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SMILES: COc1cc2nccc(Oc3ccc(CC(=O)Nc4cn(C)nc4C)cc3)c2cc1OC

InChI Key: InChIKey=LJZDAUHIEXUPMS-UHFFFAOYSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50381951   
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
Platelet-derived growth factor receptor beta


(Homo sapiens (Human))
BDBM50381951
PNG
(CHEMBL2023490)
Show SMILES COc1cc2nccc(Oc3ccc(CC(=O)Nc4cn(C)nc4C)cc3)c2cc1OC
Show InChI InChI=1S/C24H24N4O4/c1-15-20(14-28(2)27-15)26-24(29)11-16-5-7-17(8-6-16)32-21-9-10-25-19-13-23(31-4)22(30-3)12-18(19)21/h5-10,12-14H,11H2,1-4H3,(H,26,29)
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n/an/a 10n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of PDGFRbeta


Bioorg Med Chem Lett 22: 3050-5 (2012)


Article DOI: 10.1016/j.bmcl.2012.03.074
BindingDB Entry DOI: 10.7270/Q298881Z
More data for this
Ligand-Target Pair
Macrophage colony-stimulating factor 1 receptor


(Homo sapiens (Human))
BDBM50381951
PNG
(CHEMBL2023490)
Show SMILES COc1cc2nccc(Oc3ccc(CC(=O)Nc4cn(C)nc4C)cc3)c2cc1OC
Show InChI InChI=1S/C24H24N4O4/c1-15-20(14-28(2)27-15)26-24(29)11-16-5-7-17(8-6-16)32-21-9-10-25-19-13-23(31-4)22(30-3)12-18(19)21/h5-10,12-14H,11H2,1-4H3,(H,26,29)
PDB

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antibodypedia
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AffyNet 
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PC cid
PC sid
UniChem

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Article
PubMed
n/an/a 300n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of CSF-1R


Bioorg Med Chem Lett 22: 3050-5 (2012)


Article DOI: 10.1016/j.bmcl.2012.03.074
BindingDB Entry DOI: 10.7270/Q298881Z
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50381951
PNG
(CHEMBL2023490)
Show SMILES COc1cc2nccc(Oc3ccc(CC(=O)Nc4cn(C)nc4C)cc3)c2cc1OC
Show InChI InChI=1S/C24H24N4O4/c1-15-20(14-28(2)27-15)26-24(29)11-16-5-7-17(8-6-16)32-21-9-10-25-19-13-23(31-4)22(30-3)12-18(19)21/h5-10,12-14H,11H2,1-4H3,(H,26,29)
PDB
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NCI pathway
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KEGG

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PubMed
n/an/a 183n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of KDR


Bioorg Med Chem Lett 22: 3050-5 (2012)


Article DOI: 10.1016/j.bmcl.2012.03.074
BindingDB Entry DOI: 10.7270/Q298881Z
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein kinase FLT3


(Homo sapiens (Human))
BDBM50381951
PNG
(CHEMBL2023490)
Show SMILES COc1cc2nccc(Oc3ccc(CC(=O)Nc4cn(C)nc4C)cc3)c2cc1OC
Show InChI InChI=1S/C24H24N4O4/c1-15-20(14-28(2)27-15)26-24(29)11-16-5-7-17(8-6-16)32-21-9-10-25-19-13-23(31-4)22(30-3)12-18(19)21/h5-10,12-14H,11H2,1-4H3,(H,26,29)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 30n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of Flt3


Bioorg Med Chem Lett 22: 3050-5 (2012)


Article DOI: 10.1016/j.bmcl.2012.03.074
BindingDB Entry DOI: 10.7270/Q298881Z
More data for this
Ligand-Target Pair