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. 2022 Apr 26;37(1):1120–1195. doi: 10.1080/14756366.2022.2061966

Table 22.

Structure and activity of coumarin against tyrosinase.

Structure Name IC50 (μM) Ref.
Inline graphic
Coumarin
8100
Masamoto et al.143
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Esculetin
43/6.9
Masamoto et al.143; Li et al.144
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Umbelliferone
420
Masamoto et al.143
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Scopoletin
2600/0.2
Masamoto et al.143; Li et al.144
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Esculin
>14000
Masamoto et al.143
graphic file with name IENZ_A_2061966_ILG0147_B.jpg Scopoline 15.9 Li et al.144
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5,7-dihydroxycoumarin-7-(6-O-β-D-apiofuranosyl-β-Dglucopyranoside)
>400
Zheng et al.145
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xeroboside
>400
Zheng et al.145
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7-[[6-O-(6-deoxy-R-L-mannopyranosyl)-β-Dglucopyranosyl]oxy]-2H-1-benzopyran-2-one
>400
Zheng et al.145
graphic file with name IENZ_A_2061966_ILG0151_B.jpg mulberroside B >500 Zheng et al.145
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5,7-dihydroxycoumarin-7-O-β-D-glucopyranoside
>400
Zheng et al.145
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8′-epi-cleomiscosin A
1.33
Ahmad et al.146
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Cleomiscosin A
18.69
Ahmad et al.146
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aquillochin
15.69
Ahmad et al.146
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5,6,7-trimethoxycoumarin
8.65
Ahmad et al.146
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8-O-b-Dglucopyranosyl-6-hydroxy-2-methyl-4H-1-benzopyrane-4- one
256.97
Ahmad et al.146
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3-Phenylcoumarin
>1000
Matos et al.147
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3-Thiophenylcoumarin
>1000
Matos et al.147
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5,7-Dihydroxy-3-(3-thiophenyl)coumarin
0.19
Matos et al.147
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3-(4′-Bromophenyl)-5,7-dihydroxycoumarin
1.05
Matos et al.147
graphic file with name IENZ_A_2061966_ILG0162_B.jpg 2-(1-(Coumarin-3-yl)ethylidene) hydrazinecarbothioamide 3.44 Liu et al.150
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4c
118.48
Ashraf et al.151
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4e
8.96
Ashraf et al.151
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6a
123.77
Ashraf et al.151
graphic file with name IENZ_A_2061966_ILG0166_B.jpg 6b 80.20 Ashraf et al.151