Compile Data Set for Download or QSAR

Found 41 hits Enz. Inhib. hit(s) with all data for entry = 50012574   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120559 (7-Methyl-2-[2-methyl-4-(3-piperidin-1-yl-propoxy)-...) Show SMILES Cc1ccn2cc(nc2c1)-c1ccc(OCCCN2CCCCC2)cc1C Show InChI InChI=1S/C23H29N3O/c1-18-9-13-26-17-22(24-23(26)15-18)21-8-7-20(16-19(21)2)27-14-6-12-25-10-4-3-5-11-25/h7-9,13,15-17H,3-6,10-12,14H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120543 (7-Methyl-2-[4-(3-piperidin-1-yl-propoxy)-phenyl]-i...) Show SMILES Cc1ccn2cc(nc2c1)-c1ccc(OCCCN2CCCCC2)cc1 Show InChI InChI=1S/C22H27N3O/c1-18-10-14-25-17-21(23-22(25)16-18)19-6-8-20(9-7-19)26-15-5-13-24-11-3-2-4-12-24/h6-10,14,16-17H,2-5,11-13,15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120537 (8-Methyl-2-[4-(3-piperidin-1-yl-propoxy)-phenyl]-i...) Show SMILES Cc1cccn2cc(nc12)-c1ccc(OCCCN2CCCCC2)cc1 Show InChI InChI=1S/C22H27N3O/c1-18-7-5-15-25-17-21(23-22(18)25)19-8-10-20(11-9-19)26-16-6-14-24-12-3-2-4-13-24/h5,7-11,15,17H,2-4,6,12-14,16H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Antagonist activity for human histamine H3 receptor was determined				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120537 (8-Methyl-2-[4-(3-piperidin-1-yl-propoxy)-phenyl]-i...) Show SMILES Cc1cccn2cc(nc12)-c1ccc(OCCCN2CCCCC2)cc1 Show InChI InChI=1S/C22H27N3O/c1-18-7-5-15-25-17-21(23-22(18)25)19-8-10-20(11-9-19)26-16-6-14-24-12-3-2-4-13-24/h5,7-11,15,17H,2-4,6,12-14,16H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120544 (7-Methyl-2-[4-(3-pyrrolidin-1-yl-propoxy)-phenyl]-...) Show SMILES Cc1ccn2cc(nc2c1)-c1ccc(OCCCN2CCCC2)cc1 Show InChI InChI=1S/C21H25N3O/c1-17-9-13-24-16-20(22-21(24)15-17)18-5-7-19(8-6-18)25-14-4-12-23-10-2-3-11-23/h5-9,13,15-16H,2-4,10-12,14H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120542 (2-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-imidazo[1,...) Show SMILES C(COc1ccc(cc1)-c1cn2ccccc2n1)CN1CCCCC1 Show InChI InChI=1S/C21H25N3O/c1-3-12-23(13-4-1)14-6-16-25-19-10-8-18(9-11-19)20-17-24-15-5-2-7-21(24)22-20/h2,5,7-11,15,17H,1,3-4,6,12-14,16H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120562 (2-[4-(3-Azepan-1-yl-propoxy)-phenyl]-7-methyl-imid...) Show SMILES Cc1ccn2cc(nc2c1)-c1ccc(OCCCN2CCCCCC2)cc1 Show InChI InChI=1S/C23H29N3O/c1-19-11-15-26-18-22(24-23(26)17-19)20-7-9-21(10-8-20)27-16-6-14-25-12-4-2-3-5-13-25/h7-11,15,17-18H,2-6,12-14,16H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120561 (7-Methyl-2-[4-(4-piperidin-1-yl-but-1-ynyl)-phenyl...) Show SMILES Cc1ccn2cc(nc2c1)-c1ccc(cc1)C#CCCN1CCCCC1 Show InChI InChI=1S/C23H25N3/c1-19-12-16-26-18-22(24-23(26)17-19)21-10-8-20(9-11-21)7-3-6-15-25-13-4-2-5-14-25/h8-12,16-18H,2,4-6,13-15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Rattus norvegicus (rat))	BDBM50120543 (7-Methyl-2-[4-(3-piperidin-1-yl-propoxy)-phenyl]-i...) Show SMILES Cc1ccn2cc(nc2c1)-c1ccc(OCCCN2CCCCC2)cc1 Show InChI InChI=1S/C22H27N3O/c1-18-10-14-25-17-21(23-22(25)16-18)19-6-8-20(9-7-19)26-15-5-13-24-11-3-2-4-12-24/h6-10,14,16-17H,2-5,11-13,15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Compound was tested for its binding affinity for rat histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120551 (2-[2-Fluoro-4-(3-piperidin-1-yl-propoxy)-phenyl]-7...) Show SMILES Cc1ccn2cc(nc2c1)-c1ccc(OCCCN2CCCCC2)cc1F Show InChI InChI=1S/C22H26FN3O/c1-17-8-12-26-16-21(24-22(26)14-17)19-7-6-18(15-20(19)23)27-13-5-11-25-9-3-2-4-10-25/h6-8,12,14-16H,2-5,9-11,13H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120549 (CHEMBL70944 | Dimethyl-{3-[4-(8-methyl-imidazo[1,2...) Show SMILES CN(C)CCCOc1ccc(cc1)-c1cn2cccc(C)c2n1 Show InChI InChI=1S/C19H23N3O/c1-15-6-4-12-22-14-18(20-19(15)22)16-7-9-17(10-8-16)23-13-5-11-21(2)3/h4,6-10,12,14H,5,11,13H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	13	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120539 (CHEMBL113236 | [4-(8-Methyl-imidazo[1,2-a]pyridin-...) Show SMILES Cc1cccn2cc(nc12)-c1ccc(NCCCN2CCCCC2)cc1 Show InChI InChI=1S/C22H28N4/c1-18-7-5-16-26-17-21(24-22(18)26)19-8-10-20(11-9-19)23-12-6-15-25-13-3-2-4-14-25/h5,7-11,16-17,23H,2-4,6,12-15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	15	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120565 (7-Methyl-2-[4-(4-piperidin-1-yl-butyl)-phenyl]-imi...) Show SMILES Cc1ccn2cc(nc2c1)-c1ccc(CCCCN2CCCCC2)cc1 Show InChI InChI=1S/C23H29N3/c1-19-12-16-26-18-22(24-23(26)17-19)21-10-8-20(9-11-21)7-3-6-15-25-13-4-2-5-14-25/h8-12,16-18H,2-7,13-15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	17	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120556 (7-Methyl-2-[4-((E)-4-piperidin-1-yl-but-1-enyl)-ph...) Show SMILES Cc1ccn2cc(nc2c1)-c1ccc(\C=C\CCN2CCCCC2)cc1 Show InChI InChI=1S/C23H27N3/c1-19-12-16-26-18-22(24-23(26)17-19)21-10-8-20(9-11-21)7-3-6-15-25-13-4-2-5-14-25/h3,7-12,16-18H,2,4-6,13-15H2,1H3/b7-3+	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	22	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120547 (2-[3-Methyl-4-(3-piperidin-1-yl-propoxy)-phenyl]-i...) Show SMILES Cc1cc(ccc1OCCCN1CCCCC1)-c1cn2ccccc2n1 Show InChI InChI=1S/C22H27N3O/c1-18-16-19(20-17-25-14-6-3-8-22(25)23-20)9-10-21(18)26-15-7-13-24-11-4-2-5-12-24/h3,6,8-10,14,16-17H,2,4-5,7,11-13,15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	28	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120569 (CHEMBL306911 | {3-[4-(8-Methyl-imidazo[1,2-a]pyrid...) Show SMILES CCCN(CCC)CCCOc1ccc(cc1)-c1cn2cccc(C)c2n1 Show InChI InChI=1S/C23H31N3O/c1-4-13-25(14-5-2)15-7-17-27-21-11-9-20(10-12-21)22-18-26-16-6-8-19(3)23(26)24-22/h6,8-12,16,18H,4-5,7,13-15,17H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	43	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120566 (2-[3-Methoxy-4-(3-piperidin-1-yl-propoxy)-phenyl]-...) Show SMILES COc1cc(ccc1OCCCN1CCCCC1)-c1cn2ccc(C)cc2n1 Show InChI InChI=1S/C23H29N3O2/c1-18-9-13-26-17-20(24-23(26)15-18)19-7-8-21(22(16-19)27-2)28-14-6-12-25-10-4-3-5-11-25/h7-9,13,15-17H,3-6,10-12,14H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	69	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120570 (8-Methyl-2-[4-(3-morpholin-4-yl-propoxy)-phenyl]-i...) Show SMILES Cc1cccn2cc(nc12)-c1ccc(OCCCN2CCOCC2)cc1 Show InChI InChI=1S/C21H25N3O2/c1-17-4-2-10-24-16-20(22-21(17)24)18-5-7-19(8-6-18)26-13-3-9-23-11-14-25-15-12-23/h2,4-8,10,16H,3,9,11-15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120567 (CHEMBL114231 | N-[4-(8-Methyl-imidazo[1,2-a]pyridi...) Show SMILES Cc1cccn2cc(nc12)-c1ccc(NC(=O)CCN2CCCCC2)cc1 Show InChI InChI=1S/C22H26N4O/c1-17-6-5-14-26-16-20(24-22(17)26)18-7-9-19(10-8-18)23-21(27)11-15-25-12-3-2-4-13-25/h5-10,14,16H,2-4,11-13,15H2,1H3,(H,23,27)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120550 (3-Piperidin-1-yl-propane-1-sulfonic acid [4-(8-met...) Show SMILES Cc1cccn2cc(nc12)-c1ccc(NS(=O)(=O)CCCN2CCCCC2)cc1 Show InChI InChI=1S/C22H28N4O2S/c1-18-7-5-15-26-17-21(23-22(18)26)19-8-10-20(11-9-19)24-29(27,28)16-6-14-25-12-3-2-4-13-25/h5,7-11,15,17,24H,2-4,6,12-14,16H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	500	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120538 (CHEMBL445619 | Dibutyl-{3-[4-(3,8-dimethyl-imidazo...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1nc2c(C)cccn2c1C Show InChI InChI=1S/C26H37N3O/c1-5-7-16-28(17-8-6-2)18-10-20-30-24-14-12-23(13-15-24)25-22(4)29-19-9-11-21(3)26(29)27-25/h9,11-15,19H,5-8,10,16-18,20H2,1-4H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	870	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120560 (2-[4-(3-Imidazol-1-yl-propoxy)-phenyl]-8-methyl-im...) Show SMILES Cc1cccn2cc(nc12)-c1ccc(OCCCn2ccnc2)cc1 Show InChI InChI=1S/C20H20N4O/c1-16-4-2-11-24-14-19(22-20(16)24)17-5-7-18(8-6-17)25-13-3-10-23-12-9-21-15-23/h2,4-9,11-12,14-15H,3,10,13H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50022761 (CHEMBL1204265 | CHEMBL71248 | Dibutyl-{3-[4-(7-met...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2ccc(C)cc2n1 Show InChI InChI=1S/C25H35N3O/c1-4-6-14-27(15-7-5-2)16-8-18-29-23-11-9-22(10-12-23)24-20-28-17-13-21(3)19-25(28)26-24/h9-13,17,19-20H,4-8,14-16,18H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50022764 (CHEMBL1204272 | CHEMBL71352 | Dibutyl-[3-(4-imidaz...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2ccccc2n1 Show InChI InChI=1S/C24H33N3O/c1-3-5-15-26(16-6-4-2)17-9-19-28-22-13-11-21(12-14-22)23-20-27-18-8-7-10-24(27)25-23/h7-8,10-14,18,20H,3-6,9,15-17,19H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120568 (2-[4-(3-Dibutylamino-propoxy)-phenyl]-imidazo[1,2-...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2cccc(O)c2n1 Show InChI InChI=1S/C24H33N3O2/c1-3-5-14-26(15-6-4-2)16-8-18-29-21-12-10-20(11-13-21)22-19-27-17-7-9-23(28)24(27)25-22/h7,9-13,17,19,28H,3-6,8,14-16,18H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120540 (CHEMBL71693 | Dibutyl-{3-[2-methoxy-4-(8-methyl-im...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1OC)-c1cn2cccc(C)c2n1 Show InChI InChI=1S/C26H37N3O2/c1-5-7-14-28(15-8-6-2)16-10-18-31-24-13-12-22(19-25(24)30-4)23-20-29-17-9-11-21(3)26(29)27-23/h9,11-13,17,19-20H,5-8,10,14-16,18H2,1-4H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120554 (CHEMBL310907 | Dibutyl-{3-[4-(6-methyl-imidazo[1,2...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2cc(C)ccc2n1 Show InChI InChI=1S/C25H35N3O/c1-4-6-15-27(16-7-5-2)17-8-18-29-23-12-10-22(11-13-23)24-20-28-19-21(3)9-14-25(28)26-24/h9-14,19-20H,4-8,15-18H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120555 (CHEMBL113145 | Dibutyl-{3-[4-(5,7-dimethyl-imidazo...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2c(C)cc(C)cc2n1 Show InChI InChI=1S/C26H37N3O/c1-5-7-14-28(15-8-6-2)16-9-17-30-24-12-10-23(11-13-24)25-20-29-22(4)18-21(3)19-26(29)27-25/h10-13,18-20H,5-9,14-17H2,1-4H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120564 (CHEMBL70313 | Dibutyl-{3-[4-(5-methyl-imidazo[1,2-...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2c(C)cccc2n1 Show InChI InChI=1S/C25H35N3O/c1-4-6-16-27(17-7-5-2)18-9-19-29-23-14-12-22(13-15-23)24-20-28-21(3)10-8-11-25(28)26-24/h8,10-15,20H,4-7,9,16-19H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120546 (CHEMBL302591 | {3-[4-(8-Benzyloxy-imidazo[1,2-a]py...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2cccc(OCc3ccccc3)c2n1 Show InChI InChI=1S/C31H39N3O2/c1-3-5-19-33(20-6-4-2)21-11-23-35-28-17-15-27(16-18-28)29-24-34-22-10-14-30(31(34)32-29)36-25-26-12-8-7-9-13-26/h7-10,12-18,22,24H,3-6,11,19-21,23,25H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50022758 (CHEMBL1204266 | CHEMBL308142 | Dibutyl-{3-[4-(8-me...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2cccc(C)c2n1 Show InChI InChI=1S/C25H35N3O/c1-4-6-15-27(16-7-5-2)17-9-19-29-23-13-11-22(12-14-23)24-20-28-18-8-10-21(3)25(28)26-24/h8,10-14,18,20H,4-7,9,15-17,19H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50022766 (CHEMBL1204277 | CHEMBL70946 | {3-[4-(6-Bromo-imida...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2cc(Br)ccc2n1 Show InChI InChI=1S/C24H32BrN3O/c1-3-5-14-27(15-6-4-2)16-7-17-29-22-11-8-20(9-12-22)23-19-28-18-21(25)10-13-24(28)26-23/h8-13,18-19H,3-7,14-17H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120545 (CHEMBL71530 | Dibutyl-{3-[2,6-dimethoxy-4-(8-methy...) Show SMILES CCCCN(CCCC)CCCOc1c(OC)cc(cc1OC)-c1cn2cccc(C)c2n1 Show InChI InChI=1S/C27H39N3O3/c1-6-8-13-29(14-9-7-2)15-11-17-33-26-24(31-4)18-22(19-25(26)32-5)23-20-30-16-10-12-21(3)27(30)28-23/h10,12,16,18-20H,6-9,11,13-15,17H2,1-5H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120548 (CHEMBL112163 | {3-[4-(8-Methyl-imidazo[1,2-a]pyrid...) Show SMILES CC(N(CCCOc1ccc(cc1)-c1cn2cccc(C)c2n1)C(C)c1ccccc1)c1ccccc1 Show InChI InChI=1S/C33H35N3O/c1-25-12-10-21-35-24-32(34-33(25)35)30-17-19-31(20-18-30)37-23-11-22-36(26(2)28-13-6-4-7-14-28)27(3)29-15-8-5-9-16-29/h4-10,12-21,24,26-27H,11,22-23H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50022758 (CHEMBL1204266 | CHEMBL308142 | Dibutyl-{3-[4-(8-me...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2cccc(C)c2n1 Show InChI InChI=1S/C25H35N3O/c1-4-6-15-27(16-7-5-2)17-9-19-29-23-13-11-22(12-14-23)24-20-28-18-8-10-21(3)25(28)26-24/h8,10-14,18,20H,4-7,9,15-17,19H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120541 (CHEMBL70874 | Dibutyl-{3-[3-methyl-4-(8-methyl-imi...) Show SMILES CCCCN(CCCC)CCCOc1ccc(-c2cn3cccc(C)c3n2)c(C)c1 Show InChI InChI=1S/C26H37N3O/c1-5-7-14-28(15-8-6-2)16-10-18-30-23-12-13-24(22(4)19-23)25-20-29-17-9-11-21(3)26(29)27-25/h9,11-13,17,19-20H,5-8,10,14-16,18H2,1-4H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120558 (CHEMBL114470 | Dibutyl-{3-[4-(6,8-dibromo-imidazo[...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2cc(Br)cc(Br)c2n1 Show InChI InChI=1S/C24H31Br2N3O/c1-3-5-12-28(13-6-4-2)14-7-15-30-21-10-8-19(9-11-21)23-18-29-17-20(25)16-22(26)24(29)27-23/h8-11,16-18H,3-7,12-15H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120557 (Benzyl-{3-[4-(8-methyl-imidazo[1,2-a]pyridin-2-yl)...) Show SMILES Cc1cccn2cc(nc12)-c1ccc(OCCCNCc2ccccc2)cc1 Show InChI InChI=1S/C24H25N3O/c1-19-7-5-15-27-18-23(26-24(19)27)21-10-12-22(13-11-21)28-16-6-14-25-17-20-8-3-2-4-9-20/h2-5,7-13,15,18,25H,6,14,16-17H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	5.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120552 (CHEMBL70945 | {3-[4-(8-Methyl-imidazo[1,2-a]pyridi...) Show SMILES CCCCCN(CCCCC)CCCOc1ccc(cc1)-c1cn2cccc(C)c2n1 Show InChI InChI=1S/C27H39N3O/c1-4-6-8-17-29(18-9-7-5-2)19-11-21-31-25-15-13-24(14-16-25)26-22-30-20-10-12-23(3)27(30)28-26/h10,12-16,20,22H,4-9,11,17-19,21H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	7.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120563 (CHEMBL71476 | Dibutyl-{3-[2-methyl-4-(8-methyl-imi...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1C)-c1cn2cccc(C)c2n1 Show InChI InChI=1S/C26H37N3O/c1-5-7-14-28(15-8-6-2)16-10-18-30-25-13-12-23(19-22(25)4)24-20-29-17-9-11-21(3)26(29)27-24/h9,11-13,17,19-20H,5-8,10,14-16,18H2,1-4H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50120553 (CHEMBL71047 | Dibutyl-{3-[4-(8-nitro-imidazo[1,2-a...) Show SMILES CCCCN(CCCC)CCCOc1ccc(cc1)-c1cn2cccc([N+]([O-])=O)c2n1 Show InChI InChI=1S/C24H32N4O3/c1-3-5-14-26(15-6-4-2)16-8-18-31-21-12-10-20(11-13-21)22-19-27-17-7-9-23(28(29)30)24(27)25-22/h7,9-13,17,19H,3-6,8,14-16,18H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson and Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor				Bioorg Med Chem Lett 12: 3309-12 (2002) BindingDB Entry DOI: 10.7270/Q2KH0MPG
					More data for this Ligand-Target Pair