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BDBM50153116 CHEMBL3774672

SMILES: OCCc1cnn(c1)-c1nccc2c1nc[nH]c2=O

InChI Key: InChIKey=GSQZSUZKJWHBOL-UHFFFAOYSA-N

Data: 4 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 4 hits for monomerid = 50153116   
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))
BDBM50153116
PNG
(CHEMBL3774672)
Show SMILES OCCc1cnn(c1)-c1nccc2c1nc[nH]c2=O
Show InChI InChI=1S/C12H11N5O2/c18-4-2-8-5-16-17(6-8)11-10-9(1-3-13-11)12(19)15-7-14-10/h1,3,5-7,18H,2,4H2,(H,14,15,19)
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UniProtKB/SwissProt

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CHEMBL
MMDB
PC cid
PC sid
UniChem

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PubMed
n/an/a 4.60E+3n/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)


BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair
Lysine-specific demethylase 5C


(Homo sapiens (Human))
BDBM50153116
PNG
(CHEMBL3774672)
Show SMILES OCCc1cnn(c1)-c1nccc2c1nc[nH]c2=O
Show InChI InChI=1S/C12H11N5O2/c18-4-2-8-5-16-17(6-8)11-10-9(1-3-13-11)12(19)15-7-14-10/h1,3,5-7,18H,2,4H2,(H,14,15,19)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

PubMed
n/an/a 8.40E+3n/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)


BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4A


(Homo sapiens (Human))
BDBM50153116
PNG
(CHEMBL3774672)
Show SMILES OCCc1cnn(c1)-c1nccc2c1nc[nH]c2=O
Show InChI InChI=1S/C12H11N5O2/c18-4-2-8-5-16-17(6-8)11-10-9(1-3-13-11)12(19)15-7-14-10/h1,3,5-7,18H,2,4H2,(H,14,15,19)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
MMDB
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a 2.18E+4n/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)


BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4B


(Homo sapiens (Human))
BDBM50153116
PNG
(CHEMBL3774672)
Show SMILES OCCc1cnn(c1)-c1nccc2c1nc[nH]c2=O
Show InChI InChI=1S/C12H11N5O2/c18-4-2-8-5-16-17(6-8)11-10-9(1-3-13-11)12(19)15-7-14-10/h1,3,5-7,18H,2,4H2,(H,14,15,19)
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
MMDB
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a 8.80E+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)


BindingDB Entry DOI: 10.7270/Q2W097TR
More data for this
Ligand-Target Pair