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BDBM50414315 CHEMBL565027

SMILES: CCS(=O)(=O)N1CCc2c(C1)ccc(C)c2NC(=O)Cc1ccc(c(F)c1)C(F)(F)F

InChI Key: InChIKey=TZNWYRWJMOFSOQ-UHFFFAOYSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50414315   
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
P2X purinoceptor 7


(Homo sapiens (Human))		BDBM50414315
PNG
(CHEMBL565027)
Show SMILES CCS(=O)(=O)N1CCc2c(C1)ccc(C)c2NC(=O)Cc1ccc(c(F)c1)C(F)(F)F
Show InChI InChI=1S/C21H22F4N2O3S/c1-3-31(29,30)27-9-8-16-15(12-27)6-4-13(2)20(16)26-19(28)11-14-5-7-17(18(22)10-14)21(23,24)25/h4-7,10H,3,8-9,11-12H2,1-2H3,(H,26,28)
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 25.1n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Antagonist activity at P2X7 receptor in human THP1 cells assessed as inhibition of BzATP-induced ethidium uptake

J Med Chem 52: 3123-41 (2009)


Article DOI: 10.1021/jm801528x
BindingDB Entry DOI: 10.7270/Q2251KDR
More data for this
Ligand-Target Pair