BDBM52621 (4Z)-4-(4-hydroxy-3-methoxy-5-nitro-benzylidene)-1-(m-tolyl)pyrazolidine-3,5-quinone::(4Z)-4-[(3-methoxy-5-nitro-4-oxidanyl-phenyl)methylidene]-1-(3-methylphenyl)pyrazolidine-3,5-dione::(4Z)-4-[(4-hydroxy-3-methoxy-5-nitrophenyl)methylidene]-1-(3-methylphenyl)pyrazolidine-3,5-dione::4-(4-hydroxy-3-methoxy-5-nitrobenzylidene)-1-(3-methylphenyl)-3,5-pyrazolidinedione::MLS000626744::SMR000299131::cid_2176498
SMILES COc1cc(\C=C2\C(=O)NN(C2=O)c2cccc(C)c2)cc(c1O)[N+]([O-])=O
InChI Key InChIKey=OVGKGOCKQDNRIG-QPEQYQDCSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 52621
TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: >8.00E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 2.55E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair