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Dup-721

CAS No. 104421-21-8

Dup-721 ( —— )

产品货号. M28176 CAS No. 104421-21-8

DuP-721是一种广谱、口服活性抗菌剂,可对抗多种临床敏感和耐药细菌,特别是结核分枝杆菌。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥444 有现货
5MG ¥752 有现货
10MG ¥1226 有现货
25MG ¥2055 有现货
50MG ¥2948 有现货
100MG ¥4041 有现货
200MG ¥5328 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥809 有现货

生物学信息

  • 产品名称
    Dup-721
  • 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
    DuP-721是一种广谱、口服活性抗菌剂,可对抗多种临床敏感和耐药细菌,特别是结核分枝杆菌。
  • 产品描述
    DuP-721 is a broad spectrum and orally active antibacterial agent against a variety of clinically susceptible and resistant bacteria, especially M. tuberculosis.(In Vitro):DuP-721 (1.5-4 μg/ml) inhibits equally the strains of Mycobacterium tuberculosis susceptible and resistant to conventional antituberculosis drug. And it does not show cross resistance to any of the anti-tuberculosis drugs tested.DuP-721 is inactive against M. avium and M. intracellulare at 250 μg/ml. It inhibits M. gordonoe and M. fortuitum at 3.9 μg/ml and M. kansassi and M. scrofulaceum at 1.95 μg/ml and 15.6 μg/ml, respectively.(In Vivo):DuP-721 (oral gavage; 50-160 mg/kg) is protective against M. tuberculosis infection in mice. DuP-721 protects 100% of the infected animals at 50 mg/kg p.o. dose when administered daily for 17 days, and the same effect is observed at 160 mg/kg dose when the drug is administered only on day 11 and 12 post infection.
  • 体外实验
    DuP-721 (1.5-4 μg/ml) inhibits equally the strains of Mycobacterium tuberculosis susceptible and resistant to conventional antituberculosis drug. And it does not show cross resistance to any of the anti-tuberculosis drugs tested.DuP-721 is inactive against M. avium and M. intracellulare at 250 μg/ml. It inhibits M. gordonoe and M. fortuitum at 3.9 μg/ml and M. kansassi and M. scrofulaceum at 1.95 μg/ml and 15.6 μg/ml, respectively.
  • 体内实验
    DuP-721 (oral gavage; 50-160 mg/kg) is protective against M. tuberculosis infection in mice. DuP-721 protects 100% of the infected animals at 50 mg/kg p.o. dose when administered daily for 17 days, and the same effect is observed at 160 mg/kg dose when the drug is administered only on day 11 and 12 post infection.
  • 同义词
    ——
  • 通路
    GPCR/G Protein
  • 靶点
    Antibacterial
  • 受体
    Nuclear factor of activated Tcells (NFAT)
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    104421-21-8
  • 分子量
    276.29
  • 分子式
    C14H16N2O4
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (361.94 mM)
  • SMILES
    N/A
  • 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.Colin A Bretz,?et al. The role of the NFAT signaling pathway in retinal neovascularization. Invest Ophthalmol Vis Sci.?2013 Oct 25;54(10):7020-7.
产品手册
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