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Swainsonine (Synonyms: Tridolgosir)
目录号: PC15220 纯度: ≥98%
CAS No. :72741-87-8
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PC15220-500ug 500ug ¥782.04 请登录
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PC15220-5mg 5mg ¥6228.88 请登录
PC15220-10mg 10mg ¥10893.68 请登录
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中文名称
Swainsonine
中文别名
苦马豆素;(1S,2R,8R,8AR)-1,2,8-八氢吲哚啶三醇;八倾吲嗪三醇;玛卡提取物;D-苦马豆素;苦马豆素盐酸盐
英文名称
Swainsonine
英文别名
1,2,8-Indolizinetriol,octahydro-, (1S,2R,8R,8aR)-;Swainsonine;(1S,2R,8R,8aR)-octahydro-1,2,8-indolizinetriol;(1S,2R,8R,8aR)-octahydroindolizine-1,2,8-triol;8A,B-INDOLIZIDINE-1,2A,8B-TRIOL;D-Swainsonine;SwainMoia;swainsonine synthetic;Tridolgosir;Tridolgosir Hydrochloride;(1S,2R,8R,8aR)-1,2,8-Octahydroindolizidinetriol;(-)-Swainsonine;RSY4RK37KQ;1,2,8-Indolizinetriol, octahydro-, (1S-(1alpha,2alpha,8beta,8abeta))-;1S-8AB-OCTAHYDRO-INDOLIZIDINE-1A,2A,8B-TRIOL;(1S,2R,8R,8aR)-1,2,3,5,6,7,8,8a-octahydroindolizine-1,2,8-triol;Tridolgosir [INN];SWA;Swainosine;Locoweed deriv.;NSC614553;1hww;Octahydro-1,2,8-indolizinetriol
Cas No.
72741-87-8
分子式
C8H15NO3
分子量
173.21
包装储存
Powder -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month
生物活性

Swainsonine (Tridolgosir) is an natural indolizidine alkaloid, a potent and reversible α-mannosidase inhibitor. Swainsonine induces apoptosis and cell cycle arrest at G2/M phase. Swainsonine shows anti-tumor activity.

性状

Solid

体外研究(In Vitro)

Swainsonine (0-40 μM; 12 h) shows antiproliferative activity in U251 and LN444 cells.
Swainsonine (30 μM; 12 h) induces apoptosis and cell cycle arrest at G2/M phase, and decreases the expression of CyclinD1 and CDK4 protein levels, increases the expression of p16 protein level.
Swainsonine (30 μM; 12 h) reduces glioma cell migration and invasion.

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

Cell Viability Assay

Cell Line: U251, LN444 cells
Concentration: 0, 10, 20, 30, 40 μM
Incubation Time: 12 h
Result: Inhibited cell viability in a dose-dependent manner, and shows no cytotoxicity in normal brain cells.

Cell Cycle Analysis

Cell Line: U251 cells
Concentration: 30 μM
Incubation Time: 12 h
Result: Induced cell cycle arrest at G2/M phase.

Apoptosis Analysis

Cell Line: U251 cells
Concentration: 30 μM
Incubation Time: 12 h
Result: Induced apoptosis with the cleaved-Caspase-3 and cleaved-Caspase-9 expression were obviously increased.
体内研究(In Vivo)

Swainsonine (1 mg/kg; i.p.; twice daily for ten days) and cisplatin increases the anti-tumor efficacy in mouse.

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

Animal Model: Eighty-seven sixty-day-old male C57BL/6 mice
Dosage: 1 mg/kg (cisplatin; 0.25 mg/kg, i.p., every other day for 10 days)
Administration: I.p.; twice daily for ten days
Result: Showed a significant reduction in ascites volume of 63.5% was observed in mice and a significant reduction in the percentage of cells in the G0/G1, S and G2 phases.
运输条件

Room temperature or refrigerated transportation.

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

DMSO : 10 mg/mL (57.73 mM; Need ultrasonic and warming)

Ethanol : 10 mg/mL (57.73 mM; Need ultrasonic and warming)

H2O : 3.57 mg/mL (20.61 mM; ultrasonic and warming and heat to 60°C)

配制储备溶液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 5.7733 mL 28.8667 mL 57.7334 mL
5 mM 1.1547 mL 5.7733 mL 11.5467 mL
10 mM 0.5773 mL 2.8867 mL 5.7733 mL
*

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。

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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The dilution calculator equation
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