BDBM50398968 CHEMBL2179675

SMILES Cn1cc2c(OCC3CCN(CCc4ccc(N)cc4)CC3)nc3ccccc3c2c1

InChI Key InChIKey=YOBFWRIGWQNXBS-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 = 50398968   

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

Curated by ChEMBL
LigandPNGBDBM50398968(CHEMBL2179675)
Affinity DataKi:  5.01nMAssay 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 Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Angelini Santa Palomba Research Center

Curated by ChEMBL
LigandPNGBDBM50398968(CHEMBL2179675)
Affinity DataIC50: 50nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
Target5-hydroxytryptamine receptor 2A(Human)
Angelini Santa Palomba Research Center

Curated by ChEMBL
LigandPNGBDBM50398968(CHEMBL2179675)
Affinity DataKi:  251nMAssay Description:Displacement of [3H]ketanserin from human 5HT2AR expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed