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Isovitexin 2''-O-arabinoside Sale

(Synonyms: 异牡荆素-2''-O-阿拉伯糖苷) 目录号 : GC61615 复制 一键复制产品信息

Isovitexin 2''-O-arabinoside是来自Avena sativa L.的C-糖基黄酮,具有植物毒性活性。

Isovitexin 2''-O-arabinoside Chemical Structure

Cas No.:53382-71-1

规格 价格 库存 购买数量
1mg
¥980.00
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5mg
¥2,380.00
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10mg
¥3,500.00
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Sample solution is provided at 25 µL, 10mM.

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Description

Isovitexin 2''-O-arabinoside is the C-glycosylflavone from Avena sativa L. with Phytotoxic activity [1]. Isovitexin 2''-O-arabinoside is capable of effectively reducing the accumulation of intracellular reactive oxygen species (ROS), activating the PI3K/NQO-1 pathway, thereby enhancing the antioxidant response[2]. Isovitexin 2''-O-arabinoside is widely used as an internal reference to optimize chromatographic purification conditions and nuclear magnetic resonance parameters for the efficient purification and identification of related compounds[3].

In vitro, Isovitexin 2''-O-arabinoside treatment (10μM) for 3 days significantly enhanced the alkaline phosphatase (ALP) activity in BMP-2-stimulated C2C12 cells and promoted cell differentiation[4].

References:
[1] De Bertoldi C, De Leo M, Braca A, et al. Bioassay-guided isolation of allelochemicals from Avena sativa L.: allelopathic potential of flavone C-glycosides[J]. Chemoecology, 2009, 19(3): 169-176.
[2] Huang M, Chen Q, Li S, et al. Germination-driven dynamic changes of phenolic compounds in oats and the underlying mechanisms for antioxidation enhancement[J]. Food Chemistry, 2025: 146344.
[3] Zhou G, Wu H, Wang T, et al. C-glycosylflavone with rotational isomers from Vaccaria hispanica (Miller) Rauschert seeds[J]. Phytochemistry letters, 2017, 19: 241-247.
[4] Woo S Y, Lee K S, Shin H L, et al. Two new secondary metabolites isolated from Avena sativa L.(Oat) seedlings and their effects on osteoblast differentiation[J]. Bioorganic & Medicinal Chemistry Letters, 2020, 30(14): 127250.

Isovitexin 2''-O-arabinoside是来自Avena sativa L.的C-糖基黄酮,具有植物毒性活性[1]。Isovitexin 2''-O-arabinoside能够有效减少细胞内活性氧的积累,激活PI3K/NQO-1通路,从而增强抗氧化反应[2]。Isovitexin 2''-O-arabinoside被广泛用作内参,以优化色谱纯化条件和核磁共振参数,从而高效纯化和鉴定相关化合物[3]

在体外,10μM的Isovitexin 2''-O-arabinoside处理BMP-2刺激的C2C12细胞3天,显著增强了碱性磷酸酶(ALP)活性并促进了细胞分化[4]

实验参考方法

Cell experiment [1]:

Cell lines

C2C12 cells

Preparation Method

C2C12 cells were incubated in alpha minimum essential medium (α‐MEM) that contained 10% FBS, 100U/ml penicillin, and 100μg/ml streptomycin in a humidified incubator at 37°C and 5% CO2. For differentiation into osteoblasts, the C2C12 cells were seeded and allowed to attach and grow for one day. After differentiating for three days by BMP-2 (100ng/ml) in the presence of Isovitexin 2''-O-arabinoside (0.3, 1, 3, and 10μM), the cells were washed twice with PBS, fixed with 10% formalin in PBS for 5 min, and rinsed with deionized water. The ALP staining and activity assays were conducted.

Reaction Conditions

0.3, 1, 3, and 10μM; 72h

Applications

Isovitexin 2''-O-arabinoside treatment significantly enhanced ALP activity in C2C12 cells in a concentration-dependent manner.

化学性质

Cas No. 53382-71-1 SDF
别名 异牡荆素-2''-O-阿拉伯糖苷
Canonical SMILES O=C1C=C(C2=CC=C(O)C=C2)OC3=CC(O)=C([C@H]4[C@@H]([C@H]([C@@H]([C@@H](CO)O4)O)O)O[C@H]5[C@@H]([C@H]([C@H](CO5)O)O)O)C(O)=C13
分子式 C26H28O14 分子量 564.49
溶解度 DMSO : 100 mg/mL (177.15 mM; Need ultrasonic) 储存条件 Store at 2-8°C,protect from light
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1 mg 5 mg 10 mg
1 mM 1.7715 mL 8.8576 mL 17.7151 mL
5 mM 354.3 μL 1.7715 mL 3.543 mL
10 mM 177.2 μL 885.8 μL 1.7715 mL
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