1<i>H</i>-Cyclopentapyrimidine-2,4(1<i>H</i>,3<i>H</i>)-dione-Related Ionotropic Glutamate Receptors Ligands. Structure−Activity Relationships and Identification of Potent and Selective iGluR5 Modulators
作者:Stefania Butini、Darryl S. Pickering、Elena Morelli、Salvatore Sanna Coccone、Francesco Trotta、Meri De Angelis、Egeria Guarino、Isabella Fiorini、Giuseppe Campiani、Ettore Novellino、Arne Schousboe、Jeppe K. Christensen、Sandra Gemma
DOI:10.1021/jm800865a
日期:2008.10.23
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
(S)-CPW399((S)-1)是一种有效的兴奋性AMPA受体部分激动剂。修饰(S)-1的环戊烷环,我们开发了两种最有效和选择性的功能抑制剂(5和7),用于对抗海藻酸盐受体(KA-R)亚基iGluR5。衍生物5和7具有独特的药理作用,可能导致人们更好地了解iGluR1-5亚基的不同作用和作用方式,从而为合成新的,有效的亚基选择性iGluR5调节剂铺平了道路。