Synephrine HCl
CAS No. 5985-28-4
Synephrine HCl ( Oxedrine hydrochloride )
产品货号. M18871 CAS No. 5985-28-4
SynephrineHCl (Oxedrine, p-Synephrine) 是一种作用于拟交感神经 α-肾上腺素能受体 (AR) 的激动剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 500MG | 获取报价 | 有现货 |
|
| 1G | ¥89 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥94 | 有现货 |
|
生物学信息
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产品名称Synephrine HCl
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述SynephrineHCl (Oxedrine, p-Synephrine) 是一种作用于拟交感神经 α-肾上腺素能受体 (AR) 的激动剂。
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产品描述SynephrineHCl (Oxedrine, p-Synephrine) is an agonist that acts on sympathomimetic α-adrenergic receptor (AR).(In Vivo):Synephrine (1 mg/kg; oral gavage; for 8 days; PVL and BDL rats) significantly ameliorates the hyperdynamic state in both PVL and BDL rats. The portal venous pressure in PVL and BDL rats, portal tributary blood flow and cardiac index are significantly reduced, while mean arterial pressure and systemic as well as portal territory vascular resistance are enhanced by treatment of Synephrine.
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体外实验——
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体内实验Synephrine (1 mg/kg; oral gavage; for 8 days; PVL and BDL rats) significantly ameliorates the hyperdynamic state in both PVL and BDL rats. The portal venous pressure in PVL and BDL rats, portal tributary blood flow and cardiac index are significantly reduced, while mean arterial pressure and systemic as well as portal territory vascular resistance are enhanced by treatment of Synephrine. Animal Model:Portal vein ligation (PVL) or bile duct ligation (BDL) rats Dosage:1 mg/kg per 12 hours Administration:Oral gavage; for 8 days Result:The portal venous pressure in PVL and BDL rats, portal tributary blood flow and cardiac index were significantly reduced, while mean arterial pressure and systemic as well as portal territory vascular resistance were enhanced.
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同义词Oxedrine hydrochloride
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通路Others
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靶点Other Targets
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受体α-adrenergic receptor
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研究领域Neurological Disease
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适应症——
化学信息
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CAS Number5985-28-4
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分子量203.67
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分子式C9H13NO2·HCl
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纯度>98% (HPLC)
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溶解度DMSO : ≥ 52 mg/mL; 255.31 mM
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SMILESC(c1ccc(cc1)O)(CNC)O.Cl
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Huang YT, et al. Jpn J Pharmacol, 2001, 85(2), 183-188.
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