DC Field | Value | Language |
---|---|---|
dc.contributor.author | H J Yuk | - |
dc.contributor.author | J H Lee | - |
dc.contributor.author | M J Curtis-Long | - |
dc.contributor.author | J W Lee | - |
dc.contributor.author | Y S Kim | - |
dc.contributor.author | Hyung Won Ryu | - |
dc.contributor.author | C G Park | - |
dc.contributor.author | Tae Sook Jeong | - |
dc.contributor.author | K H Park | - |
dc.date.accessioned | 2017-04-19T09:21:23Z | - |
dc.date.available | 2017-04-19T09:21:23Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 0308-8146 | - |
dc.identifier.uri | 10.1016/j.foodchem.2010.11.125 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/9968 | - |
dc.description.abstract | The leaves of soybean (Glycine max) were extracted into four different polar solvents: ethylacetate, butanol, ethanol and water. The ethylacetate extract (EE) showed the lowest IC50 value against α-glucosidase (70.1 μg/ml). To investigate the compounds responsible for this effect, activity guided fractionation of soybean leaves by chromatography yielded seven phenolic compounds which were identified as formononetin (1), afromosin (2), coumestrol (3), isotrifoliol (4), phaseol (5), glyceofuran (6) and a new compound, glyceollin V (7). Importantly, coumestrol 3 was not only the most potent component with IC50 = 6.0 μM, but also the most abundant polyphenol in soybean leaves. There was shown to be an increasing inhibition across the developmental stage of the plant, which correlated strongly with an increase in compound 3 in the leaves. In fact, we have shown it can comprise up to 65% of the polyphenols in the leaves by HPLC analysis. | - |
dc.publisher | Elsevier | - |
dc.title | The most abundant polyphenol of soy leaves, coumestrol, displays potent α-glucosidase inhibitory activity | - |
dc.title.alternative | The most abundant polyphenol of soy leaves, coumestrol, displays potent α-glucosidase inhibitory activity | - |
dc.type | Article | - |
dc.citation.title | Food Chemistry | - |
dc.citation.number | 3 | - |
dc.citation.endPage | 1063 | - |
dc.citation.startPage | 1057 | - |
dc.citation.volume | 126 | - |
dc.contributor.affiliatedAuthor | Hyung Won Ryu | - |
dc.contributor.affiliatedAuthor | Tae Sook Jeong | - |
dc.contributor.alternativeName | 육흥주 | - |
dc.contributor.alternativeName | 이진환 | - |
dc.contributor.alternativeName | Curtis-Long | - |
dc.contributor.alternativeName | 이지원 | - |
dc.contributor.alternativeName | 김영수 | - |
dc.contributor.alternativeName | 류형원 | - |
dc.contributor.alternativeName | 박청교 | - |
dc.contributor.alternativeName | 정태숙 | - |
dc.contributor.alternativeName | 박기훈 | - |
dc.identifier.bibliographicCitation | Food Chemistry, vol. 126, no. 3, pp. 1057-1063 | - |
dc.identifier.doi | 10.1016/j.foodchem.2010.11.125 | - |
dc.subject.keyword | α-Glucosidase | - |
dc.subject.keyword | Coumestrol | - |
dc.subject.keyword | Isoflavones | - |
dc.subject.keyword | Pterocarpans | - |
dc.subject.keyword | Soy leaf | - |
dc.subject.local | α-glucosidase | - |
dc.subject.local | α-Glucosidase | - |
dc.subject.local | Alpha-glucosidase | - |
dc.subject.local | alpha-glucosidases | - |
dc.subject.local | Coumestrol | - |
dc.subject.local | Isoflavone | - |
dc.subject.local | Isoflavones | - |
dc.subject.local | Pterocarpan | - |
dc.subject.local | Pterocarpans | - |
dc.subject.local | pterocarpan | - |
dc.subject.local | Soy leaf | - |
dc.subject.local | soy leaf | - |
dc.description.journalClass | Y | - |
There are no files associated with this item.
Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.