119 related articles for article (PubMed ID: 21982895)
1. An essential difference in the reactivity of the glutathione adducts of the structurally closely related flavonoids monoHER and quercetin.
Jacobs H; Moalin M; van Gisbergen MW; Bast A; van der Vijgh WJ; Haenen GR
Free Radic Biol Med; 2011 Dec; 51(11):2118-23. PubMed ID: 21982895
[TBL] [Abstract][Full Text] [Related]
2. An essential difference between the flavonoids monoHER and quercetin in their interplay with the endogenous antioxidant network.
Jacobs H; Moalin M; Bast A; van der Vijgh WJ; Haenen GR
PLoS One; 2010 Nov; 5(11):e13880. PubMed ID: 21079733
[TBL] [Abstract][Full Text] [Related]
3. Characterization of the glutathione conjugate of the semisynthetic flavonoid monoHER.
Jacobs H; van der Vijgh WJ; Koek GH; Draaisma GJ; Moalin M; van Strijdonck GP; Bast A; Haenen GR
Free Radic Biol Med; 2009 Jun; 46(12):1567-73. PubMed ID: 19272444
[TBL] [Abstract][Full Text] [Related]
4. Quenching of quercetin quinone/quinone methides by different thiolate scavengers: stability and reversibility of conjugate formation.
Awad HM; Boersma MG; Boeren S; Van Bladeren PJ; Vervoort J; Rietjens IM
Chem Res Toxicol; 2003 Jul; 16(7):822-31. PubMed ID: 12870884
[TBL] [Abstract][Full Text] [Related]
5. The reversibility of the glutathionyl-quercetin adduct spreads oxidized quercetin-induced toxicity.
Boots AW; Balk JM; Bast A; Haenen GR
Biochem Biophys Res Commun; 2005 Dec; 338(2):923-9. PubMed ID: 16246300
[TBL] [Abstract][Full Text] [Related]
6. Identification of the metabolites of the antioxidant flavonoid 7-mono-O-(β-hydroxyethyl)-rutoside in mice.
Jacobs H; Peters R; den Hartog GJ; van der Vijgh WJ; Bast A; Haenen GR
Drug Metab Dispos; 2011 May; 39(5):750-6. PubMed ID: 21266594
[TBL] [Abstract][Full Text] [Related]
7. The contribution of the major metabolite 4'-O-methylmonoHER to the antioxidant activity of the flavonoid monoHER.
Lemmens KJ; Herst PM; Housmans BA; Moalin M; van der Vijgh WJ; Bast A; Haenen GR
Chem Biol Interact; 2015 Sep; 239():146-52. PubMed ID: 26163455
[TBL] [Abstract][Full Text] [Related]
8. The flavonoid 7-mono-O-(β-hydroxyethyl)-rutoside is able to protect endothelial cells by a direct antioxidant effect.
Lemmens KJ; van de Wier B; Vaes N; Ghosh M; van Zandvoort MA; van der Vijgh WJ; Bast A; Haenen GR
Toxicol In Vitro; 2014 Jun; 28(4):538-43. PubMed ID: 24412621
[TBL] [Abstract][Full Text] [Related]
9. Peroxidase-catalyzed formation of quercetin quinone methide-glutathione adducts.
Awad HM; Boersma MG; Vervoort J; Rietjens IM
Arch Biochem Biophys; 2000 Jun; 378(2):224-33. PubMed ID: 10860540
[TBL] [Abstract][Full Text] [Related]
10. Competition between ascorbate and glutathione for the oxidized form of methylated quercetin metabolites and analogues: tamarixetin, 4'O-methylquercetin, has the lowest thiol reactivity.
Moalin M; van Strijdonck GP; Bast A; Haenen GR
J Agric Food Chem; 2012 Sep; 60(36):9292-7. PubMed ID: 22860763
[TBL] [Abstract][Full Text] [Related]
11. Differences in pharmacological activities of the antioxidant flavonoid monoHER in humans and mice are caused by variations in its metabolic profile.
Jacobs H; Koek GH; Peters R; Moalin M; Tack J; van der Vijgh WJ; Bast A; Haenen GR
Clin Pharmacol Ther; 2011 Dec; 90(6):852-9. PubMed ID: 22048223
[TBL] [Abstract][Full Text] [Related]
12. Oxidized quercetin reacts with thiols rather than with ascorbate: implication for quercetin supplementation.
Boots AW; Kubben N; Haenen GR; Bast A
Biochem Biophys Res Commun; 2003 Aug; 308(3):560-5. PubMed ID: 12914787
[TBL] [Abstract][Full Text] [Related]
13. The regioselectivity of glutathione adduct formation with flavonoid quinone/quinone methides is pH-dependent.
Awad HM; Boersma MG; Boeren S; van Bladeren PJ; Vervoort J; Rietjens IM
Chem Res Toxicol; 2002 Mar; 15(3):343-51. PubMed ID: 11896681
[TBL] [Abstract][Full Text] [Related]
14. The semisynthetic flavonoid monoHER sensitises human soft tissue sarcoma cells to doxorubicin-induced apoptosis via inhibition of nuclear factor-κB.
Jacobs H; Bast A; Peters GJ; van der Vijgh WJ; Haenen GR
Br J Cancer; 2011 Feb; 104(3):437-40. PubMed ID: 21245867
[TBL] [Abstract][Full Text] [Related]
15. The maize benzoxazinone DIMBOA reacts with glutathione and other thiols to form spirocyclic adducts.
Dixon DP; Sellars JD; Kenwright AM; Steel PG
Phytochemistry; 2012 May; 77():171-8. PubMed ID: 22342783
[TBL] [Abstract][Full Text] [Related]
16. Polycyclic aromatic hydrocarbon (PAH) ortho-quinone conjugate chemistry: kinetics of thiol addition to PAH ortho-quinones and structures of thioether adducts of naphthalene-1,2-dione.
Murty VS; Penning TM
Chem Biol Interact; 1992 Sep; 84(2):169-88. PubMed ID: 1394622
[TBL] [Abstract][Full Text] [Related]
17. The thiol reactivity of the oxidation product of 3,5,7-trihydroxy-4H-chromen-4-one containing flavonoids.
Michels G; Haenen GR; Wätjen W; Rietjens S; Bast A
Toxicol Lett; 2004 Jun; 151(1):105-11. PubMed ID: 15177646
[TBL] [Abstract][Full Text] [Related]
18. Monohydroxyethylrutoside, a dose-dependent cardioprotective agent, does not affect the antitumor activity of doxorubicin.
van Acker SA; Boven E; Kuiper K; van den Berg DJ; Grimbergen JA; Kramer K; Bast A; van der Vijgh WJ
Clin Cancer Res; 1997 Oct; 3(10):1747-54. PubMed ID: 9815559
[TBL] [Abstract][Full Text] [Related]
19. Identification and quantification of adducts between oxidized rosmarinic acid and thiol compounds by UHPLC-LTQ-Orbitrap and MALDI-TOF/TOF tandem mass spectrometry.
Tang CB; Zhang WG; Dai C; Li HX; Xu XL; Zhou GH
J Agric Food Chem; 2015 Jan; 63(3):902-11. PubMed ID: 25541907
[TBL] [Abstract][Full Text] [Related]
20. Peroxidative metabolism of apigenin and naringenin versus luteolin and quercetin: glutathione oxidation and conjugation.
Galati G; Moridani MY; Chan TS; O'Brien PJ
Free Radic Biol Med; 2001 Feb; 30(4):370-82. PubMed ID: 11182292
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]