BDBM50279923 CHEMBL69572::N-[1-(4-Nitro-phenyl)-meth-(E)-ylidene]-N'-phenyl-hydrazine::cid_252617

SMILES [O-][N+](=O)c1ccc([CH-]\N=[NH+]\c2ccccc2)cc1

InChI Key InChIKey=BPAGOBKFQMQMLG-CCEZHUSRSA-O

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50279923   

TargetSentrin-specific protease 1(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM50279923(CHEMBL69572 | N-[1-(4-Nitro-phenyl)-meth-(E)-ylide...)
Affinity DataIC50:  7.20E+3nMMore data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50279923(CHEMBL69572 | N-[1-(4-Nitro-phenyl)-meth-(E)-ylide...)
Affinity DataIC50: >3.32E+6nMAssay Description:Inhibitory concentration against phosphoylation of angiotensin I catalyzed by protein-tyrosine kinase p56lckMore data for this Ligand-Target Pair
In DepthDetails Article
TargetSentrin-specific protease 1(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM50279923(CHEMBL69572 | N-[1-(4-Nitro-phenyl)-meth-(E)-ylide...)
Affinity DataIC50:  2.15E+4nMMore data for this Ligand-Target Pair
In DepthDetails PCBioAssay