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Cat. No. Product Name Information
PC-21247

AH7614

GPR120 (FFAR4) inhibitor

AH-7614 is a potent and selective FFA4 (GPR120) antagonist with pIC50 of 7.1, 8.1, and 8.1 for human, mouse, and rat FFA4, respectively.
PC-20767

TUG-2304

FFA2 (GPR43) antagonist

TUG-2304 (TUG2304) is a highly potent FFA2 (GPR43) antagonist with IC50 of 3-4 nM in both cAMP and GTPγS assays.
PC-49032

AR420626

GPR41 agonist

AR420626 is a potent, selective GPR41/FFA3 agonist with pEC50 of 5.74 in [35S]GTPγS-binding assays, induces apoptosis in HCC cells, including HepG2 and HLE cells.
PC-72422

CFMB

FFAR2 (GPR43) agonist

CFMB (FFA2R agonist 58) is a potent, allosteric FFAR2 (GPR43) agonist/modulator.
PC-72119

CPL207280

GPR40 agonist

CPL207280 (CPL 207280) is a novel potent, selective GPR40/FFA1 agonist with EC50 of 80 nM in a Ca2+ influx assay, shows greater potency than fasiglifam (EC50=270 nM).
PC-38228

MK-8666

GPR40 agonist

MK-8666 is a potent, selective partial GPR40 agonist with EC50 of 0.9 nM, shows potential for the treatment of type 2 diabetes mellitus.
PC-35696

(S)-4CMTB

FFA2 agonist

(S)-4CMTB (AMG 7703, Phenylacetamide 1) is a potent, specific and allosteric agonist of FFA2 (GPR43) with cAMP IC50 of 0.7 and 0.96 uM for hFFA2 and mFFA2, respectively.
PC-35695

TUG-1375

FFA2 agonist

TUG-1375 (TUG1375, TUG 1375) is a potent, selective free fatty acid receptor 2 (FFA2/GPR43) agonist with β-arrestin-2 pEC50 of 6.1 and cAMP pEC50 of 7.11.
PC-35510

GPR40 AgoPAM AP5

GPR40 agonist

GPR40 AgoPAM AP5 is a potent, selective GPR40 AgoPAM (full agonist with positive allosteric modulation) with hIP1 EC50 of 0.8 nM, high selectivity over the GPR120 receptor (EC50>30 uM).
PC-35465

PBI-4050 sodium

GPR40 agonist, GPR84 antagonist

PBI-4050 (Setogepram, Fezagepras) sodium is a synthetic analog of a medium-chain fatty acid that displays agonist and antagonist ligand affinity toward GPR40 and GPR84, respectively.
PC-35464

PBI-4050

GPR40 agonist, GPR84 antagonist

PBI-4050 (Setogepram, Fezagepras) is a synthetic analog of a medium-chain fatty acid that displays agonist and antagonist ligand affinity toward GPR40 and GPR84, respectively.
PC-63157

AZ1729

FFA2 agonist

AZ1729 is a novel direct, positive allosteric modulator of fatty acid receptor FFA2 (pEC50=6.9), selectively activates Gi signaling but lacks the capacity to activate FFA2 Gq/G11-mediated signaling pathways.

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