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BDBM50127769 4-Iodo-N-[2-(2,2,2-trifluoro-1-hydroxy-1-trifluoromethyl-ethyl)-naphthalen-1-yl]-benzamide::CHEMBL51460

SMILES: OC(c1ccc2ccccc2c1NC(=O)c1ccc(I)cc1)(C(F)(F)F)C(F)(F)F

InChI Key: InChIKey=NKOQDJNKUIVVCI-UHFFFAOYSA-N

Data: 1 EC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50127769   
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
Sulfonylurea receptor 2, Kir6.2


(Homo sapiens (Human))
BDBM50127769
PNG
(4-Iodo-N-[2-(2,2,2-trifluoro-1-hydroxy-1-trifluoro...)
Show SMILES OC(c1ccc2ccccc2c1NC(=O)c1ccc(I)cc1)(C(F)(F)F)C(F)(F)F
Show InChI InChI=1S/C20H12F6INO2/c21-19(22,23)18(30,20(24,25)26)15-10-7-11-3-1-2-4-14(11)16(15)28-17(29)12-5-8-13(27)9-6-12/h1-10,30H,(H,28,29)
PDB

KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/an/an/a 154n/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Potassium channel opening activity in vitro using LtK cells transfected with Kir6.2/SUR2B exon 17


Bioorg Med Chem Lett 13: 1741-4 (2003)


BindingDB Entry DOI: 10.7270/Q28S4P9V
More data for this
Ligand-Target Pair