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BDBM50207497 1-(4-(3-amino-7-(2-(pyrrolidin-1-yl)ethoxy)-1H-indazol-4-yl)phenyl)-3-m-tolylurea::CHEMBL223790::N-{4-[3-amino-7-(2-pyrrolidin-1-yl-ethoxy)-1H-indazol-4-yl]-phenyl}-N'-(3-methylphenyl)urea

SMILES: Cc1cccc(NC(=O)Nc2ccc(cc2)-c2ccc(OCCN3CCCC3)c3[nH]nc(N)c23)c1

InChI Key: InChIKey=CQQHPXAPMGAALV-UHFFFAOYSA-N

Data: 4 IC50

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 = 50207497   
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
Mast/stem cell growth factor receptor Kit


(Homo sapiens (Human))
BDBM50207497
PNG
(1-(4-(3-amino-7-(2-(pyrrolidin-1-yl)ethoxy)-1H-ind...)
Show SMILES Cc1cccc(NC(=O)Nc2ccc(cc2)-c2ccc(OCCN3CCCC3)c3[nH]nc(N)c23)c1
Show InChI InChI=1S/C27H30N6O2/c1-18-5-4-6-21(17-18)30-27(34)29-20-9-7-19(8-10-20)22-11-12-23(25-24(22)26(28)32-31-25)35-16-15-33-13-2-3-14-33/h4-12,17H,2-3,13-16H2,1H3,(H3,28,31,32)(H2,29,30,34)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 26n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibition of c-Kit by HTRF assay


J Med Chem 50: 1584-97 (2007)


Article DOI: 10.1021/jm061280h
BindingDB Entry DOI: 10.7270/Q2DJ5F95
More data for this
Ligand-Target Pair
Mast/stem cell growth factor receptor Kit


(Homo sapiens (Human))
BDBM50207497
PNG
(1-(4-(3-amino-7-(2-(pyrrolidin-1-yl)ethoxy)-1H-ind...)
Show SMILES Cc1cccc(NC(=O)Nc2ccc(cc2)-c2ccc(OCCN3CCCC3)c3[nH]nc(N)c23)c1
Show InChI InChI=1S/C27H30N6O2/c1-18-5-4-6-21(17-18)30-27(34)29-20-9-7-19(8-10-20)22-11-12-23(25-24(22)26(28)32-31-25)35-16-15-33-13-2-3-14-33/h4-12,17H,2-3,13-16H2,1H3,(H3,28,31,32)(H2,29,30,34)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 26n/an/an/an/an/an/a



Punjabi University

Curated by ChEMBL


Assay Description
Inhibition of c-Kit by HTRF method


Eur J Med Chem 45: 393-404 (2010)


Article DOI: 10.1016/j.ejmech.2009.09.013
BindingDB Entry DOI: 10.7270/Q2RX9C6D
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein kinase FLT3


(Homo sapiens (Human))
BDBM50207497
PNG
(1-(4-(3-amino-7-(2-(pyrrolidin-1-yl)ethoxy)-1H-ind...)
Show SMILES Cc1cccc(NC(=O)Nc2ccc(cc2)-c2ccc(OCCN3CCCC3)c3[nH]nc(N)c23)c1
Show InChI InChI=1S/C27H30N6O2/c1-18-5-4-6-21(17-18)30-27(34)29-20-9-7-19(8-10-20)22-11-12-23(25-24(22)26(28)32-31-25)35-16-15-33-13-2-3-14-33/h4-12,17H,2-3,13-16H2,1H3,(H3,28,31,32)(H2,29,30,34)
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 120n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibition of FLT3 by HTRF assay


J Med Chem 50: 1584-97 (2007)


Article DOI: 10.1021/jm061280h
BindingDB Entry DOI: 10.7270/Q2DJ5F95
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50207497
PNG
(1-(4-(3-amino-7-(2-(pyrrolidin-1-yl)ethoxy)-1H-ind...)
Show SMILES Cc1cccc(NC(=O)Nc2ccc(cc2)-c2ccc(OCCN3CCCC3)c3[nH]nc(N)c23)c1
Show InChI InChI=1S/C27H30N6O2/c1-18-5-4-6-21(17-18)30-27(34)29-20-9-7-19(8-10-20)22-11-12-23(25-24(22)26(28)32-31-25)35-16-15-33-13-2-3-14-33/h4-12,17H,2-3,13-16H2,1H3,(H3,28,31,32)(H2,29,30,34)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 31n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibition of VEGF-induced human KDR phosphorylation in mouse 3T3 cells by ELISA


J Med Chem 50: 1584-97 (2007)


Article DOI: 10.1021/jm061280h
BindingDB Entry DOI: 10.7270/Q2DJ5F95
More data for this
Ligand-Target Pair