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S88178

E-64c

源叶(MedMol) 98%
  • 英文名:
  • E-64c
  • 别名:
  • 阿洛司他丁酸
  • CAS号:
  • 76684-89-4
  • 分子式:
  • C15H26N2O5
  • 分子量:
  • 314.38
  • MDL:
  • MFCD00132882
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) S88178-1mg 98% ¥308.00元 10 - - - EA 加入购物车
源叶(MedMol) S88178-5mg 98% ¥610.00元 10 - - - EA 加入购物车
源叶(MedMol) S88178-10mg 98% ¥820.00元 10 - - - EA 加入购物车
源叶(MedMol) S88178-50mg 98% ¥2060.00元 9 - - - EA 加入购物车
源叶(MedMol) S88178-100mg 98% ¥3089.00元 10 - - - EA 加入购物车
源叶(MedMol) S88178-250mg 98% ¥5150.00元 5 - - - EA 加入购物车
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参考文献

质检证书(COA)

摩尔浓度计算器

相关产品

  • 产品描述: E 64c is a derivative of naturally occurring epoxide inhibitor of cysteine proteases, a Calcium-activated neutral protease (CANP) inhibitor and a very weak irreversible cathepsin C inhibitor. E 64c exhibits entry-blocking effect for MERS-CoV.
  • 靶点: Cysteine proteases, CANP, Cathepsin C;SARS-CoV; CysteineProtease
  • 体内研究:
    The t-1/2 of plasma E-64c is 0.48 hours. The hemodynamic effects of E-64c are absent at this dose. Using two way analysis of variance, the effects of reperfusion (p=0.0016) or E-64c (p=0.0226) per se on infarct size are significant. In comparing Group A with Group B and Group C with Group D, the depletion of CPK in the E-64c treated groups (Groups A and C) is slightly less than in the vehicle-injected groups (Groups B and D). The insufficient effect of E-64c alone may be explained by the early administration and relatively short t-1/2. Since the effectiveness of NCO-700 has been established,6),7) our findings might indicate a small but beneficial effect of E-64c on infarct size and CPK content
  • 参考文献:
    1. Khan MS, et al. Design, synthesis, evaluation and thermodynamics of 1-substituted pyridylimidazo[1,5-a]pyridine derivatives as cysteine protease inhibitors. PLoS One. 2013 Aug 5;8(8):e69982. 2. Toda G, et al. Calcium-activated neutral protease inhibitor (E-64c) and reperfusion for experimental myocardial infarction. Jpn Heart J. 1989 May;30(3):375-86. 3. Radzey H, et al. E-64c-hydrazide: a lead structure for the development of irreversible cathepsin C inhibitors. ChemMedChem. 2013 Aug;8(8):1314-21. 4. Ji Yeun Kim, et al. Safe, High-Throughput Screening of Natural Compounds of MERS-CoV Entry Inhibitors Using a Pseudovirus Expressing MERS-CoV Spike Protein. Int J Antimicrob Agents. 2018 Nov;52(5):730-732.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 3.181 ml 15.904 ml 31.809 ml
    5 mM 0.636 ml 3.181 ml 6.362 ml
    10 mM 0.318 ml 1.59 ml 3.181 ml
    50 mM 0.064 ml 0.318 ml 0.636 ml
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