2008
DOI: 10.1365/s10337-008-0722-3
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New Components from Silybum marianum L. Fruits: A Theory Comes True

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Cited by 10 publications
(9 citation statements)
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“…Similarly, milk thistle is commercially cultivated for its remarkable medicinal values [ 6 ]. It has been reported that polyphenols existing in milk thistle seeds have antioxidant, anti-inflammatory, hypolipidemic, and anti-carcinogenic properties, all at once [ 7 , 8 , 9 , 10 ]. Milk thistle seed oil has also been documented as a potential natural source of vitamin E (fat-soluble vitamin covering a set of eight organic molecules, four tocopherols, and four tocotrienols) [ 11 , 12 ], and has often been recommended as a favorable edible oil [ 13 ].…”
Section: Introductionmentioning
confidence: 99%
“…Similarly, milk thistle is commercially cultivated for its remarkable medicinal values [ 6 ]. It has been reported that polyphenols existing in milk thistle seeds have antioxidant, anti-inflammatory, hypolipidemic, and anti-carcinogenic properties, all at once [ 7 , 8 , 9 , 10 ]. Milk thistle seed oil has also been documented as a potential natural source of vitamin E (fat-soluble vitamin covering a set of eight organic molecules, four tocopherols, and four tocotrienols) [ 11 , 12 ], and has often been recommended as a favorable edible oil [ 13 ].…”
Section: Introductionmentioning
confidence: 99%
“…Silymarin mainly comprises of silybin and usually contains several minor components with an important biological activities including isosilybin, silychristin, silydianin, 2,3-dehydrosilybin (DHSB), quercetin and dihydroquercetin (taxifolin) and a poorly characterized polymer fraction. Furthermore, the presence and concentration of minor components in silymarin fluctuate depending on subspecies of S. marianum, growing conditions of the plants and age of the extract (Kurkin et al, 2001;Nyiredy et al, 2008;Biedermann et al, 2014). As such, the characterization of the effect of each of the compounds found in silymarin is pertinent to selecting the 'correct' extract for each application.…”
Section: Introductionmentioning
confidence: 99%
“…They are therefore, a priori, non-stereospecific and non-regioselective, which implies a wide variety of possibilities at the coupling level, and therefore of the isomers formed. Based on this information, the diastereomers of silybin and isosilybin are described as equimolar mixtures reflecting the lack of stereospecificity of the initial radical couplings [76,95]. Among the available experimental data, none confirms the 1: 1 ratio between these diastereoisomeric couples [31,37,88,96,97].…”
Section: Flavonolignans Biosynthesis In Silybum Marianummentioning
confidence: 99%