2019
DOI: 10.1007/s00217-019-03276-2
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Characterization of polyphenolic constituents from Sanguisorba officinalis L. and its antibacterial activity

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Cited by 25 publications
(24 citation statements)
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“…In a recent study, Su et al (2019) also reported that bioactive compounds isolated from dried roots extracts of S. officinalis exhibited inhibitory effects against the Gram (−) bacterium Vibrio vulnificus in a dose dependent manner. Similarly to the present study, Zhu et al (2019) observed that purified phenolic compounds extract (PE) from S. officinalis exhibited better activity against Gram (−) bacteria (Escherichia coli and Salmonella typhimurium) than against Gram (+) bacteria (S. aureus, L. monocytogenes and B. subtilis).…”
Section: Antimicrobial Activitysupporting
confidence: 84%
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“…In a recent study, Su et al (2019) also reported that bioactive compounds isolated from dried roots extracts of S. officinalis exhibited inhibitory effects against the Gram (−) bacterium Vibrio vulnificus in a dose dependent manner. Similarly to the present study, Zhu et al (2019) observed that purified phenolic compounds extract (PE) from S. officinalis exhibited better activity against Gram (−) bacteria (Escherichia coli and Salmonella typhimurium) than against Gram (+) bacteria (S. aureus, L. monocytogenes and B. subtilis).…”
Section: Antimicrobial Activitysupporting
confidence: 84%
“…(small burnet) and Sanguisorba officinalis L. (great burnet) which are native in the Mediterranean basin and other areas of the world (Gawron-Gzella et al, 2016;Karkanis et al, 2019). The leaves and roots of these species contain a wide variety of bioactive compounds such as gallic acid, ellagic acid, (+)-catechin, lambertianin C, sanguiin H-10, and ziyuglycoside II (Karkanis et al, 2019;Lkhagvasuren & Kim, 2019;Tan et al, 2019;Zhu et al, 2019). So far, it has been well documented that isolated bioactive compounds and/or extracts of both species exert a broad spectrum of medicinal properties.…”
Section: Introductionmentioning
confidence: 99%
“…Fragmentation of the primary ions resulted in losses of hexose (162 Da), pentose (146 Da), and deoxyhexose (308 Da) [24]. Of the 9 flavonols initially suggested for S. officinalis L., only [2,3,12]. In turn, 3 compounds have not been previously described according to the available literature.…”
Section: Introductionmentioning
confidence: 99%
“…Among the 77 compounds, only 36 had previously been identified in S. officinalis L., and they all were methyl-6-O-galloyl-β-d-glucopyranoside (peak 17, 64; m/z 345), pedunculagin1 (18,23,29; m/z 785), galloyl-HHDP-glucose otherwise called corilagin isomer (25,44,55; m/z 633), di-galloyl-glucoside (37; m/z 483), methyl-4,6-digalloyl-β-d-glucopyranoside (50, 62, 71, 88; m/z 497), HHDP-galloyl-glucose (53; m/z 633), ellagic acid pentoside (60, 99; m/z 433), ellagic acid hexoside (67, 68, 102; m/z 463), di-galloyl hexoside (72, 118; m/z 483), galloyl-bis-HHDP-glucose otherwise called potentilin/casuarictin isomer (84,85,95,97,104,106; m/z 935), lambertianin C (86; m/z 1401), ellagic acid (108; m/z 300.99), trigalloyl-HHDP-glucose (92, 114; m/z 937), trigalloyl-β-D-methyl glucoside (115; m/z 649), 3,3 ,4 -O-trimethyl ellagic acid (127, 128; m/z 343), and 3,4 -O-dimethyl ellagic acid (129, 130; m/z 329) [2,3,12]. In turn, 16 compounds had earlier been detected and identified in flowers and fruits of Punica granatum but in this study were for the first time detected in the morphological parts of S. officinalis L. These compounds were referred to as: 2,3-HHDP-(α/β)-glucose (1; m/z 481), HHDP-hexoside(2,3-(S)-Hexahydroxydiphenoyl-d-glucose) (2,4; m/z 481), HHDP-hexoside(1-galloyl-2,3-hexahydroxydiphenoyl-α-glucose) (3; m/z 481), galloyl-hexoside(β-glucogallin) (5; m/z 331), galloyl-hexoside (7)(8)(9)(10)13; m/z 331), di-HHDP-glucoside (34; m/z 783), di-galloyl-HHDP-glucose (14,56,66; m/z 785), galloyl-HHDP-hexoside (77; m/z 633), and pentagalloyl-glucoside (111; m/z 939) [10,13]. Another 6 compounds belonging to the group of hydrolyzable tannins were detected during identification of Duchesnea indica and they were: di-HHDP-glucose also known as pedunculalagin isomer (15,20,24,26,27,…”
Section: Introductionmentioning
confidence: 99%
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