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SMILES: C1Cc2c(C1)c1cccc3CNCCn2c13

InChI Key: InChIKey=DPHFYUMHDPCCRU-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50145568   

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))	BDBM50145568 (4,5,6,7,9,10-Hexahydro-8H-5,7a-diaza-benzo[cd]cycl...) Show SMILES C1Cc2c(C1)c1cccc3CNCCn2c13 Show InChI InChI=1S/C14H16N2/c1-3-10-9-15-7-8-16-13-6-2-4-11(13)12(5-1)14(10)16/h1,3,5,15H,2,4,6-9H2	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	97	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wyeth Research Curated by ChEMBL					Assay Description Agonistic binding affinity against human 5-hydroxytryptamine 2C receptor in CHO cells using [125I]- DOI				Bioorg Med Chem Lett 14: 2603-7 (2004) Article DOI: 10.1016/j.bmcl.2004.02.100 BindingDB Entry DOI: 10.7270/Q2QZ29F3
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Homo sapiens (Human))	BDBM50145568 (4,5,6,7,9,10-Hexahydro-8H-5,7a-diaza-benzo[cd]cycl...) Show SMILES C1Cc2c(C1)c1cccc3CNCCn2c13 Show InChI InChI=1S/C14H16N2/c1-3-10-9-15-7-8-16-13-6-2-4-11(13)12(5-1)14(10)16/h1,3,5,15H,2,4,6-9H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	922	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Wyeth Research Curated by ChEMBL					Assay Description Agonistic binding affinity of the compound against human 5-hydroxytryptamine 2A receptor in CHO cells using 8-OH-DPA radioligand				Bioorg Med Chem Lett 14: 2603-7 (2004) Article DOI: 10.1016/j.bmcl.2004.02.100 BindingDB Entry DOI: 10.7270/Q2QZ29F3
					More data for this Ligand-Target Pair