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S83862

Ezatiostat

源叶(MedMol) 96%
  • 英文名:
  • (S)-ethyl 2-amino-5-(((R)-3-(benzylthio)-1-(((S)-2-ethoxy-2-oxo-1-phenylethyl)amino)-1-oxopropan-2-yl)amino)-5-oxopentanoate
  • 别名:
  • Telintra; Ezatiostat; TLK-199; UNII-057D10I8S8; Terrapin 199; Ter-199;
  • CAS号:
  • 168682-53-9
  • 分子式:
  • C27H35N3O6S
  • 分子量:
  • 529.6483
  • 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) S83862-5mg 96% ¥440.00元 7 - - - EA 加入购物车
源叶(MedMol) S83862-10mg 96% ¥820.00元 5 - - - EA 加入购物车
源叶(MedMol) S83862-50mg 96% ¥2550.00元 2 - - - EA 加入购物车
源叶(MedMol) S83862-100mg 96% ¥4200.00元 预计交期:2-3天 - - - EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: Ezatiostat (TER199 free base; TLK199) is a tripeptide analog of glutathione and is a selective and orally active glutathione S-transferase P1-1 (GSTP1) inhibitor. Ezatiostat leads to JNK activation by inhibiting GSTP1. Ezatiostat stimulates both lymphocyte production and bone marrow progenitor proliferation. Ezatiostat has the potential for myelodysplastic syndrome (MDS) treatment
  • 靶点: Glutathione S-transferase P1-1 (GSTP1);Apoptosis; GlutathionePeroxidase; GST
  • 体外研究:
    Ezatiostat causes dissociation of the enzyme from the jun-N-terminal kinase/c-Jun (JNK/JUN) complex, leading to JNK activation by phosphorylation. The therapeutic action of ezatiostat appears to include both proliferation of normal myeloid progenitors as well as apoptosis of the malignant clone.
    Selection of a resistant clone of an HL60 tumor cell line through chronic exposure to Ezatiostat (TLK199) results in cells with elevated activities of c-Jun NH2 terminal kinase (JNK1) and ERK1/ERK2, and allowes the cells to proliferate under stress conditions that induced high levels of apoptosis in the wild type cells.
  • 体内研究:
    Administration of Ezatiostat (TLK199), stimulates both lymphocyte production and bone marrow progenitor (colony-forming unit-granulocyte macrophage) proliferation, but only in glutathione S-transferase P1-1 (GSTP1+/+) and not in GSTP1-/- animals.
  • 参考文献:
    1. Galili N, et al. Prediction of response to therapy with ezatiostat in lower risk myelodysplastic syndrome. J Hematol Oncol. 2012 May 6;5:20 2. Ruscoe JE, et al. Pharmacologic or genetic manipulation of glutathione S-transferase P1-1 (GSTpi) influences cell proliferation pathways. J Pharmacol Exp Ther. 2001 Jul;298(1):339-45.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 1.888 ml 9.44 ml 18.88 ml
    5 mM 0.378 ml 1.888 ml 3.776 ml
    10 mM 0.189 ml 0.944 ml 1.888 ml
    50 mM 0.038 ml 0.189 ml 0.378 ml
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