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Peldesine

CAS No. 133432-71-0

Peldesine ( BCX 34 )

产品货号. M26363 CAS No. 133432-71-0

Peldesine is an effective, competitive, reversible, and orally active inhibitor of purine nucleoside phosphorylase.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥2341 有现货
10MG ¥3750 有现货
25MG ¥6205 有现货
50MG ¥8667 有现货
100MG ¥11745 有现货
500MG ¥23328 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Peldesine
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Peldesine is an effective, competitive, reversible, and orally active inhibitor of purine nucleoside phosphorylase.
  • 产品描述
    Peldesine is an effective, competitive, reversible, and orally active inhibitor of purine nucleoside phosphorylase. Peldesine inhibits T-cell proliferation with an IC50 of 800 nM. Peldesine can be used in research on cutaneous T-cell lymphoma, psoriasis and HIV infection.(In Vitro):The IC50s are 36 nM, 5 nM, and 32 nM for human, rat, and mouse red blood cell purine nucleoside phosphorylase, respectively. In Jurkat cells, Peldesine (BCX 34; 0-50 μM; 72 hours) inhibits the T-cell proliferation completely at a concentration of less than 10 μM, in the presence of dGuo (10 μM). In contrast, the B-cell proliferation is not affected by Peldesine.(In Vivo):Peldesine is orally active in elevating plasma inosine in rats (2-fold at 30 mg/kg), in suppressing ex vivo RBC PNP activity in rats (98% at 3 h. 100 mg/kg), and in suppressing ex vivo skin PNP in mice (39% at 3 h, 100 mg/kg). Oral bioavailability of Peldesine in rats is 76%.
  • 同义词
    BCX 34
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    GSTP1; Gutathione S-transferase
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    133432-71-0
  • 分子量
    241.3
  • 分子式
    C12H11N5O
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    Nc1nc2c(Cc3cccnc3)c[nH]c2c(=O)[nH]1
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.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.
产品手册
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