2009
DOI: 10.1080/14756360802188081
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In vitroantioxidant activity of silymarin

Abstract: Silymarin, a known standardized extract obtained from seeds of Silybum marianum is widely used in treatment of several diseases of varying origin. In the present paper, we clarified the antioxidant activity of silymarin by employing various in vitro antioxidant assay such as 1,1-diphenyl-2-picryl-hydrazyl free radical (DPPH·) scavenging, 2,2 0 -azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) radical scavenging activity, total antioxidant activity determination by ferric thiocyanate, total reducing abil… Show more

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Cited by 197 publications
(125 citation statements)
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“…Free radicals intrinsically exist in living organisms; however, much amount of free radicals and lipid peroxides can lead to tissue damage, cell death or degenerative processes, including aspects of ageing, inflammation, neural disorders, cancer, and the circulatory system diseases by oxidise biomolecules and they are mainly responsible for oxidative stress [6][7][8] . Free radicals can change the structures of cellular molecules such as DNA, proteins, lipids and carbohydrates [9][10][11][12] . The effect of oxidants can be deactivated or inhibited in various ways by antioxidant compounds, scavenging and suppressing the free radicals [13][14][15][16] .…”
Section: Introductionmentioning
confidence: 99%
“…Free radicals intrinsically exist in living organisms; however, much amount of free radicals and lipid peroxides can lead to tissue damage, cell death or degenerative processes, including aspects of ageing, inflammation, neural disorders, cancer, and the circulatory system diseases by oxidise biomolecules and they are mainly responsible for oxidative stress [6][7][8] . Free radicals can change the structures of cellular molecules such as DNA, proteins, lipids and carbohydrates [9][10][11][12] . The effect of oxidants can be deactivated or inhibited in various ways by antioxidant compounds, scavenging and suppressing the free radicals [13][14][15][16] .…”
Section: Introductionmentioning
confidence: 99%
“…Antioxidants respond to DPPH• by giving electron or hydrogen particle, in this way reducing it to 1,1-diphenyl-2-hydrazine (DPPH-H) or a substitute practically equivalent to hydrazine. The profound violet shade of DPPH at most extreme absorption of 515 nm is changed to light yellow, colorless or bleached product, resulting in decrease in absorption (18,19). The hexane extract of L. humilis displayed noteworthy antioxidant activity of 95% at 240 µg.mL -1 ( Figure. (20,21,22), which is accepted to add to their electron exchange/hydrogen giving capacity.…”
Section: Resultsmentioning
confidence: 99%
“…The bromophenol 11, which had two methoxy (-OH) and a bromine (-Br) groups, was the best hCA II inhibitor (K i : 2.01 ± 0.52 nM). Phenolic compounds have a lot of nutritional and pharmacological properties including anti-oxidant properties [62][63][64][65][66][67][68][69][70][71][72][73][74][75][76][77][78][79][80][81] and enzymes inhibition [82][83][84][85][86] . However, all bromophenol derivatives (1-12) have shown similar hCA II inhibition properties.…”
Section: Resultsmentioning
confidence: 99%