1. MAPK/ERK Pathway Epigenetics PI3K/Akt/mTOR Anti-infection Immunology/Inflammation Cell Cycle/DNA Damage Vitamin D Related/Nuclear Receptor Metabolic Enzyme/Protease Apoptosis NF-κB
  2. p38 MAPK AMPK Bacterial Fungal Interleukin Related PPAR CDK PI3K Akt mTOR Apoptosis Reactive Oxygen Species (ROS)
  3. Sinigrin hydrate

Sinigrin hydrate  (Synonyms: 黑芥子硫苷酸钾一水; Allyl-glucosinolate hydrate; 2-Propenyl-glucosinolate hydrate)

目录号: HY-N2423 纯度: 99.77%
COA 产品使用指南 技术支持

Sinigrin (Allyl-glucosinolate) hydrate 是一种口服有效的存在于十字花科植物中的硫代葡萄糖苷。Sinigrin hydrate 具有抗癌、抗菌、抗真菌、抗炎抗氧化和抑制脂肪合成等多种活性。Sinigrin hydrate 可用于肿瘤、炎症性和代谢性等疾病的研究。

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Sinigrin hydrate

Sinigrin hydrate Chemical Structure

CAS No. : 64550-88-5

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Other Forms of Sinigrin hydrate:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Sinigrin (Allyl-glucosinolate) hydrate is an orally active glucosinolate found in cruciferous plants. Sinigrin hydrate possesses multiple activities such as anti-cancer, antibacterial, antifungal, anti-inflammatory, antioxidant, and inhibition of fat synthesis. Sinigrin hydrate can be used in the research of tumors, inflammatory, and metabolic diseases[1][2][3][4].

IC50 & Target[1][2]

PPARγ

 

IL-6

 

IL-1β

 

CDK4

 

CDK6

 

体外研究
(In Vitro)

Sinigrin (1-100 μg/mL; 1-8 days) hydrate 在 3T3-L1 细胞中可抑制脂质积累,下调脂肪生成相关基因的表达,抑制促炎细胞因子 (TNF-α、IL-6、IL-1β、IL-18) 的产生,并诱导细胞周期阻滞。机制涉及对 AMPK 通路的激活和 MAPK 通路的抑制[1]
Sinigrin (5-30 μM; 24-48 h) hydrate 在 MCF-7 细胞中通过抑制 PI3K/AKT/mTOR 磷酸化,诱导细胞周期阻滞于 S 期并促进凋亡,同时引发 ROS 依赖性氧化应激损伤[2]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cycle Analysis[1]

Cell Line: 3T3-L1 adipocytes
Concentration: 100 μg/mL
Incubation Time: 24 h
Result: Arrested cells in the G0/G1phase of the cell cycle and increased the expression of p21 and p27.

Western Blot Analysis[1]

Cell Line: 3T3-L1 adipocytes
Concentration: 1, 10, and 100 μg/mL
Incubation Time: 8 days
Result: Remarkably inhibited the accumulation of lipid droplets and adipogenesis by downregulating the expression of CCAAT-enhancer-binding protein α (C/EBPα), PPARγ, leptin and aP2.

RT-PCR[1]

Cell Line: 3T3-L1 adipocytes
Concentration: 100 μg/mL
Incubation Time: 24 h
Result: Inhibited the production of pro-inflammatory cytokines including TNF-α and IL-6, IL-1β and IL-18.

Western Blot Analysis[2]

Cell Line: MCF-7 cells
Concentration: 20 μM
Incubation Time: 24 and 48 h
Result: Inhibited the levels of cyclin-D1, PCNA, CDK4, and CDK6.
体内研究
(In Vivo)

Sinigrin (15-30 mg/kg; 口服; 12 天) hydrate 在 DSS (HY-116282C) 诱导的溃疡性结肠炎小鼠模型中具有抗炎和改善作用[3]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male BALB/c mice (20-25 gm) treated DSS (HY-116282C)[3]
Dosage: 15 and 30 mg/kg
Administration: Oral administration; 12 days
Result: Significantly mitigated the DSS-induced body weight loss, attenuated the colon length shrinkage, and improved the disease index score.
Successfully abrogated the DSS-induced IL-17 levels and improved the colonic barrier in colon tissues.
分子量

415.48

Formula

C10H18KNO10S2

CAS 号
性状

固体

颜色

White to off-white

中文名称

黑芥子硫苷酸钾一水; 芥子甙单水合物

结构分类
初始来源
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
细胞实验: 

H2O 中的溶解度 : ≥ 50 mg/mL (120.34 mM)

* "≥" means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.4069 mL 12.0343 mL 24.0685 mL
5 mM 0.4814 mL 2.4069 mL 4.8137 mL
查看完整储备液配制表

* 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, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-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。

* 备注:如您选择水作为储备液,请稀释至工作液后,再用 0.22 μm 的滤膜过滤除菌后使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
该产品水溶性佳,请具体参考实测 水 / PBS / Saline 中的溶解度数据。
您所需的储备液浓度超过该产品的实测溶解度,如有需要,请与 MCE 中国技术支持联系。
纯度 & 产品资料
参考文献

完整储备液配制表

* 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, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-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。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
H2O 1 mM 2.4069 mL 12.0343 mL 24.0685 mL 60.1714 mL
5 mM 0.4814 mL 2.4069 mL 4.8137 mL 12.0343 mL
10 mM 0.2407 mL 1.2034 mL 2.4069 mL 6.0171 mL
15 mM 0.1605 mL 0.8023 mL 1.6046 mL 4.0114 mL
20 mM 0.1203 mL 0.6017 mL 1.2034 mL 3.0086 mL
25 mM 0.0963 mL 0.4814 mL 0.9627 mL 2.4069 mL
30 mM 0.0802 mL 0.4011 mL 0.8023 mL 2.0057 mL
40 mM 0.0602 mL 0.3009 mL 0.6017 mL 1.5043 mL
50 mM 0.0481 mL 0.2407 mL 0.4814 mL 1.2034 mL
60 mM 0.0401 mL 0.2006 mL 0.4011 mL 1.0029 mL
80 mM 0.0301 mL 0.1504 mL 0.3009 mL 0.7521 mL
100 mM 0.0241 mL 0.1203 mL 0.2407 mL 0.6017 mL

* 备注:如您选择水作为储备液,请稀释至工作液后,再用 0.22 μm 的滤膜过滤除菌后使用。

Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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HY-N2423
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