2022
DOI: 10.1016/j.heliyon.2022.e10103
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HPTLC/HPLC-mass spectrometry identification and NMR characterization of major flavonoids of wild lemongrass (Cymbopogon giganteus) collected in Burkina Faso

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Cited by 3 publications
(5 citation statements)
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“…For flavonoid compounds, the order of mobility is as follows: acyl derivatives (Rf ≈ 0.6-0.7) followed by monoglucosides (R f ≈ 0.5-0.6) then diglucosids (R f ≈ 0.4-0.3) and finally triglucosides (R f ≈ 0.1-03). In some cases, the triglucosid derivatives may not migrate onto silica (R f ≈ 0.00) (Bationo, 2019). Thus, the compounds present in our samples may be diglucosid, triglucosid and/or acylated anthocyanin derivatives.…”
Section: Compound Identification By Hptlc and Hptlc-msmentioning
confidence: 95%
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“…For flavonoid compounds, the order of mobility is as follows: acyl derivatives (Rf ≈ 0.6-0.7) followed by monoglucosides (R f ≈ 0.5-0.6) then diglucosids (R f ≈ 0.4-0.3) and finally triglucosides (R f ≈ 0.1-03). In some cases, the triglucosid derivatives may not migrate onto silica (R f ≈ 0.00) (Bationo, 2019). Thus, the compounds present in our samples may be diglucosid, triglucosid and/or acylated anthocyanin derivatives.…”
Section: Compound Identification By Hptlc and Hptlc-msmentioning
confidence: 95%
“…Our extracts would be either a mixture of several anthocyanin derivatives or a mixture of anthocyanins and other pigments. Intense spot front reference values analysis shows that these values are characteristic of polar compounds (Bationo, 2019;Remy et al, 2022a, b). Indeed, mobility varies with polarity on the normal phases (NPs) of silica F 254 .…”
Section: Compound Identification By Hptlc and Hptlc-msmentioning
confidence: 99%
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“…Lund et al [96] quantized four flavonoids (naringenin, hyperoside, rutin, and vitexin-2 ′′ -O-rhamnoside) and chlorogenic acid in leaf extracts of four Crataegus species by 1 H-NMR, revealing chemical differences between the four biological samples. Bationo et al [97] isolated three flavonoids from the leaves of the Burkina Faso species and identified the chemical structures of several flavonoids using 1 H-NMR. Kontogianni et al [98] used 1-D 1 H NMR, 1-D total correlation spectroscopy, 2-D 1 H- 13 C heteronuclear single quantum coherence, and 1 H- 13 C heteronuclear multiple bond correlation nuclear magnetic resonance techniques for the simultaneous identification and quantification of artemisinin and five of its analogs, along with five flavonoids, an aromatic ketone, and camphor (in total, 13 compounds) in crude diethyl ether Artemisia annua.…”
Section: Nuclear Magnetic Resonancementioning
confidence: 99%