Vitexin3X 积分

目录号: GN10806纯度: >99.50%同义词: 牡荆素,Apigenin 8-C-glucoside; Vitexina; 4H-1-Benzopyran-4-one, 8-β-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-
Vitexin是许多传统中药的有效成分,在各种药用植物中都有发现。

Vitexin
Cas No.: 3681-93-4
规格价格库存数量操作
5mg¥420.00现货
1
10mg¥700.00现货
1
20mg¥1,260.00现货
1
10mM (in 1mL DMSO)¥400.00现货
1

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产品描述 Description

Vitexin is an active components of many traditional Chinese medicines, and were found in various medicinal plants. Vitexin (apigenin-8-C-glucoside) has recently received increased attention due to its wide range of pharmacological effects, including but not limited to anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects [1]. vitexin has recently received increased attention due to its wide range of pharmacological effects, including anti-cancer, anti-oxidant, anti-inflammatory, anti-nociceptive, anti-AD (AD, Alzheimer's disease), anti-hypertensive, anti-spasmodic, anti-hypoxia/ischemia injury, anti-depressant-like actions and anti-viral activities [1].

Vitexin (20 µM, 24h) significantly reduced the HIF-1α level in rat pheochromocytoma PC12 cells, not in human hepatocellular carcinoma HepG2 or in human osteosarcoma HOS cells under hypoxia [2]. Vitexin reduced the levels of VEGF (the major angiogenic factor) protein and mRNA in a dose-dependent manner [2]. 20 µM of vitexin inhibited PC12 cells invasion by approximately 66% [2]. Vitexin-induced (100 µM, 48h) apoptosis was p53 dependent in human oral cancer OC2 cells [3]. Vitexin (100 µM, 48h) induced the expression of ERK 1/2 in OC2 cells [3].

Vitexin (40 mg/kg i.g.) increased the brain weights of D-galactose-aged mice [4]. vitexin (10-40 mg/kg i.g.) increased the activity of the antioxidase system and levels of ATPase in the serum and tissue of D-galactose-aged mice [4]. Vitexin (0.3-10 mg/kg, i.p.) inhibits the mice writhing response induced by acetic acid and phenyl-p-benzoquinone (PBQ) [5]. Vitexin (1-10 mg/kg, i.p.) inhibits carrageenan-, capsaicin-, and CFA-Induced mechanical and thermal hyperalgesia [5]. Vitexin (10 mg/kg, ip, 30 min before the ipl injection of carrageenan) inhibits pro-inflammatory cytokine (TNF-α, IL-1β, IL-6, and IL-33) and enhances anti-inflammatory cytokine (IL-10) production induced by carrageenan [5].

References:
[1]. He M, Min J W, Kong W L, et al. A review on the pharmacological effects of vitexin and isovitexin[J]. Fitoterapia, 2016, 115: 74-85.
[2]. Choi H J, Eun J S, Kim B G, et al. Vitexin, an HIF-1α Inhibitor, Has Anti-metastatic Potential in PC12 Cells[J]. Molecules & Cells (Springer Science & Business Media BV), 2006, 22(3).
[3]. Yang S H, Liao P H, Pan Y F, et al. The novel p53‐dependent metastatic and apoptotic pathway induced by vitexin in human oral cancer OC2 cells[J]. Phytotherapy Research, 2013, 27(8): 1154-1161.
[4]. Dong L Y, Li S, Zhen Y L, et al. Cardioprotection of vitexin on myocardial ischemia/reperfusion injury in rat via regulating inflammatory cytokines and MAPK pathway[J]. The American Journal of Chinese Medicine, 2013, 41(06): 1251-1266.
[5]. Borghi S M, Carvalho T T, Staurengo-Ferrari L, et al. Vitexin inhibits inflammatory pain in mice by targeting TRPV1, oxidative stress, and cytokines[J]. Journal of Natural Products, 2013, 76(6): 1141-1149.

实验参考方法 Experimental Reference Method

Cell experiment [1]:

Cell lines

Human oral cancer cell line (OC2)

Preparation Method

A total of 1000 cells were seeded in a 96-well plate for 24 h before treatment with vitexin (0, 12.5, 25, 50, 100 µM). At the end of incubation, add alamarBlue reagent in an amount equal to 10% of the volume in the well. Cultures were incubated for 4 h, and then cytotoxicty was measured by using spectrophotometry at 570 and 600 nm.

Reaction Conditions

0, 12.5, 25, 50, 100 µM for for 48 h.

Applications

Increasing concentration of vitexin drastic decreased cell viability of OC2 cells.

Animal experiment [2]:

Animal models

male adult Sprague-Dawley (SD) rats

Preparation Method

rats were randomly divided into the following six groups with 16 rats in each group: (1) sham group, sham-operated without occludes the artery, (2) I/R group, I/R alone with normal saline (NS) treatment, (3) I/R + puerarin group, puerarin was administered intravenously at a dose of 30 mg/kg, beginning at coronary ischemia and again at reperfusion, (4) I/R + vitexin 6 mg/kg group, vitexin was administered intravenously at a dose of 6 mg/kg, beginning at coronary ischemia and again at reperfusion, (5) I/R + vitexin 3 mg/kg group, vitexin was administered intravenously at a dose of 3 mg/kg, beginning at coronary ischemia and again at reperfusion, (6) I/R + vitexin 1.5 mg/kg group, vitexin was administered intravenously at a dose of 1.5 mg/kg, beginning at coronary ischemia and again at reperfusion.

Dosage form

Intravenous injection, 1.5, 3, 6 mg/kg

Applications

The elevation of the ST segment was significantly enhanced in I/R group 30 min after ischemia, 30 and 60 min after reperfusion compared with sham group. Vitexin 6 mg/kg and puerarin have a significant inhibiting effect against the elevation of the ST segment 30 and 60 min after reperfusion compared with I/R group.

References:

[1]: Yang S H, Liao P H, Pan Y F, et al. The novel p53‐dependent metastatic and apoptotic pathway induced by vitexin in human oral cancer OC2 cells[J]. Phytotherapy Research, 2013, 27(8): 1154-1161.
[2]: Dong L Y, Li S, Zhen Y L, et al. Cardioprotection of vitexin on myocardial ischemia/reperfusion injury in rat via regulating inflammatory cytokines and MAPK pathway[J]. The American Journal of Chinese Medicine, 2013, 41(06): 1251-1266.

产品文档 Product Documents

Purity:>99.50%

化学性质Chemical Properties

CAS 号
3681-93-4
同义词
牡荆素,Apigenin 8-C-glucoside; Vitexina; 4H-1-Benzopyran-4-one, 8-β-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-
化学名
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
SMILES
C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O
分子式
C21H20O10
分子量
432.38 g/mol
溶解性
DMSO:47 mg/mL (108.7 mM)
保存条件
Store at 4°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol