MC-VC-PAB-Tubulysin M is a potent antibody-drug conjugate used in the treatment of various cancers, including breast, lung, and ovarian cancers. It combines the targeted delivery of an antibody with the cytotoxic effects of Tubulysin M, inhibiting microtubule formation and inducing cell death.
Catalog Number | Size | Price | Quantity | |
---|---|---|---|---|
BADC-01535 | -- | $-- | Inquiry |
MC-VC-PAB-Tubulysin M is a potent antibody-drug conjugate (ADC) that combines the highly targeted delivery of an antibody with the powerful cytotoxic effects of Tubulysin M. Tubulysin M is a potent antitumor agent that inhibits microtubule formation, a crucial component of cell division. By halting microtubule dynamics, Tubulysin M induces cell cycle arrest and ultimately leads to apoptosis, effectively killing cancer cells. The ability to selectively deliver Tubulysin M to tumor cells via an antibody increases the specificity of treatment, allowing for more effective tumor destruction while minimizing harm to healthy tissues. This makes MC-VC-PAB-Tubulysin M an essential tool in targeted cancer therapy.
The cleavable linker, MC-VC-PAB, plays a vital role in the effectiveness of MC-VC-PAB-Tubulysin M by ensuring that the cytotoxic payload is only released once the ADC reaches the target cancer cells. The MC-VC-PAB linker is designed to be cleaved in the acidic tumor microenvironment, which is rich in proteolytic enzymes such as cathepsins. This cleavable mechanism ensures that Tubulysin M is released specifically within the tumor site, where it can exert its cytotoxic effects on rapidly dividing cancer cells. By limiting the activation of Tubulysin M to the tumor microenvironment, MC-VC-PAB-Tubulysin M reduces systemic toxicity and increases the overall therapeutic index of the drug.
MC-VC-PAB-Tubulysin M has significant applications in the treatment of a variety of cancers, including breast, lung, and ovarian cancers. These cancers often exhibit aggressive growth and can be resistant to conventional chemotherapy. By utilizing the targeted approach of ADCs, MC-VC-PAB-Tubulysin M can overcome some of the limitations of traditional treatments, such as poor drug penetration and systemic side effects. The antibody component of the ADC specifically targets tumor-associated antigens, ensuring that Tubulysin M is delivered directly to the cancer cells. This targeted delivery significantly enhances the drug's potency while reducing the risk of damaging healthy tissues.
In addition to its use in solid tumors, MC-VC-PAB-Tubulysin M is also being explored for its potential in treating hematological cancers. The versatility of this ADC makes it adaptable to a range of malignancies, where it can be used to target specific cell surface markers expressed by leukemia or lymphoma cells. By exploiting the unique molecular characteristics of these cancers, MC-VC-PAB-Tubulysin M offers a personalized treatment option that could improve outcomes for patients who do not respond well to standard therapies. Its potential to target both solid and liquid tumors makes it a promising candidate for broader cancer therapy applications.
Customer Support
Providing excellent 24/7 customer service and support
Project Management
Offering 100% high-quality services at all stages
Quality Assurance
Ensuring the quality and reliability of products or services
Global Delivery
Ensuring timely delivery of products worldwide
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.