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MC-vc-PAB-(PEG2)-duocarmycin DM is a drug-linker conjugate for ADC by using Duocarmycin DM (a potent antitumor antibiotic), linked via MA-MC-vc-PAB-(PEG2).
| Catalog Number | Size | Price | Quantity | |
|---|---|---|---|---|
| BADC-00746 | -- | $-- | Inquiry |
MC-vc-PAB-(PEG2)-duocarmycin DM is a novel peptide-drug conjugate (PDC) designed to enhance targeted drug delivery and reduce off-target toxicity. One of its key applications lies in targeted cancer therapy. The conjugate consists of the potent cytotoxic agent duocarmycin DM, which is linked to a peptide sequence via a cleavable valine-citrulline (vc) linker. This design allows for selective activation of the drug within cancer cells, where the linker is cleaved by tumor-specific enzymes, leading to localized and precise cytotoxicity, thereby sparing healthy tissues and minimizing systemic side effects.
Another significant application of MC-vc-PAB-(PEG2)-duocarmycin DM is in drug delivery systems with improved pharmacokinetics. The incorporation of PEG2 (a polyethylene glycol derivative) enhances the solubility and stability of the conjugate in circulation, prolonging its half-life and improving bioavailability. This PEGylation also reduces the likelihood of immune recognition, which can lead to faster clearance of non-PEGylated drugs from the body. As a result, the conjugate remains active in the bloodstream longer, allowing for efficient accumulation in tumor tissues.
MC-vc-PAB-(PEG2)-duocarmycin DM also demonstrates potential in combination therapies to increase therapeutic efficacy. When used in conjunction with other anticancer agents, such as immune checkpoint inhibitors or targeted biologics, the conjugate can work synergistically to overcome tumor resistance mechanisms. The targeted release of duocarmycin DM within cancer cells enhances the overall treatment effect, making it a valuable tool in multi-modal cancer therapy approaches. This ability to combine with other treatments enhances the overall therapeutic outcome and potentially reduces the risk of relapse.
Lastly, the versatility of MC-vc-PAB-(PEG2)-duocarmycin DM makes it an important candidate for personalized cancer therapy. The peptide component of the conjugate can be modified to target specific biomarkers expressed on various tumor types. This adaptability allows for the design of customized therapies that address the unique molecular characteristics of individual cancers, leading to more precise and effective treatment strategies. Personalized approaches using this conjugate hold promise for improving patient outcomes and advancing 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.
