null

SMILES: Fc1ccc(cc1)C(=O)NCCNCc1c[nH]c2ccccc12

InChI Key: InChIKey=ISXRMTZDLBSXGP-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50021092   

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))	BDBM50021092 (CHEMBL3287639) Show SMILES Fc1ccc(cc1)C(=O)NCCNCc1c[nH]c2ccccc12 Show InChI InChI=1S/C18H18FN3O/c19-15-7-5-13(6-8-15)18(23)21-10-9-20-11-14-12-22-17-4-2-1-3-16(14)17/h1-8,12,20,22H,9-11H2,(H,21,23)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.34E+3	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]SS14 from human SST3 expressed in CHO membrane after 60 to 90 mins by scintillation counting				ACS Med Chem Lett 5: 690-5 (2014) Article DOI: 10.1021/ml500079u BindingDB Entry DOI: 10.7270/Q22N53V4
					More data for this Ligand-Target Pair
Somatostatin receptor type 3 (Homo sapiens (Human))	BDBM50021092 (CHEMBL3287639) Show SMILES Fc1ccc(cc1)C(=O)NCCNCc1c[nH]c2ccccc12 Show InChI InChI=1S/C18H18FN3O/c19-15-7-5-13(6-8-15)18(23)21-10-9-20-11-14-12-22-17-4-2-1-3-16(14)17/h1-8,12,20,22H,9-11H2,(H,21,23)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	9.58E+3	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Agonist activity at human SST3 expressed in CHO-K1 cells assessed as foreskin-stimulated cAMP accumulation after 45 mins by TR-FRET assay				ACS Med Chem Lett 5: 690-5 (2014) Article DOI: 10.1021/ml500079u BindingDB Entry DOI: 10.7270/Q22N53V4
					More data for this Ligand-Target Pair