BDBM50434117 CHEMBL2381488

SMILES Clc1cccc2CC(=O)Nc12

InChI Key InChIKey=FPDLUAACCNVSQA-UHFFFAOYSA-N

Data  1 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50434117   

TargetAryl hydrocarbon receptor(Human)
Palacky University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50434117BDBM50434117(CHEMBL2381488)
Affinity DataEC50:  5.60E+3nMAssay Description:Inhibition of mouse SGLT2-mediated [14C]alpha-methylglucopyranoside uptake by cell based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/3/2026
Entry Details PubMed
TargetAryl hydrocarbon receptor(Human)
Palacky University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50434117BDBM50434117(CHEMBL2381488)
Affinity DataEC50:  5.29E+4nMAssay Description:Inhibition of EGFR in human A431 cells by phosphotyrosine cell-based ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/3/2026
Entry Details PubMed
TargetChymase(Human)
Boehringer Ingelheim Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50434117BDBM50434117(CHEMBL2381488)
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of recombinant human chymase using bis(succinoyl-L-alanyl-L-prolyl-L-phenylalanylamide) as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed