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BDBM50092231 (4-Phenoxy-phenyl)-quinazolin-4-yl-amine::CHEMBL304760

SMILES: N(c1ccc(Oc2ccccc2)cc1)c1ncnc2ccccc12

InChI Key: InChIKey=RJOICMFRJBMONF-UHFFFAOYSA-N

Data: 3 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50092231   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Angiopoietin-1 receptor


(Homo sapiens (Human))
BDBM50092231
PNG
((4-Phenoxy-phenyl)-quinazolin-4-yl-amine | CHEMBL3...)
Show SMILES N(c1ccc(Oc2ccccc2)cc1)c1ncnc2ccccc12
Show InChI InChI=1S/C20H15N3O/c1-2-6-16(7-3-1)24-17-12-10-15(11-13-17)23-20-18-8-4-5-9-19(18)21-14-22-20/h1-14H,(H,21,22,23)
PDB
MMDB

KEGG

UniProtKB/SwissProt

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DrugBank
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CHEMBL
PC cid
PC sid
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PubMed
n/an/a 1.79E+4n/an/an/an/an/an/a



BASF Bioresearch Corporation

Curated by ChEMBL


Assay Description
Inhibition of tie-2 at 5 uM ATP


Bioorg Med Chem Lett 10: 2167-70 (2001)


BindingDB Entry DOI: 10.7270/Q2J38RTH
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50092231
PNG
((4-Phenoxy-phenyl)-quinazolin-4-yl-amine | CHEMBL3...)
Show SMILES N(c1ccc(Oc2ccccc2)cc1)c1ncnc2ccccc12
Show InChI InChI=1S/C20H15N3O/c1-2-6-16(7-3-1)24-17-12-10-15(11-13-17)23-20-18-8-4-5-9-19(18)21-14-22-20/h1-14H,(H,21,22,23)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a<8n/an/an/an/an/an/a



BASF Bioresearch Corporation

Curated by ChEMBL


Assay Description
Inhibition of p56 Lck tyrosine kinase at 1 mM ATP


Bioorg Med Chem Lett 10: 2167-70 (2001)


BindingDB Entry DOI: 10.7270/Q2J38RTH
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50092231
PNG
((4-Phenoxy-phenyl)-quinazolin-4-yl-amine | CHEMBL3...)
Show SMILES N(c1ccc(Oc2ccccc2)cc1)c1ncnc2ccccc12
Show InChI InChI=1S/C20H15N3O/c1-2-6-16(7-3-1)24-17-12-10-15(11-13-17)23-20-18-8-4-5-9-19(18)21-14-22-20/h1-14H,(H,21,22,23)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a 2.72E+3n/an/an/an/an/an/a



BASF Bioresearch Corporation

Curated by ChEMBL


Assay Description
Inhibition of Vascular endothelial growth factor receptor 2 at 5 uM ATP


Bioorg Med Chem Lett 10: 2167-70 (2001)


BindingDB Entry DOI: 10.7270/Q2J38RTH
More data for this
Ligand-Target Pair