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Disitamab vedotin

(別名: RC48)
5 Cited Publications
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Based on 5 publication(s) in Google Scholar

Disitamab vedotin (RC48) is an antibody-drug conjugate (ADC) comprising a monoclonal antibody against human epidermal growth factor receptor 2 (HER2) conjugated via a cleavable linker to the cytotoxic agent Monomethyl auristatin E (MMAE) (HY-15162), and the drug-linker conjugate for ADC is Deruxtecan (HY-13631E). Disitamab vedotin enhances antitumor immunity.

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  • 純度: 98.90%
  • CAS 番号: 2136633-23-1
  • 分子量:149000 (average)
  • 保管条件:

    Please store the product under the recommended conditions in the Certificate of Analysis.

  • Disitamab vedotin Chemical Structure
    Disitamab vedotin 構造式
  • Experimental Validation Results for Disitamab vedotin
  • Experimental Validation Results for Disitamab vedotin
  • Experimental Validation Results for Disitamab vedotin
  • Experimental Validation Results for Disitamab vedotin
  • Experimental Validation Results for Disitamab vedotin
CAS 番号: 2136633-23-1
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  • Disitamab vedotin Chemical Structure
    Disitamab vedotin Chemical Structure
    1/16
  • 1/16

    Disitamab vedotin purchased from MedChemExpress. Usage Cited in: Cancer Lett. 2025 Oct 10:630:217900. [Abstract]

    Customer Validation
     Disitamab vedotin (DV, 0.25 μg/mL) reduced the overall cell number of HER2-positive JIMT-1 breast cancer cells.

  • 1/16

    Disitamab vedotin purchased from MedChemExpress. Usage Cited in: Cancer Lett. 2025 Oct 10:630:217900. [Abstract]

    Customer Validation
     Unlike the parental cells, which were sensitive to XMT-1522 and Disitamab vedotin (DV, 0.0001, 0.0006, 0.003, 0.016, 0.08, 0.4, 1, 2, and 10 μg/mL; 5 days), both D1 and D2 daughter cells that emerged from the DTP-PGCC were resistant to these drugs. D1, daughter-1 cells (one prior ADC treatment); D2, daughter-2 cells (two prior ADC treatments). ∗∗, p < 0.01; ∗∗∗, p < 0.001.

  • 1/16

    Disitamab vedotin purchased from MedChemExpress. Usage Cited in: Transl Oncol. 2025 Mar:53:102284. [Abstract]

    Customer Validation
     Disitamab vedotin (DV, 50 μg/mL, 15 or 30 min) increased T-DM1 internalization into JIMT-1 breast cancer cells.

  • 1/16

    Disitamab vedotin purchased from MedChemExpress. Usage Cited in: Transl Oncol. 2025 Mar:53:102284. [Abstract]

    Customer Validation
     In JIMT-1 xenografts, the combination of Disitamab vedotin (DV, 0.5 mg/kg or 5 mg/kg, administered intravenously twice at 7-day intervals) plus T-DM1, as well as DV plus T-DXd, inhibited tumor growth more effectively than the corresponding single treatments.

  • 1/16

    Disitamab vedotin purchased from MedChemExpress. Usage Cited in: Transl Oncol. 2025 Mar:53:102284. [Abstract]

    Customer Validation
     In macroscopic JIMT-1 xenografts, tumors that relapsed after T-DM1 treatment and subsequently responded to Disitamab vedotin (DV, 0.5 mg/kg or 5 mg/kg, administered intravenously twice at 7-day intervals) but later progressed had lost HER2 expression. A: PBS; B: relapsed after T-DM1, progressed on T-DM1; C: relapsed after T-DM1, progressed on DV; D: relapsed after T-DM1, progressed on T-DXd.

  • Disitamab vedotin