null

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

InChI Key: InChIKey=NKARZGURZMIRMA-RBSFLKMASA-N

PDB links: 2 PDB IDs match this monomer.

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50194702   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM50194702 ((3R,4R,5R)-5-(HYDROXYMETHYL)-1-(3-PHENYLPROPYL)PIP...) Show SMILES OC[C@H]1CN(CCCc2ccccc2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C15H23NO3/c17-11-13-9-16(10-14(18)15(13)19)8-4-7-12-5-2-1-3-6-12/h1-3,5-6,13-15,17-19H,4,7-11H2/t13-,14-,15-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents	MMDB PDB Article PubMed	n/a	n/a	840	n/a	n/a	n/a	n/a	n/a	n/a
The National Hellenic Research Foundation Curated by ChEMBL					Assay Description Inhibition of non-phosphorylated form of rabbit muscle glycogen phosphorylase				J Med Chem 49: 5687-701 (2006) Article DOI: 10.1021/jm060496g BindingDB Entry DOI: 10.7270/Q25Q4VQP
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50194702 ((3R,4R,5R)-5-(HYDROXYMETHYL)-1-(3-PHENYLPROPYL)PIP...) Show SMILES OC[C@H]1CN(CCCc2ccccc2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C15H23NO3/c17-11-13-9-16(10-14(18)15(13)19)8-4-7-12-5-2-1-3-6-12/h1-3,5-6,13-15,17-19H,4,7-11H2/t13-,14-,15-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents	Article PubMed	n/a	n/a	850	n/a	n/a	n/a	n/a	n/a	n/a
The National Hellenic Research Foundation Curated by ChEMBL					Assay Description Inhibition of phosphorylated form of pig liver glycogen phosphorylase				J Med Chem 49: 5687-701 (2006) Article DOI: 10.1021/jm060496g BindingDB Entry DOI: 10.7270/Q25Q4VQP
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50194702 ((3R,4R,5R)-5-(HYDROXYMETHYL)-1-(3-PHENYLPROPYL)PIP...) Show SMILES OC[C@H]1CN(CCCc2ccccc2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C15H23NO3/c17-11-13-9-16(10-14(18)15(13)19)8-4-7-12-5-2-1-3-6-12/h1-3,5-6,13-15,17-19H,4,7-11H2/t13-,14-,15-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents	Article PubMed	n/a	n/a	1.22E+3	n/a	n/a	n/a	n/a	n/a	n/a
The National Hellenic Research Foundation Curated by ChEMBL					Assay Description Inhibition of phosphorylated form of rat liver glycogen phosphorylase				J Med Chem 49: 5687-701 (2006) Article DOI: 10.1021/jm060496g BindingDB Entry DOI: 10.7270/Q25Q4VQP
					More data for this Ligand-Target Pair