BDBM50135549 4-[3-Fluoro-2-(3-nitro-benzoylamino)-phenoxy]-phthalic acid::CHEMBL133745

SMILES OC(=O)c1ccc(Oc2cccc(F)c2NC(=O)c2cccc(c2)[N+]([O-])=O)cc1C(O)=O

InChI Key InChIKey=XKPFJBJRMRYLPA-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 = 50135549   

TargetGlycogen phosphorylase, liver form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135549(4-[3-Fluoro-2-(3-nitro-benzoylamino)-phenoxy]-phth...)
Affinity DataIC50: 250nMAssay Description:Inhibitory activity against HLGP(human liver glycogen phosphorylase)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, liver form(Mouse)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135549(4-[3-Fluoro-2-(3-nitro-benzoylamino)-phenoxy]-phth...)
Affinity DataIC50: 207nMAssay Description:Inhibitory activity against mouse liver glycogen phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, liver form(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135549(4-[3-Fluoro-2-(3-nitro-benzoylamino)-phenoxy]-phth...)
Affinity DataIC50: 302nMAssay Description:Inhibitory activity against rat liver glycogen phosphorylaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135549(4-[3-Fluoro-2-(3-nitro-benzoylamino)-phenoxy]-phth...)
Affinity DataIC50: 1.86E+3nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed