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BDBM50044652 CHEMBL3353352::US10358436, Example A208::US9907800, Example A208

SMILES: CN(C)Cc1ccc(\C=C\c2n[nH]c3cc(ccc23)[C@@H]2C[C@@]22C(=O)Nc3ccc(F)cc23)cc1

InChI Key:

Data: 6 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 6 hits for monomerid = 50044652   
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
Serine/threonine-protein kinase PLK4


(Homo sapiens (Human))
BDBM50044652
PNG
(CHEMBL3353352 | US10358436, Example A208 | US99078...)
Show SMILES CN(C)Cc1ccc(\C=C\c2n[nH]c3cc(ccc23)[C@@H]2C[C@@]22C(=O)Nc3ccc(F)cc23)cc1 |r|
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Article
PubMed
n/an/a 0.790n/an/an/an/an/an/a



EntreMed Inc.

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged PLK4 (1 to 391 residues) expressed in Escherichia coli incubated for 30 mins by ELISA method


J Med Chem 58: 130-46 (2015)


Article DOI: 10.1021/jm5005336
BindingDB Entry DOI: 10.7270/Q2125V9W
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK4


(Homo sapiens (Human))
BDBM50044652
PNG
(CHEMBL3353352 | US10358436, Example A208 | US99078...)
Show SMILES CN(C)Cc1ccc(\C=C\c2n[nH]c3cc(ccc23)[C@@H]2C[C@@]22C(=O)Nc3ccc(F)cc23)cc1 |r|
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US Patent
n/an/a<100n/an/an/an/an/an/a



The Scripps Research Institute



Assay Description
PLK4 activity was measured using an indirect ELISA detection system. Dephosphorylated GST-PLK4 (4 nM) was incubated in the presence of 15 μM ATP...


J Med Chem 50: 3359-68 (2007)


BindingDB Entry DOI: 10.7270/Q2KD216W
More data for this
Ligand-Target Pair
Aurora kinase B


(Homo sapiens (Human))
BDBM50044652
PNG
(CHEMBL3353352 | US10358436, Example A208 | US99078...)
Show SMILES CN(C)Cc1ccc(\C=C\c2n[nH]c3cc(ccc23)[C@@H]2C[C@@]22C(=O)Nc3ccc(F)cc23)cc1 |r|
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US Patent
n/an/a<100n/an/an/an/an/an/a



University Health Network

US Patent


Assay Description
Aurora B inhibition was determined using the Z-Lyte assay kit from Invitrogen. The assay was performed using the recommended manufacturer's instr...


US Patent US10358436 (2019)


BindingDB Entry DOI: 10.7270/Q2K939WH
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK4


(Homo sapiens (Human))
BDBM50044652
PNG
(CHEMBL3353352 | US10358436, Example A208 | US99078...)
Show SMILES CN(C)Cc1ccc(\C=C\c2n[nH]c3cc(ccc23)[C@@H]2C[C@@]22C(=O)Nc3ccc(F)cc23)cc1 |r|
PDB

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PC sid
UniChem

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US Patent
n/an/a<100n/an/an/an/an/an/a



University Health Network

US Patent


Assay Description
Active PLK4 was purified from an E. coli expression system as an amino terminal GST fusion of residues 1-391 of human PLK4. The protein was purified ...


US Patent US10358436 (2019)


BindingDB Entry DOI: 10.7270/Q2K939WH
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50044652
PNG
(CHEMBL3353352 | US10358436, Example A208 | US99078...)
Show SMILES CN(C)Cc1ccc(\C=C\c2n[nH]c3cc(ccc23)[C@@H]2C[C@@]22C(=O)Nc3ccc(F)cc23)cc1 |r|
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US Patent
n/an/a<500n/an/an/an/an/an/a



University Health Network

US Patent


Assay Description
Aurora A inhibition was determined using the Z-Lyte assay kit from Invitrogen. The assay was performed using the recommended manufacturer's instr...


US Patent US10358436 (2019)


BindingDB Entry DOI: 10.7270/Q2K939WH
More data for this
Ligand-Target Pair
Aurora kinase B


(Homo sapiens (Human))
BDBM50044652
PNG
(CHEMBL3353352 | US10358436, Example A208 | US99078...)
Show SMILES CN(C)Cc1ccc(\C=C\c2n[nH]c3cc(ccc23)[C@@H]2C[C@@]22C(=O)Nc3ccc(F)cc23)cc1 |r|
PDB

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KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
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CHEMBL
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PC sid
UniChem

Patents


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US Patent
n/an/a<100n/an/an/an/an/an/a



The Scripps Research Institute



Assay Description
Aurora B inhibition was determined using the Z-Lyte assay kit from Invitrogen. The assay was performed using the recommended manufacturer's instr...


J Med Chem 50: 3359-68 (2007)


BindingDB Entry DOI: 10.7270/Q2KD216W
More data for this
Ligand-Target Pair