Subnanomolar Affinity and Selective Antagonism at α7 Nicotinic Receptor by Combined Modifications of 2-Triethylammonium Ethyl Ether of 4-Stilbenol (MG624)
Subnanomolar Affinity and Selective Antagonism at α7 Nicotinic Receptor by Combined Modifications of 2-Triethylammonium Ethyl Ether of 4-Stilbenol (MG624)
Two oligo(phenylenevinylene)s with cyanobiphenyl terminates were synthesized as non-covalent modifiers of single walled carbon nanotubes (SWNTs). The wrapping of SWNTs with synthesized oligomers enhanced the dispersibility in CHCl3 by the dissociation of SWNT bundle structures. It was found that the addition of oligomers caused self-organized precipitation from a homogeneous dispersed solution of SWNT complexes. The self-organized precipitates exhibited thermotropic liquid-crystalline properties.
Veschambre,H. et al., Bulletin de la Societe Chimique de France, 1967, p. 2846 - 2854
作者:Veschambre,H. et al.
DOI:——
日期:——
4, 5-DIHYDRO-OXAZOL-2-YL AMINE DERIVATIVES
申请人:F. Hoffmann-La Roche AG
公开号:EP2245019A1
公开(公告)日:2010-11-03
[EN] 4, 5-DIHYDRO-OXAZOL-2-YL AMINE DERIVATIVES<br/>[FR] DÉRIVÉS DE 4,5-DIHYDROOXAZOL-2-YLAMINE
申请人:HOFFMANN LA ROCHE
公开号:WO2009103626A1
公开(公告)日:2009-08-27
The present invention relates to a compounds of formula I or a pharmaceutically active acid addition salts thereof. It has been found that the present compounds have Asp2 (β-sccretasc, BACE 1 or Mcmapsin-2) inhibitory activity and that the compounds may therefore be used in the treatment of diseases characterised by elevated β-amyloid levels or β-amyloid deposits, particularly Alzheimer's disease.
Subnanomolar Affinity and Selective Antagonism at α7 Nicotinic Receptor by Combined Modifications of 2-Triethylammonium Ethyl Ether of 4-Stilbenol (MG624)