null

SMILES: CN(c1ccccc1)S(=O)(=O)c1ccc2CCNCCc2c1

InChI Key: InChIKey=DIZZADVCOPMWQC-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50257566   

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
5-hydroxytryptamine receptor 2C (Homo sapiens (Human))	BDBM50257566 (CHEMBL492950 | N-methyl-N-phenyl-2,3,4,5-tetrahydr...) Show SMILES CN(c1ccccc1)S(=O)(=O)c1ccc2CCNCCc2c1 Show InChI InChI=1S/C17H20N2O2S/c1-19(16-5-3-2-4-6-16)22(20,21)17-8-7-14-9-11-18-12-10-15(14)13-17/h2-8,13,18H,9-12H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Displacement of [3H]mesulergine form human recombinant 5HT2C receptor expressed in mouse Swiss 3T3 cells by scintillation proximity assay				Bioorg Med Chem Lett 19: 1871-5 (2009) Article DOI: 10.1016/j.bmcl.2009.02.071 BindingDB Entry DOI: 10.7270/Q2GB23XH
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2B (Homo sapiens (Human))	BDBM50257566 (CHEMBL492950 | N-methyl-N-phenyl-2,3,4,5-tetrahydr...) Show SMILES CN(c1ccccc1)S(=O)(=O)c1ccc2CCNCCc2c1 Show InChI InChI=1S/C17H20N2O2S/c1-19(16-5-3-2-4-6-16)22(20,21)17-8-7-14-9-11-18-12-10-15(14)13-17/h2-8,13,18H,9-12H2,1H3	PDB 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	478	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Agonist activity at human recombinant 5HT2B receptor by cell-based system				Bioorg Med Chem Lett 19: 1871-5 (2009) Article DOI: 10.1016/j.bmcl.2009.02.071 BindingDB Entry DOI: 10.7270/Q2GB23XH
					More data for this Ligand-Target Pair