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BDBM50424617 CHEMBL2313160

SMILES: COC(=O)c1ccc2cc(NC(=O)C3CCN(CC3)S(=O)(=O)c3ccc(C)cc3C)ccc2c1

InChI Key: InChIKey=DATGOSDUXLFFBA-UHFFFAOYSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50424617   
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
EBifunctional epoxide hydrolase 2


(Homo sapiens (Human))
BDBM50424617
PNG
(CHEMBL2313160)
Show SMILES COC(=O)c1ccc2cc(NC(=O)C3CCN(CC3)S(=O)(=O)c3ccc(C)cc3C)ccc2c1
Show InChI InChI=1S/C26H28N2O5S/c1-17-4-9-24(18(2)14-17)34(31,32)28-12-10-19(11-13-28)25(29)27-23-8-7-20-15-22(26(30)33-3)6-5-21(20)16-23/h4-9,14-16,19H,10-13H2,1-3H3,(H,27,29)
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 110n/an/an/an/an/an/a



Columbia University

Curated by ChEMBL


Assay Description
Inhibition of human sEH assessed as 6-methoxy-2-naphthaldehyde generation preincubated for 10 before addition of cyano(2-methyl-oxynaphthalen-6-yl)me...


Bioorg Med Chem Lett 23: 417-21 (2012)


Article DOI: 10.1016/j.bmcl.2012.11.084
BindingDB Entry DOI: 10.7270/Q2Z60QBJ
More data for this
Ligand-Target Pair