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MC-vc-PAB-(PEG2)-duocarmycin TM is a drug-linker conjugate for ADC by using Duocarmycin TM (a potent antitumor antibiotic), linked via MA-MC-vc-PAB-(PEG2).
| Catalog Number | Size | Price | Quantity | |
|---|---|---|---|---|
| BADC-00744 | -- | $-- | Inquiry |
MC-vc-PAB-(PEG2)-duocarmycin TM is a powerful peptide-drug conjugate (PDC) that combines the targeting specificity of a peptide with the potent cytotoxicity of duocarmycin TM. One key application is in targeted cancer therapy. The conjugate uses a valine-citrulline (vc) linker to ensure selective cleavage by enzymes found in the tumor microenvironment. This enables the release of duocarmycin TM directly within the cancer cells, leading to efficient DNA damage and cell death while minimizing exposure to healthy tissues. This highly targeted approach reduces systemic toxicity and enhances therapeutic efficacy.
Another important application of MC-vc-PAB-(PEG2)-duocarmycin TM is in enhancing pharmacokinetics and stability. The addition of PEG2 (polyethylene glycol) to the conjugate improves its solubility, stability, and circulation time in the bloodstream. PEGylation helps to evade recognition by the immune system, thus preventing rapid clearance and allowing for prolonged drug exposure. This modification optimizes the drug’s bioavailability and improves its accumulation in the tumor site, which is essential for maximizing the therapeutic benefit of duocarmycin TM.
MC-vc-PAB-(PEG2)-duocarmycin TM also shows promise in combination therapies. The conjugate can be used alongside other anticancer treatments, such as immunotherapies or chemotherapy agents, to enhance the overall therapeutic response. By delivering duocarmycin TM directly to the tumor, it can work synergistically with other drugs to increase the likelihood of overcoming resistance mechanisms and achieving sustained tumor regression. This multi-pronged therapeutic approach offers a promising strategy to improve treatment outcomes in complex cancer cases.
Lastly, MC-vc-PAB-(PEG2)-duocarmycin TM is well-suited for personalized medicine applications. The peptide component of the conjugate can be tailored to bind to specific receptors or biomarkers expressed on various cancer types. This customization allows for the design of highly targeted therapies, providing an opportunity for more effective and personalized treatment regimens. By aligning the drug delivery with the unique molecular profile of a patient's cancer, MC-vc-PAB-(PEG2)-duocarmycin TM holds potential for advancing precision oncology and improving patient outcomes.
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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.
