null

SMILES: COc1cc2CCN(C(=O)Nc3cccc(Cl)c3F)c2cc1N1C[C@H](C)N(C)[C@H](C)C1

InChI Key: InChIKey=VJHAAOFTCZHNAY-GASCZTMLSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50475413   

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 1B (Homo sapiens (Human))	BDBM50475413 (CHEMBL381035) Show SMILES COc1cc2CCN(C(=O)Nc3cccc(Cl)c3F)c2cc1N1C[C@H](C)N(C)[C@H](C)C1 Show InChI InChI=1S/C23H28ClFN4O2/c1-14-12-28(13-15(2)27(14)3)20-11-19-16(10-21(20)31-4)8-9-29(19)23(30)26-18-7-5-6-17(24)22(18)25/h5-7,10-11,14-15H,8-9,12-13H2,1-4H3,(H,26,30)/t14-,15+	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	7.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity against cloned human 5-hydroxytryptamine 1B receptor				Bioorg Med Chem Lett 15: 4708-12 (2005) Article DOI: 10.1016/j.bmcl.2005.07.085 BindingDB Entry DOI: 10.7270/Q2CC13F8
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1D (Homo sapiens (Human))	BDBM50475413 (CHEMBL381035) Show SMILES COc1cc2CCN(C(=O)Nc3cccc(Cl)c3F)c2cc1N1C[C@H](C)N(C)[C@H](C)C1 Show InChI InChI=1S/C23H28ClFN4O2/c1-14-12-28(13-15(2)27(14)3)20-11-19-16(10-21(20)31-4)8-9-29(19)23(30)26-18-7-5-6-17(24)22(18)25/h5-7,10-11,14-15H,8-9,12-13H2,1-4H3,(H,26,30)/t14-,15+	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	200	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Binding affinity against cloned human 5-hydroxytryptamine 1D receptor				Bioorg Med Chem Lett 15: 4708-12 (2005) Article DOI: 10.1016/j.bmcl.2005.07.085 BindingDB Entry DOI: 10.7270/Q2CC13F8
					More data for this Ligand-Target Pair