Chemistry of silybin
Language English Country Great Britain, England Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
24977260
DOI
10.1039/c3np70122k
Knihovny.cz E-resources
- MeSH
- Molecular Structure MeSH
- Silybum marianum chemistry MeSH
- Seeds chemistry MeSH
- Silybin MeSH
- Silymarin chemistry isolation & purification pharmacology MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Silybin MeSH
- Silymarin MeSH
Silybin, a secondary metabolite isolated from the seeds of the blessed milk thistle (Silybum marianum) was discovered as the first member of a new family of natural compounds called flavonolignans in 1959. Over the years it has received the research attention of many organic chemists. This research has resulted in a number of semisynthetic derivatives prepared in an effort to modulate and better target the biological activities of silybin or to improve its physical properties, such as its solubility. A fundamental breakthrough in silybin chemistry was the determination of the absolute configurations of silybin A and silybin B, and the development of methods for their separation. This review covers articles dealing with silybin chemistry and also summarizes all the derivatives prepared.
References provided by Crossref.org
Selectively Halogenated Flavonolignans-Preparation and Antibacterial Activity
Chirality Matters: Biological Activity of Optically Pure Silybin and Its Congeners
Dual SMO/BRAF Inhibition by Flavonolignans from Silybum marianum †
Modulation of Skin Inflammatory Response by Active Components of Silymarin
Sulfated Metabolites of Flavonolignans and 2,3-Dehydroflavonolignans: Preparation and Properties
Isoquercitrin Esters with Mono- or Dicarboxylic Acids: Enzymatic Preparation and Properties
Flavonolignans As a Novel Class of Sodium Pump Inhibitors
Regioselective alcoholysis of silychristin acetates catalyzed by lipases