BDBM50194702 (3R,4R,5R)-5-(HYDROXYMETHYL)-1-(3-PHENYLPROPYL)PIPERIDINE-3,4-DIOL::(3R,4R,5R)-5-hydroxymethyl-1-(3-phenylpropyl)-3,4-piperidinediol::CHEMBL213661

SMILES OC[C@H]1CN(CCCc2ccccc2)C[C@@H](O)[C@@H]1O

InChI Key InChIKey=NKARZGURZMIRMA-UHFFFAOYSA-N

Data  3 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 3 hits for monomerid = 50194702   

TargetGlycogen phosphorylase, liver form(Rat)
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50194702((3R,4R,5R)-5-(HYDROXYMETHYL)-1-(3-PHENYLPROPYL)PIP...)
Affinity DataIC50: 1.22E+3nMAssay Description:Inhibition of phosphorylated form of rat liver glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, liver form(Human)
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50194702((3R,4R,5R)-5-(HYDROXYMETHYL)-1-(3-PHENYLPROPYL)PIP...)
Affinity DataIC50: 850nMAssay Description:Inhibition of phosphorylated form of pig liver glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50194702((3R,4R,5R)-5-(HYDROXYMETHYL)-1-(3-PHENYLPROPYL)PIP...)
Affinity DataIC50: 840nMAssay Description:Inhibition of non-phosphorylated form of rabbit muscle glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed