174/1568026023393787
Price: $58