BDBM50610696 CHEMBL5281064

SMILES c1cc2c(cc1F)sc(c2Cl)C(=O)O

InChI Key InChIKey=HSRSWUJIPYUCSE-UHFFFAOYSA-N

Data  3 IC50

PDB links: 1 PDB ID matches this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50610696   

LigandChemical structure of BindingDB Monomer ID 50610696BDBM50610696(CHEMBL5281064)
Affinity DataIC50: 920nMAssay Description:Inhibition of human BDK using LBD-Tev-PhosphoPep/Lipoyl as substrate preincubated for 15 mins followed by substrate/ATP addition and measured after 9...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
LigandChemical structure of BindingDB Monomer ID 50610696BDBM50610696(CHEMBL5281064)
Affinity DataIC50: 5.60E+3nMAssay Description:Inhibition of BDK in human skeletal myocyte using BCKDHA as substrate assessed as inhibition of substrate phosphorylation incubated for 60 mins by Al...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetC-type lectin domain family 4 member M(Human)
National Institute of Pharmaceutical Education and Research (NIPER)

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50610696BDBM50610696(CHEMBL5281064)
Affinity DataIC50: 1.96E+6nMAssay Description:Inhibition of human DC-SIGN overexpressed in human Raji cells incubated for 30 mins by flow cytometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/21/2024
Entry Details
PubMed