TUG-469,99.90%
产品编号:Bellancom-123297| CAS NO:1236109-67-3| 分子式:C23H23NO2| 分子量:345.43
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TUG-469
产品介绍 | TUG-469 是选择性的游离脂肪酸受体 1 (FFA1/GPR40) 激动剂,EC50 值为 19 nM。TUG-469 对 FFA1 的选择性是 FFA4 的 200 倍。TUG-469 显著改善糖尿病早期小鼠的糖耐量。TUG-469 可用于糖尿病的研究。 | ||||||||||||||||
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生物活性 | TUG-469 is a selective free fatty acid receptor 1 (FFA1/GPR40) agonist with an EC50 value of 19 nM. TUG-469 is >200-fold selective for FFA1 over FFA4. TUG-469 significantly improves glucose tolerance in pre-diabetic mice. TUG-469 can be used for the research of diabetes. | ||||||||||||||||
体外研究 |
TUG-469 (0-10 μM) shows efficacy to hFFA1 with a pEC50 value of 7.73. TUG-469 (10 μM) increases the insulin secretion under 10 mM glucose stimulation. TUG-469 (0-100 μM) is >200-fold selective for FFA1 over FFA4 with EC50 values of 19 nM and 4.4 μM for FFA1 and FFA4, respectively. TUG-469 (5 μM; 30 min) significantly increases insulin secretion of INS-1 cells with the presence of high glucose concentration (16.7 mM). 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 |
TUG-469 (5 mg/kg; i.p.; 60 and 90 min after glucose administration) affects blood glucose level. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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体内研究 |
TUG-469 (5 mg/kg; i.p.; 60 and 90 min after glucose administration) affects blood glucose level. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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性状 | Solid | ||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : 100 mg/mL (289.49 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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参考文献 |
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