BDBM50311392 CHEMBL1079335::N-[3-(3-Bromophenylamino)-4-pyridinyl]trifluoromethanesulfonamide

SMILES FC(F)(F)S(=O)(=O)Nc1ccncc1Nc1cccc(Br)c1

InChI Key InChIKey=WYMPMNZWERFHGE-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50311392   

TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
University Of Liege

Curated by ChEMBL
LigandPNGBDBM50311392(CHEMBL1079335 | N-[3-(3-Bromophenylamino)-4-pyridi...)
Affinity DataIC50:  120nMAssay Description:Inhibition of COX2 in LPS-stimulated human whole blood assessed as PGE2 production by enzyme immunoassayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50311392(CHEMBL1079335 | N-[3-(3-Bromophenylamino)-4-pyridi...)
Affinity DataIC50:  910nMAssay Description:Inhibition of COX1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
University Of Liege

Curated by ChEMBL
LigandPNGBDBM50311392(CHEMBL1079335 | N-[3-(3-Bromophenylamino)-4-pyridi...)
Affinity DataIC50:  120nMAssay Description:Inhibition of COX2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50311392(CHEMBL1079335 | N-[3-(3-Bromophenylamino)-4-pyridi...)
Affinity DataIC50:  910nMAssay Description:Inhibition of COX1 in human whole blood assessed as TXB2 production by enzyme immunoassayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed