BindingDB logo
myBDB logout

BDBM19144 (2S)-2-[(tert-butylcarbamoyl)amino]-N-cyclopentyl-7-sulfanylheptanamide::thiolate analogue, 35a

SMILES: CC(C)(C)NC(=O)N[C@@H](CCCCCS)C(=O)NC1CCCC1

InChI Key: InChIKey=CBRFYHIFCHDUDU-AWEZNQCLSA-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 = 19144   
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 6 (HDAC6)


(Mus musculus)
BDBM19144
PNG
((2S)-2-[(tert-butylcarbamoyl)amino]-N-cyclopentyl-...)
Show SMILES CC(C)(C)NC(=O)N[C@@H](CCCCCS)C(=O)NC1CCCC1 |r|
Show InChI InChI=1S/C17H33N3O2S/c1-17(2,3)20-16(22)19-14(11-5-4-8-12-23)15(21)18-13-9-6-7-10-13/h13-14,23H,4-12H2,1-3H3,(H,18,21)(H2,19,20,22)/t14-/m0/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 100n/an/an/an/a8.037



Nagoya City University



Assay Description
The enzyme activity was assayed using recombinant HDAC and [3H] acetyl-labeled histones as substrate. The released [3H]acetic acid was extracted and ...


J Med Chem 50: 5425-38 (2007)


Article DOI: 10.1021/jm7009217
BindingDB Entry DOI: 10.7270/Q2XK8CT6
More data for this
Ligand-Target Pair
Histone deacetylase 4


(Homo sapiens (Human))
BDBM19144
PNG
((2S)-2-[(tert-butylcarbamoyl)amino]-N-cyclopentyl-...)
Show SMILES CC(C)(C)NC(=O)N[C@@H](CCCCCS)C(=O)NC1CCCC1 |r|
Show InChI InChI=1S/C17H33N3O2S/c1-17(2,3)20-16(22)19-14(11-5-4-8-12-23)15(21)18-13-9-6-7-10-13/h13-14,23H,4-12H2,1-3H3,(H,18,21)(H2,19,20,22)/t14-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 310n/an/an/an/an/an/a



Nagoya City University



Assay Description
The enzyme activity was assayed using recombinant HDAC and [3H] acetyl-labeled histones as substrate. The released [3H]acetic acid was extracted and ...


J Med Chem 50: 5425-38 (2007)


Article DOI: 10.1021/jm7009217
BindingDB Entry DOI: 10.7270/Q2XK8CT6
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM19144
PNG
((2S)-2-[(tert-butylcarbamoyl)amino]-N-cyclopentyl-...)
Show SMILES CC(C)(C)NC(=O)N[C@@H](CCCCCS)C(=O)NC1CCCC1 |r|
Show InChI InChI=1S/C17H33N3O2S/c1-17(2,3)20-16(22)19-14(11-5-4-8-12-23)15(21)18-13-9-6-7-10-13/h13-14,23H,4-12H2,1-3H3,(H,18,21)(H2,19,20,22)/t14-/m0/s1
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 460n/an/an/an/an/an/a



Nagoya City University



Assay Description
The enzyme activity was assayed using recombinant HDAC and [3H] acetyl-labeled histones as substrate. The released [3H]acetic acid was extracted and ...


J Med Chem 50: 5425-38 (2007)


Article DOI: 10.1021/jm7009217
BindingDB Entry DOI: 10.7270/Q2XK8CT6
More data for this
Ligand-Target Pair