null

SMILES: OC(=O)c1ccccc1OCCN1CCC(CC1)c1cn(CC=C)c2ccccc12

InChI Key: InChIKey=KTEZZEXASTZNJG-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50156850   

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))	BDBM50156850 (2-{2-[4-(1-allyl-1H-indol-3-yl)piperidin-1-yl]etho...) Show SMILES OC(=O)c1ccccc1OCCN1CCC(CC1)c1cn(CC=C)c2ccccc12 Show InChI InChI=1S/C25H28N2O3/c1-2-13-27-18-22(20-7-3-5-9-23(20)27)19-11-14-26(15-12-19)16-17-30-24-10-6-4-8-21(24)25(28)29/h2-10,18-19H,1,11-17H2,(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	>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))	BDBM50156850 (2-{2-[4-(1-allyl-1H-indol-3-yl)piperidin-1-yl]etho...) Show SMILES OC(=O)c1ccccc1OCCN1CCC(CC1)c1cn(CC=C)c2ccccc12 Show InChI InChI=1S/C25H28N2O3/c1-2-13-27-18-22(20-7-3-5-9-23(20)27)19-11-14-26(15-12-19)16-17-30-24-10-6-4-8-21(24)25(28)29/h2-10,18-19H,1,11-17H2,(H,28,29)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	97	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