null

SMILES: OC(=O)c1ccccc1OCCN1CCC(CC1)c1cn(CC2CC2)c2ccccc12

InChI Key: InChIKey=VBXUDFDAMGGOQA-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50156869   

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))	BDBM50156869 (2-{2-[4-(1-cyclopropylmethyl-1H-indol-3-yl)piperid...) Show SMILES OC(=O)c1ccccc1OCCN1CCC(CC1)c1cn(CC2CC2)c2ccccc12 Show InChI InChI=1S/C26H30N2O3/c29-26(30)22-6-2-4-8-25(22)31-16-15-27-13-11-20(12-14-27)23-18-28(17-19-9-10-19)24-7-3-1-5-21(23)24/h1-8,18-20H,9-17H2,(H,29,30)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+4	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))	BDBM50156869 (2-{2-[4-(1-cyclopropylmethyl-1H-indol-3-yl)piperid...) Show SMILES OC(=O)c1ccccc1OCCN1CCC(CC1)c1cn(CC2CC2)c2ccccc12 Show InChI InChI=1S/C26H30N2O3/c29-26(30)22-6-2-4-8-25(22)31-16-15-27-13-11-20(12-14-27)23-18-28(17-19-9-10-19)24-7-3-1-5-21(23)24/h1-8,18-20H,9-17H2,(H,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	140	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