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Kira8

CAS No. 1630086-20-2

Kira8 ( AMG-18 )

产品货号. M26271 CAS No. 1630086-20-2

Kira8 是一种单选择性 IRE1α 抑制剂,可变构减弱 IRE1α RNase 活性(IC50:5.9 nM)。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥1725 有现货
10MG ¥2608 有现货
25MG ¥4836 有现货
50MG ¥6901 有现货
100MG ¥9477 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
    Kira8
  • 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
    Kira8 是一种单选择性 IRE1α 抑制剂,可变构减弱 IRE1α RNase 活性(IC50:5.9 nM)。
  • 产品描述
    Kira8 is a mono-selective IRE1α inhibitor that allosterically attenuates IRE1α RNase activity (IC50: 5.9 nM).(In Vitro):Kira8 more effectively causes IRE1α-driven apoptosis in INS-1 cells than KIRA6 and also reverses XBP1 splicing promoted by GNF-2. Kira8 blocks IRE1α oligomerization and effectively inhibits IRE1α RNase activity against XBP1 and Ins2 RNAs.(In Vivo):One week of treatment of pre-diabetic NODs mice with Kira8 (50 mg/kg; i.p.; once a day) causes obvious reductions in islet XBP1 splicing and TXNIP mRNAs. It also preserves Ins1/Ins2, BiP, and MANF mRNAs. Male Ins2+/Akita mice are injected i.p. with KIRA8 (50 mg/kg; daily; for 35 days), obviously reduction of hyperglycemia becomes apparent over several weeks.
  • 体外实验
    Kira8 blocks IRE1α oligomerization, and potently inhibits IRE1α RNase activity against XBP1 and Ins2 RNAs. Kira8 more potently reduces IRE1α-driven apoptosis in INS-1 cells than KIRA6 and also reverses XBP1 splicing promoted by GNF-2.
  • 体内实验
    Male Ins2+/Akita mice are injected i.p. with KIRA8 (50 mg/kg; daily; for 35 days), significant reduction of hyperglycemia become apparent over several weeks. One week treatment of pre-diabetic NODs mice with Kira8 (50 mg/kg; i.p.; once a day) leads to significant reductions in islet XBP1 splicing and TXNIP mRNAs, and preserves Ins1/Ins2, BiP and MANF mRNAs. Animal Model:Male Ins2+/Akita mice Dosage:50 mg/kg Administration:Injected i.p.; daily; for 35 days Result:Significant reduction of hyperglycemia became apparent over several weeks.
  • 同义词
    AMG-18
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    antiprotozoal
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1630086-20-2
  • 分子量
    601.12
  • 分子式
    C31H29ClN6O3S
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?Ethanol : 76.92 mg/mL (127.96)
  • SMILES
    Cc1ccc2c(NS(=O)(=O)c3ccccc3Cl)cccc2c1Oc1ncccc1-c1ccnc(N[C@H]2CCCNC2)n1
  • 化学全称
    ——

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.Dianzani C, Collino M, Gallicchio M, Di Braccio M, Roma G, Fantozzi R. Effects of anti-inflammatory [1, 2, 4]triazolo[4, 3-a] [1, 8]naphthyridine derivatives on human stimulated PMN and endothelial cells: an in vitro study. J Inflamm (Lond). 2006 Mar 28;3:4.
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