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The Effects of Conformational Constraints in the Polyamine Moiety of Philanthotoxins on AMPAR Inhibition
Author(s) -
Franzyk Henrik,
Grzeskowiak John W.,
Tikhonov Denis B.,
Jaroszewski Jerzy W.,
Mellor Ian R.
Publication year - 2014
Publication title -
chemmedchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.817
H-Index - 100
eISSN - 1860-7187
pISSN - 1860-7179
DOI - 10.1002/cmdc.201402109
Subject(s) - moiety , stereochemistry , ampa receptor , chemistry , polyamine , allosteric regulation , steric effects , xenopus , biophysics , biochemistry , glutamate receptor , receptor , biology , gene
Philanthotoxin‐433 (PhTX‐433) is a known potent inhibitor of ionotropic glutamate receptors, and analogues have been synthesised to identify more potent and selective antagonists. Herein we report the synthesis of four PhTXs with a cyclopropane moiety introduced into their polyamine chain, and their inhibition of an α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid (AMPA) receptor subtype by using two‐electrode voltage‐clamp assays on Xenopus oocytes expressing the GluA1flop subunit. All analogues were found to be more potent than PhTX‐343, with trans ‐cyclopropyl‐PhTX‐343 being the most potent (∼28‐fold) and cis ‐cyclopropyl‐PhTX‐343 least potent (∼4‐fold). Both cis ‐ and trans ‐cyclopropyl‐PhTX‐444 had intermediate potency (both ∼12‐fold). Molecular modelling indicates that a cyclopropane moiety confers a favourable steric constraint to the polyamine part, but this is compromised by a cis conformation due to enhanced intramolecular folding. Elongated PhTX‐444 analogues alleviate this to some extent, but optimal positioning of the amines is not permitted.