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Cat. No. Product Name Information
PC-60167

GPR120 agonist 4x

GPR120 (FFAR4) agonist

GPR120 agonist 4x is a potent, selective, orally bioavailable GPR120 agonist with EC50 of 42 nM in calcium flux assays.
PC-70042

DC260126

GPR40 agonist

DC260126 is a potent GPR40 (FFAR1) agonist with IC50 of 6.28 uM for inhibition of Ca2+ stimulated by linoleic acid.
PC-42610

TAK-875

GPR40 agonist

TAK-875 (Fasiglifam) is a potent, selective, orally bioavailable GPR40 (FFA1) agonist with EC50 of 14 nM.
PC-42283

TUG-891

GPR120 agonist

TUG-891 (TUG891) is a potent, selective human GPR120 (FFA4) agonist with pEC50 of 7.22.
PC-45843

GW-1100

GPR40 inhibitor

GW-1100 (SB-376752) is a potent, selective GPR40 antagonist that dose dependently inhibits GPR40-mediated Ca2+ elevations stimulated by GW9508 and linoleic acid with pIC50 of 5.99.
PC-45779

GSK137647A

GPR120 (FFAR4) agonist

GSK-137647 (GSK-137647A) is a potent, selective GPR120 (FFA4) agonist with pEC50 of 6.3, >100-fold selectivity over the FFA1, FFA2, and FFA3 receptors.
PC-42400

GPR120 agonist 1

GPR120 (FFAR4) agonist

GPR120 agonist 1 is a potent, fully selective, orally available GPR120 (FFA4) agonist with pEC50 of 7.62.
PC-43813

AMG 837

GPR40 agonist

AMG 837 is a potent partial GPR40 (FFA1) agonist (EC50=13 nM for hGPR40).
PC-24882

HWL-088

FFA1 agonist

HWL-088 is a potent, selective and orally active FFAR1 (FFA1, GPR40) agonist with EC50 of 19 nM, has moderate PPARδ activity (EC50=570.9 nM).
PC-24881

ZLY032

FFA1/PPARδ agonist

ZLY032 (ZLY-032) is a potent, selective dual FFA1/PPARδ agonist with EC50 of 68 nM and 102 nM for hFFA1 and hPPARδ respectively.
PC-24798

TUG-1958

GPR43 antagonist

TUG-1958 is a potent, selective antagonist of GPR43 (FFA2R, free fatty acid receptor 2) with pIC50 of 7.41 uM (hFFA2) in [35S]GTPγS-based binding assays.
PC-24797

BTI-A-404

hGPR43 antagonist

BTI-A-404 is a selective and potent competitive inverse agonist / antagonist of human GPR43 (FFA2R) with cAMP IC50 of 9.5 uM.

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