BDBM50398965 CHEMBL2179670

SMILES CC(=O)Nc1ccc(CCN2CCC(COc3nc4ccccc4c4cn(C)cc34)CC2)cc1

InChI Key InChIKey=YJAIZWWQRYKSON-UHFFFAOYSA-N

Data  2 KI  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 = 50398965   

Target5-hydroxytryptamine receptor 4(Homo sapiens (Human))
Angelini Santa Palomba Research Center

Curated by ChEMBL
LigandPNGBDBM50398965(CHEMBL2179670)
Affinity DataKi:  2nMAssay Description:Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Angelini Santa Palomba Research Center

Curated by ChEMBL
LigandPNGBDBM50398965(CHEMBL2179670)
Affinity DataKi:  3.16E+3nMAssay Description:Displacement of [3H]ketanserin from human 5HT2AR expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Angelini Santa Palomba Research Center

Curated by ChEMBL
LigandPNGBDBM50398965(CHEMBL2179670)
Affinity DataIC50:  20nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed