2007
DOI: 10.1007/s11418-007-0194-z
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Assessment of the antibacterial activity of phenylethanoid glycosides from Phlomis lanceolata against multiple-drug-resistant strains of Staphylococcus aureus

Abstract: Three phenylethanoid glycosides, forsythoside B (1), phlinoside C (2) and verbascoside (3), were isolated from the methanol extract of the leaves of Phlomis lanceolata, an Iranian medicinal plant, by reversed-phase preparative high-performance liquid chromatography (HPLC), and the structures of these compounds were elucidated conclusively by ultraviolet (UV), mass spectrometry (MS) and a series of 1D and 2D nuclear magnetic resonance (NMR) analyses. The antibacterial properties of 1-3 against five multi-drug-r… Show more

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Cited by 54 publications
(36 citation statements)
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“…UV, 1 H NMR (200 MHz, CD 3 OD) and 13 C NMR (50 MHz, CD 3 OD) data were in agreement with the published data (Nazemiyeh et al, 2008c;Delazar et al, 2005Delazar et al, , 2012.…”
Section: Isolation Of Compoundssupporting
confidence: 89%
See 1 more Smart Citation
“…UV, 1 H NMR (200 MHz, CD 3 OD) and 13 C NMR (50 MHz, CD 3 OD) data were in agreement with the published data (Nazemiyeh et al, 2008c;Delazar et al, 2005Delazar et al, , 2012.…”
Section: Isolation Of Compoundssupporting
confidence: 89%
“…Solid-phase extraction (SPE) of the MeOH extract of the aerial parts of Pedicularis sibthorpii Boiss., Scrophulariaceae, followed by reversed-phase prep-HPLC analyses of the SPE fractions (10, 20, 40 and 60% aqueous MeOH fractions) afforded three phenylethanoids, verbascoside (1, Nazemiyeh et al, 2008c;Delazar et al, 2005, martynoside (2, Toth et al, 2007) and isomartynoside (3, Calis et al, 1984), an iridoid, aucubin (4, Bernini et al, 1984;Rønsted et al, 2000), a flavonoid glycoside, luteolin 7-O-β-D-glucopyranoside (5, (Mabry et al, 1970;Suntar et al, 2012), and a monosaccharide mannitol (6, Bock & Pedersen, 1983;SDBS, 2012). All isolated compounds were identified unequivocally by UV and NMR analyses.…”
Section: Resultsmentioning
confidence: 99%
“…Isolated glycosides were identified unequivocally as the phenylethanoid glycoside, acteoside (1; Delazar et al, 2005;Nazemiyeh et al, 2008c), and two flavone glycosides, chrysoeriol 7-O-glucopyranoside (2; Mabry et al, 1970;Wagner et al, 1976;Wenkert & Gottlieb, 1977;Zhang & Li, 2008;Zhao et al, 2009;Zhou et al, 2009) and apigenin 7-O-rhamnopyranoside (3; Mabry et al, 1970;Wagner et al, 1976;Wenkert & Gottlieb, 1977;Iwashina & Matsumoto, 1994;Chunsriimyatav et al, 2009), by extensive UV spectroscopic analyses using various shift reagents (Mabry et al, 1970) and NMR analyses (Tables 1 and 2). All spectroscopic data were comparable with respective published data.…”
Section: Resultsmentioning
confidence: 99%
“…Compounds 121 and 125 showed considerable antibacterial activities against all strains of S. aureus with the minimum inhibitory concentration (MIC) values ranging from 64 µg/L to 256 µg/L. Particularly, the activities of 121 (MIC = 2.1ˆ10´4 and 4.1ˆ10´4 M) and 125 (MIC = 3.4ˆ10´4 M) against SA 1199B (NorA) and XU 212 (TetK/MecA), respectively, were comparable to those of the positive control, norfloxacin (MIC = 1.0ˆ10´4 and 2.5ˆ10´5 M) [90]. In addition, 4 111 -O-acetylacteoside (133) and 121 possessed significant inhibition of the formation of bacterial biofilms by E. coli UTI89 [91].…”
Section: Antibacterial and Antivirus Activitymentioning
confidence: 99%