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TUG-424

CAT: 0804-HY-14363-01Size: 1 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-14363-01Size:1 mg
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Description
TUG-424 is a potent and selective free fatty acid receptor 1 (FFA1/GPR40) agonist with an EC50 of 32 nM. TUG-424 significantly increases glucose-stimulated insulin secretion at 100 nM. TUG-424 may serve to explore the role of FFA1 in metabolic diseases such as diabetes or obesity[1]. TUG-424 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
CAS Number
1082058-99-8
UNSPSC
12352005
Hazard Statement
H319, H410
Target
Free Fatty Acid Receptor
Type
Reference compound
Related Pathways
GPCR/G Protein
Applications
Neuroscience-Neuromodulation
Field of Research
Metabolic Disease
Assay Protocol
https://www.medchemexpress.com/tug-424.html
Purity
99.68
Solubility
10 mM in DMSO|DMSO : ≥ 10mg/mL
Smiles
OC(CCC(C=C1)=CC=C1C#CC2=C(C)C=CC=C2)=O
Molecular Formula
C18H16O2
Molecular Weight
264.32
Precautions
H319, H410
References & Citations
[1]Discovery of Potent and Selective Agonists for the Free Fatty Acid Receptor 1 (FFA1/GPR40), a Potential Target for the Treatment of Type II Diabetes J. Med. Chem., 2008, 51 (22), pp 7061-7064|[2]Christiansen E, et al. Discovery of potent and selective agonists for the free fatty acid receptor 1 (FFA (1) /GPR40), a potential target for the treatment of type II diabetes. J Med Chem. 2008 Nov 27;51 (22) :7061-4.
Shipping Conditions
Blue Ice
Storage Conditions
-20°C, 3 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported

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