Search Results - "Land, Edward J."
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Scavenging of Cation Radicals of the Visual Cycle Retinoids by Lutein, Zeaxanthin, Taurine, and Melanin
Published in International journal of molecular sciences (29-12-2023)“…In the retina, retinoids involved in vision are under constant threat of oxidation, and their oxidation products exhibit deleterious properties. Using pulse…”
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2
Scavenging of Retinoid Cation Radicals by Urate, Trolox, and α-, β-, γ-, and δ-Tocopherols
Published in International journal of molecular sciences (07-06-2019)“…Retinoids are present in human tissues exposed to light and under increased risk of oxidative stress, such as the retina and skin. Retinoid cation radicals can…”
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3
Free Radical Coupling of o‑Semiquinones Uncovered
Published in Journal of the American Chemical Society (14-08-2013)“…As a rule, o-semiquinones decay through disproportionation leading to equimolar amounts of catechol and o-quinone products. However, the o-semiquinone 1S…”
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4
Tyrosinase Autoactivation and the Chemistry of ortho-Quinone Amines
Published in Accounts of chemical research (01-05-2003)“…Tyrosinase oxidizes tyrosine to dopaquinone, which undergoes nonenzymatic reactions leading to precursors of melanin pigments. Cyclization of dopaquinone gives…”
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5
Cyclic Structural Motifs in 5,6-Dihydroxyindole Polymerization Uncovered: Biomimetic Modular Buildup of a Unique Five-Membered Macrocycle
Published in Organic letters (16-07-2010)“…An unprecedented 5,6-dihydroxyindole macrocycle (4) featuring a rigid twisted backbone was obtained by biomimetic oxidative cross-coupling of the 2,2′-biindole…”
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6
The Mechanism of Suicide-Inactivation of Tyrosinase: A Substrate Structure Investigation
Published in The Tohoku Journal of Experimental Medicine (2007)“…Tyrosinase is a copper-containing mono-oxygenase, widely distributed in nature, able to catalyze the oxidation of both phenols and catechols to the…”
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7
Evidence Consistent with the Requirement of Cresolase Activity for Suicide Inactivation of Tyrosinase
Published in The Tohoku Journal of Experimental Medicine (01-11-2008)“…Tyrosinase is a mono-oxygenase with a dinuclear copper catalytic center which is able to catalyze both the ortho-hydroxylation of monophenols (cresolase…”
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8
Short-Lived Quinonoid Species from 5,6-Dihydroxyindole Dimers en Route to Eumelanin Polymers: Integrated Chemical, Pulse Radiolytic, and Quantum Mechanical Investigation
Published in Journal of the American Chemical Society (06-12-2006)“…The transient species formed by oxidation of three dimers of 5,6-dihydroxyindole (1), a major building block of the natural biopolymer eumelanin, have been…”
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9
Lack of Visible Chromophore Development in the Pulse Radiolysis Oxidation of 5,6-Dihydroxyindole-2-carboxylic Acid Oligomers: DFT Investigation and Implications for Eumelanin Absorption Properties
Published in Journal of organic chemistry (15-05-2009)“…The structural factors underlying the peculiar optical properties and visible chromophore of eumelanin biopolymers are largely uncharted. It is known that…”
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10
Potency of inhibition of human DNA topoisomerase I by flavones assessed through physicochemical parameters
Published in Free radical biology & medicine (01-10-2011)“…DNA topoisomerases, enzymes involved in DNA replication and transcription, are known as targets for anticancer drugs. Among the various types of topoisomerase…”
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11
Investigation of the anomalous action of 5-hydroxyresorcinol on tyrosinase
Published in Pigment cell and melanoma research (01-07-2016)Get full text
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12
Quinone chemistry and melanogenesis
Published in Methods in enzymology (2004)Get more information
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13
Chemical, Pulse Radiolysis and Density Functional Studies of a New, Labile 5,6-Indolequinone and Its Semiquinone
Published in Journal of organic chemistry (02-03-2007)“…The chemical and spectroscopic characterization of 5,6-indolequinones and their semiquinones, key transient intermediates in the oxidative conversion of…”
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14
Dopamine quinone chemistry: a study of the influence of amide, amidine and guanidine substituents [-NH-CX-Y] on the mode of reaction
Published in Organic & biomolecular chemistry (01-01-2009)“…The influence of N-substituents on the mode of reaction of ortho-quinones generated by oxidation of N-substituted dopamine derivatives has been studied…”
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15
Studies of carotenoid one-electron reduction radicals
Published in Archives of biochemistry and biophysics (15-02-2007)“…The relative reduction potentials of a variety of carotenoids have been established by monitoring the reaction of carotenoid radical anion (CAR1 − ) with…”
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16
Evidence of the Indirect Formation of the Catecholic Intermediate Substrate Responsible for the Autoactivation Kinetics of Tyrosinase
Published in The Journal of biological chemistry (17-10-1997)“…Tyrosinase (EC 1.14.18.1) exhibits unusual kinetic properties in the oxidation of monohydric phenol substrates consisting of a lag period that increases with…”
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17
Carotenoid Radical Anions and Their Protonated Derivatives
Published in Organic letters (14-09-2006)“…In this study, we report the protonation reactions for astaxanthin and canthaxanthin radical anions in methanol, alkaline methanol, and aqueous 2% Triton X-100…”
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18
Pulse radiolysis study of the interaction of retinoids with peroxyl radicals
Published in Free radical biology & medicine (15-11-2005)“…Vitamin A (retinol) and its derivatives—retinal and retinoic acid—are known for their ability to inhibit lipid peroxidation. Antioxidant actions of retinoids…”
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Relative One-Electron Reduction Potentials of Carotenoid Radical Cations and the Interactions of Carotenoids with the Vitamin E Radical Cation
Published in Journal of the American Chemical Society (06-05-1998)“…Pulse radiolysis studies have been used to determine the electron-transfer rate constants between various pairs of carotenoids, one of which is present as the…”
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20
An MO study of regioselective amine addition to ortho-quinones relevant to melanogenesis
Published in Tetrahedron (15-05-2006)“…Energy profiles for alternative intramolecular cyclisations of 4-(aminoalkyl)- ortho-quinones have been calculated using the AM1 method and ab initio energies…”
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