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SMILES: CCOCCn1cc(C2CCN(Cc3ccccc3C(O)=O)CC2)c2ccccc12

InChI Key: InChIKey=WDWGPVKQXKUYMD-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50156854   

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
Histamine H2 receptor (Homo sapiens (Human))	BDBM50156854 (2-((4-(1-(2-ethoxyethyl)-1H-indol-3-yl)piperidin-1...) Show SMILES CCOCCn1cc(C2CCN(Cc3ccccc3C(O)=O)CC2)c2ccccc12 Show InChI InChI=1S/C25H30N2O3/c1-2-30-16-15-27-18-23(22-9-5-6-10-24(22)27)19-11-13-26(14-12-19)17-20-7-3-4-8-21(20)25(28)29/h3-10,18-19H,2,11-17H2,1H3,(H,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.05E+3	n/a	n/a	n/a	n/a	n/a	n/a
Rhône-Poulenc Rorer Curated by ChEMBL					Assay Description Displacement of [3H]ketanserine from histamine H2 receptor in human cortex membranes				J Med Chem 47: 6326-37 (2004) Article DOI: 10.1021/jm0498203 BindingDB Entry DOI: 10.7270/Q2HM57XC
					More data for this Ligand-Target Pair
Histamine H1 receptor (Cavia porcellus (domestic guinea pig))	BDBM50156854 (2-((4-(1-(2-ethoxyethyl)-1H-indol-3-yl)piperidin-1...) Show SMILES CCOCCn1cc(C2CCN(Cc3ccccc3C(O)=O)CC2)c2ccccc12 Show InChI InChI=1S/C25H30N2O3/c1-2-30-16-15-27-18-23(22-9-5-6-10-24(22)27)19-11-13-26(14-12-19)17-20-7-3-4-8-21(20)25(28)29/h3-10,18-19H,2,11-17H2,1H3,(H,28,29)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	330	n/a	n/a	n/a	n/a	n/a	n/a
Rhône-Poulenc Rorer Curated by ChEMBL					Assay Description Displacement of [3H]mepyramine from histamine H1 receptor in guinea pig cerebellum membranes				J Med Chem 47: 6326-37 (2004) Article DOI: 10.1021/jm0498203 BindingDB Entry DOI: 10.7270/Q2HM57XC
					More data for this Ligand-Target Pair