BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 12859624)

  • 1. 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]  

  • 2. Tyrosinase autoactivation and the chemistry of ortho-quinone amines.
    Land EJ; Ramsden CA; Riley PA
    Acc Chem Res; 2003 May; 36(5):300-8. PubMed ID: 12755639
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Mechanistic aspects of the tyrosinase oxidation of hydroquinone.
    Ramsden CA; Riley PA
    Bioorg Med Chem Lett; 2014 Jun; 24(11):2463-4. PubMed ID: 24767847
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Catalytic oxidation of 2-aminophenols and ortho hydroxylation of aromatic amines by tyrosinase.
    Toussaint O; Lerch K
    Biochemistry; 1987 Dec; 26(26):8567-71. PubMed ID: 2964867
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Tyrosinase: the four oxidation states of the active site and their relevance to enzymatic activation, oxidation and inactivation.
    Ramsden CA; Riley PA
    Bioorg Med Chem; 2014 Apr; 22(8):2388-95. PubMed ID: 24656803
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Model sclerotization studies. 4. Generation of N-acetylmethionyl catechol adducts during tyrosinase-catalyzed oxidation of catechols in the presence of N-acetylmethionine.
    Sugumaran M; Nelson E
    Arch Insect Biochem Physiol; 1998; 38(1):44-52. PubMed ID: 9589603
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mechanistic studies of melanogenesis: the influence of N-substitution on dopamine quinone cyclization.
    Borovansky J; Edge R; Land EJ; Navaratnam S; Pavel S; Ramsden CA; Riley PA; Smit NP
    Pigment Cell Res; 2006 Apr; 19(2):170-8. PubMed ID: 16524433
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Formation of a new quinone methide intermediate during the oxidative transformation of 3,4-dihydroxyphenylacetic acids: implication for eumelanin biosynthesis.
    Sugumaran M; Duggaraju P; Jayachandran E; Kirk KL
    Arch Biochem Biophys; 1999 Nov; 371(1):98-106. PubMed ID: 10525294
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. The Metabolic Fate of ortho-Quinones Derived from Catecholamine Metabolites.
    Ito S; Yamanaka Y; Ojika M; Wakamatsu K
    Int J Mol Sci; 2016 Jan; 17(2):. PubMed ID: 26828480
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Oxidation of 3,4-dihydroxybenzylamine affords 3,4-dihydroxybenzaldehyde via the quinone methide intermediate.
    Sugumaran M
    Pigment Cell Res; 1995 Oct; 8(5):250-4. PubMed ID: 8789199
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence consistent with the requirement of cresolase activity for suicide inactivation of tyrosinase.
    Land EJ; Ramsden CA; Riley PA; Stratford MR
    Tohoku J Exp Med; 2008 Nov; 216(3):231-8. PubMed ID: 18987457
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 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. Tyrosinase-catalyzed oxidation of dopa and related catechol(amine)s: a kinetic electron spin resonance investigation using spin-stabilization and spin label oximetry.
    Korytowski W; Sarna T; Kalyanaraman B; Sealy RC
    Biochim Biophys Acta; 1987 Jun; 924(3):383-92. PubMed ID: 3036239
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.