BDBM50388669 CHEMBL2059319

SMILES Fc1ccc2CCC(=O)N(CCCN3CCC(CC3)n3c4ccccc4[nH]c3=O)c2c1

InChI Key InChIKey=ABUDXXYFKLCSKO-UHFFFAOYSA-N

Data  1 KI  1 IC50

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50388669   

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

Curated by ChEMBL

LigandBDBM50388669(CHEMBL2059319)Copy SMILESCopy InChI

Affinity DataIC50: 5.70E+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

LigandBDBM50388669(CHEMBL2059319)Copy SMILESCopy InChI

Affinity DataKi:  90nMAssay 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