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BDBM50352302 CHEMBL1822489

SMILES: Cc1cc(Nc2nc(Sc3ccc(NC(=O)C4CC4)cc3)nn3cc(NC(=O)CN4CCC[C@@H]4CO)cc23)[nH]n1

InChI Key: InChIKey=LSEOXFVSQOHSDK-HXUWFJFHSA-N

Data: 1 IC50  3 Kd

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 4 hits for monomerid = 50352302   
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
Aurora kinase B


(Homo sapiens (Human))
BDBM50352302
PNG
(CHEMBL1822489)
Show SMILES Cc1cc(Nc2nc(Sc3ccc(NC(=O)C4CC4)cc3)nn3cc(NC(=O)CN4CCC[C@@H]4CO)cc23)[nH]n1
Show InChI InChI=1S/C27H31N9O3S/c1-16-11-23(33-32-16)30-25-22-12-19(28-24(38)14-35-10-2-3-20(35)15-37)13-36(22)34-27(31-25)40-21-8-6-18(7-9-21)29-26(39)17-4-5-17/h6-9,11-13,17,20,37H,2-5,10,14-15H2,1H3,(H,28,38)(H,29,39)(H2,30,31,32,33,34)/t20-/m1/s1
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Article
PubMed
n/an/a 6.30E+3n/an/an/an/an/an/a



Ambit Biosciences Corporation

Curated by ChEMBL


Assay Description
Inhibition of Aurora B kinase assessed as reduction in histone H3 phosphorylation in human HCT116 cells


Bioorg Med Chem Lett 21: 5296-300 (2011)


Article DOI: 10.1016/j.bmcl.2011.07.027
BindingDB Entry DOI: 10.7270/Q20P10D8
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase Aurora-C


(Homo sapiens (human))
BDBM50352302
PNG
(CHEMBL1822489)
Show SMILES Cc1cc(Nc2nc(Sc3ccc(NC(=O)C4CC4)cc3)nn3cc(NC(=O)CN4CCC[C@@H]4CO)cc23)[nH]n1
Show InChI InChI=1S/C27H31N9O3S/c1-16-11-23(33-32-16)30-25-22-12-19(28-24(38)14-35-10-2-3-20(35)15-37)13-36(22)34-27(31-25)40-21-8-6-18(7-9-21)29-26(39)17-4-5-17/h6-9,11-13,17,20,37H,2-5,10,14-15H2,1H3,(H,28,38)(H,29,39)(H2,30,31,32,33,34)/t20-/m1/s1
NCI pathway
KEGG

UniProtKB/SwissProt

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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/a 80n/an/an/an/an/a



Ambit Biosciences Corporation

Curated by ChEMBL


Assay Description
Binding affinity to Aurora C kinase catalytic domain by competitive binding assay


Bioorg Med Chem Lett 21: 5296-300 (2011)


Article DOI: 10.1016/j.bmcl.2011.07.027
BindingDB Entry DOI: 10.7270/Q20P10D8
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (human))
BDBM50352302
PNG
(CHEMBL1822489)
Show SMILES Cc1cc(Nc2nc(Sc3ccc(NC(=O)C4CC4)cc3)nn3cc(NC(=O)CN4CCC[C@@H]4CO)cc23)[nH]n1
Show InChI InChI=1S/C27H31N9O3S/c1-16-11-23(33-32-16)30-25-22-12-19(28-24(38)14-35-10-2-3-20(35)15-37)13-36(22)34-27(31-25)40-21-8-6-18(7-9-21)29-26(39)17-4-5-17/h6-9,11-13,17,20,37H,2-5,10,14-15H2,1H3,(H,28,38)(H,29,39)(H2,30,31,32,33,34)/t20-/m1/s1
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Article
PubMed
n/an/an/a 10n/an/an/an/an/a



Ambit Biosciences Corporation

Curated by ChEMBL


Assay Description
Binding affinity to Aurora A kinase catalytic domain by competitive binding assay


Bioorg Med Chem Lett 21: 5296-300 (2011)


Article DOI: 10.1016/j.bmcl.2011.07.027
BindingDB Entry DOI: 10.7270/Q20P10D8
More data for this
Ligand-Target Pair
Aurora kinase B


(Homo sapiens (Human))
BDBM50352302
PNG
(CHEMBL1822489)
Show SMILES Cc1cc(Nc2nc(Sc3ccc(NC(=O)C4CC4)cc3)nn3cc(NC(=O)CN4CCC[C@@H]4CO)cc23)[nH]n1
Show InChI InChI=1S/C27H31N9O3S/c1-16-11-23(33-32-16)30-25-22-12-19(28-24(38)14-35-10-2-3-20(35)15-37)13-36(22)34-27(31-25)40-21-8-6-18(7-9-21)29-26(39)17-4-5-17/h6-9,11-13,17,20,37H,2-5,10,14-15H2,1H3,(H,28,38)(H,29,39)(H2,30,31,32,33,34)/t20-/m1/s1
PDB

Reactome pathway
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UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/a 16n/an/an/an/an/a



Ambit Biosciences Corporation

Curated by ChEMBL


Assay Description
Binding affinity to Aurora B kinase catalytic domain by competitive binding assay


Bioorg Med Chem Lett 21: 5296-300 (2011)


Article DOI: 10.1016/j.bmcl.2011.07.027
BindingDB Entry DOI: 10.7270/Q20P10D8
More data for this
Ligand-Target Pair