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Assay Detail

CHEMBL2050449

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

Binding
Inhibition of mushroom tyrosinase activity using L-tyrosine as substrate after 30 mins by spectrophotometric analysis
6
Total Activities
3
Compounds Tested
2
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 5-(substituted benzylidene)thiazolidine-2,4-dione derivatives as novel tyrosinase inhibitors.
Ha YM, Park YJ, Kim JA, Park D, Park JY, Lee HJ, Lee JY, Moon HR, Chung HY.
Eur J Med Chem (2012) 49 : 245 -252
PubMed 22301213 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 4.83 5.01
Inhibition 3 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL233375 2 5.01
CHEMBL87706 2 4.87
CHEMBL287556 KOJIC ACID 2 4.61

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL233375 IC50 = 9870.0 nM 5.01
CHEMBL87706 IC50 = 13360.0 nM 4.87
CHEMBL287556 KOJIC ACID IC50 = 24720.0 nM 4.61
CHEMBL87706 Inhibition - % -
CHEMBL233375 Inhibition - % -
CHEMBL287556 KOJIC ACID Inhibition - % -