Compile Data Set for Download or QSAR

Found 188 hits with Last Name = 'cowden' and Initial = 'j'   

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 H4 receptor (Homo sapiens (Human))	BDBM50356873 (CHEMBL1914541) Show SMILES CN1CCN(CC1)c1nc(N)nc2c3cc(Cl)ccc3oc12 Show InChI InChI=1S/C15H16ClN5O/c1-20-4-6-21(7-5-20)14-13-12(18-15(17)19-14)10-8-9(16)2-3-11(10)22-13/h2-3,8H,4-7H2,1H3,(H2,17,18,19)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	0.100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356794 (CHEMBL1914462) Show SMILES CN1CCN(CC1)c1nc(N)nc2c3cc(Cl)ccc3sc12 Show InChI InChI=1S/C15H16ClN5S/c1-20-4-6-21(7-5-20)14-13-12(18-15(17)19-14)10-8-9(16)2-3-11(10)22-13/h2-3,8H,4-7H2,1H3,(H2,17,18,19)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	0.300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50315348 ((R)-8-chloro-4-(3-(methylamino)pyrrolidin-1-yl)ben...) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(Cl)ccc3oc12 |r| Show InChI InChI=1S/C15H16ClN5O/c1-18-9-4-5-21(7-9)14-13-12(19-15(17)20-14)10-6-8(16)2-3-11(10)22-13/h2-3,6,9,18H,4-5,7H2,1H3,(H2,17,19,20)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	0.400	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356815 (CHEMBL1914781) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(Br)ccc3oc12 |r| Show InChI InChI=1S/C15H16BrN5O/c1-18-9-4-5-21(7-9)14-13-12(19-15(17)20-14)10-6-8(16)2-3-11(10)22-13/h2-3,6,9,18H,4-5,7H2,1H3,(H2,17,19,20)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	0.700	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356788 (CHEMBL1914755) Show SMILES CN1CCN(CC1)c1nc(N)nc2c3cc(ccc3oc12)C(F)(F)F Show InChI InChI=1S/C16H16F3N5O/c1-23-4-6-24(7-5-23)14-13-12(21-15(20)22-14)10-8-9(16(17,18)19)2-3-11(10)25-13/h2-3,8H,4-7H2,1H3,(H2,20,21,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	0.800	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50315348 ((R)-8-chloro-4-(3-(methylamino)pyrrolidin-1-yl)ben...) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(Cl)ccc3oc12 |r| Show InChI InChI=1S/C15H16ClN5O/c1-18-9-4-5-21(7-9)14-13-12(19-15(17)20-14)10-6-8(16)2-3-11(10)22-13/h2-3,6,9,18H,4-5,7H2,1H3,(H2,17,19,20)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	0.900	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006745 (CHEMBL3236556) Show SMILES N[C@@H]1CCN(C1)c1cc(nc(N)n1)C1CCCC1 |r| Show InChI InChI=1S/C13H21N5/c14-10-5-6-18(8-10)12-7-11(16-13(15)17-12)9-3-1-2-4-9/h7,9-10H,1-6,8,14H2,(H2,15,16,17)/t10-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.920	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356793 (CHEMBL1914760) Show SMILES CN1CCN(CC1)c1nc(N)nc2c3cc(Br)ccc3sc12 Show InChI InChI=1S/C15H16BrN5S/c1-20-4-6-21(7-5-20)14-13-12(18-15(17)19-14)10-8-9(16)2-3-11(10)22-13/h2-3,8H,4-7H2,1H3,(H2,17,18,19)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356817 (CHEMBL1914783) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(ccc3oc12)C(F)(F)F |r| Show InChI InChI=1S/C16H16F3N5O/c1-21-9-4-5-24(7-9)14-13-12(22-15(20)23-14)10-6-8(16(17,18)19)2-3-11(10)25-13/h2-3,6,9,21H,4-5,7H2,1H3,(H2,20,22,23)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356872 (CHEMBL1914540) Show SMILES Nc1nc(N2CCCNCC2)c2oc3ccc(Cl)cc3c2n1 Show InChI InChI=1S/C15H16ClN5O/c16-9-2-3-11-10(8-9)12-13(22-11)14(20-15(17)19-12)21-6-1-4-18-5-7-21/h2-3,8,18H,1,4-7H2,(H2,17,19,20)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356874 (CHEMBL1914542) Show SMILES Nc1nc(N2CCNCC2)c2oc3ccc(Cl)cc3c2n1 Show InChI InChI=1S/C14H14ClN5O/c15-8-1-2-10-9(7-8)11-12(21-10)13(19-14(16)18-11)20-5-3-17-4-6-20/h1-2,7,17H,3-6H2,(H2,16,18,19)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006743 (CHEMBL3236554) Show SMILES CN[C@@H]1CCN(C1)c1cc(nc(N)n1)C1CCCC1 |r| Show InChI InChI=1S/C14H23N5/c1-16-11-6-7-19(9-11)13-8-12(17-14(15)18-13)10-4-2-3-5-10/h8,10-11,16H,2-7,9H2,1H3,(H2,15,17,18)/t11-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006742 (CHEMBL3236553) Show SMILES Nc1nc(cc(n1)N1CCNCC1)C1CCCC1 Show InChI InChI=1S/C13H21N5/c14-13-16-11(10-3-1-2-4-10)9-12(17-13)18-7-5-15-6-8-18/h9-10,15H,1-8H2,(H2,14,16,17)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006739 (CHEMBL3236552) Show SMILES CN1CCN(CC1)c1cc(nc(N)n1)C1CCCC1 Show InChI InChI=1S/C14H23N5/c1-18-6-8-19(9-7-18)13-10-12(16-14(15)17-13)11-4-2-3-5-11/h10-11H,2-9H2,1H3,(H2,15,16,17)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006761 (CHEMBL3236571) Show SMILES CCCCc1cc(nc(N)n1)N1CC[C@H](C1)NC |r| Show InChI InChI=1S/C13H23N5/c1-3-4-5-10-8-12(17-13(14)16-10)18-7-6-11(9-18)15-2/h8,11,15H,3-7,9H2,1-2H3,(H2,14,16,17)/t11-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006769 (CHEMBL3236579) Show SMILES CN[C@@H]1CCN(C1)c1cc(nc(N)n1)C12CC3CC(CC(C3)C1)C2 |r,TLB:9:14:17:21.19.20,THB:19:18:15:21.20.22,19:20:17.18.23:15,22:20:17:23.14.15,22:14:17:21.19.20| Show InChI InChI=1S/C19H29N5/c1-21-15-2-3-24(11-15)17-7-16(22-18(20)23-17)19-8-12-4-13(9-19)6-14(5-12)10-19/h7,12-15,21H,2-6,8-11H2,1H3,(H2,20,22,23)/t12?,13?,14?,15-,19?/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006749 (CHEMBL3236560) Show SMILES [H][C@@]12CN(C[C@]1([H])NCCC2)c1cc(nc(N)n1)C1CCCC1 |r| Show InChI InChI=1S/C16H25N5/c17-16-19-13(11-4-1-2-5-11)8-15(20-16)21-9-12-6-3-7-18-14(12)10-21/h8,11-12,14,18H,1-7,9-10H2,(H2,17,19,20)/t12-,14+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50315349 ((S)-8-chloro-4-(3-(methylamino)pyrrolidin-1-yl)ben...) Show SMILES CN[C@H]1CCN(C1)c1nc(N)nc2c3cc(Cl)ccc3oc12 |r| Show InChI InChI=1S/C15H16ClN5O/c1-18-9-4-5-21(7-9)14-13-12(19-15(17)20-14)10-6-8(16)2-3-11(10)22-13/h2-3,6,9,18H,4-5,7H2,1H3,(H2,17,19,20)/t9-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356816 (CHEMBL1914782) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(F)ccc3oc12 |r| Show InChI InChI=1S/C15H16FN5O/c1-18-9-4-5-21(7-9)14-13-12(19-15(17)20-14)10-6-8(16)2-3-11(10)22-13/h2-3,6,9,18H,4-5,7H2,1H3,(H2,17,19,20)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356822 (CHEMBL1914788) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(Br)ccc3sc12 |r| Show InChI InChI=1S/C15H16BrN5S/c1-18-9-4-5-21(7-9)14-13-12(19-15(17)20-14)10-6-8(16)2-3-11(10)22-13/h2-3,6,9,18H,4-5,7H2,1H3,(H2,17,19,20)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006766 (CHEMBL3236576) Show SMILES CN[C@@H]1CCN(C1)c1cc(nc(N)n1)C1CCCCC1 |r| Show InChI InChI=1S/C15H25N5/c1-17-12-7-8-20(10-12)14-9-13(18-15(16)19-14)11-5-3-2-4-6-11/h9,11-12,17H,2-8,10H2,1H3,(H2,16,18,19)/t12-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006765 (CHEMBL3236575) Show SMILES CN[C@@H]1CCN(C1)c1cc(nc(N)n1)C1CCC1 |r| Show InChI InChI=1S/C13H21N5/c1-15-10-5-6-18(8-10)12-7-11(9-3-2-4-9)16-13(14)17-12/h7,9-10,15H,2-6,8H2,1H3,(H2,14,16,17)/t10-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356771 (CHEMBL1914543) Show SMILES N[C@@H]1CCN(C1)c1nc(N)nc2c1oc1ccc(Cl)cc21 |r| Show InChI InChI=1S/C14H14ClN5O/c15-7-1-2-10-9(5-7)11-12(21-10)13(19-14(17)18-11)20-4-3-8(16)6-20/h1-2,5,8H,3-4,6,16H2,(H2,17,18,19)/t8-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006750 (CHEMBL3236561) Show SMILES [H][C@]12CCN[C@@]1([H])CN(C2)c1cc(nc(N)n1)C1CCCC1 |r| Show InChI InChI=1S/C15H23N5/c16-15-18-12(10-3-1-2-4-10)7-14(19-15)20-8-11-5-6-17-13(11)9-20/h7,10-11,13,17H,1-6,8-9H2,(H2,16,18,19)/t11-,13+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356775 (CHEMBL1914547) Show SMILES NCC1CN(C1)c1nc(N)nc2c3cc(Cl)ccc3oc12 Show InChI InChI=1S/C14H14ClN5O/c15-8-1-2-10-9(3-8)11-12(21-10)13(19-14(17)18-11)20-5-7(4-16)6-20/h1-3,7H,4-6,16H2,(H2,17,18,19)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	3.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356810 (CHEMBL1914776) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3ccccc3oc12 |r| Show InChI InChI=1S/C15H17N5O/c1-17-9-6-7-20(8-9)14-13-12(18-15(16)19-14)10-4-2-3-5-11(10)21-13/h2-5,9,17H,6-8H2,1H3,(H2,16,18,19)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	3.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356779 (CHEMBL1914745) Show SMILES Nc1nc(N2CC3CCNC3C2)c2oc3ccc(Cl)cc3c2n1 Show InChI InChI=1S/C16H16ClN5O/c17-9-1-2-12-10(5-9)13-14(23-12)15(21-16(18)20-13)22-6-8-3-4-19-11(8)7-22/h1-2,5,8,11,19H,3-4,6-7H2,(H2,18,20,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	3.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50315314 (8-chloro-4-(4-methylpiperazin-1-yl)benzofuro[3,2-d...) Show SMILES CN1CCN(CC1)c1ncnc2c3cc(Cl)ccc3oc12 Show InChI InChI=1S/C15H15ClN4O/c1-19-4-6-20(7-5-19)15-14-13(17-9-18-15)11-8-10(16)2-3-12(11)21-14/h2-3,8-9H,4-7H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356780 (CHEMBL1914746) Show SMILES Nc1nc(N2C[C@H]3CCCN[C@H]3C2)c2oc3ccc(Cl)cc3c2n1 |r| Show InChI InChI=1S/C17H18ClN5O/c18-10-3-4-13-11(6-10)14-15(24-13)16(22-17(19)21-14)23-7-9-2-1-5-20-12(9)8-23/h3-4,6,9,12,20H,1-2,5,7-8H2,(H2,19,21,22)/t9-,12+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	4.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006788 (CHEMBL3236548) Show SMILES CN1CCC(CCCCOc2cc(-c3nc4c(C)c(F)ccc4[nH]3)c(C)cn2)CC1 Show InChI InChI=1S/C24H31FN4O/c1-16-15-26-22(30-13-5-4-6-18-9-11-29(3)12-10-18)14-19(16)24-27-21-8-7-20(25)17(2)23(21)28-24/h7-8,14-15,18H,4-6,9-13H2,1-3H3,(H,27,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM22566 (5-chloro-2-[(4-methylpiperazin-1-yl)carbonyl]-1H-i...) Show SMILES CN1CCN(CC1)C(=O)c1cc2cc(Cl)ccc2[nH]1 Show InChI InChI=1S/C14H16ClN3O/c1-17-4-6-18(7-5-17)14(19)13-9-10-8-11(15)2-3-12(10)16-13/h2-3,8-9,16H,4-7H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50315314 (8-chloro-4-(4-methylpiperazin-1-yl)benzofuro[3,2-d...) Show SMILES CN1CCN(CC1)c1ncnc2c3cc(Cl)ccc3oc12 Show InChI InChI=1S/C15H15ClN4O/c1-19-4-6-20(7-5-19)15-14-13(17-9-18-15)11-8-10(16)2-3-12(11)21-14/h2-3,8-9H,4-7H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356875 (CHEMBL1914792) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3ccc(Cl)cc3sc12 |r| Show InChI InChI=1S/C15H16ClN5S/c1-18-9-4-5-21(7-9)14-13-12(19-15(17)20-14)10-3-2-8(16)6-11(10)22-13/h2-3,6,9,18H,4-5,7H2,1H3,(H2,17,19,20)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	5.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Mus musculus (mouse))	BDBM50006789 (CHEMBL3236549) Show SMILES CC(C)c1cc(nc(N)n1)N1CC[C@@H](N)C1 |r| Show InChI InChI=1S/C11H19N5/c1-7(2)9-5-10(15-11(13)14-9)16-4-3-8(12)6-16/h5,7-8H,3-4,6,12H2,1-2H3,(H2,13,14,15)/t8-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	5.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from mouse histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006747 (CHEMBL3236558) Show SMILES NC1CN(C1)c1cc(nc(N)n1)C1CCCC1 Show InChI InChI=1S/C12H19N5/c13-9-6-17(7-9)11-5-10(15-12(14)16-11)8-3-1-2-4-8/h5,8-9H,1-4,6-7,13H2,(H2,14,15,16)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	5.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356776 (CHEMBL1914548) Show SMILES N[C@H]1CCCN(C1)c1nc(N)nc2c1oc1ccc(Cl)cc21 |r| Show InChI InChI=1S/C15H16ClN5O/c16-8-3-4-11-10(6-8)12-13(22-11)14(20-15(18)19-12)21-5-1-2-9(17)7-21/h3-4,6,9H,1-2,5,7,17H2,(H2,18,19,20)/t9-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	5.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356808 (CHEMBL1914774) Show SMILES Nc1nc(N2CCNCC2)c2oc3ccc(Cl)c(Cl)c3c2n1 Show InChI InChI=1S/C14H13Cl2N5O/c15-7-1-2-8-9(10(7)16)11-12(22-8)13(20-14(17)19-11)21-5-3-18-4-6-21/h1-2,18H,3-6H2,(H2,17,19,20)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	7.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356790 (CHEMBL1914757) Show SMILES CN1CCN(CC1)c1nc(N)nc2c1oc1ccc(Cl)c(Cl)c21 Show InChI InChI=1S/C15H15Cl2N5O/c1-21-4-6-22(7-5-21)14-13-12(19-15(18)20-14)10-9(23-13)3-2-8(16)11(10)17/h2-3H,4-7H2,1H3,(H2,18,19,20)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	7.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006767 (CHEMBL3236577) Show SMILES CN[C@@H]1CCN(C1)c1cc(nc(N)n1)C(C)(C)C |r| Show InChI InChI=1S/C13H23N5/c1-13(2,3)10-7-11(17-12(14)16-10)18-6-5-9(8-18)15-4/h7,9,15H,5-6,8H2,1-4H3,(H2,14,16,17)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356819 (CHEMBL1914785) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(Cl)cc(Cl)c3oc12 |r| Show InChI InChI=1S/C15H15Cl2N5O/c1-19-8-2-3-22(6-8)14-13-11(20-15(18)21-14)9-4-7(16)5-10(17)12(9)23-13/h4-5,8,19H,2-3,6H2,1H3,(H2,18,20,21)/t8-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356859 (CHEMBL1915048) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(Cl)cnc3oc12 |r| Show InChI InChI=1S/C14H15ClN6O/c1-17-8-2-3-21(6-8)12-11-10(19-14(16)20-12)9-4-7(15)5-18-13(9)22-11/h4-5,8,17H,2-3,6H2,1H3,(H2,16,19,20)/t8-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356777 (CHEMBL1914549) Show SMILES N[C@@H]1CCCN(C1)c1nc(N)nc2c1oc1ccc(Cl)cc21 |r| Show InChI InChI=1S/C15H16ClN5O/c16-8-3-4-11-10(6-8)12-13(22-11)14(20-15(18)19-12)21-5-1-2-9(17)7-21/h3-4,6,9H,1-2,5,7,17H2,(H2,18,19,20)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	9.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006768 (CHEMBL3236578) Show SMILES CC(C)(C)c1cc(nc(N)n1)N1CC[C@@H](N)C1 |r| Show InChI InChI=1S/C12H21N5/c1-12(2,3)9-6-10(16-11(14)15-9)17-5-4-8(13)7-17/h6,8H,4-5,7,13H2,1-3H3,(H2,14,15,16)/t8-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	9.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356859 (CHEMBL1915048) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(Cl)cnc3oc12 |r| Show InChI InChI=1S/C14H15ClN6O/c1-17-8-2-3-21(6-8)12-11-10(19-14(16)20-12)9-4-7(15)5-18-13(9)22-11/h4-5,8,17H,2-3,6H2,1H3,(H2,16,19,20)/t8-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	9.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356812 (CHEMBL1914778) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c1oc1cccc(F)c21 |r| Show InChI InChI=1S/C15H16FN5O/c1-18-8-5-6-21(7-8)14-13-12(19-15(17)20-14)11-9(16)3-2-4-10(11)22-13/h2-4,8,18H,5-7H2,1H3,(H2,17,19,20)/t8-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356820 (CHEMBL1914786) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c1oc1ccc(Cl)c(Cl)c21 |r| Show InChI InChI=1S/C15H15Cl2N5O/c1-19-7-4-5-22(6-7)14-13-12(20-15(18)21-14)10-9(23-13)3-2-8(16)11(10)17/h2-3,7,19H,4-6H2,1H3,(H2,18,20,21)/t7-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356823 (CHEMBL1914789) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(Cl)ccc3sc12 |r| Show InChI InChI=1S/C15H16ClN5S/c1-18-9-4-5-21(7-9)14-13-12(19-15(17)20-14)10-6-8(16)2-3-11(10)22-13/h2-3,6,9,18H,4-5,7H2,1H3,(H2,17,19,20)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50356818 (CHEMBL1914784) Show SMILES CN[C@@H]1CCN(C1)c1nc(N)nc2c3cc(OC)ccc3oc12 |r| Show InChI InChI=1S/C16H19N5O2/c1-18-9-5-6-21(8-9)15-14-13(19-16(17)20-15)11-7-10(22-2)3-4-12(11)23-14/h3-4,7,9,18H,5-6,8H2,1-2H3,(H2,17,19,20)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	11	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [3H]histamine from recombinant human histamine H4 receptor				Bioorg Med Chem Lett 21: 6577-81 (2011) Article DOI: 10.1016/j.bmcl.2011.08.014 BindingDB Entry DOI: 10.7270/Q2CN749X
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006753 (CHEMBL3236564) Show SMILES Nc1nc(cc(n1)N1CCC2(CCCN2)C1)C1CCCC1 Show InChI InChI=1S/C16H25N5/c17-15-19-13(12-4-1-2-5-12)10-14(20-15)21-9-7-16(11-21)6-3-8-18-16/h10,12,18H,1-9,11H2,(H2,17,19,20)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	11	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair
Histamine H4 receptor (Homo sapiens (Human))	BDBM50006760 (CHEMBL3236570) Show SMILES CN[C@@H]1CCN(C1)c1cc(nc(N)n1)C(C)C |r| Show InChI InChI=1S/C12H21N5/c1-8(2)10-6-11(16-12(13)15-10)17-5-4-9(7-17)14-3/h6,8-9,14H,4-5,7H2,1-3H3,(H2,13,15,16)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Janssen Research& Development, LLC Curated by ChEMBL					Assay Description Displacement of [3H]histamine from human recombinant histamine H4 receptor expressed in SK-N-MC cells after 45 mins by competition binding analysis				J Med Chem 57: 2429-39 (2014) Article DOI: 10.1021/jm401727m BindingDB Entry DOI: 10.7270/Q25H7HSH
					More data for this Ligand-Target Pair

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