BDBM50388666 CHEMBL2059317

SMILES O=C1CCc2c(F)cccc2N1CCCN1CCC(n2c(=O)[nH]c3ccccc32)CC1

InChI Key InChIKey=DBXZHGCWVRWCGN-UHFFFAOYSA-N

Data  1 KI  1 IC50  1 EC50

  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 = 50388666   

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

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50388666BDBM50388666(CHEMBL2059317)
Affinity DataKi:  60nMAssay 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
In Depth
Date in BDB:
2/8/2013
Entry Details Article
PubMed
TargetMuscarinic acetylcholine receptor M1(Human)
H. Lundbeck

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50388666BDBM50388666(CHEMBL2059317)
Affinity DataEC50:  68nMAssay Description:Agonist activity at human M1 receptor expressed in CHO-K1 cells assessed as calcium mobilization for 6 mins by Calcium4-based stainingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/8/2013
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50388666BDBM50388666(CHEMBL2059317)
Affinity DataIC50: 5.30E+3nMAssay Description:Inhibition of human ERG expressed in CHO cells after 30 mins by Rb+ flux assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/8/2013
Entry Details Article
PubMed