146 related articles for article (PubMed ID: 1337996)
1. Reactivity of orthoquinones involved in tyrosinase-dependent cytotoxicity: differences between alkylthio- and alkoxy-substituents.
Cooksey CJ; Jimbow K; Land EJ; Riley PA
Melanoma Res; 1992 Dec; 2(5-6):283-93. PubMed ID: 1337996
[TBL] [Abstract][Full Text] [Related]
2. Tyrosinase-mediated cytotoxicity of 4-substituted phenols: quantitative structure-thiol-reactivity relationships of the derived o-quinones.
Cooksey CJ; Land EJ; Ramsden CA; Riley PA
Anticancer Drug Des; 1995 Mar; 10(2):119-29. PubMed ID: 7710634
[TBL] [Abstract][Full Text] [Related]
3. Melanogenesis-targeted anti-melanoma pro-drug development: effect of side-chain variations on the cytotoxicity of tyrosinase-generated ortho-quinones in a model screening system.
Riley PA; Cooksey CJ; Johnson CI; Land EJ; Latter AM; Ramsden CA
Eur J Cancer; 1997 Jan; 33(1):135-43. PubMed ID: 9071913
[TBL] [Abstract][Full Text] [Related]
4. Chemical Reactivities of
Ito S; Sugumaran M; Wakamatsu K
Int J Mol Sci; 2020 Aug; 21(17):. PubMed ID: 32846902
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. A cell-based evaluation of human tyrosinase-mediated metabolic activation of leukoderma-inducing phenolic compounds.
Nishimaki-Mogami T; Ito S; Cui H; Akiyama T; Tamehiro N; Adachi R; Wakamatsu K; Ikarashi Y; Kondo K
J Dermatol Sci; 2022 Nov; 108(2):77-86. PubMed ID: 36567223
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Tyrosinase kinetics: failure of the auto-activation mechanism of monohydric phenol oxidation by rapid formation of a quinomethane intermediate.
Cooksey CJ; Garratt PJ; Land EJ; Ramsden CA; Riley PA
Biochem J; 1998 Aug; 333 ( Pt 3)(Pt 3):685-91. PubMed ID: 9677329
[TBL] [Abstract][Full Text] [Related]
10. Evidence of the indirect formation of the catecholic intermediate substrate responsible for the autoactivation kinetics of tyrosinase.
Cooksey CJ; Garratt PJ; Land EJ; Pavel S; Ramsden CA; Riley PA; Smit NP
J Biol Chem; 1997 Oct; 272(42):26226-35. PubMed ID: 9334191
[TBL] [Abstract][Full Text] [Related]
11. Radicals and melanomas.
Riley PA
Philos Trans R Soc Lond B Biol Sci; 1985 Dec; 311(1152):679-89. PubMed ID: 2869525
[TBL] [Abstract][Full Text] [Related]
12. Analysis and interpretation of the action mechanism of mushroom tyrosinase on monophenols and diphenols generating highly unstable o-quinones.
Fenoll LG; Rodríguez-López JN; García-Sevilla F; García-Ruiz PA; Varón R; García-Cánovas F; Tudela J
Biochim Biophys Acta; 2001 Jul; 1548(1):1-22. PubMed ID: 11451433
[TBL] [Abstract][Full Text] [Related]
13. Pulse radiolysis studies of ortho-quinone chemistry relevant to melanogenesis.
Land EJ; Ramsden CA; Riley PA
J Photochem Photobiol B; 2001 Nov; 64(2-3):123-35. PubMed ID: 11744399
[TBL] [Abstract][Full Text] [Related]
14. Reaction between ortho-semiquinones and oxygen: pulse radiolysis, electron spin resonance, and oxygen uptake studies.
Kalyanaraman B; Korytowski W; Pilas B; Sarna T; Land EJ; Truscott TG
Arch Biochem Biophys; 1988 Oct; 266(1):277-84. PubMed ID: 2845864
[TBL] [Abstract][Full Text] [Related]
15. In vitro assessment of the structure-activity relationship of tyrosinase-dependent cytotoxicity of a series of substituted phenols.
Naish-Byfield S; Cooksey CJ; Latter AM; Johnson CI; Riley PA
Melanoma Res; 1991; 1(4):273-87. PubMed ID: 1823634
[TBL] [Abstract][Full Text] [Related]
16. Mechanistic studies of catechol generation from secondary quinone amines relevant to indole formation and tyrosinase activation.
Land EJ; Ramsden CA; Riley PA; Yoganathan G
Pigment Cell Res; 2003 Aug; 16(4):397-406. PubMed ID: 12859624
[TBL] [Abstract][Full Text] [Related]
17. Oxidation by mushroom tyrosinase of monophenols generating slightly unstable o-quinones.
Fenoll LG; Rodríguez-López JN; García-Sevilla F; Tudela J; García-Ruiz PA; Varón R; García-Cánovas F
Eur J Biochem; 2000 Oct; 267(19):5865-78. PubMed ID: 10998046
[TBL] [Abstract][Full Text] [Related]
18. Studies on the reactions between human tyrosinase, superoxide anion, hydrogen peroxide and thiols.
Wood JM; Schallreuter KU
Biochim Biophys Acta; 1991 Aug; 1074(3):378-85. PubMed ID: 1653610
[TBL] [Abstract][Full Text] [Related]
19. Tyrosinase-catalyzed oxidation of rhododendrol produces 2-methylchromane-6,7-dione, the putative ultimate toxic metabolite: implications for melanocyte toxicity.
Ito S; Ojika M; Yamashita T; Wakamatsu K
Pigment Cell Melanoma Res; 2014 Sep; 27(5):744-53. PubMed ID: 24903082
[TBL] [Abstract][Full Text] [Related]
20. Inhibition of reverse transcriptase by tyrosinase generated quinones related to levodopa and dopamine.
Wick MM; Fitzgerald G
Chem Biol Interact; 1981 Dec; 38(1):99-107. PubMed ID: 6173137
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]