TUG-424 是一种有效且选择性的游离脂肪酸受体 1 (FFA1/GPR40) 激动剂,EC50 为 32 nM。TUG-424 在 100 nM 处显著增加葡萄糖刺激的胰岛素分泌。
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描述 | TUG-424 is a potent and selective agonist of the free fatty acid receptor 1 (FFA1/GPR40) with an EC50 of 32 nM. It significantly enhances glucose-stimulated insulin secretion at 100 nM and may be useful for researching the role of FFA1 in metabolic diseases such as diabetes or obesity[1]. TUG-424 is a click chemistry reagent that features an alkyne group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules that possess azide groups. |
体外研究 | TUG-424, at concentrations ranging from 100 nM to 10 µM, significantly enhances glucose-stimulated insulin secretion starting at 100 nM, reaching a peak effect at 3 µM. This approximately two-fold increase in secretion in the presence of 12 mM glucose is similar to the effect seen with palmitate at the same glucose level. At a basal glucose concentration of 2.8 mM, TUG-424 slightly but significantly decreases insulin secretion[1]. |
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存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.78mL 0.76mL 0.38mL |
18.92mL 3.78mL 1.89mL |
37.83mL 7.57mL 3.78mL |
CAS号 | 1082058-99-8 |
分子式 | C18H16O2 |
分子量 | 264.318 |
别名 | CAY10587 |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,2-8°C |
溶解度 | |
动物实验配方 |