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Literature summary extracted from

  • Kim, Y.J.; Uyama, H.
    Tyrosinase inhibitors from natural and synthetic sources: structure, inhibition mechanism and perspective for the future (2005), Cell. Mol. Life Sci., 62, 1707-1723.
    View publication on PubMed

Application

EC Number Application Comment Organism
1.10.3.1 drug development the enzyme is a target for development of specific inhibitors to avoid unfavorable enzymatic browning of plant-derived foods by tyrosinase causing decrease in nutritional quality and economic loss of food products Beta vulgaris
1.10.3.1 nutrition the enzyme is a target for development of specific inhibitors to avoid unfavorable enzymatic browning of plant-derived foods by tyrosinase causing decrease in nutritional quality and economic loss of food products Beta vulgaris
1.14.18.1 drug development the enzyme is a target for development of specific inhibitors to avoid unfavorable enzymatic browning of plant-derived foods by tyrosinase causing decrease in nutritional quality and economic loss of food products Beta vulgaris
1.14.18.1 nutrition the enzyme is a target for development of specific inhibitors to avoid unfavorable enzymatic browning of plant-derived foods by tyrosinase causing decrease in nutritional quality and economic loss of food products Beta vulgaris

Inhibitors

EC Number Inhibitors Comment Organism Structure
1.10.3.1 (-)-epigallocatechin
-
Agaricus bisporus
1.10.3.1 (-)-epigallocatechin
-
Beta vulgaris
1.10.3.1 (-)-epigallocatechin
-
Homo sapiens
1.10.3.1 (-)-epigallocatechin
-
Neurospora crassa
1.10.3.1 (-)-epigallocatechin
-
Streptomyces glaucescens
1.10.3.1 (-)-epigallocatechin-3-O-gallate
-
Agaricus bisporus
1.10.3.1 (-)-epigallocatechin-3-O-gallate
-
Beta vulgaris
1.10.3.1 (-)-epigallocatechin-3-O-gallate
-
Homo sapiens
1.10.3.1 (-)-epigallocatechin-3-O-gallate
-
Neurospora crassa
1.10.3.1 (-)-epigallocatechin-3-O-gallate
-
Streptomyces glaucescens
1.10.3.1 (R)-HTCCA
-
Agaricus bisporus
1.10.3.1 (R)-HTCCA
-
Beta vulgaris
1.10.3.1 (R)-HTCCA
-
Homo sapiens
1.10.3.1 (R)-HTCCA
-
Neurospora crassa
1.10.3.1 (R)-HTCCA
-
Streptomyces glaucescens
1.10.3.1 (S)-HTCCA
-
Agaricus bisporus
1.10.3.1 (S)-HTCCA
-
Beta vulgaris
1.10.3.1 (S)-HTCCA
-
Homo sapiens
1.10.3.1 (S)-HTCCA
-
Neurospora crassa
1.10.3.1 (S)-HTCCA
-
Streptomyces glaucescens
1.10.3.1 4-hexylresorcinol
-
Agaricus bisporus
1.10.3.1 4-hexylresorcinol
-
Beta vulgaris
1.10.3.1 4-hexylresorcinol
-
Homo sapiens
1.10.3.1 4-hexylresorcinol
-
Neurospora crassa
1.10.3.1 4-hexylresorcinol
-
Streptomyces glaucescens
1.10.3.1 aloesin
-
Agaricus bisporus
1.10.3.1 aloesin
-
Beta vulgaris
1.10.3.1 aloesin
-
Homo sapiens
1.10.3.1 aloesin
-
Neurospora crassa
1.10.3.1 aloesin
-
Streptomyces glaucescens
1.10.3.1 Anisaldehyde noncompetitive, IC50: 0.320 mM Agaricus bisporus
1.10.3.1 Anisaldehyde noncompetitive, IC50: 0.320 mM Beta vulgaris
1.10.3.1 Anisaldehyde noncompetitive, IC50: 0.320 mM Homo sapiens
1.10.3.1 Anisaldehyde noncompetitive, IC50: 0.320 mM Neurospora crassa
1.10.3.1 Anisaldehyde noncompetitive, IC50: 0.320 mM Streptomyces glaucescens
1.10.3.1 ascorbic acid inhibition of tyrosinase-catalyzed enzymatic browning by trapping the dopaquinone intermediate with cysteine or ascorbic acid, overview Beta vulgaris
1.10.3.1 azelaic acid
-
Agaricus bisporus
1.10.3.1 azelaic acid
-
Beta vulgaris
1.10.3.1 azelaic acid
-
Homo sapiens
1.10.3.1 azelaic acid
-
Neurospora crassa
1.10.3.1 azelaic acid
-
Streptomyces glaucescens
1.10.3.1 captopril
-
Agaricus bisporus
1.10.3.1 captopril
-
Beta vulgaris
1.10.3.1 captopril
-
Homo sapiens
1.10.3.1 captopril
-
Neurospora crassa
1.10.3.1 captopril
-
Streptomyces glaucescens
1.10.3.1 cinnamaldehyde noncompetitive, 0.980 mM Agaricus bisporus
1.10.3.1 cinnamaldehyde noncompetitive, 0.980 mM Beta vulgaris
1.10.3.1 cinnamaldehyde noncompetitive, 0.980 mM Homo sapiens
1.10.3.1 cinnamaldehyde noncompetitive, 0.980 mM Neurospora crassa
1.10.3.1 cinnamaldehyde noncompetitive, 0.980 mM Streptomyces glaucescens
1.10.3.1 cuminaldehyde noncompetitive, IC50: 0.050 mM Agaricus bisporus
1.10.3.1 cuminaldehyde noncompetitive, IC50: 0.050 mM Beta vulgaris
1.10.3.1 cuminaldehyde noncompetitive, IC50: 0.050 mM Homo sapiens
1.10.3.1 cuminaldehyde noncompetitive, IC50: 0.050 mM Neurospora crassa
1.10.3.1 cuminaldehyde noncompetitive, IC50: 0.050 mM Streptomyces glaucescens
1.10.3.1 Cupferron
-
Agaricus bisporus
1.10.3.1 Cupferron
-
Beta vulgaris
1.10.3.1 Cupferron
-
Homo sapiens
1.10.3.1 Cupferron
-
Neurospora crassa
1.10.3.1 Cupferron
-
Streptomyces glaucescens
1.10.3.1 cysteine inhibition of tyrosinase-catalyzed enzymatic browning by trapping the dopaquinone intermediate with cysteine or ascorbic acid, overview Beta vulgaris
1.10.3.1 davanol
-
Agaricus bisporus
1.10.3.1 davanol
-
Beta vulgaris
1.10.3.1 davanol
-
Homo sapiens
1.10.3.1 davanol
-
Neurospora crassa
1.10.3.1 davanol
-
Streptomyces glaucescens
1.10.3.1 decahydro-2-naphthyl gallate
-
Agaricus bisporus
1.10.3.1 decahydro-2-naphthyl gallate
-
Beta vulgaris
1.10.3.1 decahydro-2-naphthyl gallate
-
Homo sapiens
1.10.3.1 decahydro-2-naphthyl gallate
-
Neurospora crassa
1.10.3.1 decahydro-2-naphthyl gallate
-
Streptomyces glaucescens
1.10.3.1 dopastin
-
Agaricus bisporus
1.10.3.1 dopastin
-
Beta vulgaris
1.10.3.1 dopastin
-
Homo sapiens
1.10.3.1 dopastin
-
Neurospora crassa
1.10.3.1 dopastin
-
Streptomyces glaucescens
1.10.3.1 geranyl gallate
-
Agaricus bisporus
1.10.3.1 geranyl gallate
-
Beta vulgaris
1.10.3.1 geranyl gallate
-
Homo sapiens
1.10.3.1 geranyl gallate
-
Neurospora crassa
1.10.3.1 geranyl gallate
-
Streptomyces glaucescens
1.10.3.1 glabrene mixed-type, IC50: 7.600 mM Agaricus bisporus
1.10.3.1 glabrene mixed-type, IC50: 7.600 mM Beta vulgaris
1.10.3.1 glabrene mixed-type, IC50: 7.600 mM Homo sapiens
1.10.3.1 glabrene mixed-type, IC50: 7.600 mM Neurospora crassa
1.10.3.1 glabrene mixed-type, IC50: 7.600 mM Streptomyces glaucescens
1.10.3.1 glabridin noncompetitive, IC50: 0.004 mM Agaricus bisporus
1.10.3.1 glabridin noncompetitive, IC50: 0.004 mM Beta vulgaris
1.10.3.1 glabridin noncompetitive, IC50: 0.004 mM Homo sapiens
1.10.3.1 glabridin noncompetitive, IC50: 0.004 mM Neurospora crassa
1.10.3.1 glabridin noncompetitive, IC50: 0.004 mM Streptomyces glaucescens
1.10.3.1 isoliquiritigenin mixed-type, IC50: 0.047 Agaricus bisporus
1.10.3.1 isoliquiritigenin mixed-type, IC50: 0.047 Beta vulgaris
1.10.3.1 isoliquiritigenin mixed-type, IC50: 0.047 Homo sapiens
1.10.3.1 isoliquiritigenin mixed-type, IC50: 0.047 Neurospora crassa
1.10.3.1 isoliquiritigenin mixed-type, IC50: 0.047 Streptomyces glaucescens
1.10.3.1 kaempferol
-
Agaricus bisporus
1.10.3.1 kaempferol
-
Beta vulgaris
1.10.3.1 kaempferol
-
Homo sapiens
1.10.3.1 kaempferol
-
Neurospora crassa
1.10.3.1 kaempferol
-
Streptomyces glaucescens
1.10.3.1 kojic acid mixed-type, IC50: 0.014 mM Agaricus bisporus
1.10.3.1 kojic acid mixed-type, IC50: 0.014 mM Beta vulgaris
1.10.3.1 kojic acid mixed-type, IC50: 0.014 mM Homo sapiens
1.10.3.1 kojic acid mixed-type, IC50: 0.014 mM Neurospora crassa
1.10.3.1 kojic acid mixed-type, IC50: 0.014 mM Streptomyces glaucescens
1.10.3.1 L-mimosine
-
Agaricus bisporus
1.10.3.1 L-mimosine
-
Beta vulgaris
1.10.3.1 L-mimosine
-
Homo sapiens
1.10.3.1 L-mimosine
-
Neurospora crassa
1.10.3.1 L-mimosine
-
Streptomyces glaucescens
1.10.3.1 luteolin noncompetitive, IC50: 0.190 mM Agaricus bisporus
1.10.3.1 luteolin noncompetitive, IC50: 0.190 mM Beta vulgaris
1.10.3.1 luteolin noncompetitive, IC50: 0.190 mM Homo sapiens
1.10.3.1 luteolin noncompetitive, IC50: 0.190 mM Neurospora crassa
1.10.3.1 luteolin noncompetitive, IC50: 0.190 mM Streptomyces glaucescens
1.10.3.1 luteolin 7-O-glucoside noncompetitive, IC50: 0.500 mM Agaricus bisporus
1.10.3.1 luteolin 7-O-glucoside noncompetitive, IC50: 0.500 mM Beta vulgaris
1.10.3.1 luteolin 7-O-glucoside noncompetitive, IC50: 0.500 mM Homo sapiens
1.10.3.1 luteolin 7-O-glucoside noncompetitive, IC50: 0.500 mM Neurospora crassa
1.10.3.1 luteolin 7-O-glucoside noncompetitive, IC50: 0.500 mM Streptomyces glaucescens
1.10.3.1 Methimazole
-
Agaricus bisporus
1.10.3.1 Methimazole
-
Beta vulgaris
1.10.3.1 Methimazole
-
Homo sapiens
1.10.3.1 Methimazole
-
Neurospora crassa
1.10.3.1 Methimazole
-
Streptomyces glaucescens
1.10.3.1 additional information structure, application and importance of inhibitors, overview Agaricus bisporus
1.10.3.1 additional information structure, application and importance of inhibitors, overview Beta vulgaris
1.10.3.1 additional information melanin plays a crucial protective role against skin photocarcinogenesis, however, the production of abnormal melanin pigmentation is a serious esthetic problem in humans, melanin biosynthesis can be inhibited by avoiding UV exposure, the inhibition of tyrosinase, the inhibition of melanocyte metabolism and proliferation, or the removal of melanin with corneal ablation, overview, structure, application and importance of inhibitors, overview Homo sapiens
1.10.3.1 additional information structure, application and importance of inhibitors, overview Neurospora crassa
1.10.3.1 additional information structure, application and importance of inhibitors, overview Streptomyces glaucescens
1.10.3.1 morin
-
Agaricus bisporus
1.10.3.1 morin competitive, IC50: 2.320 mM Beta vulgaris
1.10.3.1 morin
-
Homo sapiens
1.10.3.1 morin
-
Neurospora crassa
1.10.3.1 morin
-
Streptomyces glaucescens
1.10.3.1 quercetin
-
Agaricus bisporus
1.10.3.1 quercetin
-
Beta vulgaris
1.10.3.1 quercetin
-
Homo sapiens
1.10.3.1 quercetin
-
Neurospora crassa
1.10.3.1 quercetin
-
Streptomyces glaucescens
1.10.3.1 tropolone
-
Agaricus bisporus
1.10.3.1 tropolone
-
Beta vulgaris
1.10.3.1 tropolone
-
Homo sapiens
1.10.3.1 tropolone
-
Neurospora crassa
1.10.3.1 tropolone
-
Streptomyces glaucescens
1.14.18.1 (-)-epigallocatechin competitive, IC50: 0.035 mM Agaricus bisporus
1.14.18.1 (-)-epigallocatechin competitive, IC50: 0.035 mM Beta vulgaris
1.14.18.1 (-)-epigallocatechin competitive, IC50: 0.035 mM Homo sapiens
1.14.18.1 (-)-epigallocatechin competitive, IC50: 0.035 mM Neurospora crassa
1.14.18.1 (-)-epigallocatechin competitive, IC50: 0.035 mM Streptomyces glaucescens
1.14.18.1 (-)-epigallocatechin-3-O-gallate competitive, IC50: 0.034 mM Agaricus bisporus
1.14.18.1 (-)-epigallocatechin-3-O-gallate competitive, IC50: 0.034 mM Beta vulgaris
1.14.18.1 (-)-epigallocatechin-3-O-gallate competitive, IC50: 0.034 mM Homo sapiens
1.14.18.1 (-)-epigallocatechin-3-O-gallate competitive, IC50: 0.034 mM Neurospora crassa
1.14.18.1 (-)-epigallocatechin-3-O-gallate competitive, IC50: 0.034 mM Streptomyces glaucescens
1.14.18.1 (R)-HTCCA
-
Agaricus bisporus
1.14.18.1 (R)-HTCCA
-
Beta vulgaris
1.14.18.1 (R)-HTCCA
-
Homo sapiens
1.14.18.1 (R)-HTCCA
-
Neurospora crassa
1.14.18.1 (R)-HTCCA
-
Streptomyces glaucescens
1.14.18.1 (S)-HTCCA
-
Agaricus bisporus
1.14.18.1 (S)-HTCCA
-
Beta vulgaris
1.14.18.1 (S)-HTCCA
-
Homo sapiens
1.14.18.1 (S)-HTCCA
-
Neurospora crassa
1.14.18.1 (S)-HTCCA
-
Streptomyces glaucescens
1.14.18.1 4-hexylresorcinol
-
Agaricus bisporus
1.14.18.1 4-hexylresorcinol
-
Beta vulgaris
1.14.18.1 4-hexylresorcinol
-
Homo sapiens
1.14.18.1 4-hexylresorcinol
-
Neurospora crassa
1.14.18.1 4-hexylresorcinol
-
Streptomyces glaucescens
1.14.18.1 aloesin
-
Agaricus bisporus
1.14.18.1 aloesin
-
Beta vulgaris
1.14.18.1 aloesin
-
Homo sapiens
1.14.18.1 aloesin
-
Neurospora crassa
1.14.18.1 aloesin
-
Streptomyces glaucescens
1.14.18.1 Anisaldehyde
-
Agaricus bisporus
1.14.18.1 Anisaldehyde
-
Beta vulgaris
1.14.18.1 Anisaldehyde
-
Homo sapiens
1.14.18.1 Anisaldehyde
-
Neurospora crassa
1.14.18.1 Anisaldehyde
-
Streptomyces glaucescens
1.14.18.1 ascorbic acid inhibition of tyrosinase-catalyzed enzymatic browning by trapping the dopaquinone intermediate with cysteine or ascorbic acid, overview Beta vulgaris
1.14.18.1 azelaic acid
-
Agaricus bisporus
1.14.18.1 azelaic acid
-
Beta vulgaris
1.14.18.1 azelaic acid
-
Homo sapiens
1.14.18.1 azelaic acid
-
Neurospora crassa
1.14.18.1 azelaic acid
-
Streptomyces glaucescens
1.14.18.1 captopril
-
Agaricus bisporus
1.14.18.1 captopril
-
Beta vulgaris
1.14.18.1 captopril
-
Homo sapiens
1.14.18.1 captopril
-
Neurospora crassa
1.14.18.1 captopril
-
Streptomyces glaucescens
1.14.18.1 cinnamaldehyde
-
Agaricus bisporus
1.14.18.1 cinnamaldehyde
-
Beta vulgaris
1.14.18.1 cinnamaldehyde
-
Homo sapiens
1.14.18.1 cinnamaldehyde
-
Neurospora crassa
1.14.18.1 cinnamaldehyde
-
Streptomyces glaucescens
1.14.18.1 cuminaldehyde
-
Agaricus bisporus
1.14.18.1 cuminaldehyde
-
Beta vulgaris
1.14.18.1 cuminaldehyde
-
Homo sapiens
1.14.18.1 cuminaldehyde
-
Neurospora crassa
1.14.18.1 cuminaldehyde
-
Streptomyces glaucescens
1.14.18.1 Cupferron
-
Agaricus bisporus
1.14.18.1 Cupferron
-
Beta vulgaris
1.14.18.1 Cupferron
-
Homo sapiens
1.14.18.1 Cupferron
-
Neurospora crassa
1.14.18.1 Cupferron
-
Streptomyces glaucescens
1.14.18.1 cysteine inhibition of tyrosinase-catalyzed enzymatic browning by trapping the dopaquinone intermediate with cysteine or ascorbic acid, overview Beta vulgaris
1.14.18.1 davanol competitive, IC50: 0.017 mM Agaricus bisporus
1.14.18.1 davanol competitive, IC50: 0.017 mM Beta vulgaris
1.14.18.1 davanol competitive, IC50: 0.017 mM Homo sapiens
1.14.18.1 davanol competitive, IC50: 0.017 mM Neurospora crassa
1.14.18.1 davanol competitive, IC50: 0.017 mM Streptomyces glaucescens
1.14.18.1 decahydro-2-naphthyl gallate
-
Agaricus bisporus
1.14.18.1 decahydro-2-naphthyl gallate
-
Beta vulgaris
1.14.18.1 decahydro-2-naphthyl gallate
-
Homo sapiens
1.14.18.1 decahydro-2-naphthyl gallate
-
Neurospora crassa
1.14.18.1 decahydro-2-naphthyl gallate
-
Streptomyces glaucescens
1.14.18.1 dopastin
-
Agaricus bisporus
1.14.18.1 dopastin
-
Beta vulgaris
1.14.18.1 dopastin
-
Homo sapiens
1.14.18.1 dopastin
-
Neurospora crassa
1.14.18.1 dopastin
-
Streptomyces glaucescens
1.14.18.1 geranyl gallate
-
Agaricus bisporus
1.14.18.1 geranyl gallate
-
Beta vulgaris
1.14.18.1 geranyl gallate
-
Homo sapiens
1.14.18.1 geranyl gallate
-
Neurospora crassa
1.14.18.1 geranyl gallate
-
Streptomyces glaucescens
1.14.18.1 glabrene
-
Agaricus bisporus
1.14.18.1 glabrene
-
Beta vulgaris
1.14.18.1 glabrene
-
Homo sapiens
1.14.18.1 glabrene
-
Neurospora crassa
1.14.18.1 glabrene
-
Streptomyces glaucescens
1.14.18.1 glabridin
-
Agaricus bisporus
1.14.18.1 glabridin
-
Beta vulgaris
1.14.18.1 glabridin
-
Homo sapiens
1.14.18.1 glabridin
-
Neurospora crassa
1.14.18.1 glabridin
-
Streptomyces glaucescens
1.14.18.1 isoliquiritigenin
-
Agaricus bisporus
1.14.18.1 isoliquiritigenin
-
Beta vulgaris
1.14.18.1 isoliquiritigenin
-
Homo sapiens
1.14.18.1 isoliquiritigenin
-
Neurospora crassa
1.14.18.1 isoliquiritigenin
-
Streptomyces glaucescens
1.14.18.1 kaempferol competitive, IC50: 0.230 Agaricus bisporus
1.14.18.1 kaempferol competitive, IC50: 0.230 Beta vulgaris
1.14.18.1 kaempferol competitive, IC50: 0.230 Homo sapiens
1.14.18.1 kaempferol competitive, IC50: 0.230 Neurospora crassa
1.14.18.1 kaempferol competitive, IC50: 0.230 Streptomyces glaucescens
1.14.18.1 kojic acid
-
Agaricus bisporus
1.14.18.1 kojic acid
-
Beta vulgaris
1.14.18.1 kojic acid
-
Homo sapiens
1.14.18.1 kojic acid
-
Neurospora crassa
1.14.18.1 kojic acid
-
Streptomyces glaucescens
1.14.18.1 L-mimosine
-
Agaricus bisporus
1.14.18.1 L-mimosine
-
Beta vulgaris
1.14.18.1 L-mimosine
-
Homo sapiens
1.14.18.1 L-mimosine
-
Neurospora crassa
1.14.18.1 L-mimosine
-
Streptomyces glaucescens
1.14.18.1 luteolin
-
Agaricus bisporus
1.14.18.1 luteolin
-
Beta vulgaris
1.14.18.1 luteolin
-
Homo sapiens
1.14.18.1 luteolin
-
Neurospora crassa
1.14.18.1 luteolin
-
Streptomyces glaucescens
1.14.18.1 luteolin 7-O-glucoside
-
Agaricus bisporus
1.14.18.1 luteolin 7-O-glucoside
-
Beta vulgaris
1.14.18.1 luteolin 7-O-glucoside
-
Homo sapiens
1.14.18.1 luteolin 7-O-glucoside
-
Neurospora crassa
1.14.18.1 luteolin 7-O-glucoside
-
Streptomyces glaucescens
1.14.18.1 Methimazole
-
Agaricus bisporus
1.14.18.1 Methimazole
-
Beta vulgaris
1.14.18.1 Methimazole
-
Homo sapiens
1.14.18.1 Methimazole
-
Neurospora crassa
1.14.18.1 Methimazole
-
Streptomyces glaucescens
1.14.18.1 additional information structure, application and importance of inhibitors, overview Agaricus bisporus
1.14.18.1 additional information structure, application and importance of inhibitors, overview Beta vulgaris
1.14.18.1 additional information melanin plays a crucial protective role against skin photocarcinogenesis, however, the production of abnormal melanin pigmentation is a serious esthetic problem in humans, melanin biosynthesis can be inhibited by avoiding UV exposure, the inhibition of tyrosinase, the inhibition of melanocyte metabolism and proliferation, or the removal of melanin with corneal ablation, overview, structure, application and importance of inhibitors, overview Homo sapiens
1.14.18.1 additional information structure, application and importance of inhibitors, overview Neurospora crassa
1.14.18.1 additional information structure, application and importance of inhibitors, overview Streptomyces glaucescens
1.14.18.1 morin competitive, IC50: 2.320 mM Agaricus bisporus
1.14.18.1 morin competitive, IC50: 2.320 mM Beta vulgaris
1.14.18.1 morin competitive, IC50: 2.320 mM Homo sapiens
1.14.18.1 morin competitive, IC50: 2.320 mM Neurospora crassa
1.14.18.1 morin competitive, IC50: 2.320 mM Streptomyces glaucescens
1.14.18.1 quercetin competitive, IC50: 0.070 mM Agaricus bisporus
1.14.18.1 quercetin competitive, IC50: 0.070 mM Beta vulgaris
1.14.18.1 quercetin competitive, IC50: 0.070 mM Homo sapiens
1.14.18.1 quercetin competitive, IC50: 0.070 mM Neurospora crassa
1.14.18.1 quercetin competitive, IC50: 0.070 mM Streptomyces glaucescens
1.14.18.1 tropolone
-
Agaricus bisporus
1.14.18.1 tropolone
-
Beta vulgaris
1.14.18.1 tropolone
-
Homo sapiens
1.14.18.1 tropolone
-
Neurospora crassa
1.14.18.1 tropolone
-
Streptomyces glaucescens

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
1.10.3.1 membrane bound Homo sapiens 16020
-
1.14.18.1 membrane bound Homo sapiens 16020
-

Metals/Ions

EC Number Metals/Ions Comment Organism Structure
1.10.3.1 Cu2+ bound to the enzyme, presently available for any tyrosinases, the central domain contains two copper binding sites, mettyrosinase, the resting form of tyrosinase, contains two tetragonal Cu(II) ions antiferromagnetically coupled through an endogenous bridge, although hydroxide exogenous ligands other than peroxide are bound to the copper site, the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers Streptomyces glaucescens
1.10.3.1 Cu2+ bound to the enzyme, the central domain contains two copper binding sites, mettyrosinase, the resting form of tyrosinase, contains two tetragonal Cu(II) ions antiferromagnetically coupled through an endogenous bridge, although hydroxide exogenous ligands other than peroxide are bound to the copper site, the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers Beta vulgaris
1.10.3.1 Cu2+ bound to the enzyme, the central domain contains two copper binding sites, mettyrosinase, the resting form of tyrosinase, contains two tetragonal Cu(II) ions antiferromagnetically coupled through an endogenous bridge, although hydroxide exogenous ligands other than peroxide are bound to the copper site, the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers Homo sapiens
1.10.3.1 Cu2+ bound to the enzyme, the central domain contains two copper binding sites, mettyrosinase, the resting form of tyrosinase, contains two tetragonal Cu(II) ions antiferromagnetically coupled through an endogenous bridge, although hydroxide exogenous ligands other than peroxide are bound to the copper site, the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers Neurospora crassa
1.10.3.1 Cu2+ bound to the enzyme, the central domain contains two copper binding sites, mettyrosinase, the resting form of tyrosinase, contains two tetragonal Cu(II) ions antiferromagnetically coupled through an endogenous bridge, although hydroxide exogenous ligands other than peroxide are bound to the copper site, the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers Agaricus bisporus
1.10.3.1 H2O2 the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers, conferring a distinct O2-Cu(II) charge transfer Beta vulgaris
1.10.3.1 H2O2 the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers, conferring a distinct O2-Cu(II) charge transfer Homo sapiens
1.10.3.1 H2O2 the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers, conferring a distinct O2-Cu(II) charge transfer Neurospora crassa
1.10.3.1 H2O2 the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers, conferring a distinct O2-Cu(II) charge transfer Agaricus bisporus
1.10.3.1 H2O2 the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers, conferring a distinct O2-Cu(II) charge transfer Streptomyces glaucescens
1.14.18.1 Cu2+ bound to the enzyme, presently available for any tyrosinases, the central domain contains two copper binding sites, mettyrosinase, the resting form of tyrosinase, contains two tetragonal Cu(II) ions antiferromagnetically coupled through an endogenous bridge, although hydroxide exogenous ligands other than peroxide are bound to the copper site, the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers Streptomyces glaucescens
1.14.18.1 Cu2+ bound to the enzyme, the central domain contains two copper binding sites, mettyrosinase, the resting form of tyrosinase, contains two tetragonal Cu(II) ions antiferromagnetically coupled through an endogenous bridge, although hydroxide exogenous ligands other than peroxide are bound to the copper site, the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers Beta vulgaris
1.14.18.1 Cu2+ bound to the enzyme, the central domain contains two copper binding sites, mettyrosinase, the resting form of tyrosinase, contains two tetragonal Cu(II) ions antiferromagnetically coupled through an endogenous bridge, although hydroxide exogenous ligands other than peroxide are bound to the copper site, the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers Homo sapiens
1.14.18.1 Cu2+ bound to the enzyme, the central domain contains two copper binding sites, mettyrosinase, the resting form of tyrosinase, contains two tetragonal Cu(II) ions antiferromagnetically coupled through an endogenous bridge, although hydroxide exogenous ligands other than peroxide are bound to the copper site, the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers Neurospora crassa
1.14.18.1 Cu2+ bound to the enzyme, the central domain contains two copper binding sites, mettyrosinase, the resting form of tyrosinase, contains two tetragonal Cu(II) ions antiferromagnetically coupled through an endogenous bridge, although hydroxide exogenous ligands other than peroxide are bound to the copper site, the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers Agaricus bisporus
1.14.18.1 H2O2 the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers, conferring a distinct O2-Cu(II) charge transfer Beta vulgaris
1.14.18.1 H2O2 the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers, conferring a distinct O2-Cu(II) charge transfer Homo sapiens
1.14.18.1 H2O2 the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers, conferring a distinct O2-Cu(II) charge transfer Neurospora crassa
1.14.18.1 H2O2 the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers, conferring a distinct O2-Cu(II) charge transfer Agaricus bisporus
1.14.18.1 H2O2 the exogenous oxygen molecule is bound as peroxide and bridges the two copper centers, conferring a distinct O2-Æ Cu(II) charge transfer Streptomyces glaucescens

Molecular Weight [Da]

EC Number Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
1.10.3.1 30900
-
1 * 30900 Streptomyces glaucescens
1.10.3.1 40000
-
1 * 40000 Beta vulgaris
1.10.3.1 43000
-
2 * 134000 + 2 * 43000, alpha2beta2 subunit composition Agaricus bisporus
1.10.3.1 46000
-
1 * 46000 Neurospora crassa
1.10.3.1 66700
-
1 * 66700 Homo sapiens
1.10.3.1 134000
-
2 * 134000 + 2 * 43000, alpha2beta2 subunit composition Agaricus bisporus
1.14.18.1 30900
-
1 * 30900 Streptomyces glaucescens
1.14.18.1 40000
-
1 * 40000 Beta vulgaris
1.14.18.1 43000
-
2 * 134000 + 2 * 43000, alpha2beta2 subunit composition Agaricus bisporus
1.14.18.1 46000
-
1 * 46000 Neurospora crassa
1.14.18.1 66700
-
1 * 66700 Homo sapiens
1.14.18.1 134000
-
2 * 134000 + 2 * 43000, alpha2beta2 subunit composition Agaricus bisporus

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.10.3.1 3,4,5-trihydroxy-L-phenylalanine + O2 Homo sapiens cytotoxicity of TOPA ?
-
?
1.10.3.1 chlorogenic acid + O2 Beta vulgaris formation of a highly reactive o-quinone intermediate which then could interact with NH2 groups of lysine, SCH3 groups of methionines and indole rings of tryptophan in nucleophilic addition and in polymerization reactions, the so-called browning and greening reactions ?
-
?
1.10.3.1 L-tyrosine + L-dopa + O2 Beta vulgaris
-
L-dopa + dopaquinone + H2O
-
?
1.10.3.1 L-tyrosine + L-dopa + O2 Neurospora crassa
-
L-dopa + dopaquinone + H2O
-
?
1.10.3.1 L-tyrosine + L-dopa + O2 Agaricus bisporus
-
L-dopa + dopaquinone + H2O
-
?
1.10.3.1 L-tyrosine + L-dopa + O2 Streptomyces glaucescens
-
L-dopa + dopaquinone + H2O
-
?
1.10.3.1 L-tyrosine + L-dopa + O2 Homo sapiens pathway of melanin biosynthesis, detailed overview L-dopa + dopaquinone + H2O cytotoxicity of L-DOPA ?
1.10.3.1 additional information Homo sapiens tyrosinase is known to be a key enzyme in melanin biosynthesis, involved in determining the color of mammalian skin and hair, various dermatological disorders, such as melasma, age spots and sites of actinic damage, arise from the accumulation of an excessive level of epidermal pigmentation ?
-
?
1.14.18.1 3,4,5-trihydroxy-L-phenylalanine + O2 Homo sapiens cytotoxicity of TOPA ?
-
?
1.14.18.1 chlorogenic acid + O2 Beta vulgaris formation of a highly reactive o-quinone intermediate which then can interact with NH2 groups of lysine, SCH3 groups of methionines and indole rings of tryptophan in nucleophilic addition and in polymerization reactions, the so-called browning and greening reactions ?
-
?
1.14.18.1 L-tyrosine + L-dopa + O2 Beta vulgaris
-
L-dopa + dopaquinone + H2O
-
?
1.14.18.1 L-tyrosine + L-dopa + O2 Neurospora crassa
-
L-dopa + dopaquinone + H2O
-
?
1.14.18.1 L-tyrosine + L-dopa + O2 Agaricus bisporus
-
L-dopa + dopaquinone + H2O
-
?
1.14.18.1 L-tyrosine + L-dopa + O2 Streptomyces glaucescens
-
L-dopa + dopaquinone + H2O
-
?
1.14.18.1 L-tyrosine + L-dopa + O2 Homo sapiens pathway of melanin biosynthesis, detailed overview L-dopa + dopaquinone + H2O cytotoxicity of L-DOPA ?
1.14.18.1 additional information Homo sapiens tyrosinase is known to be a key enzyme in melanin biosynthesis, involved in determining the color of mammalian skin and hair, various dermatological disorders, such as melasma, age spots and sites of actinic damage, arise from the accumulation of an excessive level of epidermal pigmentation ?
-
?

Organism

EC Number Organism UniProt Comment Textmining
1.10.3.1 Agaricus bisporus
-
-
-
1.10.3.1 Beta vulgaris
-
spinach-beet
-
1.10.3.1 Homo sapiens
-
-
-
1.10.3.1 Neurospora crassa
-
-
-
1.10.3.1 Streptomyces glaucescens
-
-
-
1.14.18.1 Agaricus bisporus
-
-
-
1.14.18.1 Beta vulgaris
-
spinach-beet
-
1.14.18.1 Homo sapiens
-
-
-
1.14.18.1 Neurospora crassa
-
-
-
1.14.18.1 Streptomyces glaucescens
-
-
-

Posttranslational Modification

EC Number Posttranslational Modification Comment Organism
1.10.3.1 glycoprotein 13% carbohydrate Homo sapiens
1.14.18.1 glycoprotein 13% carbohydrate Homo sapiens

Reaction

EC Number Reaction Comment Organism Reaction ID
1.14.18.1 L-tyrosine + O2 = dopaquinone + H2O catalytic cycle, reaction mechanism, active site structure Beta vulgaris
1.14.18.1 L-tyrosine + O2 = dopaquinone + H2O catalytic cycle, reaction mechanism, active site structure Homo sapiens
1.14.18.1 L-tyrosine + O2 = dopaquinone + H2O catalytic cycle, reaction mechanism, active site structure Neurospora crassa
1.14.18.1 L-tyrosine + O2 = dopaquinone + H2O catalytic cycle, reaction mechanism, active site structure Agaricus bisporus
1.14.18.1 L-tyrosine + O2 = dopaquinone + H2O catalytic cycle, reaction mechanism, active site structure Streptomyces glaucescens

Source Tissue

EC Number Source Tissue Comment Organism Textmining
1.10.3.1 melanocyte
-
Homo sapiens
-
1.14.18.1 melanocyte
-
Homo sapiens
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.10.3.1 3,4,5-trihydroxy-L-phenylalanine + O2 cytotoxicity of TOPA Homo sapiens ?
-
?
1.10.3.1 3,4,5-trihydroxy-L-phenylalanine + O2 i.e. TOPA Homo sapiens ?
-
?
1.10.3.1 chlorogenic acid + O2 formation of a highly reactive o-quinone intermediate which then could interact with NH2 groups of lysine, SCH3 groups of methionines and indole rings of tryptophan in nucleophilic addition and in polymerization reactions, the so-called browning and greening reactions Beta vulgaris ?
-
?
1.10.3.1 chlorogenic acid + O2 formation of a highly reactive o-quinone intermediate Beta vulgaris ?
-
?
1.10.3.1 L-tyrosine + L-dopa + O2
-
Beta vulgaris L-dopa + dopaquinone + H2O
-
?
1.10.3.1 L-tyrosine + L-dopa + O2
-
Neurospora crassa L-dopa + dopaquinone + H2O
-
?
1.10.3.1 L-tyrosine + L-dopa + O2
-
Agaricus bisporus L-dopa + dopaquinone + H2O
-
?
1.10.3.1 L-tyrosine + L-dopa + O2
-
Streptomyces glaucescens L-dopa + dopaquinone + H2O
-
?
1.10.3.1 L-tyrosine + L-dopa + O2
-
Beta vulgaris L-dopa + dopaquinone + H2O o-dopaquinone is unstable in aqueous solution and rapidly suffers a non-enzymatic cyclization to leukodopachrome ?
1.10.3.1 L-tyrosine + L-dopa + O2
-
Homo sapiens L-dopa + dopaquinone + H2O o-dopaquinone is unstable in aqueous solution and rapidly suffers a non-enzymatic cyclization to leukodopachrome ?
1.10.3.1 L-tyrosine + L-dopa + O2
-
Neurospora crassa L-dopa + dopaquinone + H2O o-dopaquinone is unstable in aqueous solution and rapidly suffers a non-enzymatic cyclization to leukodopachrome ?
1.10.3.1 L-tyrosine + L-dopa + O2
-
Agaricus bisporus L-dopa + dopaquinone + H2O o-dopaquinone is unstable in aqueous solution and rapidly suffers a non-enzymatic cyclization to leukodopachrome ?
1.10.3.1 L-tyrosine + L-dopa + O2
-
Streptomyces glaucescens L-dopa + dopaquinone + H2O o-dopaquinone is unstable in aqueous solution and rapidly suffers a non-enzymatic cyclization to leukodopachrome ?
1.10.3.1 L-tyrosine + L-dopa + O2 pathway of melanin biosynthesis, detailed overview Homo sapiens L-dopa + dopaquinone + H2O cytotoxicity of L-DOPA ?
1.10.3.1 additional information tyrosinase is known to be a key enzyme in melanin biosynthesis, involved in determining the color of mammalian skin and hair, various dermatological disorders, such as melasma, age spots and sites of actinic damage, arise from the accumulation of an excessive level of epidermal pigmentation Homo sapiens ?
-
?
1.10.3.1 additional information tyrosinase is a copper-containing enzyme that catalyzes two distinct reactions of melanin synthesis: the hydroxylation of tyrosine by monophenolase action and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone by diphenolase action Beta vulgaris ?
-
?
1.10.3.1 additional information tyrosinase is a copper-containing enzyme that catalyzes two distinct reactions of melanin synthesis: the hydroxylation of tyrosine by monophenolase action and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone by diphenolase action Homo sapiens ?
-
?
1.10.3.1 additional information tyrosinase is a copper-containing enzyme that catalyzes two distinct reactions of melanin synthesis: the hydroxylation of tyrosine by monophenolase action and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone by diphenolase action Neurospora crassa ?
-
?
1.10.3.1 additional information tyrosinase is a copper-containing enzyme that catalyzes two distinct reactions of melanin synthesis: the hydroxylation of tyrosine by monophenolase action and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone by diphenolase action Agaricus bisporus ?
-
?
1.10.3.1 additional information tyrosinase is a copper-containing enzyme that catalyzes two distinct reactions of melanin synthesis: the hydroxylation of tyrosine by monophenolase action and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone by diphenolase action Streptomyces glaucescens ?
-
?
1.14.18.1 3,4,5-trihydroxy-L-phenylalanine + O2 cytotoxicity of TOPA Homo sapiens ?
-
?
1.14.18.1 3,4,5-trihydroxy-L-phenylalanine + O2 i.e. TOPA Homo sapiens ?
-
?
1.14.18.1 chlorogenic acid + O2 formation of a highly reactive o-quinone intermediate which then can interact with NH2 groups of lysine, SCH3 groups of methionines and indole rings of tryptophan in nucleophilic addition and in polymerization reactions, the so-called browning and greening reactions Beta vulgaris ?
-
?
1.14.18.1 chlorogenic acid + O2 formation of a highly reactive o-quinone intermediate Beta vulgaris ?
-
?
1.14.18.1 L-tyrosine + L-dopa + O2
-
Beta vulgaris L-dopa + dopaquinone + H2O
-
?
1.14.18.1 L-tyrosine + L-dopa + O2
-
Neurospora crassa L-dopa + dopaquinone + H2O
-
?
1.14.18.1 L-tyrosine + L-dopa + O2
-
Agaricus bisporus L-dopa + dopaquinone + H2O
-
?
1.14.18.1 L-tyrosine + L-dopa + O2
-
Streptomyces glaucescens L-dopa + dopaquinone + H2O
-
?
1.14.18.1 L-tyrosine + L-dopa + O2
-
Beta vulgaris L-dopa + dopaquinone + H2O o-dopaquinone is unstable in aqueous solution and rapidly suffers a non-enzymatic cyclization to leukodopachrome ?
1.14.18.1 L-tyrosine + L-dopa + O2
-
Homo sapiens L-dopa + dopaquinone + H2O o-dopaquinone is unstable in aqueous solution and rapidly suffers a non-enzymatic cyclization to leukodopachrome ?
1.14.18.1 L-tyrosine + L-dopa + O2
-
Neurospora crassa L-dopa + dopaquinone + H2O o-dopaquinone is unstable in aqueous solution and rapidly suffers a non-enzymatic cyclization to leukodopachrome ?
1.14.18.1 L-tyrosine + L-dopa + O2
-
Agaricus bisporus L-dopa + dopaquinone + H2O o-dopaquinone is unstable in aqueous solution and rapidly suffers a non-enzymatic cyclization to leukodopachrome ?
1.14.18.1 L-tyrosine + L-dopa + O2
-
Streptomyces glaucescens L-dopa + dopaquinone + H2O o-dopaquinone is unstable in aqueous solution and rapidly suffers a non-enzymatic cyclization to leukodopachrome ?
1.14.18.1 L-tyrosine + L-dopa + O2 pathway of melanin biosynthesis, detailed overview Homo sapiens L-dopa + dopaquinone + H2O cytotoxicity of L-DOPA ?
1.14.18.1 additional information tyrosinase is known to be a key enzyme in melanin biosynthesis, involved in determining the color of mammalian skin and hair, various dermatological disorders, such as melasma, age spots and sites of actinic damage, arise from the accumulation of an excessive level of epidermal pigmentation Homo sapiens ?
-
?
1.14.18.1 additional information tyrosinase is a copper-containing enzyme that catalyzes two distinct reactions of melanin synthesis: the hydroxylation of tyrosine by monophenolase action and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone by diphenolase action Beta vulgaris ?
-
?
1.14.18.1 additional information tyrosinase is a copper-containing enzyme that catalyzes two distinct reactions of melanin synthesis: the hydroxylation of tyrosine by monophenolase action and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone by diphenolase action Homo sapiens ?
-
?
1.14.18.1 additional information tyrosinase is a copper-containing enzyme that catalyzes two distinct reactions of melanin synthesis: the hydroxylation of tyrosine by monophenolase action and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone by diphenolase action Neurospora crassa ?
-
?
1.14.18.1 additional information tyrosinase is a copper-containing enzyme that catalyzes two distinct reactions of melanin synthesis: the hydroxylation of tyrosine by monophenolase action and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone by diphenolase action Agaricus bisporus ?
-
?
1.14.18.1 additional information tyrosinase is a copper-containing enzyme that catalyzes two distinct reactions of melanin synthesis: the hydroxylation of tyrosine by monophenolase action and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone by diphenolase action Streptomyces glaucescens ?
-
?

Subunits

EC Number Subunits Comment Organism
1.10.3.1 monomer 1 * 40000 Beta vulgaris
1.10.3.1 monomer 1 * 46000 Neurospora crassa
1.10.3.1 monomer 1 * 30900 Streptomyces glaucescens
1.10.3.1 monomer 1 * 66700 Homo sapiens
1.10.3.1 tetramer 2 * 134000 + 2 * 43000, alpha2beta2 subunit composition Agaricus bisporus
1.14.18.1 monomer 1 * 40000 Beta vulgaris
1.14.18.1 monomer 1 * 46000 Neurospora crassa
1.14.18.1 monomer 1 * 30900 Streptomyces glaucescens
1.14.18.1 monomer 1 * 66700 Homo sapiens
1.14.18.1 tetramer 2 * 134000 + 2 * 43000, alpha2beta2 subunit composition Agaricus bisporus

Synonyms

EC Number Synonyms Comment Organism
1.10.3.1 diphenolase
-
Beta vulgaris
1.10.3.1 diphenolase
-
Homo sapiens
1.10.3.1 diphenolase
-
Neurospora crassa
1.10.3.1 diphenolase
-
Agaricus bisporus
1.10.3.1 diphenolase
-
Streptomyces glaucescens
1.10.3.1 tyrosinase
-
Beta vulgaris
1.10.3.1 tyrosinase
-
Homo sapiens
1.10.3.1 tyrosinase
-
Neurospora crassa
1.10.3.1 tyrosinase
-
Agaricus bisporus
1.10.3.1 tyrosinase
-
Streptomyces glaucescens
1.14.18.1 monophenolase
-
Beta vulgaris
1.14.18.1 monophenolase
-
Homo sapiens
1.14.18.1 monophenolase
-
Neurospora crassa
1.14.18.1 monophenolase
-
Agaricus bisporus
1.14.18.1 monophenolase
-
Streptomyces glaucescens
1.14.18.1 tyrosinase
-
Beta vulgaris
1.14.18.1 tyrosinase
-
Homo sapiens
1.14.18.1 tyrosinase
-
Neurospora crassa
1.14.18.1 tyrosinase
-
Agaricus bisporus
1.14.18.1 tyrosinase
-
Streptomyces glaucescens

Cofactor

EC Number Cofactor Comment Organism Structure
1.10.3.1 additional information if L-DOPA is an active cofactor, its formation as an intermediate during o-dopaquinone production is controversial Beta vulgaris
1.10.3.1 additional information if L-DOPA is an active cofactor, its formation as an intermediate during o-dopaquinone production is controversial Homo sapiens
1.10.3.1 additional information if L-DOPA is an active cofactor, its formation as an intermediate during o-dopaquinone production is controversial Neurospora crassa
1.10.3.1 additional information if L-DOPA is an active cofactor, its formation as an intermediate during o-dopaquinone production is controversial Agaricus bisporus
1.10.3.1 additional information if L-DOPA is an active cofactor, its formation as an intermediate during o-dopaquinone production is controversial Streptomyces glaucescens
1.14.18.1 additional information if L-DOPA is an active cofactor, its formation as an intermediate during o-dopaquinone production is controversial Beta vulgaris
1.14.18.1 additional information if L-DOPA is an active cofactor, its formation as an intermediate during o-dopaquinone production is controversial Homo sapiens
1.14.18.1 additional information if L-DOPA is an active cofactor, its formation as an intermediate during o-dopaquinone production is controversial Neurospora crassa
1.14.18.1 additional information if L-DOPA is an active cofactor, its formation as an intermediate during o-dopaquinone production is controversial Agaricus bisporus
1.14.18.1 additional information if L-DOPA is an active cofactor, its formation as an intermediate during o-dopaquinone production is controversial Streptomyces glaucescens

IC50 Value

EC Number IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
1.10.3.1 0.004
-
noncompetitive, IC50: 0.004 mM Beta vulgaris glabridin
1.10.3.1 0.004
-
noncompetitive, IC50: 0.004 mM Homo sapiens glabridin
1.10.3.1 0.004
-
noncompetitive, IC50: 0.004 mM Neurospora crassa glabridin
1.10.3.1 0.004
-
noncompetitive, IC50: 0.004 mM Agaricus bisporus glabridin
1.10.3.1 0.004
-
noncompetitive, IC50: 0.004 mM Streptomyces glaucescens glabridin
1.10.3.1 0.014
-
mixed-type, IC50: 0.014 mM Beta vulgaris kojic acid
1.10.3.1 0.014
-
mixed-type, IC50: 0.014 mM Homo sapiens kojic acid
1.10.3.1 0.014
-
mixed-type, IC50: 0.014 mM Neurospora crassa kojic acid
1.10.3.1 0.014
-
mixed-type, IC50: 0.014 mM Agaricus bisporus kojic acid
1.10.3.1 0.014
-
mixed-type, IC50: 0.014 mM Streptomyces glaucescens kojic acid
1.10.3.1 0.047
-
mixed-type, IC50: 0.047 mM Beta vulgaris isoliquiritigenin
1.10.3.1 0.047
-
mixed-type, IC50: 0.047 mM Neurospora crassa isoliquiritigenin
1.10.3.1 0.047
-
mixed-type, IC50: 0.047 mM Agaricus bisporus isoliquiritigenin
1.10.3.1 0.047
-
mixed-type, IC50: 0.047 mM Streptomyces glaucescens isoliquiritigenin
1.10.3.1 0.05
-
noncompetitive, IC50: 0.050 mM Beta vulgaris cuminaldehyde
1.10.3.1 0.05
-
noncompetitive, IC50: 0.050 mM Homo sapiens cuminaldehyde
1.10.3.1 0.05
-
noncompetitive, IC50: 0.050 mM Neurospora crassa cuminaldehyde
1.10.3.1 0.05
-
noncompetitive, IC50: 0.050 mM Agaricus bisporus cuminaldehyde
1.10.3.1 0.05
-
noncompetitive, IC50: 0.050 mM Streptomyces glaucescens cuminaldehyde
1.10.3.1 0.19
-
noncompetitive, IC50: 0.190 mM Beta vulgaris luteolin
1.10.3.1 0.19
-
noncompetitive, IC50: 0.190 mM Homo sapiens luteolin
1.10.3.1 0.19
-
noncompetitive, IC50: 0.190 mM Neurospora crassa luteolin
1.10.3.1 0.19
-
noncompetitive, IC50: 0.190 mM Agaricus bisporus luteolin
1.10.3.1 0.19
-
noncompetitive, IC50: 0.190 mM Streptomyces glaucescens luteolin
1.10.3.1 0.32
-
noncompetitive, IC50: 0.320 mM Beta vulgaris Anisaldehyde
1.10.3.1 0.32
-
noncompetitive, IC50: 0.320 mM Homo sapiens Anisaldehyde
1.10.3.1 0.32
-
noncompetitive, IC50: 0.320 mM Neurospora crassa Anisaldehyde
1.10.3.1 0.32
-
noncompetitive, IC50: 0.320 mM Agaricus bisporus Anisaldehyde
1.10.3.1 0.32
-
noncompetitive, IC50: 0.320 mM Streptomyces glaucescens Anisaldehyde
1.10.3.1 0.5
-
noncompetitive, IC50: 0.500 mM Beta vulgaris luteolin 7-O-glucoside
1.10.3.1 0.5
-
noncompetitive, IC50: 0.500 mM Homo sapiens luteolin 7-O-glucoside
1.10.3.1 0.5
-
noncompetitive, IC50: 0.500 mM Neurospora crassa luteolin 7-O-glucoside
1.10.3.1 0.5
-
noncompetitive, IC50: 0.500 mM Agaricus bisporus luteolin 7-O-glucoside
1.10.3.1 0.5
-
noncompetitive, IC50: 0.500 mM Streptomyces glaucescens luteolin 7-O-glucoside
1.10.3.1 2.32
-
competitive, IC50: 2.320 mM Beta vulgaris morin
1.10.3.1 7.6
-
mixed-type, IC50: 7.600 mM Beta vulgaris glabrene
1.10.3.1 7.6
-
mixed-type, IC50: 7.600 mM Homo sapiens glabrene
1.10.3.1 7.6
-
mixed-type, IC50: 7.600 mM Neurospora crassa glabrene
1.10.3.1 7.6
-
mixed-type, IC50: 7.600 mM Agaricus bisporus glabrene
1.10.3.1 7.6
-
mixed-type, IC50: 7.600 mM Streptomyces glaucescens glabrene
1.14.18.1 0.017
-
competitive, IC50: 0.017 mM Beta vulgaris davanol
1.14.18.1 0.017
-
competitive, IC50: 0.017 mM Homo sapiens davanol
1.14.18.1 0.017
-
competitive, IC50: 0.017 mM Neurospora crassa davanol
1.14.18.1 0.017
-
competitive, IC50: 0.017 mM Agaricus bisporus davanol
1.14.18.1 0.017
-
competitive, IC50: 0.017 mM Streptomyces glaucescens davanol
1.14.18.1 0.034
-
competitive, IC50: 0.034 mM Beta vulgaris dillapiole
1.14.18.1 0.034
-
competitive, IC50: 0.034 mM Homo sapiens dillapiole
1.14.18.1 0.034
-
competitive, IC50: 0.034 mM Neurospora crassa dillapiole
1.14.18.1 0.034
-
competitive, IC50: 0.034 mM Agaricus bisporus dillapiole
1.14.18.1 0.034
-
competitive, IC50: 0.034 mM Streptomyces glaucescens dillapiole
1.14.18.1 0.035
-
competitive, IC50: 0.035 mM Beta vulgaris 3-cymene
1.14.18.1 0.035
-
competitive, IC50: 0.035 mM Homo sapiens 3-cymene
1.14.18.1 0.035
-
competitive, IC50: 0.035 mM Neurospora crassa 3-cymene
1.14.18.1 0.035
-
competitive, IC50: 0.035 mM Agaricus bisporus 3-cymene
1.14.18.1 0.035
-
competitive, IC50: 0.035 mM Streptomyces glaucescens 3-cymene
1.14.18.1 0.07
-
competitive, IC50: 0.070 mM Beta vulgaris quercetin
1.14.18.1 0.07
-
competitive, IC50: 0.070 mM Homo sapiens quercetin
1.14.18.1 0.07
-
competitive, IC50: 0.070 mM Neurospora crassa quercetin
1.14.18.1 0.07
-
competitive, IC50: 0.070 mM Agaricus bisporus quercetin
1.14.18.1 0.07
-
competitive, IC50: 0.070 mM Streptomyces glaucescens quercetin
1.14.18.1 0.23
-
competitive, IC50: 0.230 mM Neurospora crassa kaempferol
1.14.18.1 0.23
-
competitive, IC50: 0.230 mM Agaricus bisporus kaempferol
1.14.18.1 0.23
-
competitive, IC50: 0.230 mM Streptomyces glaucescens kaempferol
1.14.18.1 2.32
-
competitive, IC50: 2.320 mM Beta vulgaris morin
1.14.18.1 2.32
-
competitive, IC50: 2.320 mM Homo sapiens morin
1.14.18.1 2.32
-
competitive, IC50: 2.320 mM Neurospora crassa morin
1.14.18.1 2.32
-
competitive, IC50: 2.320 mM Agaricus bisporus morin
1.14.18.1 2.32
-
competitive, IC50: 2.320 mM Streptomyces glaucescens morin