2020
DOI: 10.17576/jsm-2020-4907-12
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High-Performance Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry (HPLC-QTOFMS) Analysis on the Ethanol:Water (80:20) Extract of Lawsonia inermis Leaves

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Cited by 3 publications
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“…Compound 12 was identified as niazinin B as it yielded a parent ion peak at m/z 342.1115 [M-H]-, generating characteristic ion peaks at m/z 310.07 and 196.04 resulting from the loss of MeOH and the rhamnosyl moiety (−146 Da), respectively [ 19 ] ( Figure 1 C). Compound 13 produced a parent ion peak [M-H] − at m/z 345.0822, yielding characteristic fragment ion peaks at m/z 301.05 and 183.02 resulting from the loss of CH 3 CHO (−44 Da) and a glucose moiety (−162 Da), respectively, and was confirmed as lalioside [ 20 ] ( Figure 1 D). Compound 14 had a precursor ion peak [M-H] − at m/z 353.0865, generating daughter ion peaks at m/z 309.09 (loss of CO 2 ), m/z 191.05 (loss of caffeic moiety), m/z 179.03 (loss of quinic moiety), and m/z 173.04 (dehydrated quinic moiety) and was characterized as 5- O -caffeoylquinic acid [ 21 ].…”
Section: Resultsmentioning
confidence: 99%
“…Compound 12 was identified as niazinin B as it yielded a parent ion peak at m/z 342.1115 [M-H]-, generating characteristic ion peaks at m/z 310.07 and 196.04 resulting from the loss of MeOH and the rhamnosyl moiety (−146 Da), respectively [ 19 ] ( Figure 1 C). Compound 13 produced a parent ion peak [M-H] − at m/z 345.0822, yielding characteristic fragment ion peaks at m/z 301.05 and 183.02 resulting from the loss of CH 3 CHO (−44 Da) and a glucose moiety (−162 Da), respectively, and was confirmed as lalioside [ 20 ] ( Figure 1 D). Compound 14 had a precursor ion peak [M-H] − at m/z 353.0865, generating daughter ion peaks at m/z 309.09 (loss of CO 2 ), m/z 191.05 (loss of caffeic moiety), m/z 179.03 (loss of quinic moiety), and m/z 173.04 (dehydrated quinic moiety) and was characterized as 5- O -caffeoylquinic acid [ 21 ].…”
Section: Resultsmentioning
confidence: 99%