Inhibition and structural reliability of prenylated flavones from the stem bark of Morus lhou on beta-secretase (BACE-1) = 뽕나무 줄기로부터 분리한 prenylated 플라보노이드의 화합물의 BACE-1 저해활성 및 구조적 연관성

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Title
Inhibition and structural reliability of prenylated flavones from the stem bark of Morus lhou on beta-secretase (BACE-1) = 뽕나무 줄기로부터 분리한 prenylated 플라보노이드의 화합물의 BACE-1 저해활성 및 구조적 연관성
Author(s)
J K Cho; Young Bae Ryu; M J Curtis-Long; J Y Kim; D Kim; S Lee; Woo Song Lee; K H Park
Bibliographic Citation
Bioorganic & Medicinal Chemistry Letters, vol. 21, no. 10, pp. 2945-2948
Publication Year
2011
Abstract
The action of β-secretase is strongly tied to the onset of Alzheimer's disease. The development of inhibitors of β-secretase is thus critical to combating this disease, which threatens an ever increasing number of the population and grows in importance as the population ages. Herein we show that flavones from Morus lhou potently inhibit β-secretase. Our aim in this manuscript is to explore the inhibitory kinetics of natural compounds and develop a phamacophore model which details the critical features responsible for inhibitory activity. The IC50 values of compounds for β-secretase inhibition were determined to range between 3.4 and 146.1 μM. Prenylated flavone 2 (IC50 = 3.4 μM) was 20 times more effective than its parent compound, noratocarpetin 1 (IC50 = 60.6 μM). The stronger activity was related with resorcinol moiety on B-ring and isoprenyl functionality at C-3. Kinetic analysis shows that the four effective compounds (1-4) have a noncompetitive mode of action. The binding affinity of flavones for β-secretase calculated using in silico docking experiments correlated well with their IC50 values and noncompetitive inhibition modes.
Keyword
BACE-1Kuwanon CMorus lhouPrenylated flavone
ISSN
0960-894X
Publisher
Elsevier
DOI
http://dx.doi.org/10.1016/j.bmcl.2011.03.060
Type
Article
Appears in Collections:
Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
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