Beta-Sitosterol (purity>80%) (Synonyms:β-谷甾醇; β-Sitosterol ;22,23-Dihydrostigmasterol)
目录号 : KM15612 CAS No. : 83-46-5 纯度 : ≥80%

Beta-Sitosterol (purity>80%) 主要包括 β-谷甾醇 (≥80%)、豆甾醇、菜油甾醇和菜籽甾醇。Beta-Sitosterol 是一种植物甾醇。Beta-Sitosterol (purity>80%) 会干扰多种细胞信号通路,包括细胞周期,细胞凋亡,增殖,存活,侵袭,血管生成和炎症等。

规格 价格 是否有货 数量
100mg
In-stock
1g
In-stock
5g
In-stock
10g 询价 In-stock
50g 询价 In-stock

Other Forms of Rapamycin:

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生物活性

Beta-Sitosterol (purity>80%) includes β-sitosterol (≥80%), stigmasterol, campesterol and brassicasterol mainly. Beta-Sitosterol is a plant sterol. Beta-Sitosterol (purity>80%) interfere with multiple cell signaling pathways, including cell cycle, apoptosis, proliferation, survival, invasion, angiogenesis, metastasis and inflammation.

体外研究

Bioactivity-guided isolation afforded three compounds from the hexane fraction of E. indica, namely, Beta-Sitosterol (β-sitosterol), Stigmasterol, and Lutein. Both compounds are found to possess very low PPL inhibition activity, that is, 2.99±0.80% (Beta-Sitosterol) of inhibition at 100 μg/mL (242 μM) and 2.68±0.38% (Stigmasterol) of inhibition at 100 μg/mL (243 μM), respectively. Weak PPL inhibition activity of Beta-Sitosterol and Stigmasterol isolated from Alpinia zerumbet with IC50 value of 99.99±1.86 μg/mL and 125.05±4.76 μg/mL, respectively, in comparison with the inhibition shown by Curcumin (IC50=4.92±0.21 μg/mL) and Quercetin (IC50=18.60±0.86 μg/mL) which are used as positive controls in their study. Beta-Sitosterol and Stigmasterol are recorded with weak PPL inhibitory activity of only 3.0±0.8% and 2.7±0.4% at 100 μg/mL, respectively, (i.e., 242 μM and 243 μM) in contrast (34.5±5.4% at 100 μg/mL), which are comparatively lower than that recorded in literature (i.e., 50% PPL inhibition at 100 μg/mL). Sitosterol is an important compound extracted from the leaves of Aloe vera. It inhibits the growth of promastigotes of L. donovani, a causative agent for life threatening visceral leishmaniasis disease.

体内研究

Beta-Sitosterol (β-sitosterol) treatment significantly reduced the immobility time at three doses (10, 20, and 30 mg/kg) in the Forced Swim Test (FST) and Tail Suspension Test (TST), indicating an antidepressant effect. This effect is similar to the positive control fluoxetine (20 mg/kg) at a dose of 30 mg/kg, where the strongest effect is observed compared with the control group (P < 0.001). The same effects are observed for three doses of Beta-Sitosterol in the TST. The % DID values are as follows: FST: 39.27% (10 mg/kg), 51.23% (20 mg/kg), and 57.48% (30 mg/kg); TST: 31.63% (10 mg/kg), 43.95% (20 mg/kg), and 53.38% (30 mg/kg). These results indicate that Beta-Sitosterol has a significant antidepressant activity in mice during the FST and TST. Furthermore, Beta-Sitosterol exhibits the antidepressant effect in a dose-dependent manner.

分子式
C29H50O
分子量
414.71
CAS号
83-46-5
中文名称
β-谷甾醇 ;谷固醇 ;谷甾醇 ;麦固醇
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°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 : 5 mg/mL (12.06 mM; ultrasonic and warming and heat to 60°C)

DMSO : < 1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble or slightly soluble)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.4113 mL 12.0566 mL 24.1132 mL
5 mM 0.4823 mL 2.4113 mL 4.8226 mL
10 mM 0.2411 mL 1.2057 mL 2.4113 mL
*

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。

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

  • 1.

    请依序添加每种溶剂: corn oil

    Solubility: 10 mg/mL (24.11 mM); Clear solution; Need ultrasonic and warming and heat to 60°C

     

  • 2.

    请依序添加每种溶剂:15% Cremophor EL → 85% Saline

    Solubility: 5 mg/mL (12.06 mM); Suspended solution; Need ultrasonic and warming and heat to 60°C

     

  • 3.

    请依序添加每种溶剂: 10% EtOH →  40% PEG300 → 5% Tween-80 → 45% saline

    Solubility:≥ 1 mg/mL (2.41 mM); Suspended solution

    此⽅案可获得 ≥ 1 mg/mL (2.41 mM,饱和度未知) 的均匀悬浊液,悬浊液可⽤于⼝服和腹腔注射。

    以 1 mL ⼯作液为例,取 100 μL 10.0 mg/mL 的澄清 EtOH 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加⼊ 50 μL  Tween-80,混合均匀;然后继续加⼊ 450 μL ⽣理盐⽔定容⾄ 1 mL

     
  • 4.

    请依序添加每种溶剂:  10% EtOH  → 90% (20% SBE-β-CD in saline)

    Solubility: 1 mg/mL (2.41 mM); Suspended solution; Need ultrasonic

    此⽅案可获得 1 mg/mL (2.41 mM) 的均匀悬浊液,悬浊液可⽤于⼝服和腹腔注射

    以 1 mL ⼯作液为例,取 100 μL 10.0 mg/mL 的澄清 EtOH 储备液加到 900 μL 20% 的 SBE-β-CD ⽣理盐⽔⽔溶液中,混合均匀 。

     
  • 5.

    请依序添加每种溶剂:  10% EtOH  →  90% corn oil

    Solubility: ≥ 1 mg/mL (2.41 mM); Clear solution

    此⽅案可获得 ≥ 1 mg/mL (2.41 mM,饱和度未知) 的澄清溶液,此⽅案不适⽤于实验周期在半个⽉以上的实验

    以 1 mL ⼯作液为例,取 100 μL 10.0 mg/mL 的澄清 EtOH 储备液加到 900 μL ⽟⽶油中,混合均匀。

科研文献
The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2
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