BDBM50022495 6,7,8,9-tetrahydro-2'H,5'H-spiro[benzo[7]annulene-5,4'-imidazolidine]-2',5'-dione::6,7,8,9-tetrahydrospiro[benzo[7]annulene-5,4'-imidazolidine]-2',5'-dione::CHEMBL39377::spiro[6,7,8,9-tetrahydro-5H-benzo[a]cycloheptene-5,4'-(tetrahydro-1'H-imidazole)]-2',5'-dione

SMILES: O=C1NC(=O)C2(CCCCc3ccccc23)N1

InChI Key: InChIKey=BCSYSQVTCKMBMK-UHFFFAOYSA-N

Data: 3 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50022495   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Aldose reductase (ALR2) (Bos taurus (Cattle))	BDBM50022495 (6,7,8,9-tetrahydro-2'H,5'H-spiro[benzo[7]annulene-...) Show SMILES O=C1NC(=O)C2(CCCCc3ccccc23)N1 Show InChI InChI=1S/C13H14N2O2/c16-11-13(15-12(17)14-11)8-4-3-6-9-5-1-2-7-10(9)13/h1-2,5,7H,3-4,6,8H2,(H2,14,15,16,17)	PDB GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Central Research Curated by ChEMBL					Assay Description In vitro inhibition of partially purified calf lens aldose reductase				J Med Chem 31: 230-43 (1988) BindingDB Entry DOI: 10.7270/Q27D2VQF
					More data for this Ligand-Target Pair
Sodium channel protein type I I alpha subunit (Rattus norvegicus)	BDBM50022495 (6,7,8,9-tetrahydro-2'H,5'H-spiro[benzo[7]annulene-...) Show SMILES O=C1NC(=O)C2(CCCCc3ccccc23)N1 Show InChI InChI=1S/C13H14N2O2/c16-11-13(15-12(17)14-11)8-4-3-6-9-5-1-2-7-10(9)13/h1-2,5,7H,3-4,6,8H2,(H2,14,15,16,17)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.51E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay 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...				J Med Chem 42: 1537-45 (1999) Article DOI: 10.1021/jm980556l BindingDB Entry DOI: 10.7270/Q2RJ4N61
					More data for this Ligand-Target Pair
Sodium channel protein type I I alpha subunit (Rattus norvegicus)	BDBM50022495 (6,7,8,9-tetrahydro-2'H,5'H-spiro[benzo[7]annulene-...) Show SMILES O=C1NC(=O)C2(CCCCc3ccccc23)N1 Show InChI InChI=1S/C13H14N2O2/c16-11-13(15-12(17)14-11)8-4-3-6-9-5-1-2-7-10(9)13/h1-2,5,7H,3-4,6,8H2,(H2,14,15,16,17)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.51E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of [3H]BTX-B binding to Neuronal voltage-dependent sodium channel of rat cerebral cortex synaptoneurosomes				J Med Chem 40: 602-7 (1997) Article DOI: 10.1021/jm960692v BindingDB Entry DOI: 10.7270/Q2J96931
					More data for this Ligand-Target Pair