Niclosamide sodium(Synonyms: BAY2353 sodium)

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Niclosamide sodium (Synonyms: BAY2353 sodium)

Niclosamide (BAY2353) sodium 是一种具有口服活性的用于寄生虫感染研究的抗蠕虫化合物。
Niclosamide sodium 是 STAT3 抑制剂，在 HeLa 细胞中的 IC50 为 0.25 μM。
Niclosamide sodium 具有抗癌的生物活性，并能抑制 Vero E6 细胞的 DNA 复制。

Niclosamide sodium(Synonyms: BAY2353 sodium)

Niclosamide sodium Chemical Structure

CAS No. : 40321-86-6

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Niclosamide sodium 的其他形式现货产品:

Niclosamide

生物活性

Niclosamide (BAY2353) sodium is an orally active antihelminthic agent used in parasitic infection research[1].
Niclosamide sodium is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells[4].
Niclosamide sodium has biological activities against cancer, and inhibits DNA replication in Vero E6 cells[2][3][5].

体外研究
(In Vitro)

Niclosamide sodium (0.6 nM-46 µM) treatment inhibits adrenocortical carcinoma cellular proliferation in BD140A, SW-13, and NCI-H295R cells[3].
Niclosamide sodium (0.05-5 μM, 24 h) treatment inhibits STAT3-mediated luciferase reporter activity in HeLa cells[4].
Niclosamide sodium (10 μM) treatment inhibits virus replication in Vero E6 cells[5].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[3]

Cell Line: BD140A, SW-13 and NCI-H295R cells
Concentration: 0.6 nM-46 µM
Incubation Time:
Result: Inhibited cellular proliferation in adrenocortical carcinoma cell lines with the IC50 of 0.12 µM, 0.15 µM, and 0.53 µM in BD140A, SW-13, and NCI-H295R, respectively.

Cell Viability Assay[4]

Cell Line: Hela cells
Concentration: 0.05-5 μM
Incubation Time: 24 hours
Result: Inhibited STAT3-mediated luciferase reporter activity with an IC50 of 0.25 μM.

Western Blot Analysis[5]

Cell Line: Vero E6 cells
Concentration: 10 μM
Incubation Time: 2 days
Result: Inhibited the synthesis of viral antigens of SARS-CoV in Vero E6 cells.

体内研究
(In Vivo)

Niclosamide sodium (oral gavage; 100 mg/kg, 200 mg/kg; once a week; 8 weeks) treatment inhibits adrenocortical carcinoma tumor growth in vivo[3].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Nu+/Nu+ mice injected with NCI-H295R cells[3]
Dosage: 100 mg/kg, 200 mg/kg
Administration: Oral gavage; 100 mg/kg, 200 mg/kg; once a week; 8 weeks
Result: Showed a 60%-80% inhibition in tumor growth, as compared to the control group.

分子量

349.10

Formula

C13H7Cl2N2NaO4
CAS 号

40321-86-6
中文名称

氯硝柳胺钠
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
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.

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