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BDBM50349104 CHEMBL1808342

SMILES: CCc1cccc(CC)c1NC(=O)c1nn(C)c-2c1CCc1cnc(Nc3ccc(cc3OC(F)(F)F)C(=O)NCCN(C)C)nc-21

InChI Key: InChIKey=MJJRBRKTAAJGIY-UHFFFAOYSA-N

Data: 4 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50349104   
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))
BDBM50349104
PNG
(CHEMBL1808342)
Show SMILES CCc1cccc(CC)c1NC(=O)c1nn(C)c-2c1CCc1cnc(Nc3ccc(cc3OC(F)(F)F)C(=O)NCCN(C)C)nc-21
Show InChI InChI=1S/C33H37F3N8O3/c1-6-19-9-8-10-20(7-2)26(19)40-31(46)28-23-13-11-22-18-38-32(41-27(22)29(23)44(5)42-28)39-24-14-12-21(17-25(24)47-33(34,35)36)30(45)37-15-16-43(3)4/h8-10,12,14,17-18H,6-7,11,13,15-16H2,1-5H3,(H,37,45)(H,40,46)(H,38,39,41)
PDB
MMDB

KEGG

UniProtKB/SwissProt

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PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 130n/an/an/an/an/an/a



Nerviano Medical Sciences srl

Curated by ChEMBL


Assay Description
Inhibition of MPS1 assessed as [33P]-gamma-ATP incorporation into substrate P38-betatide by gamma counting


Bioorg Med Chem Lett 21: 4507-11 (2011)


Article DOI: 10.1016/j.bmcl.2011.05.122
BindingDB Entry DOI: 10.7270/Q2R211RS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK1


(Homo sapiens (Human))
BDBM50349104
PNG
(CHEMBL1808342)
Show SMILES CCc1cccc(CC)c1NC(=O)c1nn(C)c-2c1CCc1cnc(Nc3ccc(cc3OC(F)(F)F)C(=O)NCCN(C)C)nc-21
Show InChI InChI=1S/C33H37F3N8O3/c1-6-19-9-8-10-20(7-2)26(19)40-31(46)28-23-13-11-22-18-38-32(41-27(22)29(23)44(5)42-28)39-24-14-12-21(17-25(24)47-33(34,35)36)30(45)37-15-16-43(3)4/h8-10,12,14,17-18H,6-7,11,13,15-16H2,1-5H3,(H,37,45)(H,40,46)(H,38,39,41)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



Nerviano Medical Sciences srl

Curated by ChEMBL


Assay Description
Inhibition of PLK1 assessed as [33P]-gamma-ATP incorporation into substrate by gamma counting


Bioorg Med Chem Lett 21: 4507-11 (2011)


Article DOI: 10.1016/j.bmcl.2011.05.122
BindingDB Entry DOI: 10.7270/Q2R211RS
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 2 (CDK2)


(Homo sapiens (Human))
BDBM50349104
PNG
(CHEMBL1808342)
Show SMILES CCc1cccc(CC)c1NC(=O)c1nn(C)c-2c1CCc1cnc(Nc3ccc(cc3OC(F)(F)F)C(=O)NCCN(C)C)nc-21
Show InChI InChI=1S/C33H37F3N8O3/c1-6-19-9-8-10-20(7-2)26(19)40-31(46)28-23-13-11-22-18-38-32(41-27(22)29(23)44(5)42-28)39-24-14-12-21(17-25(24)47-33(34,35)36)30(45)37-15-16-43(3)4/h8-10,12,14,17-18H,6-7,11,13,15-16H2,1-5H3,(H,37,45)(H,40,46)(H,38,39,41)
PDB
MMDB

NCI pathway
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KEGG

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antibodypedia
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Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



Nerviano Medical Sciences srl

Curated by ChEMBL


Assay Description
Inhibition of CDK2/Cyclin A assessed as [33P]-gamma-ATP incorporation into substrate by gamma counting


Bioorg Med Chem Lett 21: 4507-11 (2011)


Article DOI: 10.1016/j.bmcl.2011.05.122
BindingDB Entry DOI: 10.7270/Q2R211RS
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50349104
PNG
(CHEMBL1808342)
Show SMILES CCc1cccc(CC)c1NC(=O)c1nn(C)c-2c1CCc1cnc(Nc3ccc(cc3OC(F)(F)F)C(=O)NCCN(C)C)nc-21
Show InChI InChI=1S/C33H37F3N8O3/c1-6-19-9-8-10-20(7-2)26(19)40-31(46)28-23-13-11-22-18-38-32(41-27(22)29(23)44(5)42-28)39-24-14-12-21(17-25(24)47-33(34,35)36)30(45)37-15-16-43(3)4/h8-10,12,14,17-18H,6-7,11,13,15-16H2,1-5H3,(H,37,45)(H,40,46)(H,38,39,41)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.38E+3n/an/an/an/an/an/a



Nerviano Medical Sciences srl

Curated by ChEMBL


Assay Description
Inhibition of Aur-A assessed as [33P]-gamma-ATP incorporation into substrate by gamma counting


Bioorg Med Chem Lett 21: 4507-11 (2011)


Article DOI: 10.1016/j.bmcl.2011.05.122
BindingDB Entry DOI: 10.7270/Q2R211RS
More data for this
Ligand-Target Pair