BDBM50414582 CHEMBL564347

SMILES [H][C@]12CC[C@@](CN(C)CCN3CCN(C3=O)c3ccc4OCOc4c3)(CC1)C2(C)C

InChI Key InChIKey=ABSKTFYOWZQKEU-QBNMFFNISA-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 = 50414582   

TargetD(3) dopamine receptor(Homo sapiens (Human))
Cancer Therapeutics

Curated by ChEMBL
LigandPNGBDBM50414582(CHEMBL564347)
Affinity DataKi:  50.1nMAssay Description:Antagonist activity at human D3 receptor expressed in CHO cells by [35S]GTPgammaS binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
Cancer Therapeutics

Curated by ChEMBL
LigandPNGBDBM50414582(CHEMBL564347)
Affinity DataKi:  1.58E+3nMAssay Description:Antagonist activity at human D2 receptor expressed in CHO cells by [35S]GTPgammaS binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Cancer Therapeutics

Curated by ChEMBL
LigandPNGBDBM50414582(CHEMBL564347)
Affinity DataIC50:  6.31E+3nMAssay Description:Displacement of [3H]dofetilide from human ERG channel by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed