BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50297686   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Prostaglandin G/H synthase 2


(Homo sapiens (Human))
BDBM50297686
PNG
(2-(cyclohexyloxy)-4-(4-(methylsulfonyl)phenyl)-6-(...)
Show SMILES CS(=O)(=O)c1ccc(cc1)-c1cc(nc(OC2CCCCC2)n1)C(F)(F)F
Show InChI InChI=1S/C18H19F3N2O3S/c1-27(24,25)14-9-7-12(8-10-14)15-11-16(18(19,20)21)23-17(22-15)26-13-5-3-2-4-6-13/h7-11,13H,2-6H2,1H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a<10n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of human COX2 expressed in baculovirus-infected SF9 cells assessed as inhibition of arachidonic acid-stimulated PGE2 production treated 1 ...


Bioorg Med Chem Lett 19: 4504-8 (2009)


Article DOI: 10.1016/j.bmcl.2009.02.085
BindingDB Entry DOI: 10.7270/Q20Z7396
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1


(Homo sapiens (Human))
BDBM50297686
PNG
(2-(cyclohexyloxy)-4-(4-(methylsulfonyl)phenyl)-6-(...)
Show SMILES CS(=O)(=O)c1ccc(cc1)-c1cc(nc(OC2CCCCC2)n1)C(F)(F)F
Show InChI InChI=1S/C18H19F3N2O3S/c1-27(24,25)14-9-7-12(8-10-14)15-11-16(18(19,20)21)23-17(22-15)26-13-5-3-2-4-6-13/h7-11,13H,2-6H2,1H3
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.86E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of human COX1 expressed in baculovirus-infected SF9 cells assessed as inhibition of arachidonic acid-stimulated PGE2 production treated 1 ...


Bioorg Med Chem Lett 19: 4504-8 (2009)


Article DOI: 10.1016/j.bmcl.2009.02.085
BindingDB Entry DOI: 10.7270/Q20Z7396
More data for this
Ligand-Target Pair