2009
DOI: 10.1016/j.foodchem.2009.02.075
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Ursolic acid analogues: non-phenolic functional food components in Jamaican raspberry fruits

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Cited by 35 publications
(29 citation statements)
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References 23 publications
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“…The poor solubility of triterpenoids in aqueous assay conditions interferes with both LPO and COX assays. However, at lower concentrations compounds 1 and 2 showed moderate LPO and COX enzymes inhibitory activities which is in agreement with our earlier finding (Bowen-Forbes et al, 2009;Zhang, DeWitt, Murugesan, & Nair, 2009). …”
Section: Resultssupporting
confidence: 93%
See 1 more Smart Citation
“…The poor solubility of triterpenoids in aqueous assay conditions interferes with both LPO and COX assays. However, at lower concentrations compounds 1 and 2 showed moderate LPO and COX enzymes inhibitory activities which is in agreement with our earlier finding (Bowen-Forbes et al, 2009;Zhang, DeWitt, Murugesan, & Nair, 2009). …”
Section: Resultssupporting
confidence: 93%
“…Peroxidation of the lipid was initiated by adding ferrous ions. The OH radicals produced from the oxidation of the lipid then trigger the peroxidation of the embedded fluorescent probe (Bowen-Forbes, Mulabagal, Liu, & Nair, 2009). The water and methanolic extracts at 250 lg/mL showed LPO inhibition by 79% and 65%, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…Euscaphic acid, 1-b-hydroxyeuscaphic acid, and hyptatic acid B showed selective COX-1 enzyme inhibitory activity (13%, 25%, and 35% respectively) at 25 μg/mL. Similar COX inhibitory activity was demonstrated by compounds 4-epi-nigaichigoside F1 and trachelosperoside B-1, which showed moderate selectivity against the COX-1 enzyme [124]. In addition, the anti-inflammatory activity of Psidium cattleianum (strawberry guava) was analyzed using COX-1 and -2 enzyme inhibitory assays.…”
Section: Bioactivities Of Wild Fruitsmentioning
confidence: 90%
“…Estupiñan [51] reported the presence of cyanidin-3-glucoside and cyanidin-3-rutinoside, cyanidin-3-sambubioside, cyanidin-3-xylosylrutinoside, pelargonidin-3-glucoside, and pelargonidin-3-rutinoside, cyanidin glycoside, lambertianin C and sanguiin H-6, and 2 ellagitannins in various Rubus species. Bowen-Forbes et al [52] reported the presence of…”
Section: Identification Of the Isolated Bioactive Compoundsmentioning
confidence: 99%
“…Based on the TLC, the fractions with similar banding pattern were clubbed and 16 fractions were obtained. The various fractions such as F1 (34)(35)(36)(37), F2 (38)(39)(40)(41)(42)(43)(44)(45)(46)(47)(48)(49)(50)(51)(52)(53)(54), F3 (55-58), F4 (59-72), F5 (76-80), F6 (84-88), F7 (89-110), F8 (111-116), F9 (121-126), F10 (132-136), F11 (137-141), F12 (142), F13 (143-147), F14 (148-151), F15 (159-162), and F16 (163-183) were subjected to antioxidant studies. The most active fractions such as F5, F7, F9, and F16 were selected for further isolation process.…”
Section: Chromatographic Separation Of the Root Acetone Extractmentioning
confidence: 99%