1. Anti-infection
  2. SARS-CoV
  3. Ipomoeassin F

Ipomoeassin F  (Synonyms: Ipom-F)

目录号: HY-N10661
产品使用指南

Ipomoeassin F 是一种有效的、选择性内质网 (ER) 蛋白易位抑制剂,通过靶向 ER 膜上的 Sec61 复合物 (Sec61α) 的成孔亚基。Ipomoeassin F 选择性抑制 SARS-CoV-2 蛋白的 ER 膜转位。Ipomoeassin F 阻断分泌蛋白和 I 型跨膜蛋白 (TMP) 的内质网易位,但不阻断 III 型 TMP。

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Ipomoeassin F Chemical Structure

Ipomoeassin F Chemical Structure

CAS No. : 915392-44-8

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Ipomoeassin F is a potent and selective endoplasmic reticulum (ER) protein-translocation inhibitor by targeting the pore-forming subunit of the Sec61 complex (Sec61α) at the ER membrane. Ipomoeassin F selectively inhibits the ER membrane translocation of SARS-CoV-2 proteins. Ipomoeassin F block the ER translocation of secretory proteins and type I transmembrane proteins (TMPs), but not type III TMPs[1][2][3].

体外研究
(In Vitro)

Ipomoeassin F (1-500 nM; 24 小时) 有效抑制 α1AT 易位到 ER[1]
Ipomoeassin F 在人卵巢癌细胞系 A2780 中具有很强的活性,IC50 值为 0.036 μM[2]

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

Western Blot Analysis[1]

Cell Line: HepG2 cells
Concentration: 1, 5, 10, 25, 50, 75, 100, 250, 500 nM
Incubation Time: 24 h
Result: Downregulated cellular ATP levels and inhibited Sec61-mediated protein translocation with comparable potency.
分子量

830.95

Formula

C44H62O15

CAS 号
结构分类
初始来源
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.

纯度 & 产品资料
参考文献

Ipomoeassin F 相关分类

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  • 稀释计算器

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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