DBCO-PEG4-Val-Cit-PAB-MMAE

DBCO-PEG4-Val-Cit-PAB-MMAE

DBCO-PEG4-Val-Cit-PAB-MMAE is an ADC linker featuring a DBCO group, a hydrophilic PEG spacer, a Val-Cit dipeptide, a PAB motif, and an MMAE warhead. The DBCO group is a click chemistry handle which readily reacts with azide groups on a target molecule to form stable triazole linkages, while the Val-Cit dipeptide is a protease-cleavable motif which releases the MMAE warhead into cells via an elimination mechanism within the PAB structure.

Molecular structure of the compound BP-25659
    • Unit
    • Price
    • Qty
    • 10 MG
    • $680.00
    • 25 MG
    • $1350.00
    • 50 MG
    • $1950.00
    • 100 MG
    • $2900.00

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Product Citations

  1. Bernstein, Z. J., Gierke, T. R., Dammen-Brower, K., Tzeng, S. Y., Zhu, S., Chen, S. S., ... & Spangler, J. B. (2024). Production of site-specific antibody conjugates using metabolic glycoengineering and novel Fc glycovariants. Journal of Biological Chemistry, 300(12).
    https://www.jbc.org/article/S0021-9258(24)02507-9/fulltext
  2. Danielewicz, Natalia, Francesca Rosato, Jana Tomisch, Jonas Gra?ber, Birgit Wiltschi, Gerald Striedner, Winfried Ro?mer, and Juergen Mairhofer. Clickable Shiga Toxin B Subunit for Drug Delivery in Cancer Therapy.. ACS Omega. 2023
    https://pubs.acs.org/doi/pdf/10.1021/acsomega.3c00667
  3. Yang, Q., Chen, H., Ou, C., Zheng, Z., Zhang, X., Liu, Y., ... & Wang, L. X. (2023). Evaluation of Two Chemoenzymatic Glycan Remodeling Approaches to Generate Site-Specific Antibody–Drug Conjugates. Antibodies, 12(4), 71.
    https://www.mdpi.com/2073-4468/12/4/71