null

SMILES COc1ccc(Oc2nc(Cl)ccc2[N+]([O-])=O)cc1

InChI Key InChIKey=IPZJMCGPCSSZJS-UHFFFAOYSA-N

  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 = 50421322   

TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421322(CHEMBL2088178)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of MerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421322(CHEMBL2088178)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AxlMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase receptor TYRO3(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421322(CHEMBL2088178)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Tyro3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed