Literature DB >> 26429716

"Non-Taxifolin" Derived Flavonolignans: Phytochemistry and Biology.

Christopher S Chambers1, Katerina Valentova, Vladimir Kren.   

Abstract

Flavonolignans are plant natural products, composed of a flavonoid moiety and a lignan (phenylpropanoid) part. Current literature focuses on flavonolignans formed from taxifolin and coniferyl alcohol as e.g. silybin and its congeners from fruit extract from the purple variety of the milk thistle (Silybum marianum) denoted as "silymarin". This review describes chemistry and biological activity of so far neglected "non-taxifolin" based flavonolignans, derived from apigenin, luteolin, tricin, chrysoeriol, naringenin and eriodictyol, as the flavonoid part. Up-to-date knowledge on hydnocarpin, hydnocarpin-D, pseudotsuganol, hydnowightin, neohydnocarpin, palstatin, salcolins A and B, anastatins A and B, sinaiticin, silyamandin and silandrin is summarized in the present paper. Most of non-taxifolin derived flavonolignans have been shown to exhibit in vitro and/or in vivo anti-hepatotoxic, anti-oxidant, free radical scavenging, anti-inflammatory, anti-proliferative, anti-cancer, chemotherapy potentiating, anti-melanogenic, anti-bacterial, vasorelaxing, anti-platelet aggregation and/or hypotriglyceridemic activity, often stronger than silybin. Many of these compounds inhibited Staphylococcus aureus multidrug resistance pump NorA and sensitized multidrug resistant cancer cell lines showing a potential as adjuvants. Non-taxifolin derived flavonolignans are a relatively unexplored group of compounds with interesting biological activity and great application potential. Their detailed study could provide a new insight into the biomimetic synthesis in order to obtain new compounds with greater activity and identify new lead structures for the biomedicinal research.

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Year:  2015        PMID: 26429716     DOI: 10.2174/1381612821666151002112720

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  8 in total

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Authors:  Jorge Rencoret; Duarte Neiva; Gisela Marques; Ana Gutiérrez; Hoon Kim; Jorge Gominho; Helena Pereira; John Ralph; José C Del Río
Journal:  Plant Physiol       Date:  2019-04-25       Impact factor: 8.340

2.  Chemotaxonomic and biosynthetic relationships between flavonolignans produced by Silybum marianum populations.

Authors:  Sameh F AbouZid; Hayam S Ahmed; Abeer S Moawad; Asmaa I Owis; Shao-Nong Chen; Amandine Nachtergael; James B McAlpine; J Brent Friesen; Guido F Pauli
Journal:  Fitoterapia       Date:  2017-04-06       Impact factor: 3.204

3.  In Vivo Antimicrobial and Wound-Healing Activity of Resveratrol, Dihydroquercetin, and Dihydromyricetin against Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans.

Authors:  Alexei B Shevelev; Nicola La Porta; Elena P Isakova; Stefan Martens; Yulia K Biryukova; Alexander S Belous; Dmitrii A Sivokhin; Elena V Trubnikova; Marina V Zylkova; Alla V Belyakova; Maria S Smirnova; Yulia I Deryabina
Journal:  Pathogens       Date:  2020-04-17

4.  Bioconversion of Callus-Produced Precursors to Silymarin Derivatives in Silybum marianum Leaves for the Production of Bioactive Compounds.

Authors:  Dina Gad; Hamed El-Shora; Daniele Fraternale; Elisa Maricchiolo; Andrea Pompa; Karl-Josef Dietz
Journal:  Int J Mol Sci       Date:  2021-02-21       Impact factor: 5.923

5.  Flavonoids naringenin chalcone, naringenin, dihydrotricin, and tricin are lignin monomers in papyrus.

Authors:  Jorge Rencoret; Mario J Rosado; Hoon Kim; Vitaliy I Timokhin; Ana Gutiérrez; Florian Bausch; Thomas Rosenau; Antje Potthast; John Ralph; José C Del Río
Journal:  Plant Physiol       Date:  2022-01-20       Impact factor: 8.340

6.  The Sorghum (Sorghum bicolor) Brown Midrib 30 Gene Encodes a Chalcone Isomerase Required for Cell Wall Lignification.

Authors:  Hannah M Tetreault; Tammy Gries; Sarah Liu; John Toy; Zhanguo Xin; Wilfred Vermerris; John Ralph; Deanna L Funnell-Harris; Scott E Sattler
Journal:  Front Plant Sci       Date:  2021-12-02       Impact factor: 5.753

7.  Unconventional application of the Mitsunobu reaction: Selective flavonolignan dehydration yielding hydnocarpins.

Authors:  Guozheng Huang; Simon Schramm; Jörg Heilmann; David Biedermann; Vladimír Křen; Michael Decker
Journal:  Beilstein J Org Chem       Date:  2016-04-08       Impact factor: 2.883

8.  Flavonolignan 2,3-dehydrosilydianin activates Nrf2 and upregulates NAD(P)H:quinone oxidoreductase 1 in Hepa1c1c7 cells.

Authors:  Lenka Roubalová; Albena T Dinkova-Kostova; David Biedermann; Vladimír Křen; Jitka Ulrichová; Jiří Vrba
Journal:  Fitoterapia       Date:  2017-04-24       Impact factor: 3.204

  8 in total

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