BDBM50243305 (S)-2-(2-(3-(2-chloro-6-methylphenyl)ureido)-2-naphthamido)-3-cyclohexylpropanoic acid::CHEMBL507762

SMILES Cc1cccc(Cl)c1NC(=O)Nc1cc2ccccc2cc1C(=O)N[C@@H](CC1CCCCC1)C(O)=O

InChI Key InChIKey=UEAKFJHZEFJNCU-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 = 50243305   

TargetGlycogen phosphorylase, liver form(Human)
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50243305((S)-2-(2-(3-(2-chloro-6-methylphenyl)ureido)-2-nap...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of human glycogen phosphorylase alphaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetGlycogen phosphorylase, liver form(Human)
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50243305((S)-2-(2-(3-(2-chloro-6-methylphenyl)ureido)-2-nap...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of human glycogen phosphorylase alpha in presence of glucoseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetGlycogen phosphorylase, liver form(Human)
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50243305((S)-2-(2-(3-(2-chloro-6-methylphenyl)ureido)-2-nap...)
Affinity DataIC50: 7.40E+3nMAssay Description:Inhibition of human glycogen phosphorylase alpha in HepG2 cells assessed as inhibition of forskolin-induced glycogenolysis after 60 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetGlycogen phosphorylase, liver form(Human)
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50243305((S)-2-(2-(3-(2-chloro-6-methylphenyl)ureido)-2-nap...)
Affinity DataIC50: 5.10E+4nMAssay Description:Inhibition of human glycogen phosphorylase alpha in absence of glucoseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed