BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 12583751)

  • 1. Synthesis of (-)-matairesinol, (-)-enterolactone, and (-)-enterodiol from the natural lignan hydroxymatairesinol.
    Eklund P; Lindholm A; Mikkola JP; Smeds A; Lehtilä R; Sjöholm R
    Org Lett; 2003 Feb; 5(4):491-3. PubMed ID: 12583751
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A new lariciresinol-type butyrolactone lignan derived from hydroxymatairesinol and its identification in spruce wood.
    Eklund PC; Willför SM; Smeds AI; Sundell FJ; Sjöholm RE; Holmbom BR
    J Nat Prod; 2004 Jun; 67(6):927-31. PubMed ID: 15217268
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hydroxymatairesinol, a novel enterolactone precursor with antitumor properties from coniferous tree (Picea abies).
    Saarinen NM; Wärri A; Mäkelä SI; Eckerman C; Reunanen M; Ahotupa M; Salmi SM; Franke AA; Kangas L; Santti R
    Nutr Cancer; 2000; 36(2):207-16. PubMed ID: 10890032
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthesis of R-(-)-imperanene from the natural lignan hydroxymatairesinol.
    Eklund PC; Riska AI; Sjöholm RE
    J Org Chem; 2002 Oct; 67(21):7544-6. PubMed ID: 12375994
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A short semi-synthesis and complete NMR-spectroscopic characterization of the naturally occurring lignan glycoside matairesinol 4,4'-di-O-beta-D-diglucoside.
    Ekholm FS; Eklund P; Leino R
    Carbohydr Res; 2010 Sep; 345(13):1963-7. PubMed ID: 20655039
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Selective Lewis acid catalyzed transformation (gamma-butyrolactone versus cyclopropane) of 2-methoxy-4-benzyltetrahydrofuran derivatives. Efficient synthesis of lignan lactones.
    Ferrié L; Bouyssi D; Balme G
    Org Lett; 2005 Jul; 7(15):3143-6. PubMed ID: 16018606
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Estrogenic activity of 7-hydroxymatairesinol potassium acetate (HMR/lignan) from Norway spruce (Picea abies) knots and of its active metabolite enterolactone in MCF-7 cells.
    Cosentino M; Marino F; Ferrari M; Rasini E; Bombelli R; Luini A; Legnaro M; Delle Canne MG; Luzzani M; Crema F; Paracchini S; Lecchini S
    Pharmacol Res; 2007 Aug; 56(2):140-7. PubMed ID: 17572100
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 9-Norlignans: Occurrence, Properties and Their Semisynthetic Preparation from Hydroxymatairesinol.
    Eklund P; Raitanen JE
    Molecules; 2019 Jan; 24(2):. PubMed ID: 30634427
    [TBL] [Abstract][Full Text] [Related]  

  • 9. In vitro metabolism of plant lignans: new precursors of mammalian lignans enterolactone and enterodiol.
    Heinonen S; Nurmi T; Liukkonen K; Poutanen K; Wähälä K; Deyama T; Nishibe S; Adlercreutz H
    J Agric Food Chem; 2001 Jul; 49(7):3178-86. PubMed ID: 11453749
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Radical carboxyarylation approach to lignans. Total synthesis of (-)-arctigenin, (-)-matairesinol, and related natural products.
    Fischer J; Reynolds AJ; Sharp LA; Sherburn MS
    Org Lett; 2004 Apr; 6(9):1345-8. PubMed ID: 15101738
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structural determinants of plant lignans for the formation of enterolactone in vivo.
    Saarinen NM; Smeds A; Mäkelä SI; Ammälä J; Hakala K; Pihlava JM; Ryhänen EL; Sjöholm R; Santti R
    J Chromatogr B Analyt Technol Biomed Life Sci; 2002 Sep; 777(1-2):311-9. PubMed ID: 12270222
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Measurement of enterolactone and enterodiol, the first mammalian lignans, using stable isotope dilution and gas chromatography mass spectrometry.
    Setchell KD; Lawson AM; McLaughlin LM; Patel S; Kirk DN; Axelson M
    Biomed Mass Spectrom; 1983 Mar; 10(3):227-35. PubMed ID: 6405819
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Influence of different lignan compounds on enterolignan production by Bifidobacterium and Lactobacillus strains.
    Peirotén Á; Gaya P; Álvarez I; Bravo D; Landete JM
    Int J Food Microbiol; 2019 Jan; 289():17-23. PubMed ID: 30193121
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A thirteen week dietary toxicity study with 7-hydroxymatairesinol potassium acetate (HMRlignan) in rats.
    Lina B; Korte H; Nyman L; Unkila M
    Regul Toxicol Pharmacol; 2005 Feb; 41(1):28-38. PubMed ID: 15649825
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Uptake and metabolism of enterolactone and enterodiol by human colon epithelial cells.
    Jansen GH; Arts IC; Nielen MW; Müller M; Hollman PC; Keijer J
    Arch Biochem Biophys; 2005 Mar; 435(1):74-82. PubMed ID: 15680909
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Derivatives of the Lignan 7'-Hydroxymatairesinol with Antioxidant Properties and Enhanced Lipophilicity.
    Moraux T; Dumarçay S; Gérardin P; Gérardin-Charbonnier C
    J Nat Prod; 2017 Jun; 80(6):1783-1790. PubMed ID: 28590734
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Stereoselective synthesis of β-(hydroxymethylaryl/alkyl)-α-methylene-γ-butyrolactones.
    Hodgson DM; Talbot EP; Clark BP
    Org Lett; 2011 May; 13(10):2594-7. PubMed ID: 21488628
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Studies on the metabolism of the plant lignans secoisolariciresinol and matairesinol.
    Niemeyer HB; Honig DM; Kulling SE; Metzler M
    J Agric Food Chem; 2003 Oct; 51(21):6317-25. PubMed ID: 14518962
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chiral separation of the plant lignan matairesinol by capillary electrophoresis.
    Müller U; Mrestani Y; Neubert R; Dräger B
    Electrophoresis; 2008 Sep; 29(17):3582-7. PubMed ID: 18803219
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The plant lignans matairesinol and secoisolariciresinol administered to Min mice do not protect against intestinal tumor formation.
    Pajari AM; Smeds AI; Oikarinen SI; Eklund PC; Sjöholm RE; Mutanen M
    Cancer Lett; 2006 Feb; 233(2):309-14. PubMed ID: 16000235
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.