null

SMILES O=C(N[C@H]1CC[C@H](CCN2CCc3ccc(cc3C2)C#N)CC1)c1cc2ccccc2[nH]1

InChI Key InChIKey=JGLGOAQPUQITLD-OGAOHHHESA-N

  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 = 50409213   

TargetD(3) dopamine receptor(Homo sapiens (Human))
National Institute on Drug Abuse

Curated by ChEMBL
LigandPNGBDBM50409213(CHEMBL2113347)copy SMILEScopy InChI
Affinity DataKi:  3.90nMAssay Description:Displacement of [3H]N-methylspiperone from human D3 receptor expressed in HEK293 cell membranes after 1 hr by liquid scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9MRVPubMed
TargetD(2) dopamine receptor(Homo sapiens (Human))
National Institute on Drug Abuse

Curated by ChEMBL
LigandPNGBDBM50409213(CHEMBL2113347)copy SMILEScopy InChI
Affinity DataKi:  485nMAssay Description:Displacement of [3H]N-methylspiperone from human D2L receptor expressed in HEK293 cell membranes after 1 hr by liquid scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9MRVPubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50409213(CHEMBL2113347)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of cytochrome P450 2D6More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DJ5GB1PubMed