BDBM50223043 CHEMBL25205

SMILES: C[C@H]1CC[C@H](C)N1C(=O)c1ccc(cc1)-c1ccc(OCCCN2CCC(C)CC2)cc1

InChI Key: InChIKey=XLLYVFMFBVAZQF-GOTSBHOMSA-N

Data: 2 KI

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 2 hits for monomerid = 50223043   

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 (Rattus norvegicus (rat))	BDBM50223043 (CHEMBL25205) Show SMILES C[C@H]1CC[C@H](C)N1C(=O)c1ccc(cc1)-c1ccc(OCCCN2CCC(C)CC2)cc1 Show InChI InChI=1S/C28H38N2O2/c1-21-15-18-29(19-16-21)17-4-20-32-27-13-11-25(12-14-27)24-7-9-26(10-8-24)28(31)30-22(2)5-6-23(30)3/h7-14,21-23H,4-6,15-20H2,1-3H3/t22-,23-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity towards rat cortical H3 receptor				Bioorg Med Chem Lett 13: 1325-8 (2003) BindingDB Entry DOI: 10.7270/Q2HM59NM
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50223043 (CHEMBL25205) Show SMILES C[C@H]1CC[C@H](C)N1C(=O)c1ccc(cc1)-c1ccc(OCCCN2CCC(C)CC2)cc1 Show InChI InChI=1S/C28H38N2O2/c1-21-15-18-29(19-16-21)17-4-20-32-27-13-11-25(12-14-27)24-7-9-26(10-8-24)28(31)30-22(2)5-6-23(30)3/h7-14,21-23H,4-6,15-20H2,1-3H3/t22-,23-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity for human recombinant H3 receptor				Bioorg Med Chem Lett 13: 1325-8 (2003) BindingDB Entry DOI: 10.7270/Q2HM59NM
					More data for this Ligand-Target Pair