null

SMILES: Cn1ccnc1[C@@H](CC(O)=O)c1ccc(OCc2cccc(c2)-c2ccccc2Cl)cc1

InChI Key: InChIKey=XWZVTMLQUBXYLT-QHCPKHFHSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50138172   

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))	BDBM50138172 (CHEMBL3752274) Show SMILES Cn1ccnc1[C@@H](CC(O)=O)c1ccc(OCc2cccc(c2)-c2ccccc2Cl)cc1 |r| Show InChI InChI=1S/C26H23ClN2O3/c1-29-14-13-28-26(29)23(16-25(30)31)19-9-11-21(12-10-19)32-17-18-5-4-6-20(15-18)22-7-2-3-8-24(22)27/h2-15,23H,16-17H2,1H3,(H,30,31)/t23-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	43	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))	BDBM50138172 (CHEMBL3752274) Show SMILES Cn1ccnc1[C@@H](CC(O)=O)c1ccc(OCc2cccc(c2)-c2ccccc2Cl)cc1 |r| Show InChI InChI=1S/C26H23ClN2O3/c1-29-14-13-28-26(29)23(16-25(30)31)19-9-11-21(12-10-19)32-17-18-5-4-6-20(15-18)22-7-2-3-8-24(22)27/h2-15,23H,16-17H2,1H3,(H,30,31)/t23-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	5.60E+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