AMG7703
目录号: PL02166 纯度: ≥99%
CAS No. :1103523-24-5
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中文名称
AMG7703
英文名称
AMG7703
英文别名
(S)-2-(4-chlorophenyl)-3-methyl-N-(thiazol-2-yl)butanamide;BDBM50305975;B5669;(R)-2-(4-chlorophenyl)-3-methyl-N-(thiazol-2-yl)butanamide
Cas No.
1103523-24-5
分子式
C14H15ClN2Os
分子量
294.80
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
AMG7703 是一种 FFA2 (GPR43) 的选择性变构激动剂,FFA2 是短链脂肪酸 (SCFA)、醋酸盐 (acetate) 和丙酸 (methylacetic) 的受体。AMG7703可用于炎症和代谢的研究。
生物活性
AMG7703 is a selective and allosteric agonists of FFA2 (GPR43), the receptor for short-chain fatty acids (SCFAs), acetate, and propionate. AMG7703 can be used to research for in inflammatory and metabolic.
性状
Solid
体外研究(In Vitro)
AMG7703 (phenylacetamide 1) (30 μM) shows selectivity on FFA2 (GPR43) over FFA1 (GPR40) and FFA3 (GPR41) with in Chinese hamster ovary cells.
AMG7703 (0.041, 0.123, 0.37, 1.11 μM) acts as an FFA2 allosteric agonist, activates Gαi coupled signaling pathway.
AMG7703 (1, 3, 10, 30 μM) results in Gαi-dependent inhibition of lipolysis in adipocytes (3T3L1).
AMG7703 (0.041, 0.123, 0.37, 1.11 μM) exhibits allosteric activity and inhibits Gαi-coupled cAMP with IC50 values of 0.7 μM (hFFA2) and 0.96 μM (mFFA2), respectively; as for Gαq-coupled aequorin inhibition, with EC50s of 0.45 μM (hFFA2) and 1.27 μM (mFFA2), respectively.
AMG7703 (0-1 μM) shows the positive cooperating effect of acetate and stimulates calcium mobilization in a concentration-dependent manner in CHO cell stably expressing hFFA2 and ae
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Lee T, et al. Identification and functional characterization of allosteric agonists for the G protein-coupled receptor FFA2. Mol Pharmacol. 2008 Dec. 74(6):1599-609.
溶解度数据
In Vitro: DMSO : 100 mg/mL (339.21 mM; ultrasonic and warming and heat to 60°C)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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