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Literature summary extracted from

  • Ullah, F.; Hussain, H.; Hussain, J.; Bukhari, I.A.; Khan, M.T.; Choudhary, M.I.; Gilani, A.H.; Ahmad, V.U.
    Tyrosinase inhibitory pentacyclic triterpenes and analgesic and spasmolytic activities of methanol extracts of Rhododendron collettianum (2007), Phytother. Res., 21, 1076-1081.
    View publication on PubMed

Application

EC Number Application Comment Organism
1.14.18.1 drug development tyrosinase inhibitors can be clinically useful for the treatment of some dermatological disorders associated with melanin hyperpigmentation Agaricus bisporus

Inhibitors

EC Number Inhibitors Comment Organism Structure
1.14.18.1 2alpha,3alpha,23-trihydroxyolean-12-en-28-oic acid pentacyclic triterpene extracted from Rhododendron collettianum Agaricus bisporus
1.14.18.1 3beta, 23, 24-trihydroxyolean-12-en-28-oic acid pentacyclic triterpene extracted from Rhododendron collettianum Agaricus bisporus
1.14.18.1 arjungenin pentacyclic triterpene extracted from Rhododendron collettianum Agaricus bisporus
1.14.18.1 arjunilic acid pentacyclic triterpene extracted from Rhododendron collettianum, most potent inhibitor, have potential to be used for the treatment of hyperpigmentation associated with the high production of melanocytes Agaricus bisporus
1.14.18.1 bayogenin pentacyclic triterpene extracted from Rhododendron collettianum Agaricus bisporus
1.14.18.1 betulinic acid pentacyclic triterpene extracted from Rhododendron collettianum Agaricus bisporus
1.14.18.1 erythrodiol pentacyclic triterpene extracted from Rhododendron collettianum Agaricus bisporus
1.14.18.1 kojic acid used as a positive control Agaricus bisporus
1.14.18.1 L-mimosine used as a positive control Agaricus bisporus
1.14.18.1 maslinic acid pentacyclic triterpene extracted from Rhododendron collettianum Agaricus bisporus
1.14.18.1 methyl arjunolate pentacyclic triterpene extracted from Rhododendron collettianum Agaricus bisporus

Organism

EC Number Organism UniProt Comment Textmining
1.14.18.1 Agaricus bisporus
-
-
-

Source Tissue

EC Number Source Tissue Comment Organism Textmining
1.14.18.1 commercial preparation
-
Agaricus bisporus
-

Substrates and Products (Substrate)

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
-
?

Synonyms

EC Number Synonyms Comment Organism
1.14.18.1 tyrosinase
-
Agaricus bisporus

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
1.14.18.1 6.8
-
tyrosinase inhibition assay at Agaricus bisporus

IC50 Value

EC Number IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
1.14.18.1 0.001
-
-
Agaricus bisporus arjunilic acid
1.14.18.1 0.0011
-
-
Agaricus bisporus bayogenin
1.14.18.1 0.00112
-
-
Agaricus bisporus 2alpha,3alpha,23-trihydroxyolean-12-en-28-oic acid
1.14.18.1 0.0017
-
-
Agaricus bisporus maslinic acid
1.14.18.1 0.00214
-
-
Agaricus bisporus betulinic acid
1.14.18.1 0.002345
-
-
Agaricus bisporus methyl arjunolate
1.14.18.1 0.00312
-
-
Agaricus bisporus erythrodiol
1.14.18.1 0.00368
-
-
Agaricus bisporus L-mimosine
1.14.18.1 0.006577
-
-
Agaricus bisporus arjungenin
1.14.18.1 0.01102
-
-
Agaricus bisporus 3beta, 23, 24-trihydroxyolean-12-en-28-oic acid
1.14.18.1 0.01667
-
-
Agaricus bisporus kojic acid