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 PPARgamma and other diverse receptors, ion channels, and transporters. TUG-499 can be used for the research of type 2 diabetes[1]. TUG-499 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Molekulargewicht:
320.17
Reinheit:
99.78
CAS Nummer:
[1206629-08-4]
Formel:
C16H11Cl2NO2
Target-Kategorie:
Free Fatty Acid Receptor
Anwendungsbeschreibung:
MCE Product type: Reference compound
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