BDBM50602163 CHEMBL5189636

SMILES OC[C@@H]1Cc2ccc(Cl)cc2[C@@H](N1)c1cc(Cl)cc(Cl)c1

InChI Key InChIKey=HWDYWVRNXBUCEH-HOCLYGCPSA-N

Data  2 EC50

  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 2 hits for monomerid = 50602163   

TargetTransient receptor potential cation channel subfamily M member 4(Homo sapiens)
Turning Point Therapeutics

Curated by ChEMBL
LigandPNGBDBM50602163(CHEMBL5189636)
Affinity DataEC50:  8.91E+3nMAssay Description:Agonist activity at human TRPM4 expressed in CHO-K1 cells assessed as increase in relative fluorescence unit by measuring membrane potential by FLIPR...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetTransient receptor potential cation channel subfamily M member 5(Homo sapiens (Human))
Turning Point Therapeutics

Curated by ChEMBL
LigandPNGBDBM50602163(CHEMBL5189636)
Affinity DataEC50:  200nMAssay Description:Agonist activity at human TRPM5 expressed in CHO-K1 cells assessed as increase in relative fluorescence unit measured for 2 mins by FLIPR based membr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed