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β-Aminoarteether
  • 英文名称:β-Aminoarteether
  • 品牌:Chemstan
  • 货号:CS-137553
  • cas:133162-24-0
  • 价格: ¥100/mg
  • 发布日期: 2021-03-10
  • 更新日期: 2025-09-19
产品详请
产地
品牌 Chemstan
货号 CS-137553
用途 科研
英文名称 β-Aminoarteether
包装规格 100 mg
纯度 98%%
CAS编号 133162-24-0
别名
分子式
是否进口
Description

β-Aminoarteether (SM934 free base) is an Artemisinin derivative with orally active. β-Aminoarteether can be used for inflammation and autoimmune disease research, such as lupus diseases[1] .

In Vitro

β-Aminoarteether (SM934;10 μM; 24 hours) treatment directly enhances IL-10 production and suppresses IL-12/23p40 production in primary peritoneal macrophages with IFN-γ stimulation[1] .
In vitro, β-Aminoarteether (SM934) could suppress the Th1 and Th17 polarization, but exerted no influence on Treg differentiation[1] .

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

In Vivo

β-Aminoarteether (SM934; 1-10 mg/kg; oral administration; daliy; for 3 months) treatment significantly delays the progression of glomerulonephritis and increases the survival rate of NZB/W F1 mice. β-Aminoarteether treatment promots the IL-10 production of macrophages from NZB/W F1 mice[1] .

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

Animal Model: Female NZB/W F1 mice (Six and half months old)[1]
Dosage: 1 mg/kg, 3 mg/kg, and 10 mg/kg
Administration: Oral administration; daliy; for 3 months
Result: Significantly delayed the progression of glomerulonephritis and increased the survival rate of NZB/W F1 mice.
Molecular Weight

327.42

Formula

C??H??NO?

CAS No.

133162-24-0

SMILES

C[C@@H]1[C@@](CC[C@H]2C)([H])[C@@]([C@@]2([H])CC3)(OO4)[C@@](O[C@@H]1OCCN)([H])O[C@@]34C

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

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

References
  • [1]. Li-Fei Hou, et al. SM934 treated lupus-prone NZB × NZW F1 mice by enhancing macrophage interleukin-10 production and suppressing pathogenic T cell development. PLoS One. 2012;7(2):e32424.

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