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Compile Data Set for Download or QSAR

Found 7 hits of ic50 for monomerid = 50324277   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Aurora kinase B


(Homo sapiens (Human))
BDBM50324277
PNG
((Z)-N-[3-({3-[3-(Dimethylamino)propyl]-4-oxo-4,5,6...)
Show SMILES CN(C)CCCc1c(C=C2C(=O)Nc3ccc(NS(=O)(=O)c4ccccc4)cc23)[nH]c2CCCC(=O)c12 |w:8.7|
Show InChI InChI=1S/C28H30N4O4S/c1-32(2)15-7-10-20-25(29-24-11-6-12-26(33)27(20)24)17-22-21-16-18(13-14-23(21)30-28(22)34)31-37(35,36)19-8-4-3-5-9-19/h3-5,8-9,13-14,16-17,29,31H,6-7,10-12,15H2,1-2H3,(H,30,34)
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n/an/a 235n/an/an/an/an/an/a



Development Center for Biotechnology

Curated by ChEMBL


Assay Description
Inhibition of recombinant aurora B


J Med Chem 53: 5929-41 (2010)


Article DOI: 10.1021/jm1001869
BindingDB Entry DOI: 10.7270/Q2XS5VKS
More data for this
Ligand-Target Pair
Platelet-derived growth factor receptor beta


(Homo sapiens (Human))
BDBM50324277
PNG
((Z)-N-[3-({3-[3-(Dimethylamino)propyl]-4-oxo-4,5,6...)
Show SMILES CN(C)CCCc1c(C=C2C(=O)Nc3ccc(NS(=O)(=O)c4ccccc4)cc23)[nH]c2CCCC(=O)c12 |w:8.7|
Show InChI InChI=1S/C28H30N4O4S/c1-32(2)15-7-10-20-25(29-24-11-6-12-26(33)27(20)24)17-22-21-16-18(13-14-23(21)30-28(22)34)31-37(35,36)19-8-4-3-5-9-19/h3-5,8-9,13-14,16-17,29,31H,6-7,10-12,15H2,1-2H3,(H,30,34)
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n/an/a<1.00E+3n/an/an/an/an/an/a



Development Center for Biotechnology

Curated by ChEMBL


Assay Description
Inhibition of PDGFRbeta by radiometric method


J Med Chem 53: 5929-41 (2010)


Article DOI: 10.1021/jm1001869
BindingDB Entry DOI: 10.7270/Q2XS5VKS
More data for this
Ligand-Target Pair
Macrophage colony-stimulating factor 1 receptor


(Homo sapiens (Human))
BDBM50324277
PNG
((Z)-N-[3-({3-[3-(Dimethylamino)propyl]-4-oxo-4,5,6...)
Show SMILES CN(C)CCCc1c(C=C2C(=O)Nc3ccc(NS(=O)(=O)c4ccccc4)cc23)[nH]c2CCCC(=O)c12 |w:8.7|
Show InChI InChI=1S/C28H30N4O4S/c1-32(2)15-7-10-20-25(29-24-11-6-12-26(33)27(20)24)17-22-21-16-18(13-14-23(21)30-28(22)34)31-37(35,36)19-8-4-3-5-9-19/h3-5,8-9,13-14,16-17,29,31H,6-7,10-12,15H2,1-2H3,(H,30,34)
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n/an/a<1.00E+3n/an/an/an/an/an/a



Development Center for Biotechnology

Curated by ChEMBL


Assay Description
Inhibition of CSF1R by radiometric method


J Med Chem 53: 5929-41 (2010)


Article DOI: 10.1021/jm1001869
BindingDB Entry DOI: 10.7270/Q2XS5VKS
More data for this
Ligand-Target Pair
Mast/stem cell growth factor receptor Kit


(Homo sapiens (Human))
BDBM50324277
PNG
((Z)-N-[3-({3-[3-(Dimethylamino)propyl]-4-oxo-4,5,6...)
Show SMILES CN(C)CCCc1c(C=C2C(=O)Nc3ccc(NS(=O)(=O)c4ccccc4)cc23)[nH]c2CCCC(=O)c12 |w:8.7|
Show InChI InChI=1S/C28H30N4O4S/c1-32(2)15-7-10-20-25(29-24-11-6-12-26(33)27(20)24)17-22-21-16-18(13-14-23(21)30-28(22)34)31-37(35,36)19-8-4-3-5-9-19/h3-5,8-9,13-14,16-17,29,31H,6-7,10-12,15H2,1-2H3,(H,30,34)
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n/an/a<1.00E+3n/an/an/an/an/an/a



Development Center for Biotechnology

Curated by ChEMBL


Assay Description
Inhibition of c-Kit by radiometric method


J Med Chem 53: 5929-41 (2010)


Article DOI: 10.1021/jm1001869
BindingDB Entry DOI: 10.7270/Q2XS5VKS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50324277
PNG
((Z)-N-[3-({3-[3-(Dimethylamino)propyl]-4-oxo-4,5,6...)
Show SMILES CN(C)CCCc1c(C=C2C(=O)Nc3ccc(NS(=O)(=O)c4ccccc4)cc23)[nH]c2CCCC(=O)c12 |w:8.7|
Show InChI InChI=1S/C28H30N4O4S/c1-32(2)15-7-10-20-25(29-24-11-6-12-26(33)27(20)24)17-22-21-16-18(13-14-23(21)30-28(22)34)31-37(35,36)19-8-4-3-5-9-19/h3-5,8-9,13-14,16-17,29,31H,6-7,10-12,15H2,1-2H3,(H,30,34)
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n/an/a<1.00E+3n/an/an/an/an/an/a



Development Center for Biotechnology

Curated by ChEMBL


Assay Description
Inhibition of VEGFR2 by radiometric method


J Med Chem 53: 5929-41 (2010)


Article DOI: 10.1021/jm1001869
BindingDB Entry DOI: 10.7270/Q2XS5VKS
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein kinase FLT3


(Homo sapiens (Human))
BDBM50324277
PNG
((Z)-N-[3-({3-[3-(Dimethylamino)propyl]-4-oxo-4,5,6...)
Show SMILES CN(C)CCCc1c(C=C2C(=O)Nc3ccc(NS(=O)(=O)c4ccccc4)cc23)[nH]c2CCCC(=O)c12 |w:8.7|
Show InChI InChI=1S/C28H30N4O4S/c1-32(2)15-7-10-20-25(29-24-11-6-12-26(33)27(20)24)17-22-21-16-18(13-14-23(21)30-28(22)34)31-37(35,36)19-8-4-3-5-9-19/h3-5,8-9,13-14,16-17,29,31H,6-7,10-12,15H2,1-2H3,(H,30,34)
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n/an/a<1.00E+3n/an/an/an/an/an/a



Development Center for Biotechnology

Curated by ChEMBL


Assay Description
Inhibition of FLT3 by radiometric method


J Med Chem 53: 5929-41 (2010)


Article DOI: 10.1021/jm1001869
BindingDB Entry DOI: 10.7270/Q2XS5VKS
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50324277
PNG
((Z)-N-[3-({3-[3-(Dimethylamino)propyl]-4-oxo-4,5,6...)
Show SMILES CN(C)CCCc1c(C=C2C(=O)Nc3ccc(NS(=O)(=O)c4ccccc4)cc23)[nH]c2CCCC(=O)c12 |w:8.7|
Show InChI InChI=1S/C28H30N4O4S/c1-32(2)15-7-10-20-25(29-24-11-6-12-26(33)27(20)24)17-22-21-16-18(13-14-23(21)30-28(22)34)31-37(35,36)19-8-4-3-5-9-19/h3-5,8-9,13-14,16-17,29,31H,6-7,10-12,15H2,1-2H3,(H,30,34)
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n/an/a 2.19E+3n/an/an/an/an/an/a



Development Center for Biotechnology

Curated by ChEMBL


Assay Description
Inhibition of recombinant aurora A


J Med Chem 53: 5929-41 (2010)


Article DOI: 10.1021/jm1001869
BindingDB Entry DOI: 10.7270/Q2XS5VKS
More data for this
Ligand-Target Pair