Table 1. Tyrosinase inhibitory activities of new compounds.
| Compounds | R1 | R2 | IC50 value (μM) |
| 5a | H | OH | 2.0 |
| 5b | OCH3 | OH | >100 a |
| 5c | H | OCH3 | 77.4 |
| 5d | H | H | >100 a |
| 5e | H | CH3 | 39.0 |
| 5f | H | Cl | 163.8 |
| 5g | H | F | 8.3 |
| 6a | H | OH | 10.6 |
| 6b | OCH3 | OH | >100 a |
| 6c | H | OCH3 | >100 a |
| 6d | H | H | >100 a |
| 6e | H | CH3 | >100 a |
| 6f | H | Cl | >100 a |
| 6g | H | F | >100 a |
| Cinnamic acid | 209.5 | ||
| 4-Hydroxyl cinnamic acid | 4708.5 | ||
| Paeonol | 121.4 | ||
| Thymol | 5925.0 | ||
| Kojic acid | 32.2 |
aThe inhibitory percentage of these compounds at 100 μM is less than 40%.