162 related articles for article (PubMed ID: 7578916)
1. o-Methoxy-4-alkylphenols that form quinone methides of intermediate reactivity are the most toxic in rat liver slices.
Thompson DC; Perera K; Krol ES; Bolton JL
Chem Res Toxicol; 1995; 8(3):323-7. PubMed ID: 7578916
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. The enzymatic formation and chemical reactivity of quinone methides correlate with alkylphenol-induced toxicity in rat hepatocytes.
Bolton JL; Valerio LG; Thompson JA
Chem Res Toxicol; 1992; 5(6):816-22. PubMed ID: 1489934
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Influence of quinone methide reactivity on the alkylation of thiol and amino groups in proteins: studies utilizing amino acid and peptide models.
Bolton JL; Turnipseed SB; Thompson JA
Chem Biol Interact; 1997 Nov; 107(3):185-200. PubMed ID: 9448752
[TBL] [Abstract][Full Text] [Related]
7. Oxidation of 4-alkylphenols and catechols by tyrosinase: ortho-substituents alter the mechanism of quinoid formation.
Krol ES; Bolton JL
Chem Biol Interact; 1997 Apr; 104(1):11-27. PubMed ID: 9158692
[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. Comparative metabolism, covalent binding and toxicity of BHT congeners in rat liver slices.
Reed M; Fujiwara H; Thompson DC
Chem Biol Interact; 2001 Nov; 138(2):155-70. PubMed ID: 11672698
[TBL] [Abstract][Full Text] [Related]
10. Mechanism of isomerization of 4-propyl-o-quinone to its tautomeric p-quinone methide.
Bolton JL; Wu HM; Hu LQ
Chem Res Toxicol; 1996; 9(1):109-113. PubMed ID: 8924578
[TBL] [Abstract][Full Text] [Related]
11. Quinone methide formation from para isomers of methylphenol (cresol), ethylphenol, and isopropylphenol: relationship to toxicity.
Thompson DC; Perera K; London R
Chem Res Toxicol; 1995; 8(1):55-60. PubMed ID: 7703367
[TBL] [Abstract][Full Text] [Related]
12. Evidence that 4-allyl-o-quinones spontaneously rearrange to their more electrophilic quinone methides: potential bioactivation mechanism for the hepatocarcinogen safrole.
Bolton JL; Acay NM; Vukomanovic V
Chem Res Toxicol; 1994; 7(3):443-50. PubMed ID: 8075378
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Role of quinone methide in the in vitro toxicity of the skin tumor promoter butylated hydroxytoluene hydroperoxide.
Guyton KZ; Thompson JA; Kensler TW
Chem Res Toxicol; 1993; 6(5):731-8. PubMed ID: 8292753
[TBL] [Abstract][Full Text] [Related]
15. Biological and toxicological consequences of quinone methide formation.
Thompson DC; Thompson JA; Sugumaran M; Moldéus P
Chem Biol Interact; 1993 Feb; 86(2):129-62. PubMed ID: 8448810
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Dual reactivity of hydroxy- and methoxy- substituted o-quinone methides in aqueous solutions: hydration versus tautomerization.
Arumugam S; Popik VV
J Org Chem; 2010 Nov; 75(21):7338-46. PubMed ID: 20925363
[TBL] [Abstract][Full Text] [Related]
18. Skin sensitization to eugenol and isoeugenol in mice: possible metabolic pathways involving ortho-quinone and quinone methide intermediates.
Bertrand F; Basketter DA; Roberts DW; Lepoittevin JP
Chem Res Toxicol; 1997 Mar; 10(3):335-43. PubMed ID: 9084914
[TBL] [Abstract][Full Text] [Related]
19. Inhibition of mitochondrial respiration by a para-quinone methide.
Thompson DC; Perera K
Biochem Biophys Res Commun; 1995 Apr; 209(1):6-11. PubMed ID: 7726864
[TBL] [Abstract][Full Text] [Related]
20. Evidence for NQO1 and NQO2 catalyzed reduction of ortho- and para-quinone methides.
Kucera HR; Livingstone M; Moscoso CG; Gaikwad NW
Free Radic Res; 2013 Dec; 47(12):1016-26. PubMed ID: 24074361
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
