2022
DOI: 10.1016/j.arabjc.2022.104208
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UPLC-Q/TOF-MS coupled with multivariate analysis for comparative analysis of metabolomic in Dendrobium nobile from different growth altitudes

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Cited by 7 publications
(6 citation statements)
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“…The fragment ion m / z 236.20093 [M+H-2CH 2 ] + was produced by the loss of -2CH 2 from [M+H] + , and the latter was further cleaved -CO 2 and -CNH 3 to obtain m / z 163.11084 [M+H-C 4 H 5 O 2 N] + ; m / z 218.18927 [M+H-CH 2 O 2 ] + as a fragment ion was produced by the loss of -H 2 O and -CO from [M+H] + , and the latter was further cleaved -3CH 2 and -CH 3 to obtain m / z 176.14284 [M+H-C 4 H 4 O 2 ] + and m / z 203.16554 [M+H-C 2 H 5 O 2 ] + ; m / z 160.11208 [M+H-C 5 H 11 O 2 ] + was derived from m / z 176.14284 by the cleavage of -CH 3 , and the latter was further cleaved -CH 3 and -HCN to obtain m / z 145.10065 [M+H-C 6 H 14 O 2 ] + and m / z 133.10066 [M+H-C 6 H 12 O 2 N] + ; and the fragment ion m / z 133.10066 could drop -CH 2 to produce m / z 119.08548 [M+H-C 7 H 14 O 2 N] + ( Figure 2 ). After the relevant research literature comparison [ 7 , 8 ], DN 10 was inferred as dendrobine (C 16 H 25 NO 2 ). The molecular formula of DN 11 was C 15 H 23 NO 2 , as established by the [M+H] + peak at m / z 250.17961 (ppm −2.181).…”
Section: Resultsmentioning
confidence: 99%
“…The fragment ion m / z 236.20093 [M+H-2CH 2 ] + was produced by the loss of -2CH 2 from [M+H] + , and the latter was further cleaved -CO 2 and -CNH 3 to obtain m / z 163.11084 [M+H-C 4 H 5 O 2 N] + ; m / z 218.18927 [M+H-CH 2 O 2 ] + as a fragment ion was produced by the loss of -H 2 O and -CO from [M+H] + , and the latter was further cleaved -3CH 2 and -CH 3 to obtain m / z 176.14284 [M+H-C 4 H 4 O 2 ] + and m / z 203.16554 [M+H-C 2 H 5 O 2 ] + ; m / z 160.11208 [M+H-C 5 H 11 O 2 ] + was derived from m / z 176.14284 by the cleavage of -CH 3 , and the latter was further cleaved -CH 3 and -HCN to obtain m / z 145.10065 [M+H-C 6 H 14 O 2 ] + and m / z 133.10066 [M+H-C 6 H 12 O 2 N] + ; and the fragment ion m / z 133.10066 could drop -CH 2 to produce m / z 119.08548 [M+H-C 7 H 14 O 2 N] + ( Figure 2 ). After the relevant research literature comparison [ 7 , 8 ], DN 10 was inferred as dendrobine (C 16 H 25 NO 2 ). The molecular formula of DN 11 was C 15 H 23 NO 2 , as established by the [M+H] + peak at m / z 250.17961 (ppm −2.181).…”
Section: Resultsmentioning
confidence: 99%
“…All samples were processed as described previously with some modifications (Lu et al, 2022). The fresh stems of D. officinale samples were dried at 60 °C and then grounded into powder for the assay.…”
Section: Sample Preparationmentioning
confidence: 99%
“…Instrument conditions were set as described previously with some modifications (Lu et al, 2022). Agilent 1290 Infinity II UPLC liquid chromatograph system was employed for the present secondary metabolites analysis.…”
Section: Instrument Conditionsmentioning
confidence: 99%
See 1 more Smart Citation
“…DSAs share a common sesquiterpene backbone primarily synthesized through two pathways, namely the mevalonate (MVA) pathway and the MEP pathway [ 13 ]. Transcriptome sequencing of D. nobile co-cultured with endophytic fungus MF23 also identified 16 genes that were potentially involved in the synthesis of the sesquiterpene backbone [ 14 ].…”
Section: Introductionmentioning
confidence: 99%