null

SMILES: Cc1cccc(C)c1-c1cccc(COc2ccc(cc2)[C@H](CC(O)=O)c2nccn2C)c1

InChI Key: InChIKey=VOEOTYQOLLWLNZ-VWLOTQADSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50138170   

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
Free fatty acid receptor 1 (Homo sapiens (Human))	BDBM50138170 (CHEMBL3752601) Show SMILES Cc1cccc(C)c1-c1cccc(COc2ccc(cc2)[C@H](CC(O)=O)c2nccn2C)c1 |r| Show InChI InChI=1S/C28H28N2O3/c1-19-6-4-7-20(2)27(19)23-9-5-8-21(16-23)18-33-24-12-10-22(11-13-24)25(17-26(31)32)28-29-14-15-30(28)3/h4-16,25H,17-18H2,1-3H3,(H,31,32)/t25-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	n/a	n/a	58	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Partial agonist activity at human GPR40 expressed in CHO cells measured over 20 secs interval by luminometric analysis in presence of 0.01% human ser...				Bioorg Med Chem Lett 26: 15-20 (2015) BindingDB Entry DOI: 10.7270/Q21R6SBS
					More data for this Ligand-Target Pair
Free fatty acid receptor 1 (Homo sapiens (Human))	BDBM50138170 (CHEMBL3752601) Show SMILES Cc1cccc(C)c1-c1cccc(COc2ccc(cc2)[C@H](CC(O)=O)c2nccn2C)c1 |r| Show InChI InChI=1S/C28H28N2O3/c1-19-6-4-7-20(2)27(19)23-9-5-8-21(16-23)18-33-24-12-10-22(11-13-24)25(17-26(31)32)28-29-14-15-30(28)3/h4-16,25H,17-18H2,1-3H3,(H,31,32)/t25-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	n/a	n/a	2.90E+4	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Partial agonist activity at human GPR40 expressed in CHO cells measured over 20 secs interval by luminometric analysis in presence of 100% human seru...				Bioorg Med Chem Lett 26: 15-20 (2015) BindingDB Entry DOI: 10.7270/Q21R6SBS
					More data for this Ligand-Target Pair