|
Volumn 269, Issue 16, 2002, Pages 4098-4104
|
Redox reaction between amino-(3,4-dihydroxyphenyl)methyl phosphonic acid and dopaquinone is responsible for the apparent inhibitory effect on tyrosinase
|
Author keywords
3,4 dihydroxybenzaldehyde; Phosphonic amino acids; Quinone; Redox exchange; Tyrosinase
|
Indexed keywords
3,4 DIHYDROXYPHENYLETHYLENE GLYCOL;
ALPHA AMINO 3,4 DIHYDROXYBENZYLPHOSPHONIC ACID;
ALPHA AMINO 4 HYDROXYBENZYLPHOSPHONIC ACID;
DOPA;
DOPACHROME;
DOPAQUINONE;
MONOPHENOL MONOOXYGENASE;
OXFENICINE;
PHOSPHINIC ACID DERIVATIVE;
PROTOCATECHUALDEHYDE;
QUINONE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
COMPETITIVE INHIBITION;
DECOMPOSITION;
ELECTROCHEMICAL ANALYSIS;
ENZYME INACTIVATION;
ENZYME SUBSTRATE;
INHIBITION KINETICS;
OXIDATION;
OXIDATION REDUCTION POTENTIAL;
OXIDATION REDUCTION REACTION;
PRIORITY JOURNAL;
SEQUENCE HOMOLOGY;
SPECTROSCOPY;
ULTRAVIOLET SPECTROPHOTOMETRY;
AGARICALES;
BENZOQUINONES;
DIHYDROXYPHENYLALANINE;
ENZYME INHIBITORS;
MODELS, CHEMICAL;
MONOPHENOL MONOOXYGENASE;
OXIDATION-REDUCTION;
OXYGEN;
PHOSPHONIC ACIDS;
PLANT PROTEINS;
POLAROGRAPHY;
SPECTROPHOTOMETRY;
|
EID: 0036042181
PISSN: 00142956
EISSN: None
Source Type: Journal
DOI: 10.1046/j.1432-1033.2002.03103.x Document Type: Article |
Times cited : (15)
|
References (35)
|