2020
DOI: 10.1007/s11172-020-3050-x
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Polyphenol components of the knotwood extracts of Salix capreal.

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Cited by 6 publications
(2 citation statements)
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“…ESI-MS detected twelve ion peaks from 20-HM. Three of the peaks were assigned as background or contaminant peaks [ 27 ], and the remaining peaks (nine peaks) were proposed as a main fragmentation of 20-HM as presented in Figure 1 ; Figure 2 by combining a search through literature and chemical databases and a prediction from CFM-ID version 3.0 software [ 17 , 28 , 29 ]. Most of the proposed fragments were in a range of ±5 mDa from a theoretical mass calculated by ACD/Chemsketch (free version, 2015).…”
Section: Resultsmentioning
confidence: 99%
“…ESI-MS detected twelve ion peaks from 20-HM. Three of the peaks were assigned as background or contaminant peaks [ 27 ], and the remaining peaks (nine peaks) were proposed as a main fragmentation of 20-HM as presented in Figure 1 ; Figure 2 by combining a search through literature and chemical databases and a prediction from CFM-ID version 3.0 software [ 17 , 28 , 29 ]. Most of the proposed fragments were in a range of ±5 mDa from a theoretical mass calculated by ACD/Chemsketch (free version, 2015).…”
Section: Resultsmentioning
confidence: 99%
“…3 was purified by reversed-phase HPLC (Cosmosil 5C 18 -MS-Ⅱ, 20 φ × 250 mm) with 50% MeOH–1% acetic acid to obtain astragalin ( 9 , 31.0 mg, 0.0247%), rutin ( 10 , 10.0 mg, 0.0080%), and quercetin 3- O -β-cellobioside ( 11 , 14.6 mg, 0.0112%). The chemical structures of the isolated compounds were identified by a comparison of the 1 H- and 13 C- NMR spectra with References [ 2 , 19 , 20 , 54 , 55 , 56 , 57 , 58 , 59 , 60 ]. The chemical structures of the isolated compounds ( 1 – 11 ) are shown in Figure 1 .…”
Section: Methodsmentioning
confidence: 99%