2015
DOI: 10.1016/j.tetlet.2015.06.022
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Two new isopimarane diterpenoids from the endophytic fungus Xylaria sp. SNB-GTC2501

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Cited by 20 publications
(6 citation statements)
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“…No isolated endophytic fungus presented antibacterial activity. Previous studies reported that the extract of endophytic fungi belonging to genera identified in our study inhibited E. coli, S. aureus and S. enteritidis (Vieira et al, 2012;Xing et al, 2011;Sorres et al, 2015;Yue et al, 2015;Hu et al, 2015;Kurzatkowski and Gębska-kuczerowska, 2015). However, those endophytic fungi were not isolated from E. erythropappus.…”
Section: Discussionsupporting
confidence: 61%
“…No isolated endophytic fungus presented antibacterial activity. Previous studies reported that the extract of endophytic fungi belonging to genera identified in our study inhibited E. coli, S. aureus and S. enteritidis (Vieira et al, 2012;Xing et al, 2011;Sorres et al, 2015;Yue et al, 2015;Hu et al, 2015;Kurzatkowski and Gębska-kuczerowska, 2015). However, those endophytic fungi were not isolated from E. erythropappus.…”
Section: Discussionsupporting
confidence: 61%
“…However, their minimal inhibitory concentrations were more than 128 µg/mL. In addition, 4 and 12 were not cytotoxic towards MRC5 cells (IC 50 >100 µM) [65].…”
Section: Melleins From Fungimentioning
confidence: 89%
“…The other compounds were determined as 16-α-Dglucopyranosyloxyisopimar-7-en-19-oic acid (5), [9] xylabisboein B (6), [10] xylabisboein A (7), [10] xylarenolide (8), [11] methyl 4-(2-hydroxybutynoxy)benzoate ( 9), [12] 4-(2-hydroxybutynoxy)benzoic acid (10), [12] 5-hydroxymellein (11), [13] and 5-methylmellein (12). [13] Compound 13 was a yellow gum with the molecular formula C 14 H 14 O 4 established by HR-ESI-MS data.…”
Section: Resultsmentioning
confidence: 99%