null

SMILES: CC(C)Oc1ccc(F)c(c1)-c1ccc(OC[C@H]2C[C@H]2C(O)=O)cc1

InChI Key: InChIKey=YTWCODZNNZBQFV-RDTXWAMCSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 384301   

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 4 (Homo sapiens (Human))	BDBM384301 ((1R,2S)-2-(((2′-Fluoro-5′-isopropoxy-[...) Show SMILES CC(C)Oc1ccc(F)c(c1)-c1ccc(OC[C@H]2C[C@H]2C(O)=O)cc1 |r| Show InChI InChI=1S/C20H21FO4/c1-12(2)25-16-7-8-19(21)17(10-16)13-3-5-15(6-4-13)24-11-14-9-18(14)20(22)23/h3-8,10,12,14,18H,9,11H2,1-2H3,(H,22,23)/t14-,18-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	1.69E+3	n/a	n/a	n/a	n/a
Sunesis Pharmaceuticals					Assay Description For the pERK assay, 3×106 cells/mL cryopreserved human and mouse cells were thawed rapidly in a 37° C. water bath and added to a T-225 flask containi...				Bioorg Med Chem Lett 18: 4880-4 (2008) BindingDB Entry DOI: 10.7270/Q2TB1969
					More data for this Ligand-Target Pair
Free fatty acid receptor 4 (Homo sapiens (Human))	BDBM384301 ((1R,2S)-2-(((2′-Fluoro-5′-isopropoxy-[...) Show SMILES CC(C)Oc1ccc(F)c(c1)-c1ccc(OC[C@H]2C[C@H]2C(O)=O)cc1 |r| Show InChI InChI=1S/C20H21FO4/c1-12(2)25-16-7-8-19(21)17(10-16)13-3-5-15(6-4-13)24-11-14-9-18(14)20(22)23/h3-8,10,12,14,18H,9,11H2,1-2H3,(H,22,23)/t14-,18-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	2.81E+3	n/a	n/a	n/a	n/a
Sunesis Pharmaceuticals					Assay Description For the pERK assay, 3×106 cells/mL cryopreserved human and mouse cells were thawed rapidly in a 37° C. water bath and added to a T-225 flask containi...				Bioorg Med Chem Lett 18: 4880-4 (2008) BindingDB Entry DOI: 10.7270/Q2TB1969
					More data for this Ligand-Target Pair