BDBM50022454 3',4'-dihydro-2'H-spiro[imidazolidine-4,1'-naphthalene]-2,5-dione::3',4'-dihydro-2H,2'H,5H-spiro[imidazolidine-4,1'-naphthalene]-2,5-dione::CHEMBL289046::spiro[tetrahydro-1H-imidazole-4,1'-(1',2',3',4'-tetrahydronaphthalene)]-2,5-dione

SMILES O=C1NC(=O)C2(CCCc3ccccc23)N1

InChI Key InChIKey=OZYWLMZRNIFQPM-UHFFFAOYSA-N

Data  5 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 5 hits for monomerid = 50022454   

TargetAldo-keto reductase family 1 member B1 [K65Q](Bos taurus (Cattle))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50022454(3',4'-dihydro-2'H-spiro[imidazolidine-4,1'-naphtha...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of partially purified calf lens aldose reductase; value ranges from 10E-4 to 10e-5 MMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium channel protein type 1/2/3 subunit alpha(Rattus norvegicus)
University Of Alabama At Birmingham

Curated by ChEMBL
LigandPNGBDBM50022454(3',4'-dihydro-2'H-spiro[imidazolidine-4,1'-naphtha...)
Affinity DataIC50:  8.51E+5nMAssay Description:Inhibition of [3H]BTX-B binding to Neuronal voltage-dependent sodium channel of rat cerebral cortex synaptoneurosomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Kyushu University

Curated by ChEMBL
LigandPNGBDBM50022454(3',4'-dihydro-2'H-spiro[imidazolidine-4,1'-naphtha...)
Affinity DataIC50:  1.14E+5nMAssay Description:Inhibition of human Protein kinase C gammaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Kyushu University

Curated by ChEMBL
LigandPNGBDBM50022454(3',4'-dihydro-2'H-spiro[imidazolidine-4,1'-naphtha...)
Affinity DataIC50:  8.01E+4nMAssay Description:Inhibition of Protein kinase C beta 2 expressed in Sf-9 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSodium channel protein type 1/2/3 subunit alpha(Rattus norvegicus)
University Of Alabama At Birmingham

Curated by ChEMBL
LigandPNGBDBM50022454(3',4'-dihydro-2'H-spiro[imidazolidine-4,1'-naphtha...)
Affinity DataIC50:  8.51E+5nMAssay Description:In vitro inhibition of Voltage-gated sodium channel by the displacement of [3H]batrachotoxin A 20-alpha-benzoate in rat brain cerebral cortex synapto...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed