BDBM50331107 (S)-N-(8-(hydroxyamino)-1,8-dioxo-1-(quinolin-8-ylamino)octan-2-yl)-1H-indole-2-carboxamide::(S)-N8-hydroxy-2-(1H-indole-2-carboxamido)-N1-(quinolin-8-yl)octanediamide::CHEMBL221655

SMILES ONC(=O)CCCCC[C@H](NC(=O)c1cc2ccccc2[nH]1)C(=O)Nc1cccc2cccnc12

InChI Key InChIKey=IYQNLKIVMPPKFV-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50331107   

TargetHistone deacetylase 1(Human)
The University of Queensland

Curated by ChEMBL
LigandPNGBDBM50331107((S)-N-(8-(hydroxyamino)-1,8-dioxo-1-(quinolin-8-yl...)
Affinity DataIC50: 48nMAssay Description:Inhibition of recombinant human HDAC1 using Cbz-Lys(TFAc)-AMC as substrate by fluorometric analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/14/2011
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
The University of Queensland

Curated by ChEMBL
LigandPNGBDBM50331107((S)-N-(8-(hydroxyamino)-1,8-dioxo-1-(quinolin-8-yl...)
Affinity DataIC50: 107nMAssay Description:Inhibition of recombinant human HDAC6 using Boc-Lys(Ac)-AMC as substrate by fluorometric analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/14/2011
Entry Details Article
PubMed
TargetHistone deacetylase(Plasmodium falciparum (isolate 3D7))
The University of Queensland

Curated by ChEMBL
LigandPNGBDBM50331107((S)-N-(8-(hydroxyamino)-1,8-dioxo-1-(quinolin-8-yl...)
Affinity DataIC50: 78nMAssay Description:Inhibition of Plasmodium falciparum 3D7 HDAC1 in infected-human erythrocytes assessed as histone H4 hyperacetylation after 1.5 hrs by SDS-PAGE analys...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/14/2011
Entry Details Article
PubMed