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S81797

Eldecalcitol

源叶(MedMol) 99%
  • 英文名:
  • Eldecalcitol
  • 别名:
  • 2-(3-羟基丙氧基)-1,25-二羟基维他命D3; ED-71; 2-(3-羟基丙氧基)-1,25-二羟基维他命 D3;;CS-0363; UNII-I2JP8UE90H; Eldecalcitol; HY-A0020; ED 71;
  • CAS号:
  • 104121-92-8
  • 分子式:
  • C30H50O5
  • 分子量:
  • 490.72
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) S81797-1mg 99% ¥2400.00元 预计交期:2-3天 - - - EA 加入购物车
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质检证书(COA)

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  • 产品描述: Eldecalcitol (ED-71) is an orally active vitamin D3 analogue, inhibits bone resorption and increases bone mineral density. Eldecalcitol (ED-71) displays anti-tumor effect and inhibits cell proliferation, migration and induces apoptosis by suppressing GPx-1
  • 靶点: VD/VDRApoptosis;Others
  • 体内研究:
    Eldecalcitol (0.5 μg/kg; p.o.; twice a week for 4 weeks) displays anti-cancer effect by GPx-1 (glutathione peroxidase) inhibition. Eldecalcitol (10, 30, or 90 ng/kg; p.o.; 5-times per week for 12 weeks), as a more potent vitamin D3 analog, stimulates focal bone formation (minimodeling) and suppresses bone resorption more strongly than does calcitriol
  • 参考文献:
    1. Matsumoto T.Osteoporosis Treatment by a New Active Vitamin D3 Compound, Eldecalcitol, in Japan.Curr Osteoporos Rep. 2012 Aug 24. 2. Huang C, et al. Eldecalcitol Inhibits LPS-Induced NLRP3 Inflammasome-Dependent Pyroptosis in Human Gingival Fibroblasts by Activating the Nrf2/HO-1 Signaling Pathway. Drug Des Devel Ther. 2020 Nov 13;14:4901-4913. 3. Lu Y, et al. Eldecalcitol inhibits the progression of oral cancer by suppressing the expression of GPx-1. Oral Dis. 2021 Aug 24. 4. Saito H, et al. Eldecalcitol and calcitriol stimulates 'bone minimodeling,' focal bone formation without prior bone resorption, in rat trabecular bone. J Steroid Biochem Mol Biol. 2013 Jul;136:178-82.
  • 溶解性: Soluble  in  DMSO、Methanol
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.038 ml 10.189 ml 20.378 ml
    5 mM 0.408 ml 2.038 ml 4.076 ml
    10 mM 0.204 ml 1.019 ml 2.038 ml
    50 mM 0.041 ml 0.204 ml 0.408 ml
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