null

SMILES: C(NC1(CCCC1)c1nc(c[nH]1)-c1ccccc1)c1c[nH]c2ccccc12

InChI Key: InChIKey=DCVMBWUHXHBEKW-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50110460   

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
Somatostatin receptor type 3 (Homo sapiens (Human))	BDBM50110460 (CHEMBL3605788) Show SMILES C(NC1(CCCC1)c1nc(c[nH]1)-c1ccccc1)c1c[nH]c2ccccc12 Show InChI InChI=1S/C23H24N4/c1-2-8-17(9-3-1)21-16-25-22(27-21)23(12-6-7-13-23)26-15-18-14-24-20-11-5-4-10-19(18)20/h1-5,8-11,14,16,24,26H,6-7,12-13,15H2,(H,25,27)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Displacement of [125I]SS-14 from human SSTR3 expressed in CHO cells after 60 to 90 mins				Bioorg Med Chem Lett 25: 3520-5 (2015) Article DOI: 10.1016/j.bmcl.2015.06.087 BindingDB Entry DOI: 10.7270/Q29W0H9M
					More data for this Ligand-Target Pair
Somatostatin receptor type 3 (Homo sapiens (Human))	BDBM50110460 (CHEMBL3605788) Show SMILES C(NC1(CCCC1)c1nc(c[nH]1)-c1ccccc1)c1c[nH]c2ccccc12 Show InChI InChI=1S/C23H24N4/c1-2-8-17(9-3-1)21-16-25-22(27-21)23(12-6-7-13-23)26-15-18-14-24-20-11-5-4-10-19(18)20/h1-5,8-11,14,16,24,26H,6-7,12-13,15H2,(H,25,27)	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	20	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Agonist activity at human SSTR3 expressed in CHO cells assessed as intracellular cAMP level after 45 mins by time-resolved fluorescence assay				Bioorg Med Chem Lett 25: 3520-5 (2015) Article DOI: 10.1016/j.bmcl.2015.06.087 BindingDB Entry DOI: 10.7270/Q29W0H9M
					More data for this Ligand-Target Pair