null

SMILES CN(C)C\C=C\C(=O)Nc1ccc2ncnc(Nc3ccc(Br)cc3F)c2c1

InChI Key InChIKey=SLZOGARBQLIHCR-ONEGZZNKSA-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 = 50209876   

TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50209876((2E)-N-{4-[(4-bromo-2-fluorophenyl)amino]quinazoli...)copy SMILEScopy InChI
Affinity DataIC50: 4.39E+3nMAssay Description:Inhibition of human VEGFR2 in presence of 1 uM ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0VB8PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50209876((2E)-N-{4-[(4-bromo-2-fluorophenyl)amino]quinazoli...)copy SMILEScopy InChI
Affinity DataIC50: 704nMAssay Description:Inhibition of human EGFR in presence of 1 mM ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0VB8PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50209876((2E)-N-{4-[(4-bromo-2-fluorophenyl)amino]quinazoli...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human VEGFR2 in presence of 1 mM ATPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GF0VB8PubMed