Complex inhibition of tyrosinase by thiol-composed cu2+ Chelators: A Clue for Designing Whitening Agents

Journal of Biomolecular Structure and Dynamics

Volumn 24, Issue 2, 2006, Pages 131-138

  Park, Yong Doo ^a,b   Lyou, You Jeong ^b   Hahn, Hwa Sun ^a   Hahn, Myong Joon ^a   Yang, Jun Mo ^a,b  

^a Sungkyunkwan University School of Medicine   (South Korea)

^b Samsung Medical Center   (South Korea)

Author keywords

Complex inhibition; Cu2+ chelator; Dithioglycerine; Inhibition kinetics; Tyrosinase

Indexed keywords

CHELATING AGENT; COPPER ION; COSMETIC; DITHIOGLYCERINE; MONOPHENOL MONOOXYGENASE; THIOL DERIVATIVE; UNCLASSIFIED DRUG; WHITENING AGENT;

ARTICLE; BINDING AFFINITY; CELL STRAIN HEK293; CHEMICAL MODIFICATION; CONTROLLED STUDY; DRUG DESIGN; DRUG SCREENING; EMBRYO; ENZYME ACTIVE SITE; ENZYME INHIBITION; ENZYME INHIBITOR INTERACTION; GENE OVEREXPRESSION; HUMAN; HUMAN CELL; INHIBITION KINETICS; MUSHROOM; NONHUMAN; PRIORITY JOURNAL;

CELLS, CULTURED; CHELATING AGENTS; COPPER; GLYCEROL; HUMANS; MODELS, CHEMICAL; MONOPHENOL MONOOXYGENASE; SULFHYDRYL COMPOUNDS;

BASIDIOMYCOTA;

EID: 33749989366     PISSN: 07391102     EISSN: 15380254     Source Type: Journal    
DOI: 10.1080/07391102.2006.10507106     Document Type: Article

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