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-20°C, protect from light
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货期:1-2天
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MedChemExpress LLC
- CAS号:
83-46-5
- 规格:
100 mg/1 g/5 g
| 规格: | 100 mg | 产品价格: | ¥500.0 |
|---|---|---|---|
| 规格: | 1 g | 产品价格: | ¥700.0 |
| 规格: | 5 g | 产品价格: | ¥1000.0 |
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Beta-Sitosterol (purity>80%)
CAS No. : 83-46-5
MCE 国际站:Beta-Sitosterol (purity>80%)
产品活性: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。
研究领域:Apoptosis | Metabolic Enzyme/Protease
作用靶点:Apoptosis | Endogenous Metabolite
结构分类:甾体类
In Vitro: 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.
In Vivo: 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.
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文献和实验C29 H50 O。又称豆甾 -5-烯 -3β -醇, 24R-乙基胆甾 -5烯 -3β -醇。是以谷类(希文, sitos)命名的甾醇( sterol)。后来已知是α -,β -以及γ -谷甾醇等的混合物。现在知道α体是 C30 甾酵,γ体是 C2 及 C29 的甾醇混合物,因为它们已不被称为谷甾醇,所以仅留下β -谷甾醇具有谷甾醇的名称。它是植物界中分布最广的甾醇,可为毛地黄皂苷( digitonin)沉淀。
真爱满行囊 我最近在体外细胞做的关于gsk3-beta功能问题,发现药物处理以后,gsk-3-beta的总表达量下调,如果是这样的话 1、我是否能够得出gsk-3-beta的活性下调的结论? 2、是否还有必要做非活性形式的表达量?我的理解是,基础状态下,gsk-3beta维持的是低活性状态,如果总量都下调了,那应该能够得出活性降低的结论了吧? 3、另外,在这种情况下我是否有必要去做gsk-3-beta的216位点的活性形式的表达
Beta-gal Assay Adapted from Current Protocols in Molecular Biology 1. Grow 5ml YEPD cultures to mid-log phase. 2. Centrifuge and resuspend cells in 5ml Z-buffer, then place on ice. 3. Measure OD600. 4. Use straight
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