British Journal of Dermatology · 1981 · 128 citations · 10 references
AgricultureBiochemistryFood ScienceEnzymologyFood ChemistryStructure-activity RelationshipsColor ChemistryEnzyme InhibitionPhenolic Compound AnalysisCompetitive InhibitionElectron-donating GroupsElectron-withdrawing GroupsNatural Food PreservativesPhenolic CompoundsPhenolic Substrates
In order to investigate the molecular basis of substrates, and the inhibitory specificity of tyrosinase, a large series of phenolic compounds have been analysed by using a High Performance Liquid Chromatographic-Scanning Spectrophotometric system. Depending on their chemical structure, phenolic compounds may act as substrates or as competitive inhibitors of tyrosinase. The ability to act as substrates requires the presence in the molecule of electron donor groups, while competitive inhibition on the contrary requires the presence of powerful electron acceptor groups. Certain phenolic compounds used as therapeutic agents or as food preservatives are chemically capable of acting as alternative substrates or competitive inhibitors of tyrosinase in vitro; their effect on melanocytes in vivo therefore merits investigation.
10
Mechanism of Depigmentation by Hydroquinone
Kowichi Jimbow, Hiroko Obata, Madhu A. Pathak et al. · Journal of Investigative Dermatology · 1974 · 321 citations · Full text
Particulate Tyrosinase of Human Malignant Melanoma
Kenji Nishioka · European Journal of Biochemistry · 1978 · 118 citations
Hydroxyanisole depigmentation: In‐vitro studies
Patrick A. Riley · The Journal of Pathology · 1969 · 99 citations