Home>>Signaling Pathways>> Apoptosis>> Other Apoptosis>>Resveratrol

Resveratrol Sale

(Synonyms: 白藜芦醇; trans-Resveratrol; SRT501) 目录号 : GC14553

白藜芦醇(转-白藜芦醇;SRT501)是一种植物抗菌素。

Resveratrol Chemical Structure

Cas No.:501-36-0

规格 价格 库存 购买数量
10mM (in 1mL DMSO)
¥389.00
现货
200mg
¥347.00
现货
500mg
¥546.00
现货

电话:400-920-5774 Email: sales@glpbio.cn

Customer Reviews

Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.

101

客户使用产品发表文献 2

Description

Resveratrol (trans-Resveratrol; SRT501) is a phytoalexin. Resveratrol is a potent reducing agent, and can prevent carcinogenesis due to its anti-oxidant abilities [1]. Resveratrol has a broad range of targets, including cyclooxygenase (e.g., COX, IC50=1.1 μM), lipoxygenase (LOC, IC50=2.7 μM), STAT3 (IC50=20 μM), and other proteins [2,3].

Resveratrol treatment is found to exert its effect on renal cell carcinoma (RCC) proliferation, migration and invasion in a concentration dependent manner through inactivation of the Akt and ERK1/2 signaling pathways [4]. In CaCo-2 cells, treatment with 25 μM Resveratrol has shown 70% growth inhibition due to S/G2 phase arrest [5]. Resveratrol treatment lead to inhibited invasion and metastasis of colorectal cancer-derived cell lines LoVo and HCT116 by suppressing the Wnt/β-catenin signaling mediated target genes of c-Myc, MMP-7, and MALT-1[6].

Resveratrol is shown to be effective against breast cancer metastasis to lungs in mice by its inhibitory effect on Stat3 mediated signaling [7]. Resveratrol treatment reduced size and number of tumor spheres in renal carcinoma stem cells xenograft mice model [8]. Resveratrol treatment reduced Epithelial to mesenchymal transition (EMT) of glioblastoma U87 xenografted mice models [9]

References:
[1]. Bhaskara V K, Mittal B, Mysorekar V V, et al. Resveratrol, cancer and cancer stem cells: A review on past to future[J]. Current Research in Food Science, 2020, 3: 284-295.
[2]. Calamini B, Ratia K, Malkowski M G, et al. Pleiotropic mechanisms facilitated by resveratrol and its metabolites[J]. Biochemical Journal, 2010, 429(2): 273-282.
[3]. Pirola L, Fr?jd? S. Resveratrol: one molecule, many targets[J]. IUBMB life, 2008, 60(5): 323-332.
[4]. Zhao Y, Tang H, Zeng X, et al. Resveratrol inhibits proliferation, migration and invasion via Akt and ERK1/2 signaling pathways in renal cell carcinoma cells[J]. Biomedicine & Pharmacotherapy, 2018, 98: 36-44.
[5]. Schneider Y, Vincent F, Duranton B, et al. Anti-proliferative effect of resveratrol, a natural component of grapes and wine, on human colonic cancer cells[J]. Cancer letters, 2000, 158(1): 85-91.
[6]. Ji Q, Liu X, Fu X, et al. Resveratrol inhibits invasion and metastasis of colorectal cancer cells via MALAT1 mediated Wnt/β-catenin signal pathway[J]. PloS one, 2013, 8(11): e78700.
[7]. Lee-Chang C, Bodogai M, Martin-Montalvo A, et al. Inhibition of breast cancer metastasis by resveratrol-mediated inactivation of tumor-evoked regulatory B cells[J]. The Journal of Immunology, 2013, 191(8): 4141-4151.
[8]. Ji Q, Liu X, Fu X, et al. Resveratrol inhibits invasion and metastasis of colorectal cancer cells via MALAT1 mediated Wnt/β-catenin signal pathway[J]. PloS one, 2013, 8(11): e78700.
[9]. Song Y, Chen Y, Li Y, et al. Resveratrol suppresses epithelial-mesenchymal transition in GBM by regulating Smad-dependent signaling[J]. BioMed Research International, 2019, 2019.

白藜芦醇(转-白藜芦醇;SRT501)是一种植物抗菌素。它具有强大的还原剂作用,可以通过其抗氧化能力预防致癌物质的形成[1]。 白藜芦醇具有广泛的靶点,包括环氧合酶(例如COX,IC50 = 1.1μM),脂肪氧合酶(LOC,IC50 = 2.7μM),STAT3(IC50 = 20μM)和其他蛋白质[2,3]。

翻译:研究发现,白藜芦醇治疗可以通过抑制Akt和ERK1/2信号通路的活性,在浓度依赖性下对肾细胞癌(RCC)增殖、迁移和侵袭产生影响。在CaCo-2细胞中,使用25μM的白藜芦醇处理可导致70%的生长抑制,原因是S/G2期阻滞。同时,白藜芦醇治疗还能通过抑制Wnt/β-catenin信号介导的靶基因c-Myc、MMP-7和MALT-1来抑制结直肠癌衍生细胞系LoVo和HCT116的侵袭和转移。

翻译:据显示,白藜芦醇通过抑制Stat3介导的信号传递,在小鼠乳腺癌转移至肺部方面具有一定的效果。在肾癌干细胞异种移植小鼠模型中,白藜芦醇治疗减少了肿瘤球的大小和数量。在人类胶质母细胞瘤U87异种移植小鼠模型中,白藜芦醇治疗减少了上皮向间充质转化(EMT)。

实验参考方法

Cell experiment [1]:

Cell lines

ALVA-41, PC-3, and BPH-1 cells

Preparation Method

For cell viability studies, ALVA-41, PC-3, and BPH-1 cells were treated for 24 h with 10 µmol/L and 100 µmol/L concentrations of resveratrol or EGCG.

Reaction Conditions

10, 100 µM for 24 hours

Applications

Resveratrol at low doses (10 µmol/L) induced a proliferative response in ALVA-41 and BPH-1 cells at 24 h, which was not evident in PC-3 cells. However, at a higher dose (100 µmol/L), resveratrol produced a significant toxicity in prostate cancer cells, although the effect on ALVA-41 cells was relatively greater than on PC-3 cells.

Animal experiment [2]:

Animal models

CB17SC mice model injected with LAPC-4 cells

Preparation Method

In the primary LAPC-4 study, mice were fed no resveratrol (control), 50 mg/kg/day resveratrol (RV50), or 100 mg/kg/day resveratrol (RV100).

Dosage form

Fed in diet, 50 mg/kg/day and 100 mg/kg/day

Applications

In the LAPC-4 study, RV50 significantly decreased survival while RV100 did not significantly change survival.

References:

[1]: Ahmad K A, Harris N H, Johnson A D, et al. Protein kinase CK2 modulates apoptosis induced by resveratrol and epigallocatechin-3-gallate in prostate cancer cells[J]. Molecular cancer therapeutics, 2007, 6(3): 1006-1012.
[2]: Klink J C, Tewari A K, Masko E M, et al. Resveratrol worsens survival in SCID mice with prostate cancer xenografts in a cell©\line specific manner, through paradoxical effects on oncogenic pathways[J]. The Prostate, 2013, 73(7): 754-762.

化学性质

Cas No. 501-36-0 SDF
别名 白藜芦醇; trans-Resveratrol; SRT501
化学名 5-[(E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol
Canonical SMILES C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O
分子式 C14H12O3 分子量 228.24
溶解度 ≥ 100mg/mL in DMSO;≥ 50mg/mL in EtOH 储存条件 Store at -20°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℃,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。

溶解性数据

制备储备液
1 mg 5 mg 10 mg
1 mM 4.3814 mL 21.9068 mL 43.8135 mL
5 mM 0.8763 mL 4.3814 mL 8.7627 mL
10 mM 0.4381 mL 2.1907 mL 4.3814 mL
  • 摩尔浓度计算器

  • 稀释计算器

  • 分子量计算器

质量
=
浓度
x
体积
x
分子量
 
 
 
*在配置溶液时,请务必参考产品标签上、MSDS / COA(可在Glpbio的产品页面获得)批次特异的分子量使用本工具。

计算

动物体内配方计算器 (澄清溶液)

第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
给药剂量 mg/kg 动物平均体重 g 每只动物给药体积 ul 动物数量
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方)
% DMSO % % Tween 80 % saline
计算重置

产品文档

Quality Control & SDS

View current batch: