BDBM50019411 CHEMBL3290095

SMILES: COc1cccc(OC)c1-c1cc(nn1-c1ccnc2cc(Cl)ccc12)C(=O)NC1(CCCCCC1)C(O)=O

InChI Key: InChIKey=JAGBNGLKOGHGPP-UHFFFAOYSA-N

Data: 1 KI  1 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50019411   

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
Neurotensin receptor 2 (Rattus norvegicus)	BDBM50019411 (CHEMBL3290095) Show SMILES COc1cccc(OC)c1-c1cc(nn1-c1ccnc2cc(Cl)ccc12)C(=O)NC1(CCCCCC1)C(O)=O |(20.7,-18.03,;21.17,-16.57,;22.68,-16.25,;23.71,-17.39,;25.22,-17.07,;25.69,-15.61,;24.66,-14.46,;25.14,-13,;26.64,-12.68,;23.16,-14.78,;21.82,-13.29,;22.14,-11.79,;20.8,-11.02,;19.66,-12.05,;20.28,-13.46,;19.28,-15.19,;20.05,-16.52,;19.28,-17.86,;17.74,-17.86,;16.97,-16.52,;15.43,-16.52,;14.66,-15.19,;13.12,-15.19,;15.43,-13.86,;16.97,-13.86,;17.74,-15.19,;20.64,-9.49,;21.89,-8.58,;19.23,-8.86,;19.05,-7.34,;20.61,-7.52,;21.7,-6.43,;21.54,-4.9,;20.24,-4.07,;18.78,-4.57,;18.28,-6.01,;17.62,-7.83,;16.42,-6.86,;17.32,-9.34,)| Show InChI InChI=1S/C29H29ClN4O5/c1-38-24-8-7-9-25(39-2)26(24)23-17-21(27(35)32-29(28(36)37)13-5-3-4-6-14-29)33-34(23)22-12-15-31-20-16-18(30)10-11-19(20)22/h7-12,15-17H,3-6,13-14H2,1-2H3,(H,32,35)(H,36,37)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	170	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Research Triangle Institute Curated by ChEMBL					Assay Description Displacement of [125I]NT at rat NTS2 overexpressed in CHOK1 cells after 30 mins by gamma counting				J Med Chem 57: 5318-32 (2014) Article DOI: 10.1021/jm5003843 BindingDB Entry DOI: 10.7270/Q2PR7XJD
					More data for this Ligand-Target Pair
Neurotensin receptor 2 (Rattus norvegicus)	BDBM50019411 (CHEMBL3290095) Show SMILES COc1cccc(OC)c1-c1cc(nn1-c1ccnc2cc(Cl)ccc12)C(=O)NC1(CCCCCC1)C(O)=O |(20.7,-18.03,;21.17,-16.57,;22.68,-16.25,;23.71,-17.39,;25.22,-17.07,;25.69,-15.61,;24.66,-14.46,;25.14,-13,;26.64,-12.68,;23.16,-14.78,;21.82,-13.29,;22.14,-11.79,;20.8,-11.02,;19.66,-12.05,;20.28,-13.46,;19.28,-15.19,;20.05,-16.52,;19.28,-17.86,;17.74,-17.86,;16.97,-16.52,;15.43,-16.52,;14.66,-15.19,;13.12,-15.19,;15.43,-13.86,;16.97,-13.86,;17.74,-15.19,;20.64,-9.49,;21.89,-8.58,;19.23,-8.86,;19.05,-7.34,;20.61,-7.52,;21.7,-6.43,;21.54,-4.9,;20.24,-4.07,;18.78,-4.57,;18.28,-6.01,;17.62,-7.83,;16.42,-6.86,;17.32,-9.34,)| Show InChI InChI=1S/C29H29ClN4O5/c1-38-24-8-7-9-25(39-2)26(24)23-17-21(27(35)32-29(28(36)37)13-5-3-4-6-14-29)33-34(23)22-12-15-31-20-16-18(30)10-11-19(20)22/h7-12,15-17H,3-6,13-14H2,1-2H3,(H,32,35)(H,36,37)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	21	n/a	n/a	n/a	n/a
Research Triangle Institute Curated by ChEMBL					Assay Description Agonist activity at rat NTS2 stably expressed in CHOK1 cells assessed as induction of calcium release by FLIPR assay				J Med Chem 57: 5318-32 (2014) Article DOI: 10.1021/jm5003843 BindingDB Entry DOI: 10.7270/Q2PR7XJD
					More data for this Ligand-Target Pair