null

SMILES: COc1ccc(cc1OCCN1CCC(C)CC1)N1Cc2cc(C)cc(C)c2C1=O

InChI Key: InChIKey=CWYLHTHVLKCZIJ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50476490   

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))	BDBM50476490 (CHEMBL396527) Show SMILES COc1ccc(cc1OCCN1CCC(C)CC1)N1Cc2cc(C)cc(C)c2C1=O Show InChI InChI=1S/C25H32N2O3/c1-17-7-9-26(10-8-17)11-12-30-23-15-21(5-6-22(23)29-4)27-16-20-14-18(2)13-19(3)24(20)25(27)28/h5-6,13-15,17H,7-12,16H2,1-4H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Medicine Research Centre Curated by ChEMBL					Assay Description Displacement of [3H]mesulergine from 5HT2C receptor expressed in HEK293 cells				Bioorg Med Chem Lett 17: 428-33 (2007) Article DOI: 10.1016/j.bmcl.2006.10.029 BindingDB Entry DOI: 10.7270/Q2TX3J4X
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2B (Homo sapiens (Human))	BDBM50476490 (CHEMBL396527) Show SMILES COc1ccc(cc1OCCN1CCC(C)CC1)N1Cc2cc(C)cc(C)c2C1=O Show InChI InChI=1S/C25H32N2O3/c1-17-7-9-26(10-8-17)11-12-30-23-15-21(5-6-22(23)29-4)27-16-20-14-18(2)13-19(3)24(20)25(27)28/h5-6,13-15,17H,7-12,16H2,1-4H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	316	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Medicine Research Centre Curated by ChEMBL					Assay Description Displacement of [3H]5-HT from 5HT2B receptor expressed in HEK293 cells				Bioorg Med Chem Lett 17: 428-33 (2007) Article DOI: 10.1016/j.bmcl.2006.10.029 BindingDB Entry DOI: 10.7270/Q2TX3J4X
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Homo sapiens (Human))	BDBM50476490 (CHEMBL396527) Show SMILES COc1ccc(cc1OCCN1CCC(C)CC1)N1Cc2cc(C)cc(C)c2C1=O Show InChI InChI=1S/C25H32N2O3/c1-17-7-9-26(10-8-17)11-12-30-23-15-21(5-6-22(23)29-4)27-16-20-14-18(2)13-19(3)24(20)25(27)28/h5-6,13-15,17H,7-12,16H2,1-4H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.26E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Medicine Research Centre Curated by ChEMBL					Assay Description Displacement of [3H]ketanserin from 5HT2A receptor expressed in HEK293 cells				Bioorg Med Chem Lett 17: 428-33 (2007) Article DOI: 10.1016/j.bmcl.2006.10.029 BindingDB Entry DOI: 10.7270/Q2TX3J4X
					More data for this Ligand-Target Pair