null

SMILES: C[C@@H]1CCCN1CCc1ccc2nc(ccc2c1)-c1sc2nc3ccccc3n2c1C

InChI Key: InChIKey=JHZTZJQZFCCJBJ-QGZVFWFLSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50319551   

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))	BDBM50319551 ((R)-3-methyl-2-(6-(2-(2-methylpyrrolidin-1-yl)ethy...) Show SMILES C[C@@H]1CCCN1CCc1ccc2nc(ccc2c1)-c1sc2nc3ccccc3n2c1C |r| Show InChI InChI=1S/C26H26N4S/c1-17-6-5-14-29(17)15-13-19-9-11-21-20(16-19)10-12-23(27-21)25-18(2)30-24-8-4-3-7-22(24)28-26(30)31-25/h3-4,7-12,16-17H,5-6,13-15H2,1-2H3/t17-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	0.780	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]-N-alpha-methylhistamine from rat cloned histamine H3 receptor				Bioorg Med Chem Lett 20: 3295-300 (2010) Article DOI: 10.1016/j.bmcl.2010.04.045 BindingDB Entry DOI: 10.7270/Q2XW4JZN
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50319551 ((R)-3-methyl-2-(6-(2-(2-methylpyrrolidin-1-yl)ethy...) Show SMILES C[C@@H]1CCCN1CCc1ccc2nc(ccc2c1)-c1sc2nc3ccccc3n2c1C |r| Show InChI InChI=1S/C26H26N4S/c1-17-6-5-14-29(17)15-13-19-9-11-21-20(16-19)10-12-23(27-21)25-18(2)30-24-8-4-3-7-22(24)28-26(30)31-25/h3-4,7-12,16-17H,5-6,13-15H2,1-2H3/t17-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	430	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]dofetilide from human ERG expressed in HEK293 cells				Bioorg Med Chem Lett 20: 3295-300 (2010) Article DOI: 10.1016/j.bmcl.2010.04.045 BindingDB Entry DOI: 10.7270/Q2XW4JZN
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50319551 ((R)-3-methyl-2-(6-(2-(2-methylpyrrolidin-1-yl)ethy...) Show SMILES C[C@@H]1CCCN1CCc1ccc2nc(ccc2c1)-c1sc2nc3ccccc3n2c1C |r| Show InChI InChI=1S/C26H26N4S/c1-17-6-5-14-29(17)15-13-19-9-11-21-20(16-19)10-12-23(27-21)25-18(2)30-24-8-4-3-7-22(24)28-26(30)31-25/h3-4,7-12,16-17H,5-6,13-15H2,1-2H3/t17-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	0.400	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bioprojet-Biotech Curated by ChEMBL					Assay Description Displacement of [125I]Iodoproxyfan from human recombinant histamine H3 receptor by Competitive binding assay				Bioorg Med Chem Lett 21: 5378-83 (2011) Article DOI: 10.1016/j.bmcl.2011.07.006 BindingDB Entry DOI: 10.7270/Q2VX0GXK
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50319551 ((R)-3-methyl-2-(6-(2-(2-methylpyrrolidin-1-yl)ethy...) Show SMILES C[C@@H]1CCCN1CCc1ccc2nc(ccc2c1)-c1sc2nc3ccccc3n2c1C |r| Show InChI InChI=1S/C26H26N4S/c1-17-6-5-14-29(17)15-13-19-9-11-21-20(16-19)10-12-23(27-21)25-18(2)30-24-8-4-3-7-22(24)28-26(30)31-25/h3-4,7-12,16-17H,5-6,13-15H2,1-2H3/t17-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.72E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bioprojet-Biotech Curated by ChEMBL					Assay Description Displacement of [3H]dofetilide from human recombinant ERG by Competitive binding assay				Bioorg Med Chem Lett 21: 5378-83 (2011) Article DOI: 10.1016/j.bmcl.2011.07.006 BindingDB Entry DOI: 10.7270/Q2VX0GXK
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50319551 ((R)-3-methyl-2-(6-(2-(2-methylpyrrolidin-1-yl)ethy...) Show SMILES C[C@@H]1CCCN1CCc1ccc2nc(ccc2c1)-c1sc2nc3ccccc3n2c1C |r| Show InChI InChI=1S/C26H26N4S/c1-17-6-5-14-29(17)15-13-19-9-11-21-20(16-19)10-12-23(27-21)25-18(2)30-24-8-4-3-7-22(24)28-26(30)31-25/h3-4,7-12,16-17H,5-6,13-15H2,1-2H3/t17-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	0.360	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]-N-alpha-methylhistamine from human cloned histamine H3 receptor				Bioorg Med Chem Lett 20: 3295-300 (2010) Article DOI: 10.1016/j.bmcl.2010.04.045 BindingDB Entry DOI: 10.7270/Q2XW4JZN
					More data for this Ligand-Target Pair