BDBM94931 (6-bromo-4-phenyl-quinazolin-2-yl)-[(E)-(5-nitro-2-furyl)methyleneamino]amine::6-bromanyl-N-[(E)-(5-nitrofuran-2-yl)methylideneamino]-4-phenyl-quinazolin-2-amine::6-bromo-N-[(E)-(5-nitro-2-furanyl)methylideneamino]-4-phenyl-2-quinazolinamine::6-bromo-N-[(E)-(5-nitrofuran-2-yl)methylideneamino]-4-phenylquinazolin-2-amine::MLS000529204::N-(6-Bromo-4-phenyl-quinazolin-2-yl)-N'-(5-nitro-furan-2-ylmethylene)-hydrazine::SMR000121679::cid_9589687
SMILES [O-][N+](=O)c1ccc([CH-]\N=[NH+]\c2nc(-c3ccccc3)c3cc(Br)ccc3n2)o1
InChI Key InChIKey=BEGCEULEMMEBFT-UHFFFAOYSA-O
Data 3 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 94931
Affinity DataIC50: 6.57E+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
TargetLow molecular weight phosphotyrosine protein phosphatase(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
TargetLow molecular weight phosphotyrosine protein phosphatase(Human)
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
