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J Med Chem. 2008 Oct 23;51(20):6614-8. doi: 10.1021/jm800865a. Epub 2008 Sep 24.

1H-cyclopentapyrimidine-2,4(1H,3H)-dione-related ionotropic glutamate receptors ligands. structure-activity relationships and identification of potent and Selective iGluR5 modulators.

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1
European Research Centre for Drug Discovery and Development (NatSynDrugs), Banchi di Sotto 55, 53100 Siena, Italy.

Abstract

(S)-CPW399 ((S)-1) is a potent and excitotoxic AMPA receptor partial agonist. Modifying the cyclopentane ring of (S)-1, we developed two of the most potent and selective functional antagonists (5 and 7) for kainate receptor (KA-R) subunit iGluR5. Derivatives 5 and 7, with their unique pharmacological profile, may lead to a better understanding of the different roles and modes of action of iGluR1-5 subunits, paving the way for the synthesis of new potent, subunit selective iGluR5 modulators.

PMID:
18811139
DOI:
10.1021/jm800865a
[Indexed for MEDLINE]

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