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Picroside II 
Picroside II
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英文名稱 : Picroside II
貨號 : EY-01Y20252
CAS : 39012-20-9
含量 : >99.50%
規(guī)格 : 10mM (in 1mL DMSO)、20mg
品牌 : 上海一研
價(jià)格 :
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產(chǎn)品屬性:


產(chǎn)品名稱

Picroside II

規(guī)格

10mM (in 1mL DMSO)、20mg

貨號

EY-01Y20252

Cas No.: 39012-20-9

別名: 6-Vanilloylcatalpol

化學(xué)名: [1a-(hydroxymethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,5a,6,6a-tetrahydro-1bH-oxireno[5,6]cyclopenta[1,3-c]pyran-6-yl] 4-hydroxy-3-methoxybenzoate

分子式: C23H28O13
GN10778.png
分子量: 512.46

溶解度: ≥ 22.9mg/mL in DMSO

儲存條件: 4°C, protect from light
General tips:For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.

Shipping Condition:Evaluation sample solution : ship with blue ice

All other available size: ship with RT , or blue ice upon request

產(chǎn)品描述:


EC50: 50 g/mLPicrosideII is a major an iridoid glucoside isolated from Picrorhiza scrophulariiflora Pennell (Scrophulariaceae). Previous studies have shown that picroside II can protect cardiomyocytes against oxidative stress induced by hypoxia/ reoxygenation (H/R) injury.In vitro: Pretreated cardiomyocytes with picroside II was found to inhibit LDH activity in culture media and increase cell viability in a dose-dependent manner. Such protective effect was accompanied with significant reduction of GSH contents and the activities of SOD and GSH-Px. Attenuated MDA and GSSG contents in response to H/R injury were observed as well. In addition, picroside II treatment also inhibited calcium accumulation and ROS production in cardiomyocytes. [1]. In vivo: A rat focal cerebral ischemic model was established, and picroside II were given intraperitoneally. Results indicated that the damage to the structures of the neurons and the blood brain barrier (BBB) in the cortex was more severe in the model group. In the picroside II treatment group, the neurological function, the morphology and ultrastructure of the neurons, and the BBB were improved. In addition, apoptotic cell number, cerebral infarct volume, EAR and pERK1/2 expression were decreased significantly compared to the model group [2]. Clinical trial: N/A
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