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BDBM50439463 CHEMBL2420911

SMILES: C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12

InChI Key: InChIKey=ZXMGQAIKNOIWHC-UHFFFAOYSA-N

Data: 12 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 12 hits for monomerid = 50439463   
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
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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Article
PubMed
n/an/a 7.00E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of ABL (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
Ribosomal protein S6 kinase alpha 1


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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n/an/a 1.30E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of RSK1 (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
Ribosomal protein S6 kinase alpha 5


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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n/an/a 700n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of MSK1 (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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n/an/a 1.60E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of AKT1 (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase Chk1


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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n/an/a 1.80E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of CHK1 (unknown origin) by Z'-Lyte assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
Hepatocyte growth factor receptor


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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n/an/a 1.83E+5n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of MET (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase CHK2


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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n/an/a 1.30E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of CHK2 (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D2


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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n/an/a 1.30E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of PKD2 (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
MAP kinase-activated protein kinase 5


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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n/an/a 4.10E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of PRAK (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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n/an/a 9.80E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of AURA (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
Casein kinase I isoform delta


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
PDB

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Article
PubMed
n/an/a 9.70E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of CK1delta (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 1


(Homo sapiens (Human))
BDBM50439463
PNG
(CHEMBL2420911)
Show SMILES C1CNCC2(C1)CCN(CC2)c1ncnc2nc[nH]c12
Show InChI InChI=1S/C14H20N6/c1-2-14(8-15-5-1)3-6-20(7-4-14)13-11-12(17-9-16-11)18-10-19-13/h9-10,15H,1-8H2,(H,16,17,18,19)
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n/an/a 3.80E+4n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of ERK2 (unknown origin) by microfluidic mobility shift assay


Bioorg Med Chem 21: 5707-24 (2013)


Article DOI: 10.1016/j.bmc.2013.07.021
BindingDB Entry DOI: 10.7270/Q2MW2JK5
More data for this
Ligand-Target Pair