SR-18292
目录号: PL09519 纯度: ≥98.0%
CAS No. :2095432-55-4
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中文名称
SR-18292
英文名称
SR-18292
英文别名
SR-18292;SR18292;SR 18292;1-((1H-indol-4-yl)oxy)-3-(tert-butyl(4-methylbenzyl)amino)propan-2-ol;1-[Tert-butyl-[(4-methylphenyl)methyl]amino]-3-(1H-indol-4-yloxy)propan-2-ol;yloxy)-propan-2-ol;BCP29112;s8528;SR 18292;;C73955;1-[tert-Butyl-(4-methyl-benzyl)-amino]-3-(1H-indol-4-
Cas No.
2095432-55-4
分子式
C23H30N2O2
分子量
366.50
包装储存
Pure form -20°C 3 years;4°C 2 years
产品详情
SR-18292 是一种 PPARγ 共激活因子-1α (PGC-1α) 抑制剂,可促进 PGC-1α 乙酰化,抑制糖异生基因的表达,并减少肝细胞中葡萄糖的产生。
生物活性
SR-18292 is a PPAR gamma coactivator-1α (PGC-1α) inhibitor, which increases PGC-1α acetylation, suppresses gluconeogenic gene expression and reduces glucose production in hepatocytes.
性状
Oil
IC50 & Target[1][2]
PGC-1α
体外研究(In Vitro)
The transcriptional coactivator PGC-1α plays a pivotal role in energy homeostasis by co-activating transcription factors that regulate fat and glucose metabolism. SR-18292 increases the interaction of PGC-1α with the acetyl transferase GCN5 and reduces co-activation of nuclear hormone receptor HNF4α by PGC-1α. SR-18292 suppresses HNF4α/PGC-1α gluconeogenic transcriptional function. By increasing the interaction of GCN5 with PGC-1α, SR-18292 increases the acetylation of specific PGC-1α lysine residues that might subsequently decrease its gluconeogenic activity. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
SR-18292 reduces fasting blood glucose, increases hepatic insulin sensitivity and improves glucose homeostasis in diabetic mice. The high fat diet (HFD) fed mice, a dietary model of obesity and T2D, are treated with SR-18292 (45mg/kg) via I.P. injection for 3 consecutive days and again on day 4 before measuring fasting blood glucose. Strikingly, mice that are treated with SR-18292 have significantly lower levels of fasting blood glucose concentrations compared to matched vehicle-treated control mice. The induction of gluconeogenic gene expression is a regulatory component of the response to fasting. Importantly, gluconeogenic gene expression, specifically that of Pck1, is inhibited in livers isolated from mice treated with SR-18292. has not independently confirmed the accuracy of these methods. They are for refer
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Pure form -20°C 3 years;4°C 2 years
参考文献
[1]. Sharabi K, et al. Selective Chemical Inhibition of PGC-1α Gluconeogenic Activity Ameliorates Type 2 Diabetes. Cell. 2017 Mar 23;169(1):148-160.e15.
溶解度数据
In Vitro: Ethanol : 100 mg/mL (272.85 mM; Need ultrasonic)DMSO : ≥ 100 mg/mL (272.85 mM)H2O : < 0.1 mg/mL (insoluble)
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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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