ABSTRACT
BACKGROUND: o-Aminophenols have been long recognised as tyrosinase substrates. However their exact mode of interaction with the enzyme's active site is unclear. Properly vic-substituted o-aminophenols could help gain some insight into tyrosinase catalytic mechanism. METHODS: Eight vic-substituted o-aminophenols belonging to two isomeric series were systematically evaluated as tyrosinase substrates and/or activators and/or inhibitors, by means of spectrophotometric techniques and HPLC-MS analysis. Some relevant kinetic parameters have also been obtained. RESULTS: Four o-aminophenolic compounds derived from 3-hydroxyorthanilic acid (2-amino-3-hydroxybenzenesulfonic acid) and their four counterparts derived from the isomeric 2-hydroxymetanilic acid (3-amino-2-hydroxybenzenesulfonic acid) were synthesised and tested as putative substrates for mushroom tyrosinase. While the hydroxyorthanilic derivatives were quite inactive as both substrates and inhibitors, the hydroxymetanilic compounds on the contrary all acted as substrates for the enzyme, which oxidised them to the corresponding phenoxazinone derivatives. GENERAL SIGNIFICANCE: Based on the available structures of the active sites of tyrosinases, the different affinities of the four metanilic derivatives for the enzyme, and their oxidation rates, we propose a new hypothesis regarding the interaction between o-aminophenols and the active site of tyrosinase that is in agreement with the obtained experimental results.
Subject(s)
Agaricales/enzymology , Enzyme Inhibitors/chemistry , Fungal Proteins , Monophenol Monooxygenase , Sulfanilic Acids/chemistry , Catalytic Domain , Fungal Proteins/antagonists & inhibitors , Fungal Proteins/chemistry , Kinetics , Molecular Structure , Monophenol Monooxygenase/antagonists & inhibitors , Monophenol Monooxygenase/chemistry , Structure-Activity RelationshipABSTRACT
A theoretical investigation of the facial selectivity of optically active oxazolidin-2-one-substituted dienes has been realized. This analysis enabled the development of (R)-4-phenyloxazolidin-2-thione as a very effective chiral auxiliary for cycloaddition of 1-aminodiene.
ABSTRACT
A theoretical analysis of transition state stabilization in D-A reactions of substituted dienes according to the nature and position of the substituent has been carried on. Results revealed that substituents (de)stabilize TS through four effects (steric, mesomeric, inductive, and polarizability) acting principally by favoring the electronic transfer between the two partners. The correlations observed point out nevertheless that the reactivity of substituted dienes in [4 + 2] cycloadditions on ethylene may principally be predicted by the sole use of the F + R electronic parameters.
