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NGI-1

CAS No. 790702-57-7

NGI-1 ( ML414 )

产品货号. M20759 CAS No. 790702-57-7

NGI-1是一种细胞渗透性寡糖转移酶(OST)抑制剂,可有效降低病毒感染性而不影响细胞活力。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥292 有现货
5MG ¥462 有现货
10MG ¥753 有现货
50MG ¥1887 有现货
100MG ¥2803 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    NGI-1
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    NGI-1是一种细胞渗透性寡糖转移酶(OST)抑制剂,可有效降低病毒感染性而不影响细胞活力。
  • 产品描述
    NGI-1 is a a cell-permeable inhibitor of oligosaccharyltransferase (OST).can effectively reduce virus infectivity without affecting cell viability.
  • 体外实验
    NGI-1 inhibits the glycosylation of LASV GP mediated by STT3A-OST (in STT3B- and MAGT1-TUSC3- cells) or STT3B-OST (in STT3A- cells) and impaires its proteolytic cleavage in a dose-dependent manner.NGI-1 blocks EGFR N-linked glycosylation in lung adenocarcinoma cells as assessed. In controls EGFR is biotinylated, consistent with its plasma membrane expression, but in NGI-1 treated cells the EGFR is predominantly found in the non-biotinylated intracellular fraction suggesting a change in cellular localization. Western Blot Analysis Cell Line:STT3A-, STT3B- and MAGT1-TUSC3- cellsConcentration:1, 2, 5 μM Incubation Time:36 hours Result:Inhibited the glycosylation of LASV GP mediated by STT3A-OST (in STT3B- and MAGT1-TUSC3- cells) or STT3B-OST (in STT3A- cells) and impaired its proteolytic cleavage in a dose-dependent manner.
  • 体内实验
    ——
  • 同义词
    ML414
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    oligosaccharyltransferase
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    790702-57-7
  • 分子量
    394.51
  • 分子式
    C17H22N4O3S2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:160 mg/mL (405.57 mM)
  • SMILES
    CN(C)S(=O)(=O)c1ccc(N2CCCC2)c(c1)C(=O)Nc1ncc(C)s1
  • 化学全称
    5-(dimethylsulfamoyl)-N-(5-methyl-13-thiazol-2-yl)-2-(pyrrolidin-1-yl)benzamide

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Lopez-Sambrooks C Shrimal S Khodier C et al. Oligosaccharyltransferase inhibition induces senescence in RTK-driven tumor cells[J]. Nature Chemical Biology 2016.
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