| Literature DB >> 34153812 |
Yang Hee Jo1, Solip Lee1, Sang Won Yeon1, Ayman Turk1, Jae Hyuk Lee2, Seong-Min Hong2, Yoo Kyong Han3, Ki Yong Lee3, Bang Yeon Hwang1, Sun Yeou Kim2, Mi Kyeong Lee4.
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 α-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 α-glucosidase inhibition with IC50 values <10.0 μM. 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 α-glucosidase inhibition. Conclusively, diverse prenylated isoflavonoids in M. tricuspidata leaves might ameliorate glycotoxicity-induced metabolic diseases.Entities:
Keywords: Cudracusisoflavones A-P; Glycation; Masclura tricuspidata; Molecular docking analysis; Prenylated isoflavonoids; α-glucosidase
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Year: 2021 PMID: 34153812 DOI: 10.1016/j.bioorg.2021.105098
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275