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S23454

CUDA

源葉(MedMol) 98%
  • 英文名:
  • 12-(3-Cyclohexylureido)dodecanoic acid
  • 別名:
  • 12-(3-環(huán)己基脲基)十二烷酸
  • CAS號(hào):
  • 479413-68-8
  • 分子式:
  • C19H36N2O3
  • 分子量:
  • 340.50
  • 核磁/質(zhì)譜:
品牌貨號(hào)產(chǎn)品規(guī)格價(jià)格(RMB) 庫(kù)存(上海) 北京 武漢 南京 數(shù)量計(jì)量單位 加入購(gòu)物車(chē)...
源葉(MedMol) S23454-10mg 98% ¥400.00元 10 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S23454-25mg 98% ¥580.00元 5 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S23454-50mg 98% ¥1000.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購(gòu)物車(chē)
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產(chǎn)品介紹

參考文獻(xiàn)

質(zhì)檢證書(shū)(COA)

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相關(guān)產(chǎn)品

  • 產(chǎn)品描述: CUDA is a potent inhibitor of soluble epoxide hydrolase (sEH), with IC50s of 11.1 nM and 112 nM for mouse sEH and human sEH, respectively. CUDA selectively increases peroxisome proliferator-activated receptor (PPAR) alpha activity. CUDA may be valuable for the research of cardiovascular disease
  • 靶點(diǎn): PPARα;mouse she:11.1 nM (IC50);human she:112 nM (IC50);PPAR;EpoxideHydrolase
  • 體外研究:
    CUDA (10 μM; 18 hours) produces 6- and 3-fold increases of PPARalpha in COS-7 cells.

    CUDA does not alter PPARalpha protein expression, and it competitively inhibits the binding of Wy-14643 (pirinixic acid) to the ligand binding domain of PPARalpha, suggesting that it functions as a PPARalpha ligand.
  • 參考文獻(xiàn):
    1. Morisseau C, et al. Structural refinement of inhibitors of urea-based soluble epoxide hydrolases. Biochem Pharmacol. 2002 May 1;63(9):1599-608.

    2. Fang X, et al. Activation of peroxisome proliferator-activated receptor alpha by substituted urea-derived soluble epoxide hydrolase inhibitors. J Pharmacol Exp Ther. 2005 Jul;314(1):260-70.
  • 溶解性: Soluble  in  DMSO
  • 保存條件: 2-8℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.937 ml 14.684 ml 29.369 ml
    5 mM 0.587 ml 2.937 ml 5.874 ml
    10 mM 0.294 ml 1.468 ml 2.937 ml
    50 mM 0.059 ml 0.294 ml 0.587 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(hù)參考交流研究之用。
  • 產(chǎn)品描述: CUDA is a potent inhibitor of soluble epoxide hydrolase (sEH), with IC50s of 11.1 nM and 112 nM for mouse sEH and human sEH, respectively. CUDA selectively increases peroxisome proliferator-activated receptor (PPAR) alpha activity. CUDA may be valuable for the research of cardiovascular disease
  • 靶點(diǎn): PPARα;mouse she:11.1 nM (IC50);human she:112 nM (IC50);PPAR;EpoxideHydrolase
  • 體外研究:
    CUDA (10 μM; 18 hours) produces 6- and 3-fold increases of PPARalpha in COS-7 cells.

    CUDA does not alter PPARalpha protein expression, and it competitively inhibits the binding of Wy-14643 (pirinixic acid) to the ligand binding domain of PPARalpha, suggesting that it functions as a PPARalpha ligand.
  • 參考文獻(xiàn):
    1. Morisseau C, et al. Structural refinement of inhibitors of urea-based soluble epoxide hydrolases. Biochem Pharmacol. 2002 May 1;63(9):1599-608.

    2. Fang X, et al. Activation of peroxisome proliferator-activated receptor alpha by substituted urea-derived soluble epoxide hydrolase inhibitors. J Pharmacol Exp Ther. 2005 Jul;314(1):260-70.
  • 溶解性: Soluble  in  DMSO
  • 保存條件: 2-8℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.937 ml 14.684 ml 29.369 ml
    5 mM 0.587 ml 2.937 ml 5.874 ml
    10 mM 0.294 ml 1.468 ml 2.937 ml
    50 mM 0.059 ml 0.294 ml 0.587 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(hù)參考交流研究之用。
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