BDBM50341780 4-{5-[(2-Phenyl-5-trifluoromethyloxazole-4-carbonyl)amino]-3',4',5',6'-tetrahydro-2'H-[2,4']bipyridinyl-1'-carbonyl}-transcyclohexanecarboxylic Acid::CHEMBL1766808

SMILES: OC(=O)[C@H]1CC[C@@H](CC1)C(=O)N1CCC(CC1)c1ccc(NC(=O)c2nc(oc2C(F)(F)F)-c2ccccc2)cn1

InChI Key: InChIKey=KVNKQIPSGBJKDN-MXVIHJGJSA-N

Data: 1 IC50  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 = 50341780   

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
Diacylglycerol O-acyltransferase 1 (DGAT1) (Homo sapiens (Human))	BDBM50341780 (4-{5-[(2-Phenyl-5-trifluoromethyloxazole-4-carbony...) Show SMILES OC(=O)[C@H]1CC[C@@H](CC1)C(=O)N1CCC(CC1)c1ccc(NC(=O)c2nc(oc2C(F)(F)F)-c2ccccc2)cn1 |r,wU:6.9,wD:3.2,(20.62,-31.22,;19.28,-30.47,;19.26,-28.93,;17.96,-31.25,;16.61,-30.5,;15.28,-31.29,;15.32,-32.82,;16.65,-33.57,;17.97,-32.79,;14,-33.61,;14.02,-35.14,;12.65,-32.86,;11.33,-33.65,;9.99,-32.9,;9.97,-31.36,;11.28,-30.56,;12.63,-31.32,;8.63,-30.62,;8.6,-29.08,;7.25,-28.33,;5.93,-29.12,;4.58,-28.38,;3.27,-29.18,;3.32,-30.72,;1.91,-28.45,;.69,-29.41,;-.59,-28.55,;-.17,-27.06,;1.38,-27,;2.14,-25.66,;3.68,-25.66,;1.37,-24.34,;2.77,-24.26,;-1.94,-29.29,;-3.26,-28.48,;-4.61,-29.23,;-4.65,-30.76,;-3.33,-31.57,;-1.98,-30.83,;5.96,-30.66,;7.31,-31.41,)| Show InChI InChI=1S/C29H29F3N4O5/c30-29(31,32)24-23(35-26(41-24)18-4-2-1-3-5-18)25(37)34-21-10-11-22(33-16-21)17-12-14-36(15-13-17)27(38)19-6-8-20(9-7-19)28(39)40/h1-5,10-11,16-17,19-20H,6-9,12-15H2,(H,34,37)(H,39,40)/t19-,20-	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	128	n/a	n/a	n/a	n/a	n/a	n/a
Hoffmann-La Roche Inc. Curated by ChEMBL					Assay Description Inhibition of human DGAT1 expressed in baculovirus infected insect cells after 1 hr using palmitoyl-1-14C-coenzyme A by phospholipid flashplate assay				J Med Chem 54: 2433-46 (2011) Article DOI: 10.1021/jm101580m BindingDB Entry DOI: 10.7270/Q2S182TQ
					More data for this Ligand-Target Pair
Diacylglycerol O-acyltransferase 1 (DGAT1) (Homo sapiens (Human))	BDBM50341780 (4-{5-[(2-Phenyl-5-trifluoromethyloxazole-4-carbony...) Show SMILES OC(=O)[C@H]1CC[C@@H](CC1)C(=O)N1CCC(CC1)c1ccc(NC(=O)c2nc(oc2C(F)(F)F)-c2ccccc2)cn1 |r,wU:6.9,wD:3.2,(20.62,-31.22,;19.28,-30.47,;19.26,-28.93,;17.96,-31.25,;16.61,-30.5,;15.28,-31.29,;15.32,-32.82,;16.65,-33.57,;17.97,-32.79,;14,-33.61,;14.02,-35.14,;12.65,-32.86,;11.33,-33.65,;9.99,-32.9,;9.97,-31.36,;11.28,-30.56,;12.63,-31.32,;8.63,-30.62,;8.6,-29.08,;7.25,-28.33,;5.93,-29.12,;4.58,-28.38,;3.27,-29.18,;3.32,-30.72,;1.91,-28.45,;.69,-29.41,;-.59,-28.55,;-.17,-27.06,;1.38,-27,;2.14,-25.66,;3.68,-25.66,;1.37,-24.34,;2.77,-24.26,;-1.94,-29.29,;-3.26,-28.48,;-4.61,-29.23,;-4.65,-30.76,;-3.33,-31.57,;-1.98,-30.83,;5.96,-30.66,;7.31,-31.41,)| Show InChI InChI=1S/C29H29F3N4O5/c30-29(31,32)24-23(35-26(41-24)18-4-2-1-3-5-18)25(37)34-21-10-11-22(33-16-21)17-12-14-36(15-13-17)27(38)19-6-8-20(9-7-19)28(39)40/h1-5,10-11,16-17,19-20H,6-9,12-15H2,(H,34,37)(H,39,40)/t19-,20-	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	2.36E+3	n/a	n/a	n/a	n/a
Hoffmann-La Roche Inc. Curated by ChEMBL					Assay Description Inhibition of human DGAT1 expressed in CHO-K1 cells after 1 hr using palmitoyl-1-14C-coenzyme A by phospholipid flashplate assay				J Med Chem 54: 2433-46 (2011) Article DOI: 10.1021/jm101580m BindingDB Entry DOI: 10.7270/Q2S182TQ
					More data for this Ligand-Target Pair