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BDBM50338873 CHEMBL1684800::N-(5-Amino-1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-5-(3-(4-chloro-3-(trifluoromethyl)phenyl)ureido)-2-methylbenzamide

SMILES: COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1

InChI Key: InChIKey=ZJDFSKSBQBPOSK-UHFFFAOYSA-N

Data: 20 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 20 hits for monomerid = 50338873   
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
CDK2/Cyclin E/G1/S-specific cyclin E2


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 2.13n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
Inhibition of CDK2/cyclin E


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of JNK3


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Glycogen synthase kinase-3 beta


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 2.73n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of GSK3-beta


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
RAF proto-oncogene serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 2.87n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of RAF1


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Cyclin B/Cyclin-Dependent Kinase 1 (CDK1)/G2/mitotic-specific cyclin B2/G2/mitotic-specific cyclin B3


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 3.20n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
Inhibition of CDK1/cyclin B


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Focal adhesion kinase 1


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 4.13n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
Inhibition of FAK


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 4.79n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
Inhibition of c-Src


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 9.42n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of KDR


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Dual specificity mitogen-activated protein kinase kinase 1


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 18.2n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of MEK1


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Fibroblast growth factor receptor 3


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 21.5n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of FGFR3


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Insulin-like growth factor I receptor


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 51.6n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of IGF-1R


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 101n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
Inhibition of EGFR


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
RAF proto-oncogene serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 107n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
Inhibition of C-Raf assessed as [33P]gamma-ATP incorporation into substrate after 40 mins by scintillation counting


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK1


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 167n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of PLK1


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Hepatocyte growth factor receptor


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 194n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
Inhibition of c-MET


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Macrophage-stimulating protein receptor


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 277n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of RON


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 8


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 1.59E+3n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of JNK1a1 at 10 uM


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase mTOR


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 3.02E+3n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
inhibition of mTOR


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 1.14E+4n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
Inhibition of ERK2


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair
ALK tyrosine kinase receptor


(Homo sapiens (Human))
BDBM50338873
PNG
(CHEMBL1684800 | N-(5-Amino-1-(4-methoxybenzyl)-1H-...)
Show SMILES COc1ccc(Cn2ncc(NC(=O)c3cc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)ccc3C)c2N)cc1
Show InChI InChI=1S/C27H24ClF3N6O3/c1-15-3-6-17(34-26(39)35-18-7-10-22(28)21(12-18)27(29,30)31)11-20(15)25(38)36-23-13-33-37(24(23)32)14-16-4-8-19(40-2)9-5-16/h3-13H,14,32H2,1-2H3,(H,36,38)(H2,34,35,39)
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n/an/a 2.71n/an/an/an/an/an/a



Hanyang University

Curated by ChEMBL


Assay Description
Inhibition of ALK


Bioorg Med Chem 19: 1915-23 (2011)


Article DOI: 10.1016/j.bmc.2011.01.067
BindingDB Entry DOI: 10.7270/Q2D79CD3
More data for this
Ligand-Target Pair