BDBM50327475 (S)-8-(1-isopropylpiperidin-4-yloxy)-3-methyl-3,4-dihydropyrazino[1,2-a]indol-1(2H)-one::CHEMBL1257850

SMILES: CC(C)N1CCC(CC1)Oc1ccc2n3C[C@H](C)NC(=O)c3cc2c1

InChI Key: InChIKey=GUBYCKMGWYDLAE-AWEZNQCLSA-N

Data: 1 KI  3 IC50  1 EC50

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 5 hits for monomerid = 50327475   

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))	BDBM50327475 ((S)-8-(1-isopropylpiperidin-4-yloxy)-3-methyl-3,4-...) Show SMILES CC(C)N1CCC(CC1)Oc1ccc2n3C[C@H](C)NC(=O)c3cc2c1 |r| Show InChI InChI=1S/C20H27N3O2/c1-13(2)22-8-6-16(7-9-22)25-17-4-5-18-15(10-17)11-19-20(24)21-14(3)12-23(18)19/h4-5,10-11,13-14,16H,6-9,12H2,1-3H3,(H,21,24)/t14-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
F Hoffmann-La Roche Ltd Curated by ChEMBL					Assay Description Displacement of [3H]-RAMH from human histamine H3 receptor				Bioorg Med Chem Lett 20: 5713-7 (2010) Article DOI: 10.1016/j.bmcl.2010.08.009 BindingDB Entry DOI: 10.7270/Q2571C7N
					More data for this Ligand-Target Pair
Cytochrome P450 2C9 (Homo sapiens (Human))	BDBM50327475 ((S)-8-(1-isopropylpiperidin-4-yloxy)-3-methyl-3,4-...) Show SMILES CC(C)N1CCC(CC1)Oc1ccc2n3C[C@H](C)NC(=O)c3cc2c1 |r| Show InChI InChI=1S/C20H27N3O2/c1-13(2)22-8-6-16(7-9-22)25-17-4-5-18-15(10-17)11-19-20(24)21-14(3)12-23(18)19/h4-5,10-11,13-14,16H,6-9,12H2,1-3H3,(H,21,24)/t14-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
F Hoffmann-La Roche Ltd Curated by ChEMBL					Assay Description Inhibition of CYP2C9				Bioorg Med Chem Lett 20: 5713-7 (2010) Article DOI: 10.1016/j.bmcl.2010.08.009 BindingDB Entry DOI: 10.7270/Q2571C7N
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50327475 ((S)-8-(1-isopropylpiperidin-4-yloxy)-3-methyl-3,4-...) Show SMILES CC(C)N1CCC(CC1)Oc1ccc2n3C[C@H](C)NC(=O)c3cc2c1 |r| Show InChI InChI=1S/C20H27N3O2/c1-13(2)22-8-6-16(7-9-22)25-17-4-5-18-15(10-17)11-19-20(24)21-14(3)12-23(18)19/h4-5,10-11,13-14,16H,6-9,12H2,1-3H3,(H,21,24)/t14-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	14	n/a	n/a	n/a	n/a
F Hoffmann-La Roche Ltd Curated by ChEMBL					Assay Description Inverse agonist activity at human recombinant histamine H3 receptor assessed as effect on [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5713-7 (2010) Article DOI: 10.1016/j.bmcl.2010.08.009 BindingDB Entry DOI: 10.7270/Q2571C7N
					More data for this Ligand-Target Pair
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50327475 ((S)-8-(1-isopropylpiperidin-4-yloxy)-3-methyl-3,4-...) Show SMILES CC(C)N1CCC(CC1)Oc1ccc2n3C[C@H](C)NC(=O)c3cc2c1 |r| Show InChI InChI=1S/C20H27N3O2/c1-13(2)22-8-6-16(7-9-22)25-17-4-5-18-15(10-17)11-19-20(24)21-14(3)12-23(18)19/h4-5,10-11,13-14,16H,6-9,12H2,1-3H3,(H,21,24)/t14-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
F Hoffmann-La Roche Ltd Curated by ChEMBL					Assay Description Inhibition of CYP2D6				Bioorg Med Chem Lett 20: 5713-7 (2010) Article DOI: 10.1016/j.bmcl.2010.08.009 BindingDB Entry DOI: 10.7270/Q2571C7N
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50327475 ((S)-8-(1-isopropylpiperidin-4-yloxy)-3-methyl-3,4-...) Show SMILES CC(C)N1CCC(CC1)Oc1ccc2n3C[C@H](C)NC(=O)c3cc2c1 |r| Show InChI InChI=1S/C20H27N3O2/c1-13(2)22-8-6-16(7-9-22)25-17-4-5-18-15(10-17)11-19-20(24)21-14(3)12-23(18)19/h4-5,10-11,13-14,16H,6-9,12H2,1-3H3,(H,21,24)/t14-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
F Hoffmann-La Roche Ltd Curated by ChEMBL					Assay Description Inhibition of CYP3A4				Bioorg Med Chem Lett 20: 5713-7 (2010) Article DOI: 10.1016/j.bmcl.2010.08.009 BindingDB Entry DOI: 10.7270/Q2571C7N
					More data for this Ligand-Target Pair