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SMILES: ONC(=O)CCCCCCCN(c1ncns1)c1ccccn1

InChI Key: InChIKey=WGULHDOTIUCDOF-UHFFFAOYSA-N

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 2 hits for monomerid = 310716   
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


(Homo sapiens (Human))
BDBM310716
PNG
(N-Hydroxy-8-(pyridin-2-yl(1,2,4-thiadiazol-5-yl)am...)
Show SMILES ONC(=O)CCCCCCCN(c1ncns1)c1ccccn1
Show InChI InChI=1S/C15H21N5O2S/c21-14(19-22)9-4-2-1-3-7-11-20(15-17-12-18-23-15)13-8-5-6-10-16-13/h5-6,8,10,12,22H,1-4,7,9,11H2,(H,19,21)
PDB
MMDB

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KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a<500n/an/an/an/an/an/a



Karus Therapeutics Limited

US Patent


Assay Description
The assay is described in WO2008/062201.


US Patent US10150763 (2018)


BindingDB Entry DOI: 10.7270/Q2C82CC1
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM310716
PNG
(N-Hydroxy-8-(pyridin-2-yl(1,2,4-thiadiazol-5-yl)am...)
Show SMILES ONC(=O)CCCCCCCN(c1ncns1)c1ccccn1
Show InChI InChI=1S/C15H21N5O2S/c21-14(19-22)9-4-2-1-3-7-11-20(15-17-12-18-23-15)13-8-5-6-10-16-13/h5-6,8,10,12,22H,1-4,7,9,11H2,(H,19,21)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 5.50E+3n/an/an/an/an/an/a



Karus Therapeutics Limited

US Patent


Assay Description
The assay is described in WO2008/062201.


US Patent US10150763 (2018)


BindingDB Entry DOI: 10.7270/Q2C82CC1
More data for this
Ligand-Target Pair