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BDBM50474339 CHEMBL141236

SMILES: ONC(=O)\C=C\c1ccc(CNCCc2cn(CC3CC3)c3ccccc23)cc1

InChI Key: InChIKey=FAGBOEVMPXWLID-VAWYXSNFSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50474339   
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 1/2/3/4/5/6/7/8/9/11/Polyamine deacetylase HDAC10


(Homo sapiens (Human))
BDBM50474339
PNG
(CHEMBL141236)
Show SMILES ONC(=O)\C=C\c1ccc(CNCCc2cn(CC3CC3)c3ccccc23)cc1
Show InChI InChI=1S/C24H27N3O2/c28-24(26-29)12-11-18-5-7-19(8-6-18)15-25-14-13-21-17-27(16-20-9-10-20)23-4-2-1-3-22(21)23/h1-8,11-12,17,20,25,29H,9-10,13-16H2,(H,26,28)/b12-11+
PDB

UniProtKB/SwissProt

antibodypedia
antibodypedia
antibodypedia
antibodypedia
antibodypedia
antibodypedia
antibodypedia
antibodypedia
antibodypedia
antibodypedia
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 84n/an/an/an/an/an/a



Novartis Institute for Biomedical Research

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC) enzyme obtained from H1299 human lung carcinoma cell lysates


J Med Chem 46: 4609-24 (2003)


Article DOI: 10.1021/jm030235w
BindingDB Entry DOI: 10.7270/Q2736TP0
More data for this
Ligand-Target Pair