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Anti-diabetic potential of Masclura tricuspidata leaves: Prenylated isoflavonoids with alpha-glucosidase inhibitory and anti-glycation activity

Authors
Jo, Yang HeeLee, SolipYeon, Sang WonTurk, AymanLee, Jae HyukHong, Seong-MinHan, Yoo KyongLee, Ki YongHwang, Bang YeonKim, Sun YeouLee, Mi Kyeong
Issue Date
9월-2021
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Cudracusisoflavones A-P; Glycation; Masclura tricuspidata; Molecular docking analysis; Prenylated isoflavonoids; alpha-glucosidase
Citation
BIOORGANIC CHEMISTRY, v.114
Indexed
SCIE
SCOPUS
Journal Title
BIOORGANIC CHEMISTRY
Volume
114
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/136474
DOI
10.1016/j.bioorg.2021.105098
ISSN
0045-2068
Abstract
Investigation of chemical constituents of Masclura tricuspidata leaves resulted in the isolation of 47 isoflavonoids possessing prenyl groups with different numbers and structures. Among them, sixteen compounds named cudracusisoflavones A-P (1-16) were first isolated from nature. The isoflavonoids isolated from M. tricuspidata leaves showed anti-diabetic effects as measured by inhibition on alpha-glucosidase activity and advanced glycation end-products (AGEs) formations. Especially, cudracusisoflavone L (12), a new compound, together with gancaonin M (27), erysenegalensein E (41) and millewanin G (44) showed strong a-glucosidase inhibition with IC50 values <10.0 mu M. In addition, cudracusisoflavones A (1), D (4), M (13) and N (14), together with known prenylated isoflavonoids efficiently inhibited methylglyoxal (MGO)- or glyoxal (GO)-induced AGE formations. Structure activity relationship together with molecular docking analysis suggested the importance of hydroxy group and linear type of prenyl moiety for alpha-glucosidase inhibition. Conclusively, diverse prenylated isoflavonoids in M. tricuspidata leaves might ameliorate glycotoxicity-induced metabolic diseases.
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