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3 similar compounds to monomer 50446457

Compile data set for download or QSAR
Wt: 403.8
BDBM50446434
Wt: 394.8
BDBM50446437
Wt: 309.7
BDBM50446467

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 13 hits for monomerid = 50446434,50446437,50446467   
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
Dual specificity protein kinase TTK


(Homo sapiens (Human))
BDBM50446434
PNG
(CHEMBL3109942)
Show SMILES Cn1cc(cn1)-c1cc2cnc(Nc3ccc(cc3Cl)-c3cnn(C)c3)cc2[nH]1
Show InChI InChI=1S/C21H18ClN7/c1-28-11-15(9-24-28)13-3-4-18(17(22)5-13)27-21-7-20-14(8-23-21)6-19(26-20)16-10-25-29(2)12-16/h3-12,26H,1-2H3,(H,23,27)
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PubMed
n/an/a 6.90E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of Myc-tagged wild type MPS1 autophosphorylation in human HCT116 cells after 2 hrs in presence of proteosome inhibitor MG132


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Dual specificity protein kinase TTK


(Homo sapiens (Human))
BDBM50446437
PNG
(CHEMBL3109967)
Show SMILES CN(C)C(=O)c1ccc(Nc2cc3[nH]c(cc3cn2)-c2cnn(C)c2)c(Cl)c1
Show InChI InChI=1S/C20H19ClN6O/c1-26(2)20(28)12-4-5-16(15(21)6-12)25-19-8-18-13(9-22-19)7-17(24-18)14-10-23-27(3)11-14/h4-11,24H,1-3H3,(H,22,25)
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PubMed
n/an/a 4.10E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of Myc-tagged wild type MPS1 autophosphorylation in human HCT116 cells after 2 hrs in presence of proteosome inhibitor MG132


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 2 (CDK2)


(Homo sapiens (Human))
BDBM50446434
PNG
(CHEMBL3109942)
Show SMILES Cn1cc(cn1)-c1cc2cnc(Nc3ccc(cc3Cl)-c3cnn(C)c3)cc2[nH]1
Show InChI InChI=1S/C21H18ClN7/c1-28-11-15(9-24-28)13-3-4-18(17(22)5-13)27-21-7-20-14(8-23-21)6-19(26-20)16-10-25-29(2)12-16/h3-12,26H,1-2H3,(H,23,27)
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n/an/a>1.00E+5n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of full length CDK2/Cyclin A (unknown origin) using 5FAMQSPKKG-CONH2 as substrate after 60 mins by fluorescence assay


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50446437
PNG
(CHEMBL3109967)
Show SMILES CN(C)C(=O)c1ccc(Nc2cc3[nH]c(cc3cn2)-c2cnn(C)c2)c(Cl)c1
Show InChI InChI=1S/C20H19ClN6O/c1-26(2)20(28)12-4-5-16(15(21)6-12)25-19-8-18-13(9-22-19)7-17(24-18)14-10-23-27(3)11-14/h4-11,24H,1-3H3,(H,22,25)
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n/an/a>4.00E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of N-terminal His-tagged Aurora A (unknown origin) using 5FAM-LRRASLG-CONH2 as substrate after 60 mins by fluorescence assay


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Dual specificity protein kinase TTK


(Homo sapiens (Human))
BDBM50446434
PNG
(CHEMBL3109942)
Show SMILES Cn1cc(cn1)-c1cc2cnc(Nc3ccc(cc3Cl)-c3cnn(C)c3)cc2[nH]1
Show InChI InChI=1S/C21H18ClN7/c1-28-11-15(9-24-28)13-3-4-18(17(22)5-13)27-21-7-20-14(8-23-21)6-19(26-20)16-10-25-29(2)12-16/h3-12,26H,1-2H3,(H,23,27)
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PubMed
n/an/a 17n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of N-terminal 6XHis-tagged/GST-tagged full length human MPS1 expressed in recombinant baculovirus infected sf9 insect cells using 5FAM-DHT...


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Dual specificity protein kinase TTK


(Homo sapiens (Human))
BDBM50446437
PNG
(CHEMBL3109967)
Show SMILES CN(C)C(=O)c1ccc(Nc2cc3[nH]c(cc3cn2)-c2cnn(C)c2)c(Cl)c1
Show InChI InChI=1S/C20H19ClN6O/c1-26(2)20(28)12-4-5-16(15(21)6-12)25-19-8-18-13(9-22-19)7-17(24-18)14-10-23-27(3)11-14/h4-11,24H,1-3H3,(H,22,25)
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n/an/a 15n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of N-terminal 6XHis-tagged/GST-tagged full length human MPS1 expressed in recombinant baculovirus infected sf9 insect cells using 5FAM-DHT...


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Dual specificity protein kinase TTK


(Homo sapiens (Human))
BDBM50446467
PNG
(CHEMBL3109955)
Show SMILES Clc1ccccc1Nc1cc2[nH]c(cc2cn1)-c1cn[nH]c1
Show InChI InChI=1S/C16H12ClN5/c17-12-3-1-2-4-13(12)22-16-6-15-10(7-18-16)5-14(21-15)11-8-19-20-9-11/h1-9,21H,(H,18,22)(H,19,20)
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n/an/a 28n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of N-terminal 6XHis-tagged/GST-tagged full length human MPS1 expressed in recombinant baculovirus infected sf9 insect cells using 5FAM-DHT...


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 2 (CDK2)


(Homo sapiens (Human))
BDBM50446437
PNG
(CHEMBL3109967)
Show SMILES CN(C)C(=O)c1ccc(Nc2cc3[nH]c(cc3cn2)-c2cnn(C)c2)c(Cl)c1
Show InChI InChI=1S/C20H19ClN6O/c1-26(2)20(28)12-4-5-16(15(21)6-12)25-19-8-18-13(9-22-19)7-17(24-18)14-10-23-27(3)11-14/h4-11,24H,1-3H3,(H,22,25)
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n/an/a 7.80E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of full length CDK2/Cyclin A (unknown origin) using 5FAMQSPKKG-CONH2 as substrate after 60 mins by fluorescence assay


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 2 (CDK2)


(Homo sapiens (Human))
BDBM50446467
PNG
(CHEMBL3109955)
Show SMILES Clc1ccccc1Nc1cc2[nH]c(cc2cn1)-c1cn[nH]c1
Show InChI InChI=1S/C16H12ClN5/c17-12-3-1-2-4-13(12)22-16-6-15-10(7-18-16)5-14(21-15)11-8-19-20-9-11/h1-9,21H,(H,18,22)(H,19,20)
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n/an/a 800n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of full length CDK2/Cyclin A (unknown origin) using 5FAMQSPKKG-CONH2 as substrate after 60 mins by fluorescence assay


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Aurora kinase B


(Homo sapiens (Human))
BDBM50446437
PNG
(CHEMBL3109967)
Show SMILES CN(C)C(=O)c1ccc(Nc2cc3[nH]c(cc3cn2)-c2cnn(C)c2)c(Cl)c1
Show InChI InChI=1S/C20H19ClN6O/c1-26(2)20(28)12-4-5-16(15(21)6-12)25-19-8-18-13(9-22-19)7-17(24-18)14-10-23-27(3)11-14/h4-11,24H,1-3H3,(H,22,25)
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n/an/a>1.00E+5n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of full length Aurora B (unknown origin) using 5FAM-LRRASLG-CONH2 as substrate after 60 mins by fluorescence assay


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Aurora kinase B


(Homo sapiens (Human))
BDBM50446467
PNG
(CHEMBL3109955)
Show SMILES Clc1ccccc1Nc1cc2[nH]c(cc2cn1)-c1cn[nH]c1
Show InChI InChI=1S/C16H12ClN5/c17-12-3-1-2-4-13(12)22-16-6-15-10(7-18-16)5-14(21-15)11-8-19-20-9-11/h1-9,21H,(H,18,22)(H,19,20)
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n/an/a>1.00E+5n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of full length Aurora B (unknown origin) using 5FAM-LRRASLG-CONH2 as substrate after 60 mins by fluorescence assay


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50446434
PNG
(CHEMBL3109942)
Show SMILES Cn1cc(cn1)-c1cc2cnc(Nc3ccc(cc3Cl)-c3cnn(C)c3)cc2[nH]1
Show InChI InChI=1S/C21H18ClN7/c1-28-11-15(9-24-28)13-3-4-18(17(22)5-13)27-21-7-20-14(8-23-21)6-19(26-20)16-10-25-29(2)12-16/h3-12,26H,1-2H3,(H,23,27)
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n/an/a>1.00E+5n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of N-terminal His-tagged Aurora A (unknown origin) using 5FAM-LRRASLG-CONH2 as substrate after 60 mins by fluorescence assay


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50446467
PNG
(CHEMBL3109955)
Show SMILES Clc1ccccc1Nc1cc2[nH]c(cc2cn1)-c1cn[nH]c1
Show InChI InChI=1S/C16H12ClN5/c17-12-3-1-2-4-13(12)22-16-6-15-10(7-18-16)5-14(21-15)11-8-19-20-9-11/h1-9,21H,(H,18,22)(H,19,20)
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n/an/a 4.90E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of N-terminal His-tagged Aurora A (unknown origin) using 5FAM-LRRASLG-CONH2 as substrate after 60 mins by fluorescence assay


J Med Chem 56: 10045-65 (2013)


Article DOI: 10.1021/jm401395s
BindingDB Entry DOI: 10.7270/Q2JM2C4W
More data for this
Ligand-Target Pair