2013
DOI: 10.1016/j.foodchem.2012.09.089
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In vitro studies of α-glucosidase inhibitors and antiradical constituents of Glandora diffusa (Lag.) D.C. Thomas infusion

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Cited by 18 publications
(10 citation statements)
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“…As the fragmentation (MS 3 [535 / 359] À ) observed matched with the one of ion at m/z 537, losses of DSS (À198, m/z 339 base peak) and of a carbonyl group (À44) coincident with the fragmentation observed for salvianolic acid H (SAH). 26 As for compound 13, an isomer of compound 4, it was observed a characteristic UV spectrum of caffeic acid derivatives ( Table 2). 26 As for compound 13, an isomer of compound 4, it was observed a characteristic UV spectrum of caffeic acid derivatives ( Table 2).…”
Section: Phenolic Compounds Characterizationmentioning
confidence: 93%
“…As the fragmentation (MS 3 [535 / 359] À ) observed matched with the one of ion at m/z 537, losses of DSS (À198, m/z 339 base peak) and of a carbonyl group (À44) coincident with the fragmentation observed for salvianolic acid H (SAH). 26 As for compound 13, an isomer of compound 4, it was observed a characteristic UV spectrum of caffeic acid derivatives ( Table 2). 26 As for compound 13, an isomer of compound 4, it was observed a characteristic UV spectrum of caffeic acid derivatives ( Table 2).…”
Section: Phenolic Compounds Characterizationmentioning
confidence: 93%
“…The chromatographic behavior of compound 8, as well as its UV and MS spectra (Rt 26.03 min; UV 309 nm; [M-H] − at m/z 163, MS 2 [163]: 119 (100%)) was coincident with those of p-coumaric acid standard (Ferreres et al, 2013), a compound already reported in this species (George et al, 2015).…”
Section: Hplc-dad-esi-ms N and Hplc-dad Analysesmentioning
confidence: 82%
“…DPPH • is a stable free radical which has an unpaired valence electron at the nitrogen atom. It is one of the most commonly used substrates to evaluate antioxidant activity . Figure A shows the DPPH • ‐scavenging activity of PP and FP.…”
Section: Resultsmentioning
confidence: 99%
“…It is one of the most commonly used substrates to evaluate antioxidant activity. 34,35 Figure 3A shows the DPPH • -scavenging activity of PP and FP. The results clearly indicated that PP had higher radical-scavenging activity than ascorbic acid and FP when the sample concentration was below 200 μg mL −1 .…”
Section: Antioxidant Activity Of Pp and Fpmentioning
confidence: 99%