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Assay Detail

CHEMBL3810522

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of monophenolase activity of mushroom tyrosinase using L-tyrosine as substrate incubated for 10 mins by UV-Visible spectrophotometric analysis
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Agaricus bisporus
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Tyrosinase (CHEMBL3318)
Type SINGLE PROTEIN
Organism Agaricus bisporus

Publication

Design and synthesis of novel hydroxypyridinone derivatives as potential tyrosinase inhibitors.
Zhao DY, Zhang MX, Dong XW, Hu YZ, Dai XY, Wei X, Hider RC, Zhang JC, Zhou T.
Bioorg Med Chem Lett (2016) 26 : 3103 -3108
PubMed 27185329 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 5.04 5.71

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3810334 1 5.71
CHEMBL3809975 1 5.55
CHEMBL3810170 1 5.16
CHEMBL3808924 1 4.93
CHEMBL287556 KOJIC ACID 1 4.90
CHEMBL3808959 1 4.90
CHEMBL3809951 1 4.85
CHEMBL3808964 1 4.81
CHEMBL3809467 1 4.54

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3810334 IC50 = 1950.0 nM 5.71
CHEMBL3809975 IC50 = 2790.0 nM 5.55
CHEMBL3810170 IC50 = 6930.0 nM 5.16
CHEMBL3808924 IC50 = 11760.0 nM 4.93
CHEMBL287556 KOJIC ACID IC50 = 12500.0 nM 4.90
CHEMBL3808959 IC50 = 12480.0 nM 4.90
CHEMBL3809951 IC50 = 14260.0 nM 4.85
CHEMBL3808964 IC50 = 15620.0 nM 4.81
CHEMBL3809467 IC50 = 28710.0 nM 4.54