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New high affinity H3 receptor agonists without a basic side chain.

Ruengwit Kitbunnadaj·Marcel Hoffmann·Silvina A Fratantoni·Gerold Bongers·Remko A Bakker·Kerstin Wieland·Ahmed el Jilali·Iwan J P De Esch·Wiro M P B Menge·Henk Timmerman·Rob Leurs
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Abstract

In this study, we replaced the basic amine function of the known histamine H(3) receptor agonists imbutamine or immepip with non-basic alcohol or hydrocarbon moieties. All compounds in this study show a moderate to high affinity for the cloned human H(3) receptor and, unexpectedly, almost all of them act as potent agonists. Moreover, in the alcohol series, we consistently observed an increased selectivity for the human H(3) receptor over the human H(4) receptor, but none of the compounds in this series possess increased affinity and functional activity compared to their alkylamine congeners. In this new series of compounds VUF5657, 5-(1H-imidazol-4-yl)-pentan-1-ol, is the most potent histamine H(3) receptor agonist (pK(i) = 8.0 and pEC(50) = 8.1) with a 320-fold selectivity at the human H(3) receptor over the human H(4) receptor.

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Cell Line, TumorHistamine AgonistsHumansMolecular StructureReceptors, HistamineStructure-Activity RelationshipJournal Article

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Ruengwit Kitbunnadaj, Marcel Hoffmann, Silvina A Fratantoni, Gerold Bongers, Remko A Bakker, Kerstin Wieland, Ahmed el Jilali, Iwan J P De Esch, Wiro M P B Menge, Henk Timmerman, Rob Leurs. 2005-10-05. New high affinity H3 receptor agonists without a basic side chain.. https://doi.org/10.1016/j.bmc.2005.09.002

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