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S82902

MKC9989

源葉(MedMol) 98%
  • 英文名:
  • MKC9989
  • 別名:
  • CAS號:
  • 1338934-20-5
  • 分子式:
  • C17H20O7
  • 分子量:
  • 336.3365
品牌貨號產(chǎn)品規(guī)格價格(RMB) 庫存(上海) 北京 武漢 南京 數(shù)量計量單位 加入購物車...
源葉(MedMol) S82902-1mg 98% ¥1100.00元 預(yù)計交期:2-3天 - - - EA 加入購物車
源葉(MedMol) S82902-5mg 98% ¥3300.00元 預(yù)計交期:2-3天 - - - EA 加入購物車
源葉(MedMol) S82902-10mg 98% ¥5000.00元 預(yù)計交期:2-3天 - - - EA 加入購物車
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產(chǎn)品介紹

參考文獻

質(zhì)檢證書(COA)

摩爾濃度計算器

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  • 提示:詳情請下載說明書。
  • 產(chǎn)品描述: MKC9989 is a Hydroxy aryl aldehydes (HAA) inhibitor and also inhibits IRE1α with an IC50 of 0.23 to 44 μM
  • 靶點: IC50: 0.23 to 44 μM (IRE1α);IRE1
  • 體外研究:
    At 10 μM concentration, MKC9989 completely inhibits both basal and thapsigargin induced splicing of XBP1 mRNA. These effects are observed even in cells pre-treated with thapsigargin, indicating that MKC9989 can fully reverse the onset of XPB1 splicing after the UPR is initiated. In parallel analysis, MKC9989, significantly stabilizes the RIDD target CD59 mRNA when co-administered with thapsigargin relative to thapsigargin treatment alone and modestly increases levels of CD59 mRNA in non-stressed cells, the latter likely reflects the inhibition of baseline RIDD activity. In contrast to effects on XBP1 splicing, MKC9989 moderately stabilizes CD59 levels when administered 2 hour post treatment with thapsigargin. Finally, the potency of MKC9989 against the splicing of XBP1 mRNA (EC50=0.33 μM) is comparable to its potency against RNA cleavage in vitro
  • 參考文獻:
    1. Sanches M, et al. Structure and mechanism of action of the hydroxy-aryl-aldehyde class of IRE1 endoribonuclease inhibitors. Nat Commun. 2014 Aug 28;5:4202.
  • 溶解性: soluble  in  DMSO
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.973 ml 14.866 ml 29.732 ml
    5 mM 0.595 ml 2.973 ml 5.946 ml
    10 mM 0.297 ml 1.487 ml 2.973 ml
    50 mM 0.059 ml 0.297 ml 0.595 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
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