Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/146397
Title: Cinnamoyl sucrose esters as alpha glucosidase inhibitors for the treatment of diabetes
Authors: Devaraj, Surabhi
Yip, Yew Mun
Panda, Parthasarathi
Ong, Li Lin
Wong, Kathy Pooi Wen
Zhang, Dawei
Judeh, Zaher
Keywords: Engineering::Chemical engineering
Issue Date: 2021
Source: Devaraj, S., Yip, Y. M., Panda, P., Ong, L. L., Wong, K. P. W., Zhang, D., & Judeh, Z. (2021). Cinnamoyl Sucrose Esters as Alpha Glucosidase Inhibitors for the Treatment of Diabetes. Molecules, 26(2), 469-. doi:10.3390/molecules26020469
Journal: Molecules
Abstract: Cinnamoyl sucrose esters (CSEs) were evaluated as AGIs and their enzyme inhibition activity and potency were compared with gold standard acarbose. The inhibition activity of the CSEs against α-glucosidase and α-amylase depended on their structure including the number of the cinnamoyl moieties, their position, and the presence or absence of the acetyl moieties. The inhibitory values of the CSEs 2-9 generally increases in the order of mono-cinnamoyl moieties < di-cinnamoyl ≤ tri-cinnamoyl < tetra-cinnamoyl. This trend was supported from both in vitro and in silico results. Both tetra-cinnamoyl CSEs 5 and 9 showed the highest α-glucosidase inhibitory activities of 77 ± 5%, 74 ± 9%, respectively, against acarbose at 27 ± 4%, and highest α-amylase inhibitory activities of 98 ± 2%, 99 ± 1%, respectively, against acarbose at 93 ± 2%. CSEs 3, 4, 6, 7, 8 showed desired higher inhibition of α-glucosidase than α-amylase suggesting potential for further development as AGIs with reduced side effects. Molecular docking studies on CSEs 5 and 9 attributed the high inhibition of these compounds to multiple π-π interactions and favorable projection of the cinnamoyl moieties (especially O-3 cinnamoyl) in the enzyme pockets. This work proposes CSEs as new AGIs with potentially reduced side effects.
URI: https://hdl.handle.net/10356/146397
ISSN: 1420-3049
DOI: 10.3390/molecules26020469
Rights: © 2021 The Authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SCBE Journal Articles

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