Plantagoside as Maillard reaction inhibitor—its inhibitory mechanism and application

Nobuyasu Matsuura*, Chihiro Sasaki, Tadashi Aradate, Makoto Ubukata, Hiroyuki Kojima, Mitsuharu Ohara, Junichi Hasegawa

*この論文の責任著者

研究成果: ジャーナルへの寄稿学術論文査読

1 被引用数 (Scopus)

抄録

An improvement of the Maillard reaction inhibitor screening system was carried out and led to the decrease of the background on fluorescent analysis with which we were able to perform the efficient screening, separation and purification of active compounds. As a result, plantagoside (Pl) (5,7,4′,5′-tetrahydroxyflavanone-3′-O-glucoside) from the seed of Plantago asiatica was isolated as an active compound. Plantagoside (Pl: IC50 1.2 μM) was about 90 times more potent than aminoguanidine (AG) which has been reported as a Maillard reaction inhibitor. We report on the structure–activity relationship, the effect for decline of an enzyme function by glycation and site and mechanism of action.

本文言語英語
ページ(範囲)411-412
ページ数2
ジャーナルInternational Congress Series
1245
C
DOI
出版ステータス出版済み - 2002/11/01

ASJC Scopus 主題領域

  • 医学一般

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