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Albendazole
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Albendazole图片
CAS NO:54965-21-8
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
100mg电议
500mg电议
1 g电议
5 g电议

产品名称
阿苯达唑
SKF-62979
产品介绍
Albendazole (SKF-62979) 是一种口服有效的广谱的抗寄生虫剂,具有高效、低宿主毒性的特点,可用于人类和动物胃肠道寄生虫的研究。Albendazole 可诱导癌细胞的凋亡和自噬,并抗细胞增殖和抑制细胞周期进程。Albendazole 还能抑制微管蛋白的聚合和HIF-1αVEGF的表达,具有抗氧化活性,能抑制癌细胞的糖酵解过程。
生物活性

Albendazole (SKF-62979) is an orally active and broad-spectrumparasiticidewith high effectiveness and low host toxicity, is used for the research of gastrointestinalparasitesin humans andanimals. Albendazole inducesapoptosisandautophagyincancercells. Albendazole also inhibitstubulinpolymerization andHIF-1α,VEGFexpression, has antioxidant activity, and inhibits the glycolytic process incancercells[1][2][3][4][5].

IC50& Target

parasites, tubulin[1][2].
HIF-1α, VEGF[3].

体外研究
(In Vitro)

Albendazole (100, 500, 1000 nM; 1, 3, or 5 days) inhibits cell proliferation in a dose-dependent manner[1].
Albendazole (100, 250, 500, 1000 nM; 3 days) arrests SKHEP-1 cells at both G0–G1 (250, 500 nM) and G2-M (1000 nM) phases of the cycle[1].
Albendazole (5 μM; 24, 36 h) mainly induces early apoptosis in HCT-15 cells and late apoptosis in HCT-1 16, HT29, SW480 cells accompanied with cleavage of PARP and caspase-3 in a time-dependent manner[2].
Albendazole (5 μM; 24, 36 h) induces autophagy via increasing autophagy-related protein (such as LC3, Atg7, p-beclin-1, and beclin-1) expression level in HCT-15, HCT-1 16, HT29, and SW480 cells[2].
Albendazole (500 nM, 24 h) inhibits hypoxia-induced HIF-1α expression and VEGF expression in A549 cells[3].

Cell Proliferation Assay[1]

Cell Line:SKHEP-1 cells
Concentration:100, 500, 1000 nM
Incubation Time:1, 3, or 5 days
Result:Inhibited cell proliferation in a dose-dependent manner.

Cell Cycle Analysis[1]

Cell Line:SKHEP-1 HCC cells
Concentration:100, 250, 500, 1000 nM
Incubation Time:3 days
Result:Showed dose-dependent effect on the cell cycle kinetics.

Apoptosis Analysis[2]

Cell Line:HCT-15, HCT-1 16, HT29, SW480 cells
Concentration:5 μM
Incubation Time:24, 36 h
Result:Promoted apoptosis in colon cancer cells.

Cell Autophagy Assay[2]

Cell Line:HCT-15, HCT-1 16, HT29, SW480 cells
Concentration:5 μM
Incubation Time:24, 36 h
Result:Induced autophagy in colon cancer cells.

Western Blot Analysis[2]

Cell Line:HCT-15, HCT-1 16, HT29, SW480 cells
Concentration:5 μM
Incubation Time:12, 24, 36 h
Result:Induced apoptosis-related protein (PARP, caspase-3) and autophagy-related protein (such as LC3, Atg7, p-beclin-1, and beclin-1) expression level in a time-dependent manner.
Increased phosphorylation of different MAPKs (AMPK, ERK, JNK, p38) and ULK1 protein in a time dependent manner, and up-regulated the activation of different MAPKs.
Caused the activation of both MAPK and AMPK pathways.

Western Blot Analysis[3]

Cell Line:A549 cells
Concentration:500 nM
Incubation Time:24 h
Result:Inhibited hypoxia-induced HIF-1α expression and VEGF expression in A549 cells.
体内研究
(In Vivo)

Albendazole (10 mg/kg; i.g.; once a day for 30 days) reducesEchinococcus granulosuscyst weights in mice[4].
Albendazole (300 mg/kg; p.o.; per day in two divided dose for 20 days) profoundly suppresses tumor growth in vivo[1].

Animal Model:Female BALB/c mice (10-week-age;Echinococcus granulosusinfection model)[4].
Dosage:10 mg/kg
Administration:Oral gavage; once a day for 30 days.
Result:ReducedEchinococcus granulosuscyst weights.
Animal Model:Male BALB/c Nu/Nu mice (6 to 10-week-old; inoculated subcutaneously with SKHEP-1)[1].
Dosage:50, 150, 300 mg/kg
Administration:Oral administration; per day in two divided dose for 20 days.
Result:Profoundly suppressed tumor growth in vivo.
Clinical Trial
分子量

265.33

性状

Solid

Formula

C12H15N3O2S

CAS 号

54965-21-8

中文名称

阿苯达唑;丙硫达唑;丙硫咪唑;抗蠕敏;扑尔虫;肠虫清

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : 20 mg/mL(75.38 mM;Need ultrasonic)

H2O : 0.67 mg/mL(2.53 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM3.7689 mL18.8445 mL37.6889 mL
5 mM0.7538 mL3.7689 mL7.5378 mL
10 mM0.3769 mL1.8844 mL3.7689 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℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 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: 10% DMSO    40%PEG300   5%Tween-80   45% saline

    Solubility: 2 mg/mL (7.54 mM); Suspended solution; Need ultrasonic

    此方案可获得 2 mg/mL (7.54 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 20.0 mg/mL 的澄清 DMSO 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。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH2O 中,得到澄清透明的生理盐水溶液
  • 2.

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

    Solubility: ≥ 2 mg/mL (7.54 mM); Clear solution

    此方案可获得 ≥ 2 mg/mL (7.54 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 20.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在本网站选购。