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BDBM50274171 CHEMBL4127816

SMILES: S=C(NC12CC3CC(CC(C3)C1)C2)NC12CC3CC(CC(C3)C1)C2

InChI Key: InChIKey=SDCKTNYEQQLVGV-UHFFFAOYSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50274171   
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))
BDBM50274171
PNG
(CHEMBL4127816)
Show SMILES S=C(NC12CC3CC(CC(C3)C1)C2)NC12CC3CC(CC(C3)C1)C2 |TLB:13:14:17:21.20.19,2:3:6:10.9.8,THB:22:14:17:21.20.19,22:20:17:23.15.14,4:3:6.5.10:8,4:5:8:12.3.11,11:3:6:10.9.8,11:9:6:12.3.4,15:16:19:23.14.22,15:14:17.16.21:19|
Show InChI InChI=1S/C21H32N2S/c24-19(22-20-7-13-1-14(8-20)3-15(2-13)9-20)23-21-10-16-4-17(11-21)6-18(5-16)12-21/h13-18H,1-12H2,(H2,22,23,24)
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
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PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 11n/an/an/an/an/an/a



University of California Davis

Curated by ChEMBL


Assay Description
Inhibition of recombinant human sEH expressed in baculovirus expression system using CMNPC as substrate preincubated for 5 mins followed by substrate...


Bioorg Med Chem Lett 28: 2302-2313 (2018)


Article DOI: 10.1016/j.bmcl.2018.05.024
BindingDB Entry DOI: 10.7270/Q2222X8F
More data for this
Ligand-Target Pair