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Lupeol

(Synonyms: 羽扇豆醇; Clerodol; Monogynol B; Fagarasterol)
目录号: PC13299 纯度: ≥98%
抗炎剂,Lupeol 是一种新型雄激素受体抑制剂。
CAS No. :545-47-1
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PC13299-20mg 20mg ¥226.00 请登录
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中文名称
Lupeol
中文别名
羽扇豆醇;Lupeol 羽扇豆醇 标准品;羽扇豆醇(RG)(PLEASE CALL);羽扇豆醇(标准品);羽扇豆醇,Lupeol,植物提取物,标准品,对照品;羽扇豆醇Lupeol;20(29)-羽扇烯-3β-醇;3β-羟基-20(29)-羽扇烯;蛇麻醇酯;羽扇醇;羽扇豆醇(羽扇醇,羽扇豆醇酯,蛇麻醇酯);羽扇豆醇酯;羽扇豆醇;545-47-1 ;lupeol
英文名称
Lupeol
英文别名
lupeol;Fagarasterol;Lup-20(29)-en-3b-ol;LUPEOL(AS);LUPEOL(AS) PrintBack;LUPEOL(P);LUPEOL(RG)(PLEASE CALL) PrintBack;Lupeol, froM Crataegus pinnatifida;20(29)-Lupen-3β-ol;B-VISCOL;Cautchicol;Clerodol;Fagarsterol;Lupenol;MONOGYNOL;monogynolb;β-Viscol;(3beta)-Lup-20(29)-en-3-ol;Lup-20(29)-en-3-ol;[ "Lup-20(29)-en-3-ol" ];Monogynol B
Cas No.
545-47-1
分子式
C30H50O
分子量
426.72
包装储存
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
详情描述
抗炎剂,Lupeol 是一种新型雄激素受体抑制剂。
生物活性

Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent androgen receptor (AR) inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC).

性状

Solid

IC50 & Target[1][2]

Androgen receptor

体外研究(In Vitro)

Lupeol, an effective AR inhibitor, can be developed as a potential agent to treat human prostate cancer (CaP). Lupeol (10–50 μM) treatment for 48 h results in a dose-dependent growth inhibition of androgen-dependent phenotype (ADPC) cells viz., LAPC4 and LNCaP cells with an IC50 of 15.9 and 17.3 μM, respectively. Lupeol also inhibits the growth of 22Rν_1 with an IC50 of 19.1 μM. Further, Lupeol inhibits the growth of C4-2b cells with an IC50 of 25 μM. Lupeol has the potential to inhibit the growth of CaP cells of both ADPC and CRPC phenotype. Androgens by activating AR are known to drive the growth of CaP cells.

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

体内研究(In Vivo)

Lupeol is an effective agent that has the potential to inhibit the tumorigenicity of CaP cells in vivo. At the conclusion of the study on day 56, the total circulating serum-PSA levels (secreted by the implanted tumor cells) are measured. At 56thday post-implantation, PSA levels are observed between 11.95-12.79 ng/mL in control animals with LNCaP-tumors and C4-2b-tumors, respectively. However, Lupeol-treated counterpart animals exhibits reduced serum-PSA levels in a range of 4.25-7.09 ng/mL. Tumor tissues of animals receiving Lupeol treatment exhibits reduced serum-PSA levels as compared to control.

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

运输条件

Room temperature or refrigerated transportation.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
ClinicalTrial
结构分类
来源
参考文献
溶解度数据
体外研究: 

Ethanol : 14.29 mg/mL (33.49 mM; ultrasonic and warming and heat to 60°C)

DMSO : 2 mg/mL (4.69 mM; Need ultrasonic)

配制储备溶液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.3435 mL 11.7173 mL 23.4346 mL
5 mM 0.4687 mL 2.3435 mL 4.6869 mL
10 mM 0.2343 mL 1.1717 mL 2.3435 mL
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产品不同,其溶解度不同。建议根据产品选择合适的溶剂配制储备溶液;配成溶液后,建议分装保存,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。-80°C 储存时,建议在 6 个月内使用,-20°C 储存时,建议在 1 个月内使用。

体内研究:

建议根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都建议先按照 体外研究 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.

    建议依照次序添加每种溶剂: corn oil

    Solubility: 20 mg/mL (46.87 mM); Clear solution; Need ultrasonic

  • 2.

    建议依照次序添加每种溶剂: 10% EtOH    90% corn oil

    Solubility: ≥ 1.43 mg/mL (3.35 mM); Clear solution

    此方案可获得 ≥ 1.43 mg/mL (3.35 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 14.3 mg/mL 的澄清 EtOH 储备液加到 900 μL玉米油中,混合均匀。

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搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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