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PubMed code 25680029

Compile data set for download or QSAR
Found 12 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Protein Wnt-3a


(Homo sapiens)
BDBM50073190
PNG
(CHEMBL3408213)
Show SMILES Cn1cc(cn1)-c1ccc(cc1)-c1cncc(Cl)c1N1CCC2(CCNC2=O)CC1
Show InChI InChI=1S/C23H24ClN5O/c1-28-15-18(12-27-28)16-2-4-17(5-3-16)19-13-25-14-20(24)21(19)29-10-7-23(8-11-29)6-9-26-22(23)30/h2-5,12-15H,6-11H2,1H3,(H,26,30)
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PubMed
n/an/a 7n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of ligand-induced WNT3A signaling in human PA-1 cells harboring TCF preincubated for 6 hrs before ligand addition measured after 24 hrs by...


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Glycogen synthase kinase-3


(Homo sapiens (human))
BDBM50073190
PNG
(CHEMBL3408213)
Show SMILES Cn1cc(cn1)-c1ccc(cc1)-c1cncc(Cl)c1N1CCC2(CCNC2=O)CC1
Show InChI InChI=1S/C23H24ClN5O/c1-28-15-18(12-27-28)16-2-4-17(5-3-16)19-13-25-14-20(24)21(19)29-10-7-23(8-11-29)6-9-26-22(23)30/h2-5,12-15H,6-11H2,1H3,(H,26,30)
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n/an/a 462n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of GSK3alpha (unknown origin)


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Glycogen synthase kinase-3


(Homo sapiens (human))
BDBM50073190
PNG
(CHEMBL3408213)
Show SMILES Cn1cc(cn1)-c1ccc(cc1)-c1cncc(Cl)c1N1CCC2(CCNC2=O)CC1
Show InChI InChI=1S/C23H24ClN5O/c1-28-15-18(12-27-28)16-2-4-17(5-3-16)19-13-25-14-20(24)21(19)29-10-7-23(8-11-29)6-9-26-22(23)30/h2-5,12-15H,6-11H2,1H3,(H,26,30)
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n/an/a 690n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of GSK3beta (unknown origin)


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Cytochrome P450 3A


(Homo sapiens (human))
BDBM50073188
PNG
(CHEMBL3408192)
Show SMILES Clc1cncc(-c2ccc(cc2)N2CCOCC2)c1N1CCC2(CCNC2=O)CC1
Show InChI InChI=1S/C23H27ClN4O2/c24-20-16-25-15-19(17-1-3-18(4-2-17)27-11-13-30-14-12-27)21(20)28-9-6-23(7-10-28)5-8-26-22(23)29/h1-4,15-16H,5-14H2,(H,26,29)
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n/an/a 2.10E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 (unknown origin)


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Cytochrome P450 2C9


(Homo sapiens (human))
BDBM50073188
PNG
(CHEMBL3408192)
Show SMILES Clc1cncc(-c2ccc(cc2)N2CCOCC2)c1N1CCC2(CCNC2=O)CC1
Show InChI InChI=1S/C23H27ClN4O2/c24-20-16-25-15-19(17-1-3-18(4-2-17)27-11-13-30-14-12-27)21(20)28-9-6-23(7-10-28)5-8-26-22(23)29/h1-4,15-16H,5-14H2,(H,26,29)
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n/an/a 2.90E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of CYP2C9 (unknown origin)


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Cytochrome P450 3A


(Homo sapiens (human))
BDBM50073187
PNG
(CHEMBL1673059)
Show SMILES NC(=O)C1CCN(CC1)c1c(Cl)cncc1Cl
Show InChI InChI=1S/C11H13Cl2N3O/c12-8-5-15-6-9(13)10(8)16-3-1-7(2-4-16)11(14)17/h5-7H,1-4H2,(H2,14,17)
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n/an/a 7.00E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 (unknown origin)


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Voltage-gated potassium channel


(Homo sapiens (human))
BDBM50073189
PNG
(CHEMBL3408214)
Show SMILES Clc1cncc(-c2ccc3cnccc3c2)c1N1CCC2(CCNC2=O)CC1
Show InChI InChI=1S/C22H21ClN4O/c23-19-14-25-13-18(16-1-2-17-12-24-7-3-15(17)11-16)20(19)27-9-5-22(6-10-27)4-8-26-21(22)28/h1-3,7,11-14H,4-6,8-10H2,(H,26,28)
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n/an/a>1.00E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of human ERG


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Voltage-gated potassium channel


(Homo sapiens (human))
BDBM50073187
PNG
(CHEMBL1673059)
Show SMILES NC(=O)C1CCN(CC1)c1c(Cl)cncc1Cl
Show InChI InChI=1S/C11H13Cl2N3O/c12-8-5-15-6-9(13)10(8)16-3-1-7(2-4-16)11(14)17/h5-7H,1-4H2,(H2,14,17)
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n/an/a>1.00E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of human ERG


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Human diphtheria toxin-like ADP-ribosyltransferase (ARTD5 or PARP5a)


(Homo sapiens (Human))
BDBM50073190
PNG
(CHEMBL3408213)
Show SMILES Cn1cc(cn1)-c1ccc(cc1)-c1cncc(Cl)c1N1CCC2(CCNC2=O)CC1
Show InChI InChI=1S/C23H24ClN5O/c1-28-15-18(12-27-28)16-2-4-17(5-3-16)19-13-25-14-20(24)21(19)29-10-7-23(8-11-29)6-9-26-22(23)30/h2-5,12-15H,6-11H2,1H3,(H,26,30)
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n/an/a>1.00E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged TNKS1 (1023 to 1327 aa) (unknown origin) after 90 mins by HTRF assay


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Human diphtheria toxin-like ADP-ribosyltransferase (ARTD6 or PARP5b)


(Homo sapiens (Human))
BDBM50073190
PNG
(CHEMBL3408213)
Show SMILES Cn1cc(cn1)-c1ccc(cc1)-c1cncc(Cl)c1N1CCC2(CCNC2=O)CC1
Show InChI InChI=1S/C23H24ClN5O/c1-28-15-18(12-27-28)16-2-4-17(5-3-16)19-13-25-14-20(24)21(19)29-10-7-23(8-11-29)6-9-26-22(23)30/h2-5,12-15H,6-11H2,1H3,(H,26,30)
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n/an/a 1.50E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged TNKS2 (873 to 1166 aa) (unknown origin) after 90 mins by HTRF assay


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Human diphtheria toxin-like ADP-ribosyltransferase (ARTD6 or PARP5b)


(Homo sapiens (Human))
BDBM50073188
PNG
(CHEMBL3408192)
Show SMILES Clc1cncc(-c2ccc(cc2)N2CCOCC2)c1N1CCC2(CCNC2=O)CC1
Show InChI InChI=1S/C23H27ClN4O2/c24-20-16-25-15-19(17-1-3-18(4-2-17)27-11-13-30-14-12-27)21(20)28-9-6-23(7-10-28)5-8-26-22(23)29/h1-4,15-16H,5-14H2,(H,26,29)
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n/an/a 1.60E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged TNKS2 (873 to 1166 aa) (unknown origin) after 90 mins by HTRF assay


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
Human diphtheria toxin-like ADP-ribosyltransferase (ARTD5 or PARP5a)


(Homo sapiens (Human))
BDBM50073188
PNG
(CHEMBL3408192)
Show SMILES Clc1cncc(-c2ccc(cc2)N2CCOCC2)c1N1CCC2(CCNC2=O)CC1
Show InChI InChI=1S/C23H27ClN4O2/c24-20-16-25-15-19(17-1-3-18(4-2-17)27-11-13-30-14-12-27)21(20)28-9-6-23(7-10-28)5-8-26-22(23)29/h1-4,15-16H,5-14H2,(H,26,29)
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n/an/a 1.90E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged TNKS1 (1023 to 1327 aa) (unknown origin) after 90 mins by HTRF assay


J Med Chem 58: 1717-35 (2015)


Article DOI: 10.1021/jm501436m
BindingDB Entry DOI: 10.7270/Q2H70HJ2
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%