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S87819

DMX-5084

源叶(MedMol) 98%
  • 英文名:
  • DMX5804;DMX 5804
  • 别名:
  • CAS号:
  • 2306178-56-1
  • 分子式:
  • C21H19N3O3
  • 分子量:
  • 361.39
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S87819-2mg 98% ¥1360.00元 4 - - - EA 加入购物车
源叶(MedMol) S87819-5mg 98% ¥2040.00元 6 - - - EA 加入购物车
源叶(MedMol) S87819-10mg 98% ¥3264.00元 6 - - - EA 加入购物车
源叶(MedMol) S87819-25mg 98% ¥5780.00元 6 - - - EA 加入购物车
源叶(MedMol) S87819-50mg 98% ¥8500.00元 预计交期:2-3天 - - - EA 加入购物车
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参考文献

质检证书(COA)

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相关产品

  • 产品描述: DMX-5804 is a potent, selective MAP4K4 inhibitor, with an IC50 of 3 nM.DMX-5804 enhances cardiomyocyte survival, and reduces ischemia-reperfusion injury in mice
  • 靶点: MAPK
  • 体外研究:
    DMX-5804, that rescues cell survival, mitochondrial function
  • 体内研究:
    DMX-5804 reduces ischemia-reperfusion injury in mice by more than 50%
  • 细胞实验: Mitochondrial function in hiPSC-CMs was determined using a Seahorse XFe24 Analyzer.?vCor.4U cells (60,000/well) were transferred to 0.1% gelatin-coated XF24 plates and maintained for 5 d. On day 6, DMX-5804 was added 45 min prior to challenge with menadione for 2 h. The medium was replaced 1 hr before the assay, using bicarbonate-free Seahorse assay medium (8.3 g L-1 DMEM Base , 10 mM glucose, 2 mM L-alanyl-L-glutamine dipeptide, 1 mM sodium pyruvate , pH 7.4).?Cells were maintained at 37 C without supplemental CO2 starting 1 hr before the assay.?For each state measured, three assay cycles were performed (4 min mixing, 2 min wait, and 2 min measurement periods, with readings every 15 s). The basal oxygen consumption rate (OCR) and extracellular acidification rate were determined, followed by sequential injection of 1 μM oligomycin A to inhibit ATP synthase, 0.5 μM carbonyl cyanide-4-phenylhydrazone to uncouple oxidative phosphorylation, and 1 μM antimycin A/rotenone to inhibit mitochondrial complex III and I.
  • 动物实验: n vivo pharmacokinetic profiling was performed in female CD-1 mice, using 3 animals per time point.?First, 30% w/v Kleptose as excipient was dissolved in water and vortexed gently for several min. Next, 30 mg of DMX-5084?was dissolved into 0.6 mL of DMSO, for a concentration of 50 mg ml-1, and 4.5 mL of the Kleptose solution was added to 0.5 mL of the test compound solution.?A precipitate forms, which re-dissolves over 2-5 min, leaving a clear or slightly hazy solution with a final concentration of 5 mg/ml.?The dosing solution is used as soon as practicable, vortexing immediately prior to use.?This amount was sufficient formulation for 25 doses of 200 μL (20 g mouse).?Compounds were administered orally at 50 mg/kg, with terminal blood (plasma) sampling at 10 min, 30 min, 1 h, 2.5 h, 5 h, 10 h, and 20 h
  • 参考文献:
    1. Fiedler LR, et al. MAP4K4 Inhibition Promotes Survival of Human Stem Cell-Derived Cardiomyocytes and Reduces Infarct Size In Vivo. Cell Stem Cell. 2019 Mar 1. pii: S1934-5909(19)30013-X.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20°C
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.767 ml 13.835 ml 27.671 ml
    5 mM 0.553 ml 2.767 ml 5.534 ml
    10 mM 0.277 ml 1.384 ml 2.767 ml
    50 mM 0.055 ml 0.277 ml 0.553 ml
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