4.5 Article

Design, synthesis, and biological evaluation of a scaffold for iGluR ligands based on the structure of (-)-dysiherbaine

Journal

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume 16, Issue 8, Pages 2189-2194

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2006.01.047

Keywords

excitatory amino acid receptors; KA receptor agonist; KA reeptor antagonist; NMDA receptor agonist; dysiherbaine; scaffold

Funding

  1. NIGMS NIH HHS [GM07311] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS027600, NS-27600] Funding Source: Medline

Ask authors/readers for more resources

The design and synthesis of four 2,2-disubstituted dihydrobenzofurans that are structurally related to several glutamate-containing natural products, including (-)-dysiherbaine, is described. Biological evaluation of these analogs shows that one is a KA receptor antagonist and another is an NMDA receptor agonist. (C) 2006 Elsevier Ltd. All rights reserved.

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