Insights into the inhibitory activity and mechanism of action of flavonoids from the stems and branches of Acer mono Maxim. against ?-glucosidase via kinetic analysis, molecular docking, and molecular dynamics simulations

被引:10
|
作者
Phong, Nguyen Viet [1 ,2 ,3 ]
Yang, Seo Young [4 ]
Min, Byung Sun [5 ,6 ]
Kim, Jeong Ah [1 ,2 ,3 ,7 ]
机构
[1] Kyungpook Natl Univ, Coll Pharm, Vessel Organ Interact Res Ctr, VOICE MRC, Daegu 41566, South Korea
[2] Kyungpook Natl Univ, Coll Pharm, FOUR Community Based Intelligent Novel Drug Discov, Daegu 41566, South Korea
[3] Kyungpook Natl Univ, Res Inst Pharmaceut Sci, Daegu 41566, South Korea
[4] Sangji Univ, Dept Pharmaceut Engn, Wonju 26339, South Korea
[5] Daegu Catholic Univ, Coll Pharm, Drug Res & Dev Ctr, Gyeongbuk 38430, South Korea
[6] Daegu Catholic Univ, Coll Pharm, Gyeongbuk 38430, South Korea
[7] Kyungpook Natl Univ, Coll Pharm, Daegu 41566, South Korea
基金
新加坡国家研究基金会;
关键词
Acer mono Maxim; Flavonoid; -glucosidase; Kinetic analysis; Molecular docking; Molecular dynamics; ALPHA-GLUCOSIDASE; DRYOPTERIS-CRASSIRHIZOMA; STILBENE GLYCOSIDES; PHLOROGLUCINOLS; IDENTIFICATION; DERIVATIVES; FLAVANONES; RHIZOMES; MAPLE;
D O I
10.1016/j.molstruc.2023.135188
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Acer mono Maxim. (mono maple), a deciduous tree found in temperate regions, has been reported to have a variety of pharmacological properties, including antioxidant, hepatoprotective, and osteoclastogenesis-inhibitory effects. However, the potential mechanism by which secondary metabolites inhibit alpha- glucosidase activity has not been investigated. In this study, 12 flavonoids (1 -12) were isolated from the stems and branches of A. mono Maxim. and structurally elucidated using modern spectroscopic tech-niques. The inhibitory activity and mechanism of action of the isolated flavonoids against alpha-glucosidase were studied through in vitro assays, enzyme kinetic analysis, molecular docking, and molecular dynamics simulations. Among all test compounds, two dimeric flavan-3-ols (1 and 2) exhibited strong alpha-glucosidase inhibitory effect, with IC50 values of 49.69 and 48.80 mu M, respectively, and showed non-competitive inhi-bition of alpha-glucosidase. The findings observed from in vitro and in silico studies suggests that two active compounds, 1 and 2, may be appropriate for future research into the development of new alpha-glucosidase inhibitors.(c) 2023 Elsevier B.V. All rights reserved.
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页数:11
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