BDBM50294534 (S)-2-(2-((S)-2-amino-5-guanidinopentanamido)acetamido)-N1,N8-bis(2-aminophenyl)octanediamide::CHEMBL541451

SMILES [#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#6]-[#6]-[#6](=O)-[#7]-c1ccccc1-[#7])-[#6](=O)-[#7]-c1ccccc1-[#7]

InChI Key InChIKey=KLCRKSQYVSOHGU-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50294534   

TargetHistone deacetylase 3(Human)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50294534((S)-2-(2-((S)-2-amino-5-guanidinopentanamido)aceta...)
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/26/2010
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50294534((S)-2-(2-((S)-2-amino-5-guanidinopentanamido)aceta...)
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/26/2010
Entry Details Article
PubMed