BDBM50416070 CHEMBL1084654

SMILES: OCc1cc(ccc1O)[C@@H](O)CNCCCCCCOCCOCc1ccc(Cl)cc1

InChI Key: InChIKey=FHBTZIMKHULVJR-DEOSSOPVSA-N

Data: 1 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 1 hit for monomerid = 50416070   

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
Beta-2 adrenergic receptor (Homo sapiens (Human))	BDBM50416070 (CHEMBL1084654) Show SMILES OCc1cc(ccc1O)[C@@H](O)CNCCCCCCOCCOCc1ccc(Cl)cc1 |r| Show InChI InChI=1S/C24H34ClNO5/c25-22-8-5-19(6-9-22)18-31-14-13-30-12-4-2-1-3-11-26-16-24(29)20-7-10-23(28)21(15-20)17-27/h5-10,15,24,26-29H,1-4,11-14,16-18H2/t24-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	2.5	n/a	n/a	n/a	n/a
GlaxoSmithKline Medicines Research Centre Curated by ChEMBL					Assay Description Agonist activity at human recombinant beta2 adrenergic receptor expressed in CHO cells assessed as induction of intracellular cAMP accumulation after...				J Med Chem 53: 4522-30 (2010) Article DOI: 10.1021/jm100326d BindingDB Entry DOI: 10.7270/Q23N24N1
					More data for this Ligand-Target Pair