Please use this identifier to cite or link to this item: http://dspace2020.uniten.edu.my:8080/handle/123456789/9760
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dc.contributor.authorSwaminathan, M.
dc.contributor.authorChee, C.F.
dc.contributor.authorChin, S.P.
dc.contributor.authorBuckle, M.J.C.
dc.contributor.authorRahman, N.A.
dc.contributor.authorDoughty, S.W.
dc.contributor.authorChung, L.Y.
dc.date.accessioned2018-03-06T03:49:28Z-
dc.date.available2018-03-06T03:49:28Z-
dc.date.issued2014
dc.identifier.urihttp://dspace.uniten.edu.my/jspui/handle/123456789/9760-
dc.description.abstractMuscarinic acetylcholine receptor- Active compounds have potential for the treatment of Alzheimer's disease. In this study, a series of natural and synthetic flavones and flavonols was assayed in vitro for their ability to inhibit radioligand binding at human cloned M1 muscarinic receptors. Several compounds were found to possess competitive binding affinity (K i = 40-110 μM), comparable to that of acetylcholine (Ki = 59 μM). Despite the fact that these compounds lack a positively-charged ammonium group under physiological conditions, molecular modelling studies suggested that they bind to the orthosteric site of the receptor, mainly through non-polar interactions.
dc.titleFlavonoids with M1 muscarinic acetylcholine receptor binding activity
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptUniversiti Tenaga Nasional-
Appears in Collections:COE Scholarly Publication
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