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. 2010 Feb 13;6(21):34–41. doi: 10.4103/0973-1296.59964

Table 2.

Inhibitory activities of mushroom tyrosinase and DOPA auto-oxidation by different extracts of H. globosa

Sample % Inhibition of DOPA auto-oxidation (%) at 20 μg/ml Inhibition of DOPA auto-oxidation (%) at 200 μg/ml Inhibition of tyrosinase (%) at 20 μg/ml Inhibition of tyrosinase (%) at 200 μg/ml
F.E 15.7 ± 0.03 31.7 ± 0.05 13 ± 0.01 90.4 ± 0.03
F.DC 15.5 ± 0.02 19.1 ± 0.09 0 1.8 ± 0.02
L.E 0 8.4 ± 0.06 4.8 ± 0.04 87 ± 0.02
L.DC 13.3 ± 0.03 13.6 ± 0.02 0 0
R.E 9 ± 0.03 13.7 ± 0.02 53.8 ± 0.03 86.8 ± 0.06
R.DC 14.8 ± 0.06 18.3 ± 0.02 0 0
S.E 0.9 ± 0.03 0 0 40.2 ± 0.01
S.DC 7.4 ± 0.04 10.1 ± 3 0 0
Kojic acid 42.2 ± 0.2 83.3 ± 0.2 99 ± 0.1 100 ± 0.5
Arbutin 0 0 8.7 ± 0.8 32.6 ± 0.1

F.E - Fruits, ethanol extract; F.DC - Fruits, dichloromethane extract; L. E - Leaves, ethanol extract; F.DC - Leaves, dichloromethane extract; R. E - Root, ethanol extract;R. DC - Root, dichloromethane extract; S.E - Stem, ethanol extract; S.DC - Stem, dichloromethane extract Data are mean ± SD of three separate experiments