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3 similar compounds to monomer 50153102

Wt: 251.2
BDBM50044962
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Wt: 310.3
BDBM50153104
Wt: 284.3
BDBM50153105

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50044962,50153104,50153105   
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
Lysine-specific demethylase 5B


(Homo sapiens (Human))
BDBM50153105
PNG
(CHEMBL3775454)
Show SMILES CN(C)CCc1cnn(c1)-c1nccc2c1nc[nH]c2=O
Show InChI InChI=1S/C14H16N6O/c1-19(2)6-4-10-7-18-20(8-10)13-12-11(3-5-15-13)14(21)17-9-16-12/h3,5,7-9H,4,6H2,1-2H3,(H,16,17,21)
PDB

UniProtKB/SwissProt

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UniChem

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Article
PubMed
n/an/a 350n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of KDM5B (unknown origin) using biotin-H3K4me3 as substrate preincubated for 15 mins followed by substrate addition measured after 20 mins...


J Med Chem 59: 1388-409 (2016)


Article DOI: 10.1021/acs.jmedchem.5b01635
BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair
Lysine-specific demethylase 5B


(Homo sapiens (Human))
BDBM50153104
PNG
(CHEMBL3774710)
Show SMILES O=c1[nH]cnc2c(nccc12)-n1cc(CCN2CCCC2)cn1
Show InChI InChI=1S/C16H18N6O/c23-16-13-3-5-17-15(14(13)18-11-19-16)22-10-12(9-20-22)4-8-21-6-1-2-7-21/h3,5,9-11H,1-2,4,6-8H2,(H,18,19,23)
PDB

UniProtKB/SwissProt

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PC sid
UniChem

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Article
PubMed
n/an/a 71n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of KDM5B (unknown origin) using biotin-H3K4me3 as substrate preincubated for 15 mins followed by substrate addition measured after 20 mins...


J Med Chem 59: 1388-409 (2016)


Article DOI: 10.1021/acs.jmedchem.5b01635
BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4B


(Homo sapiens)
BDBM50153105
PNG
(CHEMBL3775454)
Show SMILES CN(C)CCc1cnn(c1)-c1nccc2c1nc[nH]c2=O
Show InChI InChI=1S/C14H16N6O/c1-19(2)6-4-10-7-18-20(8-10)13-12-11(3-5-15-13)14(21)17-9-16-12/h3,5,7-9H,4,6H2,1-2H3,(H,16,17,21)
PDB

UniProtKB/SwissProt

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PC sid
UniChem

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Article
PubMed
n/an/a 2.30E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of recombinant human N-terminal GST-tagged KDM4B (1 to 500 residues) expressed in baculovirus infected sf9 cells using biotin-H3K9me3 as s...


J Med Chem 59: 1388-409 (2016)


Article DOI: 10.1021/acs.jmedchem.5b01635
BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4B


(Homo sapiens)
BDBM50153104
PNG
(CHEMBL3774710)
Show SMILES O=c1[nH]cnc2c(nccc12)-n1cc(CCN2CCCC2)cn1
Show InChI InChI=1S/C16H18N6O/c23-16-13-3-5-17-15(14(13)18-11-19-16)22-10-12(9-20-22)4-8-21-6-1-2-7-21/h3,5,9-11H,1-2,4,6-8H2,(H,18,19,23)
PDB

UniProtKB/SwissProt

GoogleScholar
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PC sid
UniChem

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Article
PubMed
n/an/a 750n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of recombinant human N-terminal GST-tagged KDM4B (1 to 500 residues) expressed in baculovirus infected sf9 cells using biotin-H3K9me3 as s...


J Med Chem 59: 1388-409 (2016)


Article DOI: 10.1021/acs.jmedchem.5b01635
BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair
Tubulin


(Bos taurus)
BDBM50044962
PNG
(7-Methoxy-2-phenyl-1H-quinolin-4-one | CHEMBL15831)
Show SMILES COc1ccc2c(O)cc(nc2c1)-c1ccccc1
Show InChI InChI=1S/C16H13NO2/c1-19-12-7-8-13-15(9-12)17-14(10-16(13)18)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)
PDB
MMDB

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CHEMBL
PC cid
PC sid
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Patents


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Article
PubMed
n/an/a 4.80E+3n/an/an/an/an/an/a



Institute of Pharmaceutical Chemistry

Curated by ChEMBL


Assay Description
Inhibition of tubulin polymerization


J Med Chem 36: 1146-56 (1993)


Article DOI: 10.1021/jm00061a005
BindingDB Entry DOI: 10.7270/Q2BV7H8S
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4A


(Homo sapiens (Human))
BDBM50153104
PNG
(CHEMBL3774710)
Show SMILES O=c1[nH]cnc2c(nccc12)-n1cc(CCN2CCCC2)cn1
Show InChI InChI=1S/C16H18N6O/c23-16-13-3-5-17-15(14(13)18-11-19-16)22-10-12(9-20-22)4-8-21-6-1-2-7-21/h3,5,9-11H,1-2,4,6-8H2,(H,18,19,23)
PDB

UniProtKB/SwissProt

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Article
PubMed
n/an/a 1.40E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal His-tagged KDM4A (1 to 359 residues) expressed in Escherichia coli using biotin-H3K9me3 as substrate preincubated for ...


J Med Chem 59: 1388-409 (2016)


Article DOI: 10.1021/acs.jmedchem.5b01635
BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair
Lysine-specific demethylase 5C


(Homo sapiens)
BDBM50153104
PNG
(CHEMBL3774710)
Show SMILES O=c1[nH]cnc2c(nccc12)-n1cc(CCN2CCCC2)cn1
Show InChI InChI=1S/C16H18N6O/c23-16-13-3-5-17-15(14(13)18-11-19-16)22-10-12(9-20-22)4-8-21-6-1-2-7-21/h3,5,9-11H,1-2,4,6-8H2,(H,18,19,23)
PDB
MMDB

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KEGG

UniProtKB/SwissProt

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PC sid
UniChem

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Article
PubMed
n/an/a 150n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of KDM5C (unknown origin) using biotin-H3K4me3 as substrate preincubated for 15 mins followed by substrate addition measured after 20 mins...


J Med Chem 59: 1388-409 (2016)


Article DOI: 10.1021/acs.jmedchem.5b01635
BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair
Lysine-specific demethylase 5C


(Homo sapiens)
BDBM50153105
PNG
(CHEMBL3775454)
Show SMILES CN(C)CCc1cnn(c1)-c1nccc2c1nc[nH]c2=O
Show InChI InChI=1S/C14H16N6O/c1-19(2)6-4-10-7-18-20(8-10)13-12-11(3-5-15-13)14(21)17-9-16-12/h3,5,7-9H,4,6H2,1-2H3,(H,16,17,21)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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PC sid
UniChem

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Article
PubMed
n/an/a 340n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of KDM5C (unknown origin) using biotin-H3K4me3 as substrate preincubated for 15 mins followed by substrate addition measured after 20 mins...


J Med Chem 59: 1388-409 (2016)


Article DOI: 10.1021/acs.jmedchem.5b01635
BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4A


(Homo sapiens (Human))
BDBM50153105
PNG
(CHEMBL3775454)
Show SMILES CN(C)CCc1cnn(c1)-c1nccc2c1nc[nH]c2=O
Show InChI InChI=1S/C14H16N6O/c1-19(2)6-4-10-7-18-20(8-10)13-12-11(3-5-15-13)14(21)17-9-16-12/h3,5,7-9H,4,6H2,1-2H3,(H,16,17,21)
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 4.10E+3n/an/an/an/an/an/a



The Institute of Cancer Research

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal His-tagged KDM4A (1 to 359 residues) expressed in Escherichia coli using biotin-H3K9me3 as substrate preincubated for ...


J Med Chem 59: 1388-409 (2016)


Article DOI: 10.1021/acs.jmedchem.5b01635
BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair