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Furthermore, other compounds such as bi-pyridine derivatives 122 , two thiadiazole derivatives 44 barbarin 123 , chlorocinnamic acids 124 , propanoic acid 125 , some N-(mono- or dihydroxybenzyl)-N-nitrosohydroxylamines 126 and p- alkylbenzaldehydes 127 inhibited catecholase activity of mushroom tyrosinase uncompetitively

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381 This oxidizing environment is enabled by systems of enzymes that maintain the redox potential and assist with the formation of the correct disulfide linkages