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MC-Val-Cit-PAB-vinblastine is a drug-linker conjugate for ADC with potent antitumor activity by using vinblastine (an microtubule protein inhibitor), linked via the ADC linker MC-Val-Cit-PAB.
| Catalog Number | Size | Price | Quantity | |
|---|---|---|---|---|
| BADC-00857 | -- | $-- | Inquiry |
MC-Val-Cit-PAB-vinblastine is a potent peptide-drug conjugate (PDC) that combines the cytotoxicity of vinblastine with the targeted delivery capabilities of a peptide sequence. One key application is in targeted cancer therapy. The conjugate leverages the specificity of the Val-Cit linker to selectively release vinblastine within cancer cells. This targeted approach minimizes systemic toxicity, enhancing the therapeutic index by ensuring the drug is predominantly active in the tumor site, where it can efficiently inhibit cancer cell division.
Another prominent application of MC-Val-Cit-PAB-vinblastine is in the field of drug delivery systems. The conjugate's design allows for the controlled release of vinblastine through enzymatic cleavage at the Val-Cit junction, which is highly sensitive to the activity of cancer-specific proteases. This ensures that the drug is only activated within the tumor microenvironment, offering a mechanism for overcoming the challenges of traditional chemotherapy, such as off-target effects and poor drug bioavailability.
MC-Val-Cit-PAB-vinblastine also plays a crucial role in improving the efficacy of combination therapies. When used alongside other therapeutic agents, it can enhance the overall treatment outcome by providing synergistic effects. For instance, combining this PDC with immune checkpoint inhibitors or other cytotoxic agents can create a multi-pronged attack on the tumor, increasing the likelihood of a sustained therapeutic response. The ability to fine-tune the drug release via the peptide linker further augments this synergism.
Lastly, MC-Val-Cit-PAB-vinblastine is a promising candidate for preclinical and clinical research in personalized medicine. The conjugate can be engineered with different peptides to target specific tumor markers, making it highly adaptable for a wide range of cancers. This customization enables more precise and effective treatment regimens tailored to individual patient profiles, which is essential for improving patient outcomes in precision oncology.
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BOC Sciences offers comprehensive services for ADC manufacturing, including antibody modification, linker chemistry, payload conjugation, and formulation development. In particular, our payload-linker customization service offers a convenient and fast raw material channel for many ADC researchers.
BOC Sciences provides one-stop site-specific conjugation services for amino acids, glycans, unnatural amino acids, and short peptide tags. In addition, cysteine conjugation, lysine conjugation, enzymatic conjugation, thio-engineered antibody can also be obtained quickly.
BOC Sciences offers a full range of linkers, including peptide linkers, PEG linkers, click chemistry, PROTAC linkers, non-cleavable linkers, etc. We also provide custom development services for chemically labile linkers and enzymatically cleavable linkers.
