Brassicasterol (Synonyms: 油菜甾醇)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Brassicasterol  (Synonyms: 油菜甾醇) 纯度: 98.71%

Brassicasterol 是 Ergosterol 的一种代谢物,具有心血管保护作用。Brassicasterol 通过双重靶向 AKT 和雄激素受体信号通路在前列腺癌中发挥抗癌作用。Brassicasterol 对 HSV-1 (IC50=1.2 μM) 和结核分枝杆菌具有抑制作用。Brassicasterol 还可以抑制固醇 δ 24 -还原酶 (δ 24-reductase),减缓动脉粥样硬化的进展。Brassicasterol 还是阿兹海默症的脑脊液生物标志物。

Brassicasterol                                          (Synonyms: 油菜甾醇)

Brassicasterol Chemical Structure

CAS No. : 474-67-9

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生物活性

Brassicasterol is a metabolite of Ergosterol and has cardiovascular protective effects. Brassicasterol exerts anticancer effects in prostate cancer through dual targeting of AKT and androgen receptor signaling pathways. Brassicasterol inhibits HSV-1 (IC50=1.2 μM) and Mycobacterium tuberculosis. Brassicasterol also inhibits sterol δ 24-reductase, slowing the progression of atherosclerosis. Brassicasterol is also a cerebrospinal fluid biomarker for Alzheimer’s disease[1][2][3][4][5][6].

IC50 & Target[2]

HSV-1

1.2 μM (IC50)

体外研究
(In Vitro)

Brassicasterol (10 μM; 24 h) 下调二氢睾酮 (DHT) 诱导的 LNCaP 细胞中雄激素受体 (AR) 和前列腺特异性抗原 (PSA) 的表达[4]
Brassicasterol (50 μM; 48 h) 将 LNCaP 的细胞周期阻滞在亚 G1 期,并诱导细胞凋亡[4]
Brassicasterol (10 μM; 48 h) 还抑制 LNCaP 细胞迁移[4]
Brassicasterol (100 μg/mL; 48 h) 在 3D 类器官模型中,能够抑制 AKT,并对 AR 不依赖的癌症以及 AR 依赖的细胞其抑制效力[4]

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Brassicasterol 相关抗体:

Cell Migration Assay [4]

Cell Line: LNCaP cells
Concentration: 0, 10, and 50 μM
Incubation Time: 5 days
Result: Showed 54% cell migration inhibitory effect.

分子量

398.66

Formula

C28H46O

CAS 号

474-67-9

性状

固体

颜色

White to light yellow

中文名称

油菜甾醇; 芜莆甾醇; 菜籽甾醇

结构分类
  • Steroids
初始来源
  • 动物

Hippocampus abdominalis

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性数据
In Vitro: 

Ethanol 中的溶解度 : 4.76 mg/mL (11.94 mM; 超声助溶)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.5084 mL 12.5420 mL 25.0840 mL
5 mM 0.5017 mL 2.5084 mL 5.0168 mL
10 mM 0.2508 mL 1.2542 mL 2.5084 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 (protect from light)。-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。

  • 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

In Vivo:

请根据您的 实验动物和给药方式 选择适当的溶解方案。

以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用
以下溶剂前显示的百分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 方案 一

    请依序添加每种溶剂: 10% EtOH    90% Corn Oil

    Solubility: ≥ 0.5 mg/mL (1.25 mM); 澄清溶液

    此方案可获得 ≥ 0.5 mg/mL(饱和度未知)的澄清溶液,此方案实验周期在半个月以上的动物实验酌情使用。

    1 mL 工作液为例,取 100 μL 5.0 mg/mL 的澄清 EtOH 储备液加到 900 μL 玉米油中,混合均匀。

扫码获得
动物溶解方案

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

纯度 & 产品资料

纯度: 98.71%

Data Sheet (630 KB) SDS (252 KB)

COA (194 KB) HNMR (291 KB) CNMR (334 KB) RP-HPLC (134 KB)

产品使用指南 (1538 KB)

参考文献
  • [1]. Yasuharu Yazawa, et al. Inhibitory effect of ergosterol on bladder carcinogenesis is due to androgen signaling inhibition by brassicasterol, a metabolite of ergosterol. J Nat Med. 2020 Sep;74(4):680-688.  [Content Brief]

    [2]. Sherif T S Hassan. Brassicasterol with Dual Anti-Infective Properties against HSV-1 and Mycobacterium tuberculosis, and Cardiovascular Protective Effect: Nonclinical In Vitro and In Silico Assessments. Biomedicines. 2020 May 24;8(5):132.  [Content Brief]

    [3]. Yinzhu Xu, et al. Brassicasterol from Edible Aquacultural Hippocampus abdominalis Exerts an Anti-Cancer Effect by Dual-Targeting AKT and AR Signaling in Prostate Cancer. Biomedicines. 2020 Sep 22;8(9):370.  [Content Brief]

    [4]. Vanmierlo T, et al. The plant sterol brassicasterol as additional CSF biomarker in Alzheimer’s disease. Acta Psychiatr Scand. 2011 Sep;124(3):184-92.  [Content Brief]

    [5]. Fernández C, et al. Inhibition of cholesterol biosynthesis by Delta22-unsaturated phytosterols via competitive inhibition of sterol Delta24-reductase in mammalian cells. Biochem J. 2002 Aug 15;366(Pt 1):109-19.  [Content Brief]

    [6]. Tansley G, et al. Sterol lipid metabolism in down syndrome revisited: down syndrome is associated with a selective reduction in serum brassicasterol levels. Curr Gerontol Geriatr Res. 2012;2012:179318.  [Content Brief]

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