BDBM50135563 4-{2-[(4-Cyano-pyridine-2-carbonyl)-amino]-phenoxy}-phthalic acid::CHEMBL132201

SMILES OC(=O)c1ccc(Oc2ccccc2NC(=O)c2cc(ccn2)C#N)cc1C(O)=O

InChI Key InChIKey=KWAQGJBZAIHRQW-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50135563   

TargetGlycogen phosphorylase, liver form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135563(4-{2-[(4-Cyano-pyridine-2-carbonyl)-amino]-phenoxy...)
Affinity DataIC50: 16nMAssay Description:Inhibitory activity against HLGP(human liver glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, liver form(Mouse)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135563(4-{2-[(4-Cyano-pyridine-2-carbonyl)-amino]-phenoxy...)
Affinity DataIC50: 14nMAssay Description:Inhibitory activity against mouse liver glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, liver form(Rat)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135563(4-{2-[(4-Cyano-pyridine-2-carbonyl)-amino]-phenoxy...)
Affinity DataIC50: 19nMAssay Description:Inhibitory activity against rat liver glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135563(4-{2-[(4-Cyano-pyridine-2-carbonyl)-amino]-phenoxy...)
Affinity DataIC50: 167nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed