计算溶液所需的质量、体积或浓度。
为什么选择此级别
，适用于对基线干扰要求严格的色谱和分析工作流程。
储存与运输
-80℃储存。特低温运输 。请查阅批次 COA 获取详细规格。
质量文档
SDS、COA、产品数据表及规格说明书均可下载。可通过批号查询获取批次 COA。
文献证明
在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。
概述
产品应用：
Synephrine (Oxedrine) hydrochloride，一种生物碱，是一种来自 Citrus aurantium 的 α-adrenergic 和 β-adrenergic 激动剂。Synephrine hydrochloride 是一种拟交感神经化合物，可用于减肥。
Information
SynephrineHCl (Oxedrine, p-Synephrine) is a sympathomimeticα-adrenergic receptor (AR)agonist.
In vitro
Synephrine (0.1-30 μM) displays potent vasoconstrictive effects on isolated rat aorta in a dose dependent manner, which can be significantly inhibited by pretreatment with prazosin, BRL15572, and ketanserin but not by pretreatment with SB216641 and propranolol, indicating that Synephrine exerts the constrictive effects via adrenergic alpha(1)-receptors, serotonergic 5-HT(1D) receptors, and 5-HT(2A) receptors. Although the Ki values of Synephrine, 1R,2S-norephedrine, and β-phenethylamine are same for all three subtypes, only Synephrine is a partial agonist of α1A-AR subtype stably expressed in HEK 293 cells with EC50 of 4 µM, giving a maximal response at 100 µM that is equal to 55.3 % of the L-phenylephrine maximum. Functional studies on the α2A- and α2C-AR subtypes stably expressed in CHO cells indicate that Synephrine may act as an antagonist rather than an agonist of the pre-synaptic α(2A)- and α(2C)-AR subtypes present in nerve terminals, although antagonist activity of synephrine is lower than its partial agonist potency. Synephrine (~100 μM) treatment increases basal glucose consumption up to 50% over the control in a dose-dependent manner, without affecting the viability of L6 skeletal muscle cells. Synephrine significantly stimulates the basal- or insulin-stimulated lactic acid production as well as glucose consumption. Synephrine treatment stimulates the phosphorylation of AMPK but not Akt, and Synephrine-induced glucose consumption and the translocation of Glut4 from the cytoplasm to the plasma membrane are sensitive to the inhibition of AMPK but not to the inhibition of PI3 kinase.
In vivo
Administration of Synephrine (1 mg/kg per 12 hours) for 8 days significantly improves the hyperdynamic state in portal hypertensive rats induced by either partial portal vein ligation (PVL) or bile duct ligation (BDL), and significantly reduces the portal venous pressure, portal tributary blood flow and cardiac index in both PVL and BDL rats.
Cell Data
cell lines：Jurkat, BALB/c 3T3, SV40-transformed MEF, L929
Concentrations：
Incubation Time：
Powder Purity:≥99%
规格
英文别名
4-(1-hydroxy-2-(methylamino)ethyl)phenol hydrochloride
规格或纯度
10mM in DMSO
英文名称
Synephrine HCl
生化机理
SynephrineHCl（Oxedrine，p-Synephrine）是一种拟交感α-肾上腺素能受体（AR）激动剂。
储存条件
-80℃储存
运输条件
特低温运输
名称和识别符
技术文档
高级数据
化学和物理性质
溶解性
Solubility (25°C) In vitro DMSO: 34 mg/mL (202.17 mM); Water: 34 mg/mL (202.17 mM); Ethanol: 34 mg/mL (202.17 mM);
安全和危险性（GHS）
信号词
警告
危险声明
H315: 引起皮肤刺激
H319: 引起严重眼睛刺激
H335: 可能引起呼吸道刺激
质检证书（CoA,COO,BSE/TSE 和分析图谱)
C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:
溶液计算器
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