1997
DOI: 10.1039/a703283h
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Glycosylation of silybin

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1997
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Cited by 65 publications
(45 citation statements)
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“…A number of silybin water-soluble semisynthetic derivatives were designed to overcome this problem, e.g., silybin bis-hemisuccinate (Legalon) [16], silybin-23-O-phosphate [17], silybin 23-O-b-glycosides [6], and silybinic acid [9]. However, modifications of silybin leading to an increase in its water-solubility usually led to an impairment of its antioxidant (antiradical) activity in the lipophilic milieu [9].…”
Section: Introductionmentioning
confidence: 99%
“…A number of silybin water-soluble semisynthetic derivatives were designed to overcome this problem, e.g., silybin bis-hemisuccinate (Legalon) [16], silybin-23-O-phosphate [17], silybin 23-O-b-glycosides [6], and silybinic acid [9]. However, modifications of silybin leading to an increase in its water-solubility usually led to an impairment of its antioxidant (antiradical) activity in the lipophilic milieu [9].…”
Section: Introductionmentioning
confidence: 99%
“…It was interesting to note that production of 3-O-glycosides was readily achieved by microbial transformation, while the secondary alcohol at C-3 has been reported to be partially substituted by chemical synthetic methods only under prolonged reaction times with formation of small amounts of 3,9 0 -diglycosides. 7 Production of silybin analogues using microbial metabolic transformation has never been reported yet. This is the first report on the presence and unambiguous structure elucidation of silybin …”
mentioning
confidence: 99%
“…13 It is interesting to note that the diastereomers of silybin, prepared recently as pure compounds by our group, clearly have different pharmacokinetic profiles. 14,15 It is possible that these diasteromers interact in different ways with receptors to which silybin is known to bind (liver receptors for ␣-amanitin, receptors for steroids?). Controversy also surrounds the activity of these compounds in animals (mostly rodents).…”
mentioning
confidence: 99%