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氯硝柳胺乙醇胺盐 /Niclosamide Ethanolamine Salt {[allProObj[0].p_purity_real_show]}

货号:A116636 同义名: Niclosamide olamine;BAY2353 olamine

Niclosamide Ethanolamine Salt是一种口服活性 P-糖蛋白 (Pgp) 和乳腺癌耐药蛋白 (BCRP) 抑制剂,用于研究外排转运蛋白对药物在脑中分布的影响,并用于癌症研究。

Niclosamide Ethanolamine Salt 化学结构 CAS号:1420-04-8
Niclosamide Ethanolamine Salt 化学结构
CAS号:1420-04-8
Niclosamide Ethanolamine Salt 3D分子结构
CAS号:1420-04-8
Niclosamide Ethanolamine Salt 化学结构 CAS号:1420-04-8
Niclosamide Ethanolamine Salt 3D分子结构 CAS号:1420-04-8
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Niclosamide Ethanolamine Salt 纯度/质量文件 产品仅供科研

货号:A116636 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 mTOR mTORC1 mTORC2 其他靶点 纯度
AZD-8055 ++++

mTOR (full length), IC50: 0.8 nM

mTOR (truncated), IC50: 0.13 nM

99%+
Gedatolisib ++++

mTOR, IC50: 1.6 nM

99%
GSK1059615 ++

mTOR, IC50: 12 nM

98%
Vistusertib +++

mTOR, IC50: 2.8 nM

99%+
Torin 1 +++

mTOR, IC50: 4.32 nM

+++

mTORC1, IC50: 2 nM

++

mTORC2, IC50: 10 nM

DNA-PK 99%+
Dactolisib +++

mTOR (p70S6K), IC50: 6 nM

98+%
PI-103 +

mTOR, IC50: 30 nM

99%+
WAY-600 ++

mTOR, IC50: 9 nM

99%
Voxtalisib +

mTOR, IC50: 157 nM

99%+
PF-04691502 ++

mTOR, Ki: 16 nM

98+%
Onatasertib ++

mTOR, IC50: 16 nM

DNA-PK 99%+
Chrysophanol EGFR 98%
Samotolisib DNA-PK 99%+
Torkinib +++

mTOR, IC50: 8 nM

PDGFR,DNA-PK 99%+
Everolimus 99%+
WYE-354 +++

mTOR, IC50: 5 nM

98%
Tacrolimus 98%
PP121 ++

mTOR, IC50: 13 nM

PDGFR,VEGFR 99%+
Torin 2 ++++

mTOR, IC50: 0.25 nM

DNA-PK 99%+
Rapamycin ++++

mTOR, IC50: ~0.1 nM

98%
GDC-0349 +++

mTOR, Ki: 3.8 nM

98%
XL388 ++

mTOR, IC50: 9.9 nM

+++

mTORC1, IC50: 8 nM

+

mTORC2, IC50: 166 nM

99%+
WYE-687 +++

mTOR, IC50: 7 nM

98+%
Apitolisib +

mTOR, Ki app: 17 nM

98%+
WYE-132 ++++

mTOR, IC50: 0.19 nM

99%+
Sapanisertib ++++

mTOR, Ki: 1.4 nM

99%+
BGT226 maleate 99%+
ETP-46464 ++++

mTOR, IC50: 0.6 nM

DNA-PK 98%
PI3K-IN-1 +

mTOR, IC50: 157 nM

98+%
Zotarolimus +++

FKBP-12, IC50: 2.8 nM

99+%
OSI-027 +++

mTOR, IC50: 4 nM

+

mTORC1, IC50: 22 nM

+

mTORC2, IC50: 65 nM

99%+
Ridaforolimus ++++

mTOR, IC50: 0.2 nM

99%+
Temsirolimus +

mTOR, IC50: 1.76 μM

95%
CZ415 ++

mTOR, pIC50: 8.07

99%+
SF2523 +

mTOR, IC50: 280 nM

DNA-PK 99%+
KU-0063794 ++

mTORC1, IC50: ~10 nM

++

mTORC2, IC50: ~10 nM

99%+
Omipalisib ++++

mTORC1, Ki: 0.18 nM

++++

mTORC2, Ki: 0.3 nM

99%+
Palomid 529 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。

Niclosamide Ethanolamine Salt 生物活性

描述 Niclosamide olamine, another form of the drug, retains the same oral activity and application in antihelminthic research[1]. Niclosamide olamin is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells[4]. Otherwise, Niclosamide olamin also shows effectiveness against cancer by inhibiting DNA replication in Vero E6 cells[2].[3].[5].
体内研究

Niclosamide sodium, when given via oral gavage at doses of 100 mg/kg and 200 mg/kg once a week for eight weeks, significantly reduces tumor growth in adrenocortical carcinoma models in vivo[3].

体外研究

Niclosamide olamine, across a range of concentrations from 0.6 nM to 46 µM, effectively inhibits cellular proliferation in adrenocortical carcinoma lines including BD140A, SW-13, and NCI-H295R cells[3].

Additionally, when administered at concentrations of 0.05 to 5 µM for 24 hours, Niclosamide olamine suppresses STAT3-mediated luciferase reporter activity in HeLa cells[4].

Niclosamide olamine also inhibits virus replication at a concentration of 10 µM in Vero E6 cells[5].

Niclosamide Ethanolamine Salt 参考文献

[1]P Andrews, et al. The biology and toxicology of molluscicides, Bayluscide. Pharmacol Ther. 1982;19(2):245-95.

[2]Wei Chen, et al. Niclosamide: Beyond an antihelminthic drug. Cell Signal. 2018 Jan;41:89-96.

[3]Kei Satoh, et al. Identification of Niclosamide as a Novel Anticancer Agent for Adrenocortical Carcinoma. Clin Cancer Res. 2016 Jul 15;22(14):3458-66.

[4]Xiaomei Ren, et al. Identification of Niclosamide as a New Small-Molecule Inhibitor of the STAT3 Signaling Pathway. ACS Med Chem Lett. 2010 Sep 7;1(9):454-9.

[5]Chang-Jer Wu, et al. Inhibition of severe acute respiratory syndrome coronavirus replication by niclosamide. Antimicrob Agents Chemother. 2004 Jul;48(7):2693-6.

Niclosamide Ethanolamine Salt 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.58mL

0.52mL

0.26mL

12.88mL

2.58mL

1.29mL

25.76mL

5.15mL

2.58mL

Niclosamide Ethanolamine Salt 技术信息

CAS号1420-04-8
分子式C15H15Cl2N3O5
分子量 388.203
别名 Niclosamide olamine;BAY2353 olamine;Niclosamide-olamine, Niclosamide (ethanolamine salt);HL 2448;Bayluscide;BAY-6076;BAY-73;Niclosamide (ethanolamine salt)
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Keep in dark place,Inert atmosphere,2-8°C

溶解度

DMSO: 120 mg/mL(309.12 mM),配合低频超声助溶,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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