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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Glycogen phosphorylase, liver form' and Ligand = 'BDBM50256269'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Glycogen phosphorylase, liver form


(Homo sapiens (Human))
BDBM50256269
PNG
(1-(3-(3-mesitylureido)-2-naphthamido)cyclopentanec...)
Show SMILES Cc1cc(C)c(NC(=O)Nc2cc3ccccc3cc2C(=O)NC2(CCCC2)C(O)=O)c(C)c1
Show InChI InChI=1S/C27H29N3O4/c1-16-12-17(2)23(18(3)13-16)29-26(34)28-22-15-20-9-5-4-8-19(20)14-21(22)24(31)30-27(25(32)33)10-6-7-11-27/h4-5,8-9,12-15H,6-7,10-11H2,1-3H3,(H,30,31)(H,32,33)(H2,28,29,34)
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Article
PubMed
n/an/a 279n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of human liver glycogen phosphorylase A by fluorescence intensity endpoint assay in presence of glucose


Bioorg Med Chem Lett 19: 976-80 (2009)


Article DOI: 10.1016/j.bmcl.2008.11.085
BindingDB Entry DOI: 10.7270/Q26T0MGG
More data for this
Ligand-Target Pair
Glycogen phosphorylase, liver form


(Homo sapiens (Human))
BDBM50256269
PNG
(1-(3-(3-mesitylureido)-2-naphthamido)cyclopentanec...)
Show SMILES Cc1cc(C)c(NC(=O)Nc2cc3ccccc3cc2C(=O)NC2(CCCC2)C(O)=O)c(C)c1
Show InChI InChI=1S/C27H29N3O4/c1-16-12-17(2)23(18(3)13-16)29-26(34)28-22-15-20-9-5-4-8-19(20)14-21(22)24(31)30-27(25(32)33)10-6-7-11-27/h4-5,8-9,12-15H,6-7,10-11H2,1-3H3,(H,30,31)(H,32,33)(H2,28,29,34)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 1.77E+3n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of human liver glycogen phosphorylase A in HepG2 cells assessed as forskolin-induced glycogenolysis


Bioorg Med Chem Lett 19: 976-80 (2009)


Article DOI: 10.1016/j.bmcl.2008.11.085
BindingDB Entry DOI: 10.7270/Q26T0MGG
More data for this
Ligand-Target Pair