2018
DOI: 10.1016/j.bse.2018.06.009
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Phytochemical investigation of Crepis incana Sm. (Asteraceae) endemic to southern Greece

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Cited by 7 publications
(9 citation statements)
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“…& SM. (Asteraceae) flowering aerial parts, expressed the best activity against Gram‐negative bacteria Enterococcus faecalis ( MIC =0.02 mg/mL; MBC =0.03 mg/mL) and P. aeruginosa ( MIC =0.03 mg/mL; MBC =0.06 mg/mL), and molds A. versicolor and T. viride ( MIC =0.045 mg/mL; MFC =0.3 mg/mL) [32] . The α ‐methylene‐ γ ‐lactone moiety is of particular importance for the manifestation of the crepiside E antimicrobial activity, i. e ., free exocyclic methylene group from this moiety causes the alkylation of cell membrane components and enzymes of microorganisms [33,34] .…”
Section: Resultsmentioning
confidence: 99%
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“…& SM. (Asteraceae) flowering aerial parts, expressed the best activity against Gram‐negative bacteria Enterococcus faecalis ( MIC =0.02 mg/mL; MBC =0.03 mg/mL) and P. aeruginosa ( MIC =0.03 mg/mL; MBC =0.06 mg/mL), and molds A. versicolor and T. viride ( MIC =0.045 mg/mL; MFC =0.3 mg/mL) [32] . The α ‐methylene‐ γ ‐lactone moiety is of particular importance for the manifestation of the crepiside E antimicrobial activity, i. e ., free exocyclic methylene group from this moiety causes the alkylation of cell membrane components and enzymes of microorganisms [33,34] .…”
Section: Resultsmentioning
confidence: 99%
“…(Asteraceae) flowering aerial parts, expressed the best activity against Gram-negative bacteria Enterococcus faecalis (MIC = 0.02 mg/mL; MBC = 0.03 mg/mL) and P. aeruginosa (MIC = 0.03 mg/mL; MBC = 0.06 mg/mL), and molds A. versicolor and T. viride (MIC = 0.045 mg/mL; MFC = 0.3 mg/mL). [32] The α-methylene-γ-lactone moiety is of particular importance for the manifestation of the crepiside E antimicrobial activity, i. e., free exocyclic methylene group from this moiety causes the alkylation of cell membrane components and enzymes of microorganisms. [33,34] However, similar antimicrobial activity of 8-epiixerisamine A (which does not contain free α-methylene group, but Nmethyl-proline instead) represents interesting finding that demands further studies of antimicrobial mode of action of this SLs.…”
Section: [C]mentioning
confidence: 99%
“…In contrast to the large diversity of sesquiterpenes reported, only a limited number of flavonoids have been observed in the genus Crepis. These are mainly luteolin derivatives, with luteolin itself (76) being the most common one, present in twenty-one species. Additionally, luteolin-7-O-glucoside (80) and luteolin 7-O-glucuronide (81) are present in several species, eighteen and thirteen, respectively, whereas luteolin 7-O-gentiobioside (82) and luteolin 4 -O-glucoside (83) occur in few cases.…”
Section: Flavonoidsmentioning
confidence: 99%
“…The HPLC-MS analysis of the aerial parts and roots of C. foetida L. subsp. rhoeadifolia showed the presence of chlorogenic acid (104) and luteonin (76). The tested extracts showed antioxidant activity in assays of DPPH (IC 50 = 0.26-1.54 mg/mL) and of the reactive substances of thiobarbituric acid (TBARS) (MDA level = 4.54-19.15 nmol/mL), thus suggesting that the activity shown by the extracts of this plant is linked to its polyphenolic content [46].…”
Section: Antioxidant Activitymentioning
confidence: 99%
“…Extracts obtained from the different parts of the Crepis spp. and their isolated constituents have undergone only limited evaluation as antitumor, anti-inflammatory, antiviral, antimicrobial, antiulcer, antioxidant and nutritional agents [ 5 , 6 ]. Moreover, within the Crepis genus, few edible representatives appear, such as C. bulbosa , C. capillaris , C. commutata , C. foetida , C. setosa and C. vesicaria [ 5 , 6 ].…”
Section: Introductionmentioning
confidence: 99%