1995
DOI: 10.1016/0031-9422(94)00571-a
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A saponin conjugated with 2,3-dihydro-2,5-dihydroxy-6-methyl-4H-pyran-4-one from Dolichos lablab

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Cited by 26 publications
(8 citation statements)
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“…In terms of the SOD‐like activity of saponins, Yoshiki & Okubo (1995) reported that 2,3‐dihydro‐2,5‐dihydroxy‐6‐methyl‐4H‐pyran‐4‐one (DDMP) saponins showed strong superoxide radical scavenging activity equivalent to 17.1 units of superoxide dismutase whereas other soysaponins lacking the DDMP moiety did not have radical scavenging effects. Yoshiki et al. (1995) also reported that maltol which has similar structure as the DDMP moiety showed SOD‐like activity beyond 5 m m .…”
Section: Resultsmentioning
confidence: 93%
“…In terms of the SOD‐like activity of saponins, Yoshiki & Okubo (1995) reported that 2,3‐dihydro‐2,5‐dihydroxy‐6‐methyl‐4H‐pyran‐4‐one (DDMP) saponins showed strong superoxide radical scavenging activity equivalent to 17.1 units of superoxide dismutase whereas other soysaponins lacking the DDMP moiety did not have radical scavenging effects. Yoshiki et al. (1995) also reported that maltol which has similar structure as the DDMP moiety showed SOD‐like activity beyond 5 m m .…”
Section: Resultsmentioning
confidence: 93%
“…The amount of DDMP‐saponin was also determined through monitoring the chromophore produced in the reaction of saponins with sulfuric acid in acetic acid (530 nm), and a linear correlation ( R 2 = 0.997) was observed in the range of 0.2 to 1 mg. We also found a linear correlation ( R 2 = 0.993) of the reducing activity of the pure saponin towards an oxidized cation radical (ABTS •+ ), in the range of 0–100 µg saponin. It was previously shown, in several other legume seeds, including soy,26 Phaseolus coccineus 34 and Dolichos lablab ,35 that a conjugated DDMP moiety will provide the saponin with reducing potential. Here we have, for the first time, demonstrated the presence of a DDMP‐conjugated saponin in chickpea.…”
Section: Resultsmentioning
confidence: 95%
“…en-28-al. [24] O OH Another saponin designated as Chikusetsu saponin IVa was isolated from the seeds of hyacinth bean (D. lablab). [25] Although D.kilimandscharicus possesses remarkable antifungal activity yet another species of this genus.…”
Section: Name Of Compounds Molecular Formulamentioning
confidence: 99%