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  • DUPA(OtBu)-OH
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DUPA(OtBu)-OH

DUPA(OtBu)-OH是一种DUPA前体。DUPA用作传递Docetaxel(DTX)的靶向基序,可用于治疗表达前列腺特异性膜抗原(PSMA)的前列腺肿瘤。

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DUPA(OtBu)-OH的二维码
  • 库存: 现货
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  • 包装
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  • 5mg
    ¥1525.00
    1220.00
    - +
  • 10mg
    ¥2375.00
    1900.00
    - +
  • 50mg
    ¥5450.00
    4360.00
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  • 100mg
    ¥7637.00
    6110.00
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  • 货号: ajce50408
  • CAS: 1026987-94-9
  • 别名: (S)-5-叔丁氧基-4-(3-((S)-1,5-二-叔丁氧基-1,5-二氧代-2-戊基)脲啶)-5-氧代戊酸
  • 分子式: C23H40N2O9
  • 分子量: 488.57
  • 纯度: >98%
  • 溶解度: DMSO : 125 mg/mL (255.85 mM)
  • 储存: Store at -20°C
  • 库存: 现货

Background

DUPA(OtBu)-OH is a DUPA precursor. DUPA is used as the targeting moiety to actively deliver Docetaxel (DTX) for treatment of Prostate-Specific Membrane Antigen (PSMA) expressing prostate cancer.


DUPA(OtBu)-OH (DUPA precursor 17) is a 2-[3-(1,3-dicarboxypropyl)ureido]pentanedioic acid (DUPA) reagent[1]. The targeting ligand DUPA enhances the transport capability and selectivity of Paclitaxel (PTX) to tumor cells via prostate-specific membrane antigen (PSMA) mediated endocytosis. Besides, DUPA is conjugated with PTX via a disulfide bond, which facilitates the rapid and differential drug release in tumor cells[2].


DUPA-targeted Docetaxel (DTX) conjugate with longer spacer has no toxicity in major organs of treated mice[3].


[1]. Roy J, et al. DUPA conjugation of a cytotoxic indenoisoquinoline topoisomerase I inhibitor for selectiveprostate cancer cell targeting. J Med Chem. 2015 Apr 9;58(7):3094-103. [2]. Lv Q, et al. Prostate-Specific Membrane Antigen Targeted Therapy of Prostate Cancer Using a DUPA-Paclitaxel Conjugate. Mol Pharm. 2018 May 7;15(5):1842-1852. [3]. Peng ZH, et al. Spacer length impacts the efficacy of targeted docetaxel conjugates in prostate-specificmembrane antigen expressing prostate cancer. J Drug Target. 2013 Dec;21(10):968-80.

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