Structure–activity relationships of small molecule inhibitors of RAGE-Aβ binding
摘要:
The Receptor for Advanced Glycation Endproducts ('RAGE') mediates transport of amyloid-beta peptide (A beta) into the brain, and is therefore an important target for the development of therapeutic agents for Alzheimer's disease. We describe structure activity relationships for inhibition of RAGE-A beta binding, derived from the analysis of a library of tertiary amides. (C) 2013 Elsevier Ltd. All rights reserved.
INHIBITING AMYLOID-BETA PEPTIDE/RAGE INTERACTION AT THE BLOOD-BRAIN BARRIER
申请人:THE UNIVERSITY OF ROCHESTER
公开号:EP1993527A2
公开(公告)日:2008-11-26
EP1993527A4
申请人:——
公开号:EP1993527A4
公开(公告)日:2009-08-05
ANTIBODIES, COMPOUNDS AND SCREENS FOR IDENTIFYING AND TREATING CACHEXIA OR PRE-CACHEXIA
申请人:The Broad Institute, Inc.
公开号:EP3307781B1
公开(公告)日:2020-10-28
Inhibiting Amyloid-Beta Peptide/Rage Interaction At The Blood-Brain Barrier
申请人:Zlokovic Berislav V.
公开号:US20110039908A1
公开(公告)日:2011-02-17
Small molecules are used to inhibit specific receptor-ligand interaction between Alzheimer's amyloid-β peptide (Aβ) and Receptor for Advanced Gly-cation Endproducts (RAGE). Objectives include treating Alzheimer's disease and other pathologies involving cerebral amyloid angiopathy; improving blood flow to or within the brain; decreasing the level of Aβ in the brain; reducing neuropathology associated with Alzheimer's disease; reducing inflammation and/or oxidant stress in the brain; improving memory and/or learning; treating other conditions involving Aβ/RAGE interaction at the blood-brain barrier, RAGE-mediated transport of Aβ into the brain, or RAGE activation in brain vasculature and/or brain parenchyma (e.g., diabetic complications); or any combination thereof.