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SMILES: Cc1nnc(o1)-c1cccc(c1)-c1nnc(s1)N1CCC(CC1)N1CCCCC1

InChI Key: InChIKey=XOBOUIANSWIUGE-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50383440   

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 H3 receptor (Homo sapiens (Human))	BDBM50383440 (CHEMBL2031600) Show SMILES Cc1nnc(o1)-c1cccc(c1)-c1nnc(s1)N1CCC(CC1)N1CCCCC1 Show InChI InChI=1S/C21H26N6OS/c1-15-22-23-19(28-15)16-6-5-7-17(14-16)20-24-25-21(29-20)27-12-8-18(9-13-27)26-10-3-2-4-11-26/h5-7,14,18H,2-4,8-13H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	22.8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]N-alpha-methylhistamine from recombinant human histamine H3 receptor expressed in HEK cell membranes after 30 mins by scintillati...				Bioorg Med Chem Lett 22: 3354-7 (2012) Article DOI: 10.1016/j.bmcl.2012.02.076 BindingDB Entry DOI: 10.7270/Q2DN462S
					More data for this Ligand-Target Pair
Histamine H3 receptor (Mus musculus)	BDBM50383440 (CHEMBL2031600) Show SMILES Cc1nnc(o1)-c1cccc(c1)-c1nnc(s1)N1CCC(CC1)N1CCCCC1 Show InChI InChI=1S/C21H26N6OS/c1-15-22-23-19(28-15)16-6-5-7-17(14-16)20-24-25-21(29-20)27-12-8-18(9-13-27)26-10-3-2-4-11-26/h5-7,14,18H,2-4,8-13H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]N-alpha-methylhistamine from mouse histamine H3 receptor				Bioorg Med Chem Lett 22: 3354-7 (2012) Article DOI: 10.1016/j.bmcl.2012.02.076 BindingDB Entry DOI: 10.7270/Q2DN462S
					More data for this Ligand-Target Pair