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(E)-5-Styryl-1H-indole and (E)-6-Styrylquinoline Derivatives Serve as Probes for β-Amyloid Plaques

We report the synthesis and biological evaluation of novel (E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives as probes for imaging β-amyloid (Aβ) plaques. These derivatives showed binding affinities for Aβ(1–40) aggregates with K(i) values varying from 4.1 to 288.4 nM. (E)-5-(4-iodostyryl...

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Detalles Bibliográficos
Autores principales: Yang, Yang, Jia, Hong-Mei, Liu, Bo-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268995/
https://www.ncbi.nlm.nih.gov/pubmed/22491675
http://dx.doi.org/10.3390/molecules17044252
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author Yang, Yang
Jia, Hong-Mei
Liu, Bo-Li
author_facet Yang, Yang
Jia, Hong-Mei
Liu, Bo-Li
author_sort Yang, Yang
collection PubMed
description We report the synthesis and biological evaluation of novel (E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives as probes for imaging β-amyloid (Aβ) plaques. These derivatives showed binding affinities for Aβ(1–40) aggregates with K(i) values varying from 4.1 to 288.4 nM. (E)-5-(4-iodostyryl)-1H-indole (8) clearly stained Aβ plaques in the brain sections of Alzheimer’s disease (AD) model mice (APP/PS1). Furthermore, autoradiography for [(125)I]8 displayed intense and specific labeling of Aβ plaques in the brain sections mentioned above with low background. In biodistribution experiments using normal mice [(125)I]8 showed high initial brain uptake followed by rapid washout (4.27 and 0.64% ID/g at 2 and 30 min post injection, respectively). These findings suggests that [(123)I]8 may be a potential SPECT imaging agent for detecting Aβ plaques in AD brain.
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spelling pubmed-62689952018-12-11 (E)-5-Styryl-1H-indole and (E)-6-Styrylquinoline Derivatives Serve as Probes for β-Amyloid Plaques Yang, Yang Jia, Hong-Mei Liu, Bo-Li Molecules Article We report the synthesis and biological evaluation of novel (E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives as probes for imaging β-amyloid (Aβ) plaques. These derivatives showed binding affinities for Aβ(1–40) aggregates with K(i) values varying from 4.1 to 288.4 nM. (E)-5-(4-iodostyryl)-1H-indole (8) clearly stained Aβ plaques in the brain sections of Alzheimer’s disease (AD) model mice (APP/PS1). Furthermore, autoradiography for [(125)I]8 displayed intense and specific labeling of Aβ plaques in the brain sections mentioned above with low background. In biodistribution experiments using normal mice [(125)I]8 showed high initial brain uptake followed by rapid washout (4.27 and 0.64% ID/g at 2 and 30 min post injection, respectively). These findings suggests that [(123)I]8 may be a potential SPECT imaging agent for detecting Aβ plaques in AD brain. MDPI 2012-04-10 /pmc/articles/PMC6268995/ /pubmed/22491675 http://dx.doi.org/10.3390/molecules17044252 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Yang, Yang
Jia, Hong-Mei
Liu, Bo-Li
(E)-5-Styryl-1H-indole and (E)-6-Styrylquinoline Derivatives Serve as Probes for β-Amyloid Plaques
title (E)-5-Styryl-1H-indole and (E)-6-Styrylquinoline Derivatives Serve as Probes for β-Amyloid Plaques
title_full (E)-5-Styryl-1H-indole and (E)-6-Styrylquinoline Derivatives Serve as Probes for β-Amyloid Plaques
title_fullStr (E)-5-Styryl-1H-indole and (E)-6-Styrylquinoline Derivatives Serve as Probes for β-Amyloid Plaques
title_full_unstemmed (E)-5-Styryl-1H-indole and (E)-6-Styrylquinoline Derivatives Serve as Probes for β-Amyloid Plaques
title_short (E)-5-Styryl-1H-indole and (E)-6-Styrylquinoline Derivatives Serve as Probes for β-Amyloid Plaques
title_sort (e)-5-styryl-1h-indole and (e)-6-styrylquinoline derivatives serve as probes for β-amyloid plaques
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268995/
https://www.ncbi.nlm.nih.gov/pubmed/22491675
http://dx.doi.org/10.3390/molecules17044252
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