Literature DB >> 22953872

Isolation and identification of phenolic compounds from the seeds of Perilla frutescens (L.) and their inhibitory activities against α-glucosidase and aldose reductase.

Tae Joung Ha1, Jin Hwan Lee, Myoung-Hee Lee, Byeong Won Lee, Hyun Sook Kwon, Chang-Hwan Park, Kang-Bo Shim, Hyun-Tae Kim, In-Youl Baek, Dae Sik Jang.   

Abstract

Five phenolic compounds were isolated from the seeds of Perilla (Perilla frutescens L.) using gradient solvent fractionation, silica gel column chromatography, and preparative high-performance liquid chromatography (HPLC). Their chemical structures were identified as caffeic acid-3-O-glucoside (1), rosmarinic acid-3-O-glucoside (2), rosmarinic acid (3), luteolin (4), and apigenin (5) using NMR spectroscopy and HPLC-ESI/MS analysis. Among them, luteolin (4) inhibited α-glucosidase (EC 3.2.1.20) with IC(50) value of 45.4μM. The inhibition kinetic analysed by Dixon plot indicate that luteolin is a noncompetitive inhibitor, and the inhibition constant K(I) was calculated at 45.0μM. Moreover, rosmarinic acid (3) and luteolin (4) inhibited recombinant human aldose reductase (EC 1.1.1.21) with IC(50) values of 11.2 and 0.6μM, respectively. Notably, the inhibition kinetic of luteolin (4) follows a hyperbolic dependence on aldose reductase inhibition by Dixon plot. Thus, inhibition kinetic indicates that luteolin (4) is a mixed-type inhibitor.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22953872     DOI: 10.1016/j.foodchem.2012.05.104

Source DB:  PubMed          Journal:  Food Chem        ISSN: 0308-8146            Impact factor:   7.514


  26 in total

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9.  Rapid identification of aldose reductase inhibitory compounds from Perilla frutescens.

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Authors:  Jose A Villa-Rodriguez; Asimina Kerimi; Laszlo Abranko; Sarka Tumova; Lauren Ford; Richard S Blackburn; Christopher Rayner; Gary Williamson
Journal:  Sci Rep       Date:  2018-04-03       Impact factor: 4.379

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