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KI2573TUG89110 mg$403
TUG89150 mg$1609.4

Chemical Characteristic

Product NameTUG891
CAS No.1374516-07-0
Molecular Weight 364.41
FormulaC23H21FO3
Chemical Name3-{4-[(4-Fluoro-4'-methyl-2-biphenylyl)methoxy]phenyl}propanoic a cid
Smilesc1(ccc(cc1)OCc1c(ccc(c1)F)c1ccc(cc1)C)CCC(=O)O
Chemical Structure

Biological activities

TUG-891 is a potent and selective agonist for FFA4. The pIC50 of TUG-891 against TNF secretion in RAW264.7 cells is 5.86 μM. TUG-891 inhibits ERK phosphorylation in HT-29 cells with pEC50 of 5.13 μM. TUG-891 displays greater potency at mFFA1 with pEC50 of 5. 92 μM than hFFA1 with pEC50 of 4.76 μM. In vitro, TUG-891 both stimulates insulin-independent glucose uptake in 3T3-L1 cells and inhibits LPS-induced TNF secretion from RAW264.7 cells.[1]

References

[1] Hudson B D, Shimpukade B, Mackenzie A E, et al. The Pharmacology of TUG-891, a Potent and Selective Agonist of the Free Fatty Acid Receptor 4 (FFA4/GPR120), Demonstrates Both Potential Opportunity and Possible Challenges to Therapeutic Agonism. Molecular pharmacology. 2013, 84 (5): 710-725.

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