TUG-499

Modify Date: 2023-01-18 16:15:20

TUG-499 structure	Common Name	TUG-499
	CAS Number	1206629-08-4	Molecular Weight	320.17
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₁₆H₁₁Cl₂NO₂	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of TUG-499

TUG-499 is a selective free fatty acid receptor 1 (FFAR1 or GPR40) (Free Fatty Acid Receptor) agonist with a pEC50 of 7.39. TUG-499 exhibits >100-fold selectivity over the related receptors FFA2, FFA3, and the nuclear receptor PPARγ and other diverse receptors, ion channels, and transporters. TUG-499 can be used for the research of type 2 diabetes[1].

Name	TUG-499

Description	TUG-499 is a selective free fatty acid receptor 1 (FFAR1 or GPR40) (Free Fatty Acid Receptor) agonist with a pEC50 of 7.39. TUG-499 exhibits >100-fold selectivity over the related receptors FFA2, FFA3, and the nuclear receptor PPARγ and other diverse receptors, ion channels, and transporters. TUG-499 can be used for the research of type 2 diabetes[1].
Related Catalog	Signaling Pathways >> GPCR/G Protein >> GPR40 Research Areas >> Metabolic Disease
Target	pEC50: 7.39 (FFAR1)[1]
In Vitro	TUG-499 (compound 7) demonstrates high chemical stability, no inhibition of selected CYP enzymes or P-glycoprotein, and excellent Caco-2 permeability. TUG-499 has potent activity on recombinant human FFA1 receptors and on the rat insulinoma cell line INS-1E[1].
References	[1]. Elisabeth Christiansen, et al. Identification of a potent and selective free fatty acid receptor 1 (FFA1/GPR40) agonist with favorable physicochemical and in vitro ADME properties. J Med Chem. 2011 Oct 13;54(19):6691-703.

Molecular Formula	C₁₆H₁₁Cl₂NO₂
Molecular Weight	320.17

TUG-499

Use of TUG-499

Names

TUG-499 Biological Activity

Chemical & Physical Properties