Bis-styrylpyridine and bis-styrylbenzene derivatives as inhibitors for A beta fibril formation

Authors
Byeon, Seong RimLee, Ji HoonSohn, Ji-HoonKim, Dong ChanShin, Kye JungYoo, Kyung HoMook-Jung, InheeLee, Won KooKim, Dong Jin
Issue Date
2007-03-01
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.17, no.5, pp.1466 - 1470
Abstract
New bis-styrylpyridine and bis-styrylbenzene derivatives were designed and synthesized. These 34 compounds were evaluated by A beta fibril formation inhibitory assay using thioflavin T as a dye (named ThT assay). Most of them showed excellent inhibitory activities for A beta fibril formation at IC50 of 0.1-2.7 mu M which is comparable to curcumin (IC50 of 0.8 mu M). Among them, nine compounds were screened for their cytotoxicities on HT-22 cell by MTT assay at 1, 10, and 50 mu M. In particular, 1-7 and II-2 exhibited the best combination of inhibitory activity and compound cytotoxicity. (c) 2006 Elsevier Ltd. All rights reserved.
Keywords
ALZHEIMERS-DISEASE; AMYLOID HYPOTHESIS; ALPHA-SYNUCLEIN; PLAQUES; MEDICINE; CURCUMIN; ALZHEIMERS-DISEASE; AMYLOID HYPOTHESIS; ALPHA-SYNUCLEIN; PLAQUES; MEDICINE; CURCUMIN; A beta fibril formation inhibitor; Alzheimer disease; bis-styrylpyridine; bis-styrylbenzene; amyloid beta
ISSN
0960-894X
URI
https://pubs.kist.re.kr/handle/201004/134549
DOI
10.1016/j.bmcl.2006.10.090
Appears in Collections:
KIST Article > 2007
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