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芬苯达唑d3 /Fenbendazole-d3 {[allProObj[0].p_purity_real_show]}

货号:A1213143 同义名: Methyl 5-(phenylthio)-2-benzimidazolecarbamate-d3

Fenbendazole-d3是氘标记的 Fenbendazole,可作为 HIF-1α 激动剂,激活与 HIF-1α 相关的 GLUT1 通路。Fenbendazole 是一种具有广泛抗寄生虫活性的口服活性苯并咪唑驱虫剂,同时也是一种微管去稳定剂。Fenbendazole 能导致细胞周期停滞和有丝分裂细胞死亡,并在野生型 p53 异种移植小鼠中展现抗肿瘤活性。

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There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Fenbendazole-d3 化学结构 CAS号:1228182-47-5
Fenbendazole-d3 化学结构
CAS号:1228182-47-5
Fenbendazole-d3 3D分子结构
CAS号:1228182-47-5
Fenbendazole-d3 化学结构 CAS号:1228182-47-5
Fenbendazole-d3 3D分子结构 CAS号:1228182-47-5
规格 价格 会员价 库存 数量
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Fenbendazole-d3 纯度/质量文件 产品仅供科研

货号:A1213143 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 HIF HIF1 PHD1 PHD2 PHD3 其他靶点 纯度
KC7F2 +

HIF-1α, IC50: 20 μM

+

HIF-1α, IC50: 20 μM

98%
Lificiguat 99%+
BAY 87-2243 99%+
PX-478·2HCl 98%+
2-Methoxyestradiol 98%
CAY10585 ++

HIF, IC50: 4.4 μM

BCRP 97%
DMOG 98%
FG 2216 ++

PHD2, IC50: 3.9 μM

99%+
MK-8617 ++++

PHD1, IC50: 1 nM

++++

PHD2, IC50: 1 nM

++++

PHD3, IC50: 14 nM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Fenbendazole-d3 生物活性

描述 Fenbendazole-d3, which is a deuterium-labeled variant of Fenbendazole, acts as a HIF-1α agonist, particularly affecting the HIF-1α-related GLUT1 pathway. Fenbendazole itself is an orally active benzimidazole anthelmintic agent known for its broad-spectrum antiparasitic activity. It is also identified as a microtubule destabilizing agent, capable of inducing cell-cycle arrest and mitotic cell death, demonstrating antitumor efficacy in mouse models xenografted with wild-type p53[1].[2].[3].[4].
体外研究

In vitro, Fenbendazole-d3 at a concentration of 20 µM over 48 hours has shown to counteract the effects of miR-143-5p on cell proliferation, colony-forming capacity, and migration[1].

At a concentration of 10 µM for 48 hours, Fenbendazole-d3 increases the protein expression levels of HIF-1α and GLUT1, thereby enhancing glucose transport and potentially contributing to its antitumor activity[1].

Fenbendazole-d3 参考文献

[1]Jia Xu, et al. miR-143-5p suppresses breast cancer progression by targeting the HIF-1α-related GLUT1 pathway. Oncol Lett. 2022 May;23(5):147.

[2]Nilambra Dogra, et al. Fenbendazole acts as a moderate microtubule destabilizing agent and causes cancer cell death by modulating multiple cellular pathways. Sci Rep. 2018 Aug 9;8(1):11926.

[3]Hossein Aleyasin, et al. Antihelminthic benzimidazoles are novel HIF activators that prevent oxidative neuronal death via binding to tubulin. Antioxid Redox Signal. 2015 Jan 10;22(2):121-34.

[4]Qiwen Duan, et al. Fenbendazole as a potential anticancer drug. Anticancer Res. 2013 Feb;33(2):355-62.

Fenbendazole-d3 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.31mL

0.66mL

0.33mL

16.54mL

3.31mL

1.65mL

33.07mL

6.61mL

3.31mL

Fenbendazole-d3 技术信息

CAS号1228182-47-5
分子式C15H13N3O2S
分子量 302.36
别名 Methyl 5-(phenylthio)-2-benzimidazolecarbamate-d3
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Sealed in dry,2-8°C

溶解度

DMSO: 4 mg/mL(13.23 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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