null

SMILES: CC\C=C1/C[C@H]2CNc3c(OC)cccc3C(=O)N2C1

InChI Key: InChIKey=VRTIPIUNHQTBEU-JVOXIWMLSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50358308   

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 2B (Homo sapiens (Human))	BDBM50358308 (CHEMBL1922537) Show SMILES CC\C=C1/C[C@H]2CNc3c(OC)cccc3C(=O)N2C1 |r| Show InChI InChI=1S/C16H20N2O2/c1-3-5-11-8-12-9-17-15-13(16(19)18(12)10-11)6-4-7-14(15)20-2/h4-7,12,17H,3,8-10H2,1-2H3/b11-5+/t12-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.89E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Suisan Kaisha, Ltd Curated by ChEMBL					Assay Description Inhibition of human 5HT2B receptor expressed in cos-7 cells assessed as [3H]5-HT uptake after 120 mins				Bioorg Med Chem Lett 21: 7099-101 (2011) Article DOI: 10.1016/j.bmcl.2011.09.086 BindingDB Entry DOI: 10.7270/Q20Z73QK
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2B (Homo sapiens (Human))	BDBM50358308 (CHEMBL1922537) Show SMILES CC\C=C1/C[C@H]2CNc3c(OC)cccc3C(=O)N2C1 |r| Show InChI InChI=1S/C16H20N2O2/c1-3-5-11-8-12-9-17-15-13(16(19)18(12)10-11)6-4-7-14(15)20-2/h4-7,12,17H,3,8-10H2,1-2H3/b11-5+/t12-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.24E+4	n/a	n/a	n/a	n/a	n/a	n/a
Nippon Suisan Kaisha, Ltd Curated by ChEMBL					Assay Description Inhibition of human 5HT2B receptor expressed in cos-7 cells assessed as [3H]5-HT uptake after 120 mins				Bioorg Med Chem Lett 21: 7099-101 (2011) Article DOI: 10.1016/j.bmcl.2011.09.086 BindingDB Entry DOI: 10.7270/Q20Z73QK
					More data for this Ligand-Target Pair