BDBM50539694 CHEMBL4633635

SMILES: CCOc1cc(Cl)c(cc1N1CCOCC1)C(=O)Nc1nc2ccc(cc2s1)S(=O)(=O)CCCN1CCN(C)CC1

InChI Key: InChIKey=BOLHPHFIRKJXMT-UHFFFAOYSA-N

Data: 1 IC50  2 EC50

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 = 50539694   

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
Hydroxycarboxylic acid receptor 1 (Homo sapiens (Human))	BDBM50539694 (CHEMBL4633635) Show SMILES CCOc1cc(Cl)c(cc1N1CCOCC1)C(=O)Nc1nc2ccc(cc2s1)S(=O)(=O)CCCN1CCN(C)CC1 Show InChI InChI=1S/C28H36ClN5O5S2/c1-3-39-25-19-22(29)21(18-24(25)34-12-14-38-15-13-34)27(35)31-28-30-23-6-5-20(17-26(23)40-28)41(36,37)16-4-7-33-10-8-32(2)9-11-33/h5-6,17-19H,3-4,7-16H2,1-2H3,(H,30,31,35)	Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	600	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Agonist activity at human GPR81 overexpressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production				Bioorg Med Chem Lett 30: (2020)
					More data for this Ligand-Target Pair
Hydroxycarboxylic acid receptor 2 (Homo sapiens (Human))	BDBM50539694 (CHEMBL4633635) Show SMILES CCOc1cc(Cl)c(cc1N1CCOCC1)C(=O)Nc1nc2ccc(cc2s1)S(=O)(=O)CCCN1CCN(C)CC1 Show InChI InChI=1S/C28H36ClN5O5S2/c1-3-39-25-19-22(29)21(18-24(25)34-12-14-38-15-13-34)27(35)31-28-30-23-6-5-20(17-26(23)40-28)41(36,37)16-4-7-33-10-8-32(2)9-11-33/h5-6,17-19H,3-4,7-16H2,1-2H3,(H,30,31,35)	Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	>6.30E+3	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Agonist activity at human GPR109A receptor				Bioorg Med Chem Lett 30: (2020)
					More data for this Ligand-Target Pair
Ghrelin receptor (Homo sapiens (Human))	BDBM50539694 (CHEMBL4633635) Show SMILES CCOc1cc(Cl)c(cc1N1CCOCC1)C(=O)Nc1nc2ccc(cc2s1)S(=O)(=O)CCCN1CCN(C)CC1 Show InChI InChI=1S/C28H36ClN5O5S2/c1-3-39-25-19-22(29)21(18-24(25)34-12-14-38-15-13-34)27(35)31-28-30-23-6-5-20(17-26(23)40-28)41(36,37)16-4-7-33-10-8-32(2)9-11-33/h5-6,17-19H,3-4,7-16H2,1-2H3,(H,30,31,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Displacement of [125I]-ghrelin from human GHS-R1a stably expressed in HEK cell membrane measured after 60 mins by gamma counter method				Bioorg Med Chem Lett 30: (2020)
					More data for this Ligand-Target Pair