BDBM42151 (5aR,9aS)-10-oxidanidyl-5-oxidanylidene-5a,6,7,8,9,9a-hexahydroindeno[1,2-b]quinoxalin-5-ium-11-one::(5aR,9aS)-10-oxido-5-oxo-5a,6,7,8,9,9a-hexahydroindeno[1,2-b]quinoxalin-5-ium-11-one::(5aR,9aS)-5-keto-10-oxido-5a,6,7,8,9,9a-hexahydroindeno[1,2-b]quinoxalin-5-ium-11-one::(5aR,9aS)-5a,6,7,8,9,9a-hexahydro-11H-indeno[1,2-b]quinoxalin-11-one 5,10-dioxide::MLS000089701::SMR000024319::cid_1886595
SMILES [O-]N1[C@H]2CCCC[C@H]2[N+](=O)C2=C1C(=O)c1ccccc21
InChI Key InChIKey=CSPAZJUKGODKGZ-NEPJUHHUSA-N
Data 13 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 42151
TargetApoptotic protease-activating factor 1(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: >1.00E+5nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBIMR, San Diego, C...More data for this Ligand-Target Pair
TargetApoptotic protease-activating factor 1(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 1.81E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBIMR, San Diego, C...More data for this Ligand-Target Pair