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SMILES: COc1cc(Oc2ncnc3cc(OC)c(OC)cc23)ccc1CC(=O)Nc1cn(C)nc1C

InChI Key: InChIKey=XBROJUXHWFXTOG-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 = 50381933   
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
Macrophage colony-stimulating factor 1 receptor


(Homo sapiens (Human))
BDBM50381933
PNG
(CHEMBL2023487)
Show SMILES COc1cc(Oc2ncnc3cc(OC)c(OC)cc23)ccc1CC(=O)Nc1cn(C)nc1C
Show InChI InChI=1S/C24H25N5O5/c1-14-19(12-29(2)28-14)27-23(30)8-15-6-7-16(9-20(15)31-3)34-24-17-10-21(32-4)22(33-5)11-18(17)25-13-26-24/h6-7,9-13H,8H2,1-5H3,(H,27,30)
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Article
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n/an/a>1.00E+3n/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
Platelet-derived growth factor receptor beta


(Homo sapiens (Human))
BDBM50381933
PNG
(CHEMBL2023487)
Show SMILES COc1cc(Oc2ncnc3cc(OC)c(OC)cc23)ccc1CC(=O)Nc1cn(C)nc1C
Show InChI InChI=1S/C24H25N5O5/c1-14-19(12-29(2)28-14)27-23(30)8-15-6-7-16(9-20(15)31-3)34-24-17-10-21(32-4)22(33-5)11-18(17)25-13-26-24/h6-7,9-13H,8H2,1-5H3,(H,27,30)
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KEGG

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n/an/a 50n/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
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50381933
PNG
(CHEMBL2023487)
Show SMILES COc1cc(Oc2ncnc3cc(OC)c(OC)cc23)ccc1CC(=O)Nc1cn(C)nc1C
Show InChI InChI=1S/C24H25N5O5/c1-14-19(12-29(2)28-14)27-23(30)8-15-6-7-16(9-20(15)31-3)34-24-17-10-21(32-4)22(33-5)11-18(17)25-13-26-24/h6-7,9-13H,8H2,1-5H3,(H,27,30)
PDB
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KEGG

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Article
PubMed
n/an/a>1.00E+4n/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))
BDBM50381933
PNG
(CHEMBL2023487)
Show SMILES COc1cc(Oc2ncnc3cc(OC)c(OC)cc23)ccc1CC(=O)Nc1cn(C)nc1C
Show InChI InChI=1S/C24H25N5O5/c1-14-19(12-29(2)28-14)27-23(30)8-15-6-7-16(9-20(15)31-3)34-24-17-10-21(32-4)22(33-5)11-18(17)25-13-26-24/h6-7,9-13H,8H2,1-5H3,(H,27,30)
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a>1.00E+3n/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