BDBM50137844 6-(1-Oxo-1,3-dihydro-isoindol-2-yl)-hexanoic acid (2-amino-phenyl)-amide::CHEMBL318821
SMILES: Nc1ccccc1NC(=O)CCCCCN1Cc2ccccc2C1=O
InChI Key: InChIKey=GYVLADWHXWFTMQ-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50137844 Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
Histone deacetylase
(Homo sapiens (Human)) | BDBM50137844
![PNG](/data/jpeg/tenK5013/BindingDB_50137844.png) (6-(1-Oxo-1,3-dihydro-isoindol-2-yl)-hexanoic acid ...)Show InChI InChI=1S/C20H23N3O2/c21-17-10-5-6-11-18(17)22-19(24)12-2-1-7-13-23-14-15-8-3-4-9-16(15)20(23)25/h3-6,8-11H,1-2,7,12-14,21H2,(H,22,24) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | n/a | n/a | 9.90E+4 | n/a | n/a | n/a | n/a |
MethylGene Inc.
Curated by ChEMBL
| Assay Description Effect on induced hyperacetylation of histones in whole cells |
Bioorg Med Chem Lett 14: 283-7 (2003)
BindingDB Entry DOI: 10.7270/Q2BV7G17 |
More data for this Ligand-Target Pair | |
Histone deacetylase 1
(Homo sapiens (Human)) | BDBM50137844
![PNG](/data/jpeg/tenK5013/BindingDB_50137844.png) (6-(1-Oxo-1,3-dihydro-isoindol-2-yl)-hexanoic acid ...)Show InChI InChI=1S/C20H23N3O2/c21-17-10-5-6-11-18(17)22-19(24)12-2-1-7-13-23-14-15-8-3-4-9-16(15)20(23)25/h3-6,8-11H,1-2,7,12-14,21H2,(H,22,24) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
MethylGene Inc.
Curated by ChEMBL
| Assay Description Ability to inhibit recombinant human histone deacetylase 1 (HDAC-1). |
Bioorg Med Chem Lett 14: 283-7 (2003)
BindingDB Entry DOI: 10.7270/Q2BV7G17 |
More data for this Ligand-Target Pair | |