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SMILES: OC(=O)CSC[C@H]1[C@@H](Cc2ccccc12)NC(=O)c1cc2sc(Cl)c(Cl)c2[nH]1

InChI Key: InChIKey=PBMXOEGUCUSDDO-VXGBXAGGSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50320328   
Target/Host
(Institution)		LigandTarget/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		pHTemp
°C
Glycogen phosphorylase, liver form


(Homo sapiens (Human))		BDBM50320328
PNG
(2-(((1R,2R)-2-(2,3-dichloro-4H-thieno[3,2-b]pyrrol...)
Show SMILES OC(=O)CSC[C@H]1[C@@H](Cc2ccccc12)NC(=O)c1cc2sc(Cl)c(Cl)c2[nH]1 |r|
Show InChI InChI=1S/C19H16Cl2N2O3S2/c20-16-17-14(28-18(16)21)6-13(22-17)19(26)23-12-5-9-3-1-2-4-10(9)11(12)7-27-8-15(24)25/h1-4,6,11-12,22H,5,7-8H2,(H,23,26)(H,24,25)/t11-,12-/m1/s1
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AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant liver glycogen phosphorylase by multienzyme-coupled reaction

Bioorg Med Chem Lett 20: 3511-4 (2010)


Article DOI: 10.1016/j.bmcl.2010.04.147
BindingDB Entry DOI: 10.7270/Q2571C66
More data for this
Ligand-Target Pair