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. 2021 Jul 15;10(7):1129. doi: 10.3390/antiox10071129

Table 2.

Tyrosinase inhibitory effects of arbutin and α-arbutin and their glucosides.

Literature Compounds Tyrosinase Inhibitory Effects Enzymes and
Substrates Used
Name Chemical Structure Monophenolase
Activity
Diphenolase
Activity
[89] α-arbutin 3 IC50 = 2.1 mM Human tyrosinase;
3.3 mM L-DOPA
Arbutin 2 IC50 > 30 mM
4-Hydroxyphenyl β-maltoside 7 IC50 = 5.7 mM
4-Hydroxyphenyl β-maltotrioside 8 IC50 = 6.1 mM
[90] 4-Hydroxyphenyl α-maltoside 11 IC50 = 4.9 mM Human tyrosinase;
3.3 mM L-DOPA
4-Hydroxyphenyl α-maltotrioside 12 IC50 = 13.9 mM
[91] Arbutin 2 Ki = 2.8 mM Mushroom tyrosinase;
3.3 mM DOPA
4-Hydroxyphenyl β-isomaltoside 9 Ki = 3.7 mM
4-Hydroxyphenyl β-isomaltotrioside 10 Not determined
[92] Arbutin 2 IC50 = 6 mM Mushroom tyrosinase;
0.03% L-tyrosine
β-D-Glucopyranosyl-(1→6)-arbutin 4 IC50 = 8 mM
β-D-Glucopyranosyl-(1→4)-arbutin 5 IC50 = 10 mM
β-D-Glucopyranosyl-(1→3)-arbutin 6 IC50 = 5 mM
α-D-Glucopyranosyl-(1→4)-arbutin 7 IC50 = 5 mM
[93] α-arbutin 3 IC50 = 2.1 mM Human tyrosinase;
3 mM L-DOPA
α-arbutin-α-glucoside 11 IC50 = 6.9 mM
α-arbutin-α-maltoside 12 IC50 = 15.6 mM
α-arbutin-α-maltotrioside 13 Not determined