Recueil des Travaux Chimiques des Pays-Bas · 1939 · 29 citations · 10 references
Life SciencesBiochemistryDermatologyEnzymologyMetabolismRedox BiochemistryColor ChemistryTannin ChemistryMelanin BiosynthesisMelanin ChemistryMelanin FormationMelanin SynthesisSkin Tannins
Abstract According to Raper's hypothesis, the quinone of 5:6‐dihydroxy‐2:3‐dihydroindole‐2‐carboxylic acid is the red coloured precursor of melanin, obtained by the oxidation of tyrosine with tyrosinase. This paper deals with some derivatives of this “red substance”, the structure of which is still unknown, with phenylhydrazine and substituted phenylhydrazines. No reaction products could be isolated, however, with hydroxylamine, or with semicarbazide. In connection with observations of Jacobs and of Breijer attention is drawn to the fact, that the “red substance” may be of importance as an anti‐pernicious principle and that premelanin of the skin‐epidermis possibly plays a rôle in blood formation.
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Henry Stanley Raper · Physiological Reviews · 1928 · 369 citations
The Tyrosinase-tyrosine Reaction
Henry Stanley Raper · Biochemical Journal · 1927 · 308 citations · Full text
The Tyrosinase-Tyrosine Reaction
Henry Stanley Raper · Biochemical Journal · 1926 · 155 citations · Full text
The Tyrosinase-Tyrosine Reaction
Henry Stanley Raper, A. Wormall · Biochemical Journal · 1923 · 109 citations · Full text
The tyrosinase-tyrosine reaction
Walter Louis Dulière, Henry Stanley Raper · Biochemical Journal · 1930 · 84 citations · Full text