BDBM50388682 CHEMBL2059318

SMILES Fc1ccc2N(CCCN3CCC(CC3)n3c4ccccc4[nH]c3=O)C(=O)CCc2c1

InChI Key InChIKey=NLKZCVSXHKODTA-UHFFFAOYSA-N

Data  1 KI  1 IC50

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50388682   

TargetPotassium voltage-gated channel subfamily H member 2(Human)
H. Lundbeck

Curated by ChEMBL

LigandBDBM50388682(CHEMBL2059318)Copy SMILESCopy InChI

Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of human ERG expressed in CHO cells after 30 mins by Rb+ flux assayMore data for this Ligand-Target Pair

Target InfoPDBKEGG
UniProtKB/SwissProtUniProtKB/TrEMBL
GoogleScholar

Ligand InfoCHEMBLPC cidPC sidSimilars

In Depth
Date in BDB:
2/8/2013
Entry Details Article
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TargetD(2) dopamine receptor(Human)
H. Lundbeck

Curated by ChEMBL

LigandBDBM50388682(CHEMBL2059318)Copy SMILESCopy InChI

Affinity DataKi:  6.5nMAssay Description:Displacement of [3H]raclopride from human D2L receptor expressed in CHO cells after 60 mins by scintillation proximity assayMore data for this Ligand-Target Pair

Target InfoPDBKEGG
UniProtKB/SwissProtUniProtKB/TrEMBL
GoogleScholar

Ligand InfoCHEMBLPC cidPC sidSimilars

In Depth
Date in BDB:
2/8/2013
Entry Details Article
Copy Entry DOIPubMed
Copy Rxn URL