174 related articles for article (PubMed ID: 10725115)
1. Regioselectivity and reversibility of the glutathione conjugation of quercetin quinone methide.
Boersma MG; Vervoort J; Szymusiak H; Lemanska K; Tyrakowska B; Cenas N; Segura-Aguilar J; Rietjens IM
Chem Res Toxicol; 2000 Mar; 13(3):185-91. PubMed ID: 10725115
[TBL] [Abstract][Full Text] [Related]
2. Identification of o-quinone/quinone methide metabolites of quercetin in a cellular in vitro system.
Awad HM; Boersma MG; Boeren S; van der Woude H; van Zanden J; van Bladeren PJ; Vervoort J; Rietjens IM
FEBS Lett; 2002 Jun; 520(1-3):30-4. PubMed ID: 12044865
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Structure-activity study on the quinone/quinone methide chemistry of flavonoids.
Awad HM; Boersma MG; Boeren S; van Bladeren PJ; Vervoort J; Rietjens IM
Chem Res Toxicol; 2001 Apr; 14(4):398-408. PubMed ID: 11304128
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Bioactivation of tamoxifen to metabolite E quinone methide: reaction with glutathione and DNA.
Fan PW; Bolton JL
Drug Metab Dispos; 2001 Jun; 29(6):891-6. PubMed ID: 11353759
[TBL] [Abstract][Full Text] [Related]
8. p-Quinone methides are the major decomposition products of catechol estrogen o-quinones.
Bolton JL; Shen L
Carcinogenesis; 1996 May; 17(5):925-9. PubMed ID: 8640939
[TBL] [Abstract][Full Text] [Related]
9. The influence of 4-alkyl substituents on the formation and reactivity of 2-methoxy-quinone methides: evidence that extended pi-conjugation dramatically stabilizes the quinone methide formed from eugenol.
Bolton JL; Comeau E; Vukomanovic V
Chem Biol Interact; 1995 Apr; 95(3):279-90. PubMed ID: 7728898
[TBL] [Abstract][Full Text] [Related]
10. 4-Hydroxylated metabolites of the antiestrogens tamoxifen and toremifene are metabolized to unusually stable quinone methides.
Fan PW; Zhang F; Bolton JL
Chem Res Toxicol; 2000 Jan; 13(1):45-52. PubMed ID: 10649966
[TBL] [Abstract][Full Text] [Related]
11. The influence of the p-alkyl substituent on the isomerization of o-quinones to p-quinone methides: potential bioactivation mechanism for catechols.
Iverson SL; Hu LQ; Vukomanovic V; Bolton JL
Chem Res Toxicol; 1995 Jun; 8(4):537-44. PubMed ID: 7548733
[TBL] [Abstract][Full Text] [Related]
12. Bioactivation of estrone and its catechol metabolites to quinoid-glutathione conjugates in rat liver microsomes.
Iverson SL; Shen L; Anlar N; Bolton JL
Chem Res Toxicol; 1996 Mar; 9(2):492-9. PubMed ID: 8839054
[TBL] [Abstract][Full Text] [Related]
13. Identification of tamoxifen-DNA adducts formed by 4-hydroxytamoxifen quinone methide.
Marques MM; Beland FA
Carcinogenesis; 1997 Oct; 18(10):1949-54. PubMed ID: 9364005
[TBL] [Abstract][Full Text] [Related]
14. Synthesis and reactivity of potential toxic metabolites of tamoxifen analogues: droloxifene and toremifene o-quinones.
Yao D; Zhang F; Yu L; Yang Y; van Breemen RB; Bolton JL
Chem Res Toxicol; 2001 Dec; 14(12):1643-53. PubMed ID: 11743747
[TBL] [Abstract][Full Text] [Related]
15. Oxidation of eugenol to form DNA adducts and 8-hydroxy-2'-deoxyguanosine: role of quinone methide derivative in DNA adduct formation.
Bodell WJ; Ye Q; Pathak DN; Pongracz K
Carcinogenesis; 1998 Mar; 19(3):437-43. PubMed ID: 9525278
[TBL] [Abstract][Full Text] [Related]
16. Glutathione transferase M2-2 catalyzes conjugation of dopamine and dopa o-quinones.
Dagnino-Subiabre A; Cassels BK; Baez S; Johansson AS; Mannervik B; Segura-Aguilar J
Biochem Biophys Res Commun; 2000 Jul; 274(1):32-6. PubMed ID: 10903891
[TBL] [Abstract][Full Text] [Related]
17. Consequences of quercetin methylation for its covalent glutathione and DNA adduct formation.
van der Woude H; Boersma MG; Alink GM; Vervoort J; Rietjens IM
Chem Biol Interact; 2006 Apr; 160(3):193-203. PubMed ID: 16516181
[TBL] [Abstract][Full Text] [Related]
18. The reactivity of o-quinones which do not isomerize to quinone methides correlates with alkylcatechol-induced toxicity in human melanoma cells.
Bolton JL; Pisha E; Shen L; Krol ES; Iverson SL; Huang Z; van Breemen RB; Pezzuto JM
Chem Biol Interact; 1997 Sep; 106(2):133-48. PubMed ID: 9366899
[TBL] [Abstract][Full Text] [Related]
19. Spontaneous hydrolysis of 4-trifluoromethylphenol to a quinone methide and subsequent protein alkylation.
Thompson DC; Perera K; London R
Chem Biol Interact; 2000 Apr; 126(1):1-14. PubMed ID: 10826650
[TBL] [Abstract][Full Text] [Related]
20. A study on the in vitro interaction between tyrosinase and glutathione S-transferase.
Miranda M; di Ilio C; Bonfigli A; Arcadi A; Pitari G; Dupre S; Federici G; del Boccio G
Biochim Biophys Acta; 1987 Jul; 913(3):386-94. PubMed ID: 3109490
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]