BDBM58130 (6E)-6-[4-[N'-[(1E)-1-(6-ketocyclohexa-2,4-dien-1-ylidene)ethyl]hydrazino]-6-methyl-1H-pyrimidin-2-ylidene]cyclohexa-2,4-dien-1-one::(6E)-6-[6-methyl-4-[2-[(1E)-1-(6-oxidanylidenecyclohexa-2,4-dien-1-ylidene)ethyl]hydrazinyl]-1H-pyrimidin-2-ylidene]cyclohexa-2,4-dien-1-one::(6E)-6-[6-methyl-4-[2-[(1E)-1-(6-oxocyclohexa-2,4-dien-1-ylidene)ethyl]hydrazinyl]-1H-pyrimidin-2-ylidene]cyclohexa-2,4-dien-1-one::(6E)-6-[6-methyl-4-[[(1E)-1-(6-oxo-1-cyclohexa-2,4-dienylidene)ethyl]hydrazo]-1H-pyrimidin-2-ylidene]-1-cyclohexa-2,4-dienone::MLS000776683::SMR000413082::cid_6517668
SMILES CC(N=Nc1cc(C)nc(n1)-c1ccccc1O)c1ccccc1O
InChI Key InChIKey=MFHDZZQMIKLPRY-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 58130
TargetBRCA1-associated RING domain protein 1(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 5.35E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...More data for this Ligand-Target Pair
Affinity DataIC50: 6.71E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...More data for this Ligand-Target Pair
Affinity DataEC50: 1.40E+4nMAssay Description:Keywords: Group A streptococcus, GAS, streptokinase, expression, virulence, inhibition, dose response, EC50 Assay Overview: The goal of this assa...More data for this Ligand-Target Pair
