Application | Comment | Organism |
---|---|---|
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 |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
anthraglycoside B | anthraquinone, isolated from the root of Polygonum cuspidatum | Agaricus bisporus | |
citreorosein | anthraquinone, isolated from the root of Polygonum cuspidatum | Agaricus bisporus | |
emodin | anthraquinone, isolated from the root of Polygonum cuspidatum | Agaricus bisporus | |
kojic acid | - |
Agaricus bisporus | |
additional information | the ranking of the inhibitory potency is physcion > citreorosein = anthraglycoside B = emodin | Agaricus bisporus | |
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 |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Agaricus bisporus | - |
- |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
commercial preparation | - |
Agaricus bisporus | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
L-dopa + 1/2 O2 | - |
Agaricus bisporus | L-dopaquinone + H2O | - |
? |
Synonyms | Comment | Organism |
---|---|---|
tyrosinase | - |
Agaricus bisporus |