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DUPA

CAS No. 302941-52-2

DUPA ( (2S,2'S)-2,2'-Carbonylbis(Azanediyl)Dipentanedioic Acid | N,N''-Carbonylbis[L-glutamic acid] )

产品货号. M27072 CAS No. 302941-52-2

DUPA 用作主动递送 DTX 的靶向部分,用于治疗表达前列腺特异性膜抗原 (PSMA) 的前列腺癌。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥300 有现货
5MG ¥478 有现货
10MG ¥786 有现货
25MG ¥1426 有现货
50MG ¥2406 有现货
100MG ¥3686 有现货
200MG ¥5322 有现货
500MG ¥7995 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    DUPA
  • 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
    DUPA 用作主动递送 DTX 的靶向部分,用于治疗表达前列腺特异性膜抗原 (PSMA) 的前列腺癌。
  • 产品描述
    DUPA is used as the targeting moiety to actively deliver DTX for treatment of Prostate-Specific Membrane Antigen (PSMA) expressing prostate cancer.(In Vitro):After binding to a DUPA-drug conjugate, PSMA internalizes, unloads the conjugate, and returns to the surface.(In Vivo):As determined by loss of body weight and death of treated mice,DUPA-indenoisoquinoline conjugate induces a complete cessation of tumor growth with no toxicity.
  • 体外实验
    DUPA is used as the targeting moiety to actively deliver Docetaxel (DTX) for treatment of prostate-specific membrane antigen (PSMA) expressing prostate cancer. The DUPA-indenoisoquinoline conjugate exhibits an IC50 in the low nanomolar range in 22RV1 cell cultures.
  • 体内实验
    The DUPA-indenoisoquinoline conjugate induces a complete cessation of tumor growth with no toxicity, as determined by loss of body weight and death of treated mice.
  • 同义词
    (2S,2'S)-2,2'-Carbonylbis(Azanediyl)Dipentanedioic Acid | N,N''-Carbonylbis[L-glutamic acid]
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    20S proteasome
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    302941-52-2
  • 分子量
    320.254
  • 分子式
    C11H16N2O9
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : ≥ 300 mg/mL (936.77 mM)
  • SMILES
    [H][C@@](CCC(O)=O)(NC(=O)N[C@@]([H])(CCC(O)=O)C(O)=O)C(O)=O
  • 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.Encouse B Golden, et al. Green Tea Polyphenols Block the Anticancer Effects of Bortezomib and Other Boronic Acid-Based Proteasome Inhibitors. Blood. 2009 Jun 4;113(23):5927-37.
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