BDBM23587 (3-Phenoxybenzoylamino)benzoic acid deriv., 33::2-hydroxy-6-[(3-phenoxy-4-phenylbenzene)amido]benzoic acid

SMILES OC(=O)c1c(O)cccc1NC(=O)c1ccc(c(Oc2ccccc2)c1)-c1ccccc1

InChI Key InChIKey=KKXSDSWMIHFYQS-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 23587   

Target3-oxoacyl-[acyl-carrier-protein] synthase 3(Enterococcus faecalis)
Quorex Pharmaceuticals

LigandPNGBDBM23587((3-Phenoxybenzoylamino)benzoic acid deriv., 33 | 2...)
Affinity DataIC50:  4nMpH: 7.0 T: 2°CAssay Description:The potency of FabH inhibition (IC50) was determined using [3H]- or [14C]-radiolabeled substrates. This was accomplished at fixed concentrations of a...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxoacyl-[acyl-carrier-protein] synthase 3(Haemophilus influenzae)
Quorex Pharmaceuticals

LigandPNGBDBM23587((3-Phenoxybenzoylamino)benzoic acid deriv., 33 | 2...)
Affinity DataIC50:  2.40E+3nMpH: 7.0 T: 2°CAssay Description:The potency of FabH inhibition (IC50) was determined using [3H]- or [14C]-radiolabeled substrates. This was accomplished at fixed concentrations of a...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxoacyl-[acyl-carrier-protein] synthase 3(Staphylococcus aureus)
Quorex Pharmaceuticals

LigandPNGBDBM23587((3-Phenoxybenzoylamino)benzoic acid deriv., 33 | 2...)
Affinity DataIC50:  3.80E+3nMpH: 7.0 T: 2°CAssay Description:The potency of FabH inhibition (IC50) was determined using [3H]- or [14C]-radiolabeled substrates. This was accomplished at fixed concentrations of a...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxoacyl-[acyl-carrier-protein] synthase 3(Streptococcus pyogenes)
Quorex Pharmaceuticals

LigandPNGBDBM23587((3-Phenoxybenzoylamino)benzoic acid deriv., 33 | 2...)
Affinity DataIC50:  4nMpH: 7.0 T: 2°CAssay Description:The potency of FabH inhibition (IC50) was determined using [3H]- or [14C]-radiolabeled substrates. This was accomplished at fixed concentrations of a...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed