白藜芦醇, COX-2 抑制剂;TAS2R14 激动剂;过氧化物酶体增殖激活受体-γ 拮抗剂

CAS: 501-36-0 货号: R408711 分子式: C14H12O3 分子量: 228.24 EC号: 610-504-8
有货
级别和纯度: Moligand™ ? Moligand™ —— 阿拉丁的配体和生物活性小分子系列。适用于需要明确小分子工具的受体、通路和结合研究。 10mM in DMSO
储存条件
-80℃储存
运输条件
特低温运输
★
规格
库存
价格
数量
1ml
R408711-1ml
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¥359.90
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为什么选择此级别

Moligand™ 级 ,适用于对基线干扰要求严格的色谱和分析工作流程。

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-80℃储存。特低温运输 。请查阅批次 COA 获取详细规格。

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文献证明

在色谱分析、有机合成和交叉偶联反应领域已被 281 篇同行评审文献引用。

概述

无味,完全溶解于乙醇。 COX−1选择性抑制剂。 白藜芦醇是一种酚类植物抗毒素,发现于葡萄皮和其他植物中。它具有细胞内抗氧化活性激活去乙酰化酶SIRT1。白藜芦醇的抗糖尿病、神经保护和抗脂特性都可能是去乙酰化酶SIRT1激活所致。

Information

Resveratrol (SRT501, trans-Resveratrol) has a wide spectrum of targets including cyclooxygenases(i.e.COX, IC50=1.1 μM), lipooxygenases(LOX, IC50=2.7 μM), kinases, sirtuins and other proteins. It has anti-cancer, anti-inflammatory, blood-sugar-lowering and
In vitro

Resveratrol inhibits the activity of Cyclooxygenase and lipooxygenase, PKCs and p56lck, ERK1, JNK1, p38, IKK β, Src, STAT3, Ribonucleotide Reductase, DNA polymerases α and δ, PKD, PKC α, Quinone reductase 2, and Aromatase with IC50 of from 0.035-60 μM. Resveratrol is also an activator of Adenylyl cyclase and AMPK with EC50 of 0.8 μM and 50 μM, respectively. The roles of Resveratrol as inhibitor or activator enable its effects on decreasing cell inflammatory associated behaviors, growth inhibition and induction of apoptosis in cancer cells, reversal of endothelin-1 stimulated cell responses, inhibition of phorbol ester-induced expression of COX-2, inhibition of DNA synthesis in cell, resistance to menadione-induced cell death, and improvement of cell mitochondrial function and glucose/lipid metabolism. Resveratrol is also an activator of sirtuins. Resveratrol lowers the Michaelis constant of SIRT1 for both the acetylated substrate and NAD+, and increases cell survival by stimulating SIRT1-dependent deacetylation of p53. In yeast, Resveratrol mimics calorie restriction by stimulating Sir2, increasing DNA stability and extending lifespan. Resveratrol is effective at protecting isolated rat hearts against ischemia/reperfusion injury via its antioxidant activity, with improved recovery of developed pressure and aortic flow, reduction of malondialdehyde concentrations and reduction of infarct size.

In vivo

Resveratrol improves health and survival of mice on a high-calorie diet. Resveratrol (22.4 mg/kg/day) shifts the physiology of middle-aged mice on a high-calorie diet towards that of mice on a standard diet and significantly increases their survival. Resveratrol produces changes associated with longer lifespan, including increased insulin sensitivity, reduced insulin-like growth factor-1 (IGF-I) levels, increased AMP-activated protein kinase (AMPK) and peroxisome proliferator-activated receptor-γcoactivator 1α(PGC-1α) activity, increased mitochondrial number, and improved motor function. Resveratrol opposed the effects of the high-calorie diet in 144 out of 153 significantly altered pathways. Resveratrol has been shown to inhibit the initiation and growth of tumors in a wide variety of rodent cancer models. Dose of Resveratrol as low as 200 μg/kg daily already shows efficacy in a rat model of colon carcinogenesis. At higher dose of 40 mg/kg, Resveratrol increases the survival of mice with subcutaneous neuroblastomas from 0% to 70%. Resveratrol inhibits vascularization in the corneal micropocket assay in mice at a dose of only 48 μg/kg when administered daily. Resveratrol shows beneficial effects on heart disease. Resveratrol blocks the increase in platelet aggregation induced by a hypercholesterolaemic diet. Resveratrol increase expression of both endothelial and inducible nitric oxide synthase. In stroke-prone, spontaneously hypertensive rats, resveratrol significantly reduces markers of oxidative stress such as glycated albumin in serum, and 8-hydroxyguanos-ine in urine. Providing Resveratrol in drinking water for 15 days (1 mg/kg) is sufficient to improve the recovery in function and coronary flow of isolated hearts. Resveratrol displays anti-inflammatory activity in vivo. Resveratrol significantly reduces both acute and chronic chemically induced oedema, lipopolysaccharide-induced airway inflammation and osteoarthritis, and helps to prevent allograft rejection. Intravenously administered Resveratrol decreases inflammation induced by ischaemia/reperfusion, oxidants generated by hypoxanthine/xanthine oxidase (HX/XO) or platelet-activating factor, but not leukotriene B4 in rats. Resveratrol shows beneficial effects on stroke and brain damage. Resveratrol administered intravenously significantly decreased ischaemic volume and brain water content at the extremely low doses of 100 ng/kg and 1 μg/kg after middle cerebral artery occlusion in rats.
Cell Data

cell lines:

Concentrations:30-300 μM

Incubation Time:2 days

Powder Purity:≥99%

规格

英文别名
trans-Resveratrol | (E)-5-(4-hydroxystyryl)benzene-1,3-diol
规格或纯度
Moligand™, 10mM in DMSO
英文名称
Resveratrol (SRT501)
生化机理
白藜芦醇(SRT501,反式白藜芦醇)具有广泛的靶标,包括环氧化酶(即 COX,IC50=1.1 μM)、脂氧化酶(LOX,IC50=2.7 μM)、激酶、sirtuins 和其他蛋白质。它具有抗癌、抗炎、降血糖和其他有益心血管的作用。白藜芦醇能诱导有丝分裂/自噬和依赖自噬的细胞凋亡。
储存条件
-80℃储存
运输条件
特低温运输
作用类型
抑制剂
作用机制
COX-2 抑制剂;TAS2R14 激动剂;过氧化物酶体增殖激活受体-γ 拮抗剂
名称和识别符
EC号
610-504-8
分子类型
小分子
Isomeric SMILES
C1=CC(=CC=C1/C=C/C2=CC(=CC(=C2)O)O)O
关联CAS
NSC Number
327430
MeSH Entry Terms
3,4',5-stilbenetriol;3,4',5-Trihydroxystilbene;3,5,4'-trihydroxystilbene;cis Resveratrol;cis-resveratrol;resveratrol;Resveratrol 3 sulfate;Resveratrol, (Z)-;resveratrol-3-sulfate;SRT 501;SRT-501;SRT501;trans Resveratrol;trans Resveratrol 3 O sulfate;trans
分子量
228.24
Reaxy-Rn
1912433
Reaxys-RN link address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1912433&ln=

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高级数据

关联靶点(人)
CYP1B1 Tchem 细胞色素 P450 1B1(Cytochrome P450 1B1) (2 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
CYP3A4 Tclin 细胞色素P450 3A4(Cytochrome P450 3A4) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
DPP4 Tclin 二肽基肽酶4(Dipeptidyl peptidase 4) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
TRPA1 Tclin 瞬时受体电位阳离子通道亚家族A成员1(Transient receptor potential cation channel subfamily A member 1) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
TTR Tclin 转甲状腺素蛋白(Transthyretin) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
PTGS1 Tclin 前列腺素 G/H 合酶 1(Prostaglandin G/H synthase 1) (2 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
PTGS2 Tclin 前列腺素 G/H 合酶 2(Prostaglandin G/H synthase 2) (5 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
CA12 Tclin 碳酸酐酶12(Carbonic anhydrase 12) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
CA14 Tclin 碳酸酐酶14(Carbonic anhydrase 14) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
CA9 Tclin 碳酸酐酶9(Carbonic anhydrase 9) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
MAOA Tclin 胺氧化酶[含黄素]A(Amine oxidase [flavin-containing] A) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
NQO2 Tchem 核糖二氢烟酰胺脱氢酶[醌](Ribosyldihydronicotinamide dehydrogenase [quinone]) (9 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
PPARG Tclin 过氧化物酶体增殖激活受体γ(Peroxisome proliferator-activated receptor gamma) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
化学和物理性质
溶解性
Solubility (25°C) In vitro DMSO: 38 mg/mL (197.74 mM);    
熔点
267 °C
安全和危险性(GHS)
象形图
信号词
警告
危险声明

H319: 引起严重眼睛刺激

预防措施声明

P264: 处理后要彻底洗手。

P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。

P405: 密闭存放

P501: 将内容物/容器处理到。。。

WGK Germany
3
RTECS
CZ8987000
Merck Index
8158
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dust mask type N95 (US),Eyeshields,Faceshields,Gloves
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批号(Lot Number) 证书类型 货号
F2417016 分析证书 R408711
技术文档和文章
RNA病毒触发信号通路
RNA Viruses Triggered Signal Pathway
白藜芦醇
Resveratrol
白黎芦醇
Resveratrol
NF-κB 通路怎么定位、抑制剂怎么选:把炎症转录输出压到“可控区间”(附表A–F)
How to Map the NF-κB Pathway and Choose Inhibitors: Bringing Inflammatory Transcriptional Output into a “Controllable Range” (Tables A–F)
皮肤细胞抗氧化酶网络及其在护肤与化妆品中的应用
Antioxidant Enzyme Networks in Skin Cells and Their Applications in Skincare and Cosmetics
乙酰基代谢酶网络与体外酶学分析
Acetyl-Group Metabolic Enzyme Network and In Vitro Enzymology Analysis
表观遗传酶的非经典功能与线粒体代谢调控
Noncanonical Functions of Epigenetic Enzymes and Regulation of Mitochondrial Metabolism
三维染色质结构重塑与生理性衰老机制
Three-Dimensional Chromatin Architecture Remodeling and Mechanisms of Physiological Aging
氧化应激相关研究进展汇总
Summary of Research Advances in Oxidative Stress
谷胱甘肽外用护肤机制解析:细胞氧化还原调节、皮肤递送难点与 SLNs 递送策略
Mechanistic Analysis of Topical Glutathione in Skincare: Cellular Redox Regulation, Skin Delivery Challenges, and SLN-Based Delivery Strategies
DNA 序列不变,基因表达为何改变?表观遗传调控的核心机制与研究方法
If the DNA Sequence Remains Unchanged, Why Does Gene Expression Change? Core Mechanisms and Research Methods of Epigenetic Regulation
α-硫辛酸的皮肤抗老机制:ALA/DHLA 氧化还原循环、抗氧化网络与胶原 AGEs 形成调控
The Skin Anti-Aging Mechanisms of α-Lipoic Acid: ALA/DHLA Redox Cycling, the Antioxidant Network, and Regulation of Collagen AGE Formation
维生素E家族中的生育酚:如何阻断皮肤脂质过氧化的链式反应
Tocopherols in the Vitamin E Family: How They Block the Chain Reaction of Lipid Peroxidation in Skin Lipids
4-MSK 的双靶向美白机制:抑制黑色素生成与减少表皮色素滞留
The Dual-Targeted Skin-Brightening Mechanism of 4-MSK: Inhibiting Melanin Production and Reducing Epidermal Pigment Retention
白藜芦醇在护肤研究中的抗氧化机制、稳定性与递送策略
Antioxidant Mechanisms, Stability, and Delivery Strategies of Resveratrol in Skincare Research
阿魏酸在护肤中的抗氧化机制、维生素C/E协同与稳定递送应用
Antioxidant Mechanisms of Ferulic Acid in Skincare, Vitamin C/E Synergy, and Stable Delivery Applications
苯乙基间苯二酚(377)的结构特征、黑色素生成调控机制及相关配方研究应用
Phenylethyl Resorcinol (377): Structural Characteristics, Melanogenesis-Regulating Mechanisms, and Related Applications in Formulation Research
传明酸在色斑护理中的作用机制:从纤溶酶系统到炎症促黑信号调节
Mechanism of Action of Tranexamic Acid in Pigmentation Care: From the Plasmin System to Regulation of Inflammation-Driven Pro-Melanogenic Signaling
衰老细胞清除剂的作用机制、代表性化合物与研究应用
Mechanisms of Action, Representative Compounds, and Research Applications of Senolytics
天然产物抗糖尿病作用机制、代表性活性成分与研究应用
Antidiabetic Mechanisms, Representative Bioactive Compounds, and Research Applications of Natural Products
衰老相关营养感知、炎症与稳态信号通路的调控机制
Regulatory Mechanisms of Aging-Related Nutrient Sensing, Inflammation, and Homeostatic Signaling Pathways
天然产物调控脂肪褐变的分子机制
Molecular Mechanisms by Which Natural Products Regulate Adipose Browning
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请于?80 °C条件下保存。需超低温保存以维持规定的有效期。
「Moligand?」是什么?
「Moligand?」是阿拉丁科学的高端产品线之一,专为多个工作流程中的高纯度应用而设计。与同类工作流程中的标准级别相比,「Moligand?」产品通常具有更严格的规格、更严谨的 QC 以及更强的批间一致性。
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本产品的 CAS 号为 501-36-0,分子式为 C14H12O3,分子量为 228.24 g/mol。
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