2021
DOI: 10.1080/10826076.2021.1948426
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An approach based on consecutive high-speed counter-current chromatography for preparation of an active compound rutin from Apocynum venetum L

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Cited by 4 publications
(8 citation statements)
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“…As a result, 28.5 mg of the target compound was isolated from 100 mg of the ethyl acetate extract. The purity of the separated compound was 95% by HPLC (Figure 5b) and the structure was identified as rutin according to the NMR results and the literature (Li et al, 2021). 1 H NMR (400 MHz, MeOD) δ : 7.57 (1H, s, H‐6′), 7.54 (1H, d, J = 8.4 Hz, H‐2′), 6.77 (1H, d, J = 8.4 Hz, H‐5′), 6.28 (1H, s, H‐8), 6.09 (1H, s, H‐6), 4.99 (1H, d, J = 7.6 Hz, H‐1″), 4.42 (1H, d, J = 1.2 Hz, H‐1″), 1.02 (3H, d, J = 6.4 Hz, H‐6″); 13 C NMR (100 MHz, MeOD): 177.8 (C‐4), 165.5 (C‐7), 161.6 (C‐5), 157.8 (C‐9), 157.2 (C‐2), 148.5 (C4’), 144.5 (C‐3′), 134.2 (C‐3), 123.1 (C‐6′), 122.6 (C‐1′), 117.2 (C‐2′), 115.6 (C‐5′), 104.0 (C‐10), 103.4 (C‐1″), 101.0 (C‐1″), 98.9 (C‐6), 93.7 (C‐8), 76.8 (C‐5″), 75.8 (C‐3″), 74.3 (C‐2″), 72.5 (C‐4″), 70.8 (C‐2″), 70.7 (C‐3″), 70.0 (C‐4″), 68.3 (C‐6″), 67.2 (C‐5″), 16.5 (C‐6″).…”
Section: Resultsmentioning
confidence: 89%
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“…As a result, 28.5 mg of the target compound was isolated from 100 mg of the ethyl acetate extract. The purity of the separated compound was 95% by HPLC (Figure 5b) and the structure was identified as rutin according to the NMR results and the literature (Li et al, 2021). 1 H NMR (400 MHz, MeOD) δ : 7.57 (1H, s, H‐6′), 7.54 (1H, d, J = 8.4 Hz, H‐2′), 6.77 (1H, d, J = 8.4 Hz, H‐5′), 6.28 (1H, s, H‐8), 6.09 (1H, s, H‐6), 4.99 (1H, d, J = 7.6 Hz, H‐1″), 4.42 (1H, d, J = 1.2 Hz, H‐1″), 1.02 (3H, d, J = 6.4 Hz, H‐6″); 13 C NMR (100 MHz, MeOD): 177.8 (C‐4), 165.5 (C‐7), 161.6 (C‐5), 157.8 (C‐9), 157.2 (C‐2), 148.5 (C4’), 144.5 (C‐3′), 134.2 (C‐3), 123.1 (C‐6′), 122.6 (C‐1′), 117.2 (C‐2′), 115.6 (C‐5′), 104.0 (C‐10), 103.4 (C‐1″), 101.0 (C‐1″), 98.9 (C‐6), 93.7 (C‐8), 76.8 (C‐5″), 75.8 (C‐3″), 74.3 (C‐2″), 72.5 (C‐4″), 70.8 (C‐2″), 70.7 (C‐3″), 70.0 (C‐4″), 68.3 (C‐6″), 67.2 (C‐5″), 16.5 (C‐6″).…”
Section: Resultsmentioning
confidence: 89%
“…Since rutin is an important natural compound with a wide range of biological activities (Li et al, 2021), it is not difficult to find evidence for rutin inhibiting α ‐amylase and α ‐glucosidase in previous studies. Most of the previous studies used acarbose as a positive control to investigate the effect of rutin on enzyme activity.…”
Section: Resultsmentioning
confidence: 99%
“…The effluent was monitored at 254 nm. The conditions of consecutive separation were consistent with those of traditional HSCCC (Kang et al, 2016;Li et al, 2021;Yang, Wang, et al, 2020). The interval loading time of the crude sample was calculated using Equation (1):…”
Section: Separation Processmentioning
confidence: 99%
“…The target compound can be repeatedly separated and enriched using a commercial counter-current chromatography (CCC) column with a volume of 300 ml (Li et al, 2021;Lv et al, 2015;Yang et al, 2020).…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, consecutive HSCCC separation is a good choice to prepare samples on a large scale (Bouju et al, 2015; Köhler & Winterhalter, 2005), because HSCCC separation has good stability. The target compound can be repeatedly separated and enriched using a commercial counter‐current chromatography (CCC) column with a volume of 300 ml (Li et al, 2021; Lv et al, 2015; Yang et al, 2020). Although 5‐HMF has been successfully separated by traditional HSCCC, its separation is still used as a case study to develop a consecutive HSCCC separation method, which can not only increase the yield of 5‐HMF, but also save time and solvent.…”
Section: Introductionmentioning
confidence: 99%