2021
DOI: 10.1080/14786419.2021.1961134
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New sesquiterpene dilactone and β-carboline alkaloid and the α-glucosidase inhibitory activity of selected phytochemicals from Neolitsea cassia (L.) Kosterm

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Cited by 11 publications
(4 citation statements)
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“…Comparison among (+)-catechin ( 16 ), quercetin ( 21 ) and luteolin ( 28 ) suggested the saturation of the 2,3-double bond in the C ring seemed to decrease the inhibitory activity [ 48 ]. In addition, among the taxifolin ( 13 ) and derivatives ( 14, 15 ), taxifolin showed the strongest inhibitory effect, indicating that the presence of a sugar moiety at C-3 may be responsible for the lowered activity [ 49 ]. In addition, galloyl moieties strengthen the inhibitory effects of flavonoids against the α-glucosidase (such as compound 26 ) [ 50 ].…”
Section: Resultsmentioning
confidence: 99%
“…Comparison among (+)-catechin ( 16 ), quercetin ( 21 ) and luteolin ( 28 ) suggested the saturation of the 2,3-double bond in the C ring seemed to decrease the inhibitory activity [ 48 ]. In addition, among the taxifolin ( 13 ) and derivatives ( 14, 15 ), taxifolin showed the strongest inhibitory effect, indicating that the presence of a sugar moiety at C-3 may be responsible for the lowered activity [ 49 ]. In addition, galloyl moieties strengthen the inhibitory effects of flavonoids against the α-glucosidase (such as compound 26 ) [ 50 ].…”
Section: Resultsmentioning
confidence: 99%
“…Further investigation of compounds 1 to 37 in terms of α-glucosidase inhibitory activity revealed taxifolin, (+)-catechin, quercetin, and luteolin (IC50 values of 40.39, 54.82, 29.47, and 35.41 μM, respectively) exhibited stronger activity than the positive control acarbose (IC50 value of 60.01 μM). From the structural analysis of the compounds, it was found that the structures of the A, B, and C rings in flavonoids were closely related to the inhibitory activity; hydroxylation at the 3-position of flavonoids could enhance the inhibitory effect, saturation of the 2,3-double bond on the C ring could reduce the inhibitory activity [ 66 ], the presence of the glycosyl portion on C-3 could reduce the activity [ 67 ], and the gallic alcohol portion could enhance the inhibitory activity of flavonoids [ 68 ].…”
Section: Extractsmentioning
confidence: 99%
“…Sesquiterpene lactones, linderalactone, pseudoneolinderane, and linderanlide C (Figure 2), demonstrated strong AG inhibition with IC 50 values of 12.72, 47.07, and 12.10 μM, respectively. As a result of the study, it was stated that the presence of an α,β‐unsaturated γ‐lactone ring fragment in the C‐ring of sesquiterpene lactones was necessary to inhibit AG activity (Jani et al, 2021).…”
Section: Promising Candidates For Ag Inhibitory Activitymentioning
confidence: 99%
“…Compounds linderalactone, pseudoneolinderane, linderanlide C, linderanine A, epicatechin, and astilbin inhibited AG with IC 50 values ranging from 12.10 to 96.77 µM (Jani et al, 2021).…”
Section: Alkaloidsmentioning
confidence: 99%