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BDBM50352306 CHEMBL1822641

SMILES: Cc1cc(Nc2nc(Sc3ccc(NC(=O)CN4C[C@H]5C[C@H]5[C@H]4CO)cc3)nn3cccc23)n[nH]1

InChI Key: InChIKey=PIBTTWIAIOIVKG-XFQXTVEOSA-N

Data: 1 IC50  2 Kd

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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50352306   
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))
BDBM50352306
PNG
(CHEMBL1822641)
Show SMILES Cc1cc(Nc2nc(Sc3ccc(NC(=O)CN4C[C@H]5C[C@H]5[C@H]4CO)cc3)nn3cccc23)n[nH]1 |r|
Show InChI InChI=1S/C24H26N8O2S/c1-14-9-21(29-28-14)26-23-19-3-2-8-32(19)30-24(27-23)35-17-6-4-16(5-7-17)25-22(34)12-31-11-15-10-18(15)20(31)13-33/h2-9,15,18,20,33H,10-13H2,1H3,(H,25,34)(H2,26,27,28,29,30)/t15-,18-,20-/m1/s1
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PC sid
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PubMed
n/an/an/a 15n/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
Aurora kinase A


(Homo sapiens (Human))
BDBM50352306
PNG
(CHEMBL1822641)
Show SMILES Cc1cc(Nc2nc(Sc3ccc(NC(=O)CN4C[C@H]5C[C@H]5[C@H]4CO)cc3)nn3cccc23)n[nH]1 |r|
Show InChI InChI=1S/C24H26N8O2S/c1-14-9-21(29-28-14)26-23-19-3-2-8-32(19)30-24(27-23)35-17-6-4-16(5-7-17)25-22(34)12-31-11-15-10-18(15)20(31)13-33/h2-9,15,18,20,33H,10-13H2,1H3,(H,25,34)(H2,26,27,28,29,30)/t15-,18-,20-/m1/s1
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PC sid
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Article
PubMed
n/an/an/a 17n/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))
BDBM50352306
PNG
(CHEMBL1822641)
Show SMILES Cc1cc(Nc2nc(Sc3ccc(NC(=O)CN4C[C@H]5C[C@H]5[C@H]4CO)cc3)nn3cccc23)n[nH]1 |r|
Show InChI InChI=1S/C24H26N8O2S/c1-14-9-21(29-28-14)26-23-19-3-2-8-32(19)30-24(27-23)35-17-6-4-16(5-7-17)25-22(34)12-31-11-15-10-18(15)20(31)13-33/h2-9,15,18,20,33H,10-13H2,1H3,(H,25,34)(H2,26,27,28,29,30)/t15-,18-,20-/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 179n/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