BDBM50319573 CHEMBL1084453::N1-(4-(2-(4-(1H-benzo[d]imidazol-2-ylamino)naphthalen-1-yloxy)pyridin-3-yl)pyrimidin-2-yl)-N3,N3,2,2-tetramethylpropane-1,3-diamine

SMILES CN(C)CC(C)(C)CNc1nccc(n1)-c1cccnc1Oc1ccc(Nc2nc3ccccc3[nH]2)c2ccccc12

InChI Key InChIKey=NMULSNNATHYGPZ-UHFFFAOYSA-N

Data  5 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 5 hits for monomerid = 50319573   

TargetAurora kinase B(Human)
Amgen

Curated by ChEMBL
LigandPNGBDBM50319573(N1-(4-(2-(4-(1H-benzo[d]imidazol-2-ylamino)naphtha...)
Affinity DataIC50: 759nMAssay Description:Inhibition of Aurora BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
TargetAurora kinase A(Human)
Amgen

Curated by ChEMBL
LigandPNGBDBM50319573(N1-(4-(2-(4-(1H-benzo[d]imidazol-2-ylamino)naphtha...)
Affinity DataIC50: 1.66E+3nMAssay Description:Inhibition of Aurora AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandPNGBDBM50319573(N1-(4-(2-(4-(1H-benzo[d]imidazol-2-ylamino)naphtha...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of KDRMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Amgen

Curated by ChEMBL
LigandPNGBDBM50319573(N1-(4-(2-(4-(1H-benzo[d]imidazol-2-ylamino)naphtha...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of LCKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
Amgen

Curated by ChEMBL
LigandPNGBDBM50319573(N1-(4-(2-(4-(1H-benzo[d]imidazol-2-ylamino)naphtha...)
Affinity DataIC50: 82nMAssay Description:Inhibition of Tie2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed