EC Number | Application | Comment | Organism |
---|---|---|---|
1.14.18.1 | drug development | commercial plant extracts containing anthraquinones are being increasingly used for pharmaceuticals, foods and cosmetics due to their wide therapeutic and pharmacological properties | Agaricus bisporus |
EC Number | Inhibitors | Comment | Organism | Structure |
---|---|---|---|---|
1.14.18.1 | anthraglycoside B | anthraquinone, isolated from the root of Polygonum cuspidatum | Agaricus bisporus | |
1.14.18.1 | citreorosein | anthraquinone, isolated from the root of Polygonum cuspidatum | Agaricus bisporus | |
1.14.18.1 | emodin | anthraquinone, isolated from the root of Polygonum cuspidatum | Agaricus bisporus | |
1.14.18.1 | kojic acid | - |
Agaricus bisporus | |
1.14.18.1 | additional information | the ranking of the inhibitory potency is physcion > citreorosein = anthraglycoside B = emodin | Agaricus bisporus | |
1.14.18.1 | physcion | anthraquinone, isolated from the root of Polygonum cuspidatum. Most potent tyrosinase inhibition among the four anthraquinones examined, which is comparable to kojic acid | Agaricus bisporus |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
1.14.18.1 | Agaricus bisporus | - |
- |
- |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
1.14.18.1 | commercial preparation | - |
Agaricus bisporus | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
1.14.18.1 | L-dopa + 1/2 O2 | - |
Agaricus bisporus | L-dopaquinone + H2O | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
1.14.18.1 | tyrosinase | - |
Agaricus bisporus |