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Journal Abstract Search

190 related items for PubMed ID: 7726864

  • 21. Possible role of salsolinol quinone methide in the decrease of RCSN-3 cell survival.
    Martinez-Alvarado P, Dagnino-Subiabre A, Paris I, Metodiewa D, Welch CJ, Olea-Azar C, Caviedes P, Caviedes R, Segura-Aguilar J.
    Biochem Biophys Res Commun; 2001 May 25; 283(5):1069-76. PubMed ID: 11355881
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  • 22. Laccase--and not tyrosinase--is the enzyme responsible for quinone methide production from 2,6-dimethoxy-4-allyl phenol.
    Sugumaran M, Bolton JL.
    Arch Biochem Biophys; 1998 May 15; 353(2):207-12. PubMed ID: 9606954
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  • 23. Electronic and structural requirements for metabolic activation of butylated hydroxytoluene analogs to their quinone methides, intermediates responsible for lung toxicity in mice.
    Yamamoto K, Kato S, Tajima K, Mizutani T.
    Biol Pharm Bull; 1997 May 15; 20(5):571-3. PubMed ID: 9178942
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  • 24. Modeling H-bonding and solvent effects in the alkylation of pyrimidine bases by a prototype quinone methide: a DFT study.
    Freccero M, Di Valentin C, Sarzi-Amadè M, DFT study.
    J Am Chem Soc; 2003 Mar 26; 125(12):3544-53. PubMed ID: 12643716
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  • 25. Chemistry of pyrrolo[1,2-a]indole- and pyrido[1,2-a]indole-based quinone methides. Mechanistic explanations for differences in cytostatic/cytotoxic properties.
    Khdour O, Skibo EB.
    J Org Chem; 2007 Nov 09; 72(23):8636-47. PubMed ID: 17927245
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  • 26. Substituent effects on carbocation stability: the pK(R) for p-quinone methide.
    Toteva MM, Moran M, Amyes TL, Richard JP.
    J Am Chem Soc; 2003 Jul 23; 125(29):8814-9. PubMed ID: 12862476
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  • 27. Trapping phosphodiester-quinone methide adducts through in situ lactonization.
    Zhou Q, Turnbull KD.
    J Org Chem; 2000 Apr 07; 65(7):2022-9. PubMed ID: 10774022
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  • 29. 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 Apr 07; 8(1):55-60. PubMed ID: 7703367
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  • 30. Comparative toxicity of eugenol and its quinone methide metabolite in cultured liver cells using kinetic fluorescence bioassays.
    Thompson DC, Barhoumi R, Burghardt RC.
    Toxicol Appl Pharmacol; 1998 Mar 07; 149(1):55-63. PubMed ID: 9512727
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  • 31. Biological and toxicological consequences of quinone methide formation.
    Thompson DC, Thompson JA, Sugumaran M, Moldéus P.
    Chem Biol Interact; 1993 Feb 07; 86(2):129-62. PubMed ID: 8448810
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  • 32. Syntheses and absolute stereochemistries of UPA0043 and UPA0044, cytotoxic antibiotics having a p-quinone-methide structure.
    Takao KI, Sasaki T, Kozaki T, Yanagisawa Y, Tadano KI, Kawashima A, Shinonaga H.
    Org Lett; 2001 Dec 27; 3(26):4291-4. PubMed ID: 11784200
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  • 33. 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 27; 14(12):1643-53. PubMed ID: 11743747
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  • 34. 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 27; 8(4):537-44. PubMed ID: 7548733
    [Abstract] [Full Text] [Related]

  • 35. Taming reactive phenol tautomers and o-quinone methides with transition metals: a structure-reactivity relationship.
    Amouri H, Le Bras J.
    Acc Chem Res; 2002 Jul 27; 35(7):501-10. PubMed ID: 12118989
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