BDBM50388665 CHEMBL2059312

SMILES O=C1CCc2ccccc2N1OCCN1CCC(CC1)n1c2ccccc2[nH]c1=O

InChI Key InChIKey=ZXXQVMFRALHHSH-UHFFFAOYSA-N

Data  1 KI  1 IC50

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50388665   

TargetD(2) dopamine receptor(Human)
H. Lundbeck

Curated by ChEMBL

LigandBDBM50388665(CHEMBL2059312)Copy SMILESCopy InChI

Affinity DataKi:  55nMAssay 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
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TargetPotassium voltage-gated channel subfamily H member 2(Human)
H. Lundbeck

Curated by ChEMBL

LigandBDBM50388665(CHEMBL2059312)Copy SMILESCopy InChI

Affinity DataIC50: 9.30E+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
Copy BDB DOIPubMed
Copy reaction URL