BDBM50229213 2-methyl-2-(4-((4-(4-methylthiazol-2-yl)benzamido)methyl)phenoxy)propanoic acid::CHEMBL253522

SMILES COc1c(-c2ccc(O)cc2)oc2cc3c(cc2c1=O)OCO3

InChI Key InChIKey=APLBIJUJEBHZMP-UHFFFAOYSA-N

Data  2 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50229213   

TargetProcathepsin L(Human)
Seoul National University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50229213BDBM50229213(CHEMBL6078249)
Affinity DataKi:  322nMAssay Description:Antagonist activity at human PPAR-alpha assessed as inhibition of GW7647-induced effect after overnight incubation by cell-based luciferase reporter ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2026
Entry Details ArticlePubMed
TargetProcathepsin L(Human)
Seoul National University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50229213BDBM50229213(CHEMBL6078249)
Affinity DataIC50: 3.20E+3nMAssay Description:Antagonist activity at human PPAR-alpha assessed as inhibition of GW7647-induced effect after overnight incubation by cell-based luciferase reporter ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/2/2026
Entry Details ArticlePubMed