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BDBM50047970 CHEMBL3314864

SMILES: Nc1ccccc1NC(=O)\C=C\c1ccc(cc1)-c1nnc(Cc2cccc3ccccc23)o1

InChI Key: InChIKey=HFZJPVYVYYPCDO-SAPNQHFASA-N

Data: 3 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 3 hits for monomerid = 50047970   
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
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50047970
PNG
(CHEMBL3314864)
Show SMILES Nc1ccccc1NC(=O)\C=C\c1ccc(cc1)-c1nnc(Cc2cccc3ccccc23)o1
Show InChI InChI=1S/C28H22N4O2/c29-24-10-3-4-11-25(24)30-26(33)17-14-19-12-15-21(16-13-19)28-32-31-27(34-28)18-22-8-5-7-20-6-1-2-9-23(20)22/h1-17H,18,29H2,(H,30,33)/b17-14+
PDB
MMDB

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KEGG

UniProtKB/SwissProt

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CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.00E+3n/an/an/an/an/a25



Sapienza University of Rome

Curated by ChEMBL


Assay Description
Inhibition of human recombinant HDAC1 using histone H3 substrate pre-incubated at room temperature for 15 mins before substrate addition by fluorimet...


J Med Chem 57: 6259-65 (2014)


Article DOI: 10.1021/jm500303u
BindingDB Entry DOI: 10.7270/Q2KK9DFZ
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Homo sapiens (Human))
BDBM50047970
PNG
(CHEMBL3314864)
Show SMILES Nc1ccccc1NC(=O)\C=C\c1ccc(cc1)-c1nnc(Cc2cccc3ccccc23)o1
Show InChI InChI=1S/C28H22N4O2/c29-24-10-3-4-11-25(24)30-26(33)17-14-19-12-15-21(16-13-19)28-32-31-27(34-28)18-22-8-5-7-20-6-1-2-9-23(20)22/h1-17H,18,29H2,(H,30,33)/b17-14+
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>2.00E+4n/an/an/an/an/a25



Sapienza University of Rome

Curated by ChEMBL


Assay Description
Inhibition of human recombinant HDAC6 pre-incubated at room temperature for 15 min before substrate addition by fluorimetric assay


J Med Chem 57: 6259-65 (2014)


Article DOI: 10.1021/jm500303u
BindingDB Entry DOI: 10.7270/Q2KK9DFZ
More data for this
Ligand-Target Pair
Histone deacetylase 4


(Homo sapiens (Human))
BDBM50047970
PNG
(CHEMBL3314864)
Show SMILES Nc1ccccc1NC(=O)\C=C\c1ccc(cc1)-c1nnc(Cc2cccc3ccccc23)o1
Show InChI InChI=1S/C28H22N4O2/c29-24-10-3-4-11-25(24)30-26(33)17-14-19-12-15-21(16-13-19)28-32-31-27(34-28)18-22-8-5-7-20-6-1-2-9-23(20)22/h1-17H,18,29H2,(H,30,33)/b17-14+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>2.00E+4n/an/an/an/an/a25



Sapienza University of Rome

Curated by ChEMBL


Assay Description
Inhibition of human recombinant HDAC4 using non-histone trifluoroacetyl lysine substrate pre-incubated at room temperature for 15 mins before substra...


J Med Chem 57: 6259-65 (2014)


Article DOI: 10.1021/jm500303u
BindingDB Entry DOI: 10.7270/Q2KK9DFZ
More data for this
Ligand-Target Pair