Chromenylchalcones with inhibitory effects on monoamine oxidase B

Authors
Jo, GeunhyeongAhn, SeunghyunKim, Bong-GyuPark, Hye RiKim, Young HwaChoo, Hyun AhKoh, DongsooChong, YouhoonAhn, Joong-HoonLim, Yoongho
Issue Date
2013-12-15
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
BIOORGANIC & MEDICINAL CHEMISTRY, v.21, no.24, pp.7890 - 7897
Abstract
Structure-activity relationship (SAR) calculations were used to find monoamine oxidase-B (MAO-B) inhibitors by identifying pharmacophores exhibiting high inhibitory activities. Several such chromenylchalcones were designed and synthesized accordingly. Their inhibitory effects on MAO-B were determined using an HPLC-based method and an MAO-B enzyme assay kit. (E)-3-(6-Methoxy-2H-chromen- 3-yl)-1-(2-methoxyphenyl) prop-2-en-1-one exhibited a half-maximal inhibitory concentration of 320 nM. Its molecular-level binding mode with the three-dimensional structure of MAO-B was elucidated using an in silico docking study. The chromenylchalcone scaffold, which is derived from natural products including isoflavonoids and chalcones, had not been previously reported as an MAO-B inhibitor. (C) 2013 Elsevier Ltd. All rights reserved.
Keywords
3-DIMENSIONAL STRUCTURE; DERIVATIVES; MAO; 3-DIMENSIONAL STRUCTURE; DERIVATIVES; MAO; Monoamine oxidase B; Chromenylchalcone; Flavonoid; In silico docking
ISSN
0968-0896
URI
https://pubs.kist.re.kr/handle/201004/127332
DOI
10.1016/j.bmc.2013.10.004
Appears in Collections:
KIST Article > 2013
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