2018
DOI: 10.1016/j.fct.2017.08.004
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Biological effects and chemical characterization of Iris schachtii Markgr. extracts: A new source of bioactive constituents

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Cited by 34 publications
(27 citation statements)
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“…The procedures of these assays were reported in our earlier work. [23][24][25][26][27] The enzyme inhibitor effects were evaluated as equivalents of acarbose for a-amylase, galantamine for acetyl cholinesterase (AChE) and butyryl cholinesterase (BChE), and kojic acid (KAE) for tyrosinase.…”
Section: Enzyme Inhibitory Activitymentioning
confidence: 99%
See 1 more Smart Citation
“…The procedures of these assays were reported in our earlier work. [23][24][25][26][27] The enzyme inhibitor effects were evaluated as equivalents of acarbose for a-amylase, galantamine for acetyl cholinesterase (AChE) and butyryl cholinesterase (BChE), and kojic acid (KAE) for tyrosinase.…”
Section: Enzyme Inhibitory Activitymentioning
confidence: 99%
“…The activity for EA may be linked with the higher level of phenolics and this approach was supported by several researchers, who reported the positive correlation between phenolic level and AChE inhibition. 27,36 However, the BChE inhibition effects can be ranked as H 2 O > EtOH > EA > MeOH. The observed BChE inhibitor effect for H 2 O can be attributed to non-phenolic inhibitors 37 since the water extract, as expected, exhibited the lowest phenolic level (see Table 2).…”
Section: Enzyme Inhibitory Effects Of the A Vulgaris Extractsmentioning
confidence: 99%
“…This results showed that inhibition of mutagenic substrates, which needs metabolic activation, such as 2-AA and 2-AF in our study can be attributed to inhibition of cytochrome P450 isoenzymes. Also Charehsaz et al [41] and Mocan et al [42] indicated that protective effects of plant extracts increased in the presence of S9 metabolic activation system by inhibiting cytochrome P450 monooxygenases.…”
Section: Discussionmentioning
confidence: 98%
“…Peaks 1-6 with deprotonated molecules at m/z: 133.01357, 191.01907, 147.02913, 205.03491, and 137.02357 were identified as malic, citric, and hydroxyglutaric acid (Schor et al, 2002) and its isomer, homo(iso)citric and hydroxybenzoic acids, (Mocan et al, 2018) respectively. Peak 7 was assigned tentatively as a dehydro-shikimic acid (C 7 H 11 O 5 − ) while peak 8 with a parent ion at m/z: 175.0243 MS 2 ions at m/z: 115.0071; 113.01269; and 87.00942, was identified as ascorbic acid (C 6 H 7 O 6 − ) (Boonpangrak et al, 2016).…”
Section: Organic Acids and Other Phenolic Derivativesmentioning
confidence: 99%