BDBM50136437 5-Chloro-1H-indole-2-carboxylic acid (2-oxo-1,2,3,4-tetrahydro-quinolin-3-yl)-amide::5-chloro-N-(2-oxo-1,2,3,4-tetrahydroquinolin-3-yl)-1H-indole-2-carboxamide::CHEMBL139461

SMILES: Clc1ccc2[nH]c(cc2c1)C(=O)NC1Cc2ccccc2NC1=O

InChI Key: InChIKey=ULRSAQLSHVWRKZ-UHFFFAOYSA-N

Data: 4 IC50

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 4 hits for monomerid = 50136437   

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
Muscle glycogen phosphorylase (Homo sapiens (Human))	BDBM50136437 (5-Chloro-1H-indole-2-carboxylic acid (2-oxo-1,2,3,...) Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)NC1Cc2ccccc2NC1=O Show InChI InChI=1S/C18H14ClN3O2/c19-12-5-6-14-11(7-12)9-15(20-14)17(23)22-16-8-10-3-1-2-4-13(10)21-18(16)24/h1-7,9,16,20H,8H2,(H,21,24)(H,22,23)	PDB MMDB Reactome pathway KEGG B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	38	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)				Bioorg Med Chem Lett 13: 4385-8 (2003) BindingDB Entry DOI: 10.7270/Q2S75FQV
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGL) (Homo sapiens (Human))	BDBM50136437 (5-Chloro-1H-indole-2-carboxylic acid (2-oxo-1,2,3,...) Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)NC1Cc2ccccc2NC1=O Show InChI InChI=1S/C18H14ClN3O2/c19-12-5-6-14-11(7-12)9-15(20-14)17(23)22-16-8-10-3-1-2-4-13(10)21-18(16)24/h1-7,9,16,20H,8H2,(H,21,24)(H,22,23)	PDB MMDB Reactome pathway KEGG B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	44	n/a	n/a	n/a	n/a	n/a	n/a
Applied Science University Curated by ChEMBL					Assay Description Inhibition of human liver glycogen phosphorylase 1a assessed as release of phosphate from glucose-1- phosphate after 20 mins				Bioorg Med Chem 19: 4746-71 (2011) Article DOI: 10.1016/j.bmc.2011.06.086 BindingDB Entry DOI: 10.7270/Q2028RXJ
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGL) (Homo sapiens (Human))	BDBM50136437 (5-Chloro-1H-indole-2-carboxylic acid (2-oxo-1,2,3,...) Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)NC1Cc2ccccc2NC1=O Show InChI InChI=1S/C18H14ClN3O2/c19-12-5-6-14-11(7-12)9-15(20-14)17(23)22-16-8-10-3-1-2-4-13(10)21-18(16)24/h1-7,9,16,20H,8H2,(H,21,24)(H,22,23)	PDB MMDB Reactome pathway KEGG B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	86	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of recombinant human liver GPa by multienzyme coupled assay				Bioorg Med Chem Lett 16: 5567-71 (2006) Article DOI: 10.1016/j.bmcl.2006.08.047 BindingDB Entry DOI: 10.7270/Q2KW5FP3
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGL) (Homo sapiens (Human))	BDBM50136437 (5-Chloro-1H-indole-2-carboxylic acid (2-oxo-1,2,3,...) Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)NC1Cc2ccccc2NC1=O Show InChI InChI=1S/C18H14ClN3O2/c19-12-5-6-14-11(7-12)9-15(20-14)17(23)22-16-8-10-3-1-2-4-13(10)21-18(16)24/h1-7,9,16,20H,8H2,(H,21,24)(H,22,23)	PDB MMDB Reactome pathway KEGG B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	44	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory concentration against recombinant human liver glycogen phosphorylase a (HLGPa)				Bioorg Med Chem Lett 13: 4385-8 (2003) BindingDB Entry DOI: 10.7270/Q2S75FQV
					More data for this Ligand-Target Pair