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MC-Val-Cit-PAB-clindamycin is a drug-linker conjugate for ADC with potent antitumor activity by using clindamycin (a protein synthesis inhibitor), linked via the ADC linker MC-Val-Cit-PAB.
| Catalog Number | Size | Price | Quantity | |
|---|---|---|---|---|
| BADC-00611 | -- | $-- | Inquiry |
MC-Val-Cit-PAB-clindamycin is a conjugate designed for targeted drug delivery, combining the antibiotic clindamycin with a peptide-based linker. Clindamycin is a well-known antibiotic that inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit, making it effective against a variety of bacterial infections. By linking clindamycin to a peptide linker like MC-Val-Cit-PAB, the drug can be selectively delivered to specific targets, potentially improving its efficacy in treating infections while minimizing side effects. This targeted delivery system has a broad range of potential applications in antimicrobial therapy and beyond.
One key application of MC-Val-Cit-PAB-clindamycin is in the development of targeted therapies for bacterial infections, particularly those that are resistant to conventional antibiotics. The conjugate can be used to deliver clindamycin more efficiently to infection sites, such as in tissues with high bacterial load. The peptide linker allows for selective targeting of bacteria or infected cells, improving the concentration of clindamycin where it is most needed. This targeted approach could reduce the risk of systemic toxicity and improve the overall therapeutic efficacy of clindamycin, especially in treating difficult-to-target infections.
MC-Val-Cit-PAB-clindamycin also offers significant promise in overcoming bacterial resistance mechanisms. Antibiotic resistance is an increasing global concern, with bacteria evolving mechanisms that render conventional antibiotics less effective. The conjugation of clindamycin to a peptide that specifically targets infected cells could bypass some of these resistance pathways by ensuring that the drug is delivered directly to the site of infection. This could enhance the antibiotic’s potency and effectiveness against resistant strains, providing a more robust solution for treating multidrug-resistant bacterial infections.
In addition, MC-Val-Cit-PAB-clindamycin has applications in the field of personalized medicine. By incorporating specific targeting peptides into the conjugate, the therapy can be tailored to address unique bacterial strains or individual patient needs. Personalized therapy allows for a more precise treatment regimen, which is crucial in managing infections caused by complex or heterogeneous bacterial populations. The targeted nature of MC-Val-Cit-PAB-clindamycin makes it a promising tool in the development of personalized antimicrobial therapies.
Finally, MC-Val-Cit-PAB-clindamycin may also be used in combination therapies, where it can be co-delivered with other antimicrobial agents or immune-modulating drugs. The targeted delivery system could allow for synergistic effects, enhancing the therapeutic outcome while minimizing the side effects of the individual drugs. This combination approach could be especially effective in treating chronic infections or those caused by biofilm-forming bacteria, which are more difficult to eradicate with standard treatments.
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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.
