Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Somatostatin receptor type 3' and Ligand = 'BDBM50103414'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/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))	BDBM50103414 (1-Cyclohexyl-1-methyl-3-(4-phenyl-1H-imidazol-2-yl...) Show SMILES CC1(NC(Cc2c1[nH]c1ccccc21)c1nc(c[nH]1)-c1ccccc1)C1CCCCC1 Show InChI InChI=1S/C27H30N4/c1-27(19-12-6-3-7-13-19)25-21(20-14-8-9-15-22(20)29-25)16-23(31-27)26-28-17-24(30-26)18-10-4-2-5-11-18/h2,4-5,8-11,14-15,17,19,23,29,31H,3,6-7,12-13,16H2,1H3,(H,28,30)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.900	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institut Henri Beaufour Curated by ChEMBL					Assay Description Inhibition of [125 I -Tyr]SRIF-14 binding to membranes isolated from CHO-K1 cells expressing cloned human SRIF receptor (sst-3) subtype				J Med Chem 44: 2990-3000 (2001) BindingDB Entry DOI: 10.7270/Q2DB82JT
					More data for this Ligand-Target Pair
Somatostatin receptor type 3 (Homo sapiens (Human))	BDBM50103414 (1-Cyclohexyl-1-methyl-3-(4-phenyl-1H-imidazol-2-yl...) Show SMILES CC1(NC(Cc2c1[nH]c1ccccc21)c1nc(c[nH]1)-c1ccccc1)C1CCCCC1 Show InChI InChI=1S/C27H30N4/c1-27(19-12-6-3-7-13-19)25-21(20-14-8-9-15-22(20)29-25)16-23(31-27)26-28-17-24(30-26)18-10-4-2-5-11-18/h2,4-5,8-11,14-15,17,19,23,29,31H,3,6-7,12-13,16H2,1H3,(H,28,30)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.40	n/a	n/a	n/a	n/a	n/a	n/a
Institut Henri Beaufour Curated by ChEMBL					Assay Description Inhibitory concentration required to inhibit SRIF-14 induced reduction of cAMP in CHO-K1 cells expressing the human sst3 receptor.				J Med Chem 44: 2990-3000 (2001) BindingDB Entry DOI: 10.7270/Q2DB82JT
					More data for this Ligand-Target Pair