2016
DOI: 10.1016/j.bjp.2015.12.004
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Isoflavone-aglycone fraction from Glycine max: a promising raw material for isoflavone-based pharmaceutical or nutraceutical products

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Cited by 27 publications
(12 citation statements)
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“…Similarly, genistein ion fragments appeared at m/z 269.0 (Figure 6C) and m/z 271.1 (Figure 6D), having the highest intensity in the negative and positive mode, respectively. These findings are in line with the results of the standard reagents and of previously reported works [3,7].…”
Section: Resultssupporting
confidence: 93%
See 1 more Smart Citation
“…Similarly, genistein ion fragments appeared at m/z 269.0 (Figure 6C) and m/z 271.1 (Figure 6D), having the highest intensity in the negative and positive mode, respectively. These findings are in line with the results of the standard reagents and of previously reported works [3,7].…”
Section: Resultssupporting
confidence: 93%
“…Structurally, the phenolic group of isoflavones is bonded to glycosides and primary hydroxyl group of glucose moiety is bonded to 6-O-acetyl or 6-O-malonyl derivatives. It has been shown that isoflavones existed in 12 isomers: three free isoflavones (aglycones) and nine linked isoflavones (glucosides) [3,4,5,6].…”
Section: Introductionmentioning
confidence: 99%
“…At such high temperatures (for example, 200 °C) there is a high conversion of malonylglycosides to acetylglycosides, β‐glycosides and aglycones, the latter increasing 3.5‐fold (Andrade and others ). The above may be of interest to the industry and medicine fields, since isoflavones absorption only occurs in aglycone forms (Yatsu and others ). Different thermal treatments have also been tested for TIs in other pulses such as peas and chickpeas, although results sometimes differ from one author to another.…”
Section: Physical Processesmentioning
confidence: 99%
“…The stability of orobol in various formulations was evaluated by determining the change of the mean particle size and orobol content. Previous studies have demonstrated that various soy isoflavones, including daidzein, glycitein, and genistein, whose chemical structures are similar to orobol, are instable when exposed to UV radiation [ 38 , 39 ]. Our preliminary study also consistently showed the color change of orobol in various solutions when exposed to sunlight ( Supplementary Figure S1 ).…”
Section: Discussionmentioning
confidence: 99%