Počet záznamů: 1  

Silybin and its congeners: from traditional medicine to molecular effects

  1. 1.
    SYSNO ASEP0558662
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevSilybin and its congeners: from traditional medicine to molecular effects
    Tvůrce(i) Křen, Vladimír (MBU-M) RID, ORCID
    Valentová, Kateřina (MBU-M) RID, ORCID
    Zdroj.dok.Natural Product Reports. - : Royal Society of Chemistry - ISSN 0265-0568
    Roč. 39, č. 6 (2022), s. 1264-1281
    Poč.str.18 s.
    Jazyk dok.eng - angličtina
    Země vyd.GB - Velká Británie
    Klíč. slovamilk thistle ; silymarin flavonolignans ; in-vitro ; silibinin ; silychristin ; isosilybin ; 2,3-dehydrosilybin ; diastereoisomers ; identification ; derivatives
    Vědní obor RIVCE - Biochemie
    Obor OECDMedicinal chemistry
    CEPGA21-00551S GA ČR - Grantová agentura ČR
    LTC20070 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Způsob publikováníOmezený přístup
    Institucionální podporaMBU-M - RVO:61388971
    UT WOS000790828700001
    EID SCOPUS85133101119
    DOI10.1039/d2np00013j
    AnotaceCovering: 2015 up to 2022 (Feb) Silymarin, an extract of milk thistle (Silybum marianum) fruits, has been used in various medicinal applications since ancient times. A major component of silymarin is the flavonolignan silybin and its relatives isosilybin, silychristin, silydianin, 2,3-dehydrosilybin, and some others. Except for silydianin, they occur in nature as two stereomers. This review focuses on recent developments in chemistry, biosynthesis, modern advanced analytical methods, and transformations of flavonolignans specifically reflecting their chirality. Recently described chemotypes of S. marianum, but also the newest findings regarding the pharmacokinetics, hepatoprotective, antiviral, neuroprotective, and cardioprotective activity, modulation of endocrine functions, modulation of multidrug resistance, and safety of flavonolignans are discussed. A growing number of studies show that the respective diastereomers of flavonolignans have significantly different activities in anisotropic biological systems. Moreover, it is now clear that flavonolignans do not act as antioxidants in vivo, but as specific ligands of biological targets and therefore their chirality is crucial. Many controversies often arise, mainly due to the non-standard composition of this phytopreparation, the use of various undefined mixtures, the misattribution of silymarin vs. silybin, and also the failure to consider the chemistry of the respective components of silymarin.
    PracovištěMikrobiologický ústav
    KontaktEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Rok sběru2023
    Elektronická adresahttps://pubs.rsc.org/en/content/articlelanding/2022/NP/D2NP00013J
Počet záznamů: 1  

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