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BDBM50162083 (5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-yl)-amine::(5-Methyl-1H-pyrazol-3-yl)-(2-phenylquinazolin-4-yl)amine::CHEMBL359482::N-(3-methyl-1H-pyrazol-5-yl)-2-phenylquinazolin-4-amine::N-(5-METHYL-1H-PYRAZOL-3-YL)-2-PHENYLQUINAZOLIN-4-AMINE

SMILES: Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1

InChI Key: InChIKey=JYCUVOXSZBECAY-UHFFFAOYSA-N

Data: 7 KI  3 IC50

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50162083   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Glycogen synthase kinase-3 beta


(Homo sapiens (Human))
BDBM50162083
PNG
((5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-...)
Show SMILES Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1
Show InChI InChI=1S/C18H15N5/c1-12-11-16(23-22-12)20-18-14-9-5-6-10-15(14)19-17(21-18)13-7-3-2-4-8-13/h2-11H,1H3,(H2,19,20,21,22,23)
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22n/an/an/an/an/an/an/an/a



Vertex Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of GSK3-beta


Bioorg Med Chem Lett 19: 3586-92 (2009)


Article DOI: 10.1016/j.bmcl.2009.04.136
BindingDB Entry DOI: 10.7270/Q28K7944
More data for this
Ligand-Target Pair
Glycogen synthase kinase-3 beta


(Homo sapiens (Human))
BDBM50162083
PNG
((5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-...)
Show SMILES Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1
Show InChI InChI=1S/C18H15N5/c1-12-11-16(23-22-12)20-18-14-9-5-6-10-15(14)19-17(21-18)13-7-3-2-4-8-13/h2-11H,1H3,(H2,19,20,21,22,23)
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22n/an/an/an/an/an/an/an/a



Vertex Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of Gsk3beta


J Med Chem 52: 2629-51 (2009)

Checked by Author
Article DOI: 10.1021/jm8012129
BindingDB Entry DOI: 10.7270/Q2B85920
More data for this
Ligand-Target Pair
Glycogen synthase kinase-3


(Homo sapiens (Human))
BDBM50162083
PNG
((5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-...)
Show SMILES Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1
Show InChI InChI=1S/C18H15N5/c1-12-11-16(23-22-12)20-18-14-9-5-6-10-15(14)19-17(21-18)13-7-3-2-4-8-13/h2-11H,1H3,(H2,19,20,21,22,23)
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24n/an/an/an/an/an/an/an/a



Vertex Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of Glycogen synthase kinase-3


J Med Chem 48: 1278-81 (2005)


Article DOI: 10.1021/jm0492249
BindingDB Entry DOI: 10.7270/Q2X92F1P
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50162083
PNG
((5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-...)
Show SMILES Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1
Show InChI InChI=1S/C18H15N5/c1-12-11-16(23-22-12)20-18-14-9-5-6-10-15(14)19-17(21-18)13-7-3-2-4-8-13/h2-11H,1H3,(H2,19,20,21,22,23)
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58n/an/an/an/an/an/an/an/a



Vertex Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of Aurora-A by coupled assay


Bioorg Med Chem Lett 19: 3586-92 (2009)


Article DOI: 10.1016/j.bmcl.2009.04.136
BindingDB Entry DOI: 10.7270/Q28K7944
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50162083
PNG
((5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-...)
Show SMILES Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1
Show InChI InChI=1S/C18H15N5/c1-12-11-16(23-22-12)20-18-14-9-5-6-10-15(14)19-17(21-18)13-7-3-2-4-8-13/h2-11H,1H3,(H2,19,20,21,22,23)
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58n/an/an/an/an/an/an/an/a



Vertex Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of aurora A kinase


J Med Chem 52: 2629-51 (2009)

Checked by Author
Article DOI: 10.1021/jm8012129
BindingDB Entry DOI: 10.7270/Q2B85920
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50162083
PNG
((5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-...)
Show SMILES Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1
Show InChI InChI=1S/C18H15N5/c1-12-11-16(23-22-12)20-18-14-9-5-6-10-15(14)19-17(21-18)13-7-3-2-4-8-13/h2-11H,1H3,(H2,19,20,21,22,23)
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81n/an/an/an/an/an/an/an/a



Vertex Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of Src


Bioorg Med Chem Lett 19: 3586-92 (2009)


Article DOI: 10.1016/j.bmcl.2009.04.136
BindingDB Entry DOI: 10.7270/Q28K7944
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50162083
PNG
((5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-...)
Show SMILES Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1
Show InChI InChI=1S/C18H15N5/c1-12-11-16(23-22-12)20-18-14-9-5-6-10-15(14)19-17(21-18)13-7-3-2-4-8-13/h2-11H,1H3,(H2,19,20,21,22,23)
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81n/an/an/an/an/an/an/an/a



Vertex Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of Src


J Med Chem 52: 2629-51 (2009)

Checked by Author
Article DOI: 10.1021/jm8012129
BindingDB Entry DOI: 10.7270/Q2B85920
More data for this
Ligand-Target Pair
Aurora kinase B


(Homo sapiens (Human))
BDBM50162083
PNG
((5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-...)
Show SMILES Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1
Show InChI InChI=1S/C18H15N5/c1-12-11-16(23-22-12)20-18-14-9-5-6-10-15(14)19-17(21-18)13-7-3-2-4-8-13/h2-11H,1H3,(H2,19,20,21,22,23)
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n/an/a 858n/an/an/an/an/an/a



Sun Yat-sen University

Curated by ChEMBL


Assay Description
Inhibition of Aurora B (unknown origin) using FAM-labelled peptide as substrate pretreated for 10 mins followed by substrate addition and measured af...


Eur J Med Chem 157: 1361-1375 (2018)


Article DOI: 10.1016/j.ejmech.2018.08.053
BindingDB Entry DOI: 10.7270/Q2CF9SSR
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50162083
PNG
((5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-...)
Show SMILES Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1
Show InChI InChI=1S/C18H15N5/c1-12-11-16(23-22-12)20-18-14-9-5-6-10-15(14)19-17(21-18)13-7-3-2-4-8-13/h2-11H,1H3,(H2,19,20,21,22,23)
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n/an/a 28n/an/an/an/an/an/a



Sun Yat-sen University

Curated by ChEMBL


Assay Description
Inhibition of Aurora A (unknown origin) using FAM-labelled peptide as substrate pretreated for 10 mins followed by substrate addition and measured af...


Eur J Med Chem 157: 1361-1375 (2018)


Article DOI: 10.1016/j.ejmech.2018.08.053
BindingDB Entry DOI: 10.7270/Q2CF9SSR
More data for this
Ligand-Target Pair
Interferon-induced, double-stranded RNA-activated protein kinase


(Homo sapiens (Human))
BDBM50162083
PNG
((5-Methyl-1H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-...)
Show SMILES Cc1cc(Nc2nc(nc3ccccc23)-c2ccccc2)[nH]n1
Show InChI InChI=1S/C18H15N5/c1-12-11-16(23-22-12)20-18-14-9-5-6-10-15(14)19-17(21-18)13-7-3-2-4-8-13/h2-11H,1H3,(H2,19,20,21,22,23)
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n/an/a 1.50E+4n/an/an/an/an/an/a



Weill Cornell Medical College

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PKR autophosphorylation using poly[I:C] after 10 mins by luminescent assay


Bioorg Med Chem Lett 21: 4108-14 (2011)


Article DOI: 10.1016/j.bmcl.2011.04.149
BindingDB Entry DOI: 10.7270/Q2KK9C4H
More data for this
Ligand-Target Pair