2017
DOI: 10.1016/j.fshw.2017.05.001
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α-Glucosidase inhibitor produced by an endophytic fungus, Xylariaceae sp. QGS 01 from Quercus gilva Blume

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Cited by 60 publications
(21 citation statements)
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“…Two unsaturated fatty acids; linoleic acid (C18:2) and α-linolenic acid (C18:3) as well as two saturated ones; stearic acid (C18:0) and palmitic acid (C16:0) in addition to its glyceryl ester, 1-monopalmitin were identified by the multivariate model as α-glucosidase inhibitors. The α-glucosidase inhibitory activity of the free fatty acids has been proposed previously by similar metabolomics studies [5] and has also been verified by an in vitro enzymatic assay in other studies [31][32][33][34][35]. Investigation of the docking results showed that the carboxylic group of the fatty acids forms 1 to 3 hydrogen bonds.…”
Section: Discussionsupporting
confidence: 69%
“…Two unsaturated fatty acids; linoleic acid (C18:2) and α-linolenic acid (C18:3) as well as two saturated ones; stearic acid (C18:0) and palmitic acid (C16:0) in addition to its glyceryl ester, 1-monopalmitin were identified by the multivariate model as α-glucosidase inhibitors. The α-glucosidase inhibitory activity of the free fatty acids has been proposed previously by similar metabolomics studies [5] and has also been verified by an in vitro enzymatic assay in other studies [31][32][33][34][35]. Investigation of the docking results showed that the carboxylic group of the fatty acids forms 1 to 3 hydrogen bonds.…”
Section: Discussionsupporting
confidence: 69%
“…Also, a handful of the identified compounds were either fatty acids or their derivatives. This is noteworthy because previous reports have documented the in vitro antidiabetic activities of palmitic acid, oleic acid, and stearic acid found in T. triandra (Collado‐González et al, 2017; Indrianingsih & Tachibana, 2017; Liu, Deseo, Morris, Winter, & Leach, 2011). Thus, the antidiabetic activity displayed may be ascribed to these compounds.…”
Section: Discussionmentioning
confidence: 72%
“…Compound 103 which was separated from Xylariaceae sp. isolated from Quercus gilva stem, possessed α-glucosidase inhibitory potential with IC 50 41.75 µg/mL, compared to quercetin (IC 50 4.80 µg/mL)[102]. The in vitro glucose consumption assay of 78 and 79 (Conc.…”
mentioning
confidence: 99%