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DBM-MMAF is composed of linker DBM and toxic molecule MMAF, which can be used to prepare antibody-conjugated drugs.
| Catalog Number | Size | Price | Quantity | ||
|---|---|---|---|---|---|
| BADC-01460 | -- | $-- | Inquiry |
DBM-MMAF, or Dolabella Marine Antibody-Drug Conjugate Monomethyl Auristatin F, is a synthetic compound employed in the creation of antibody-drug conjugates (ADCs) for cancer treatment. The utilization of DBM-MMAF is pivotal because it combines the cytotoxic potency of MMAF, a microtubule-disrupting agent, with targeted therapy offered by monoclonal antibodies. These antibodies are designed to identify and bind to specific cancer cell antigens, ensuring the delivery of MMAF directly to cancer cells while sparing normal, healthy cells from damage. This targeted approach mitigates the systemic side effects typically associated with traditional chemotherapy, representing a significant advancement in oncological therapeutics.
In the context of drug discovery, DBM-MMAF serves as a crucial drug-linker compound. Its role is to provide a stable connection between the antibody and the cytotoxic agent, allowing the ADC to circulate in the bloodstream without premature release of MMAF. Once the ADC binds to the target cancer cell, it is internalized, and the MMAF is released to exert its cytotoxic effect, leading to cell cycle arrest and apoptosis of the cancer cell. The design of DBM-MMAF ensures that the linker-payload system is stable in circulation but cleavable once inside the targeted cell, which is critical for the efficacy and safety of the ADCs.
The application of DBM-MMAF in drug discovery is pioneering the development of new therapies across various cancer types. Researchers and pharmaceutical companies invest in ADCs to leverage the selective mechanism of DBM-MMAF, improving treatment outcomes for patients with difficult-to-treat malignancies. Its adaptability to different antibodies also facilitates the exploration of treatments for varying tumor antigens, broadening the potential scope of ADC therapies. The ongoing research into optimizing linkers and conjugates seeks to enhance pharmacokinetics and reduce off-target toxicity, paving the way for more effective and personalized cancer therapies.
Moreover, DBM-MMAF is instrumental in addressing resistance issues that often arise in cancer treatment. Due to its targeted delivery mechanism, it minimizes the development of resistance seen with conventional chemotherapy. By directly attacking tumor cells with high precision, DBM-MMAF contributes to overcoming the limitations of existing therapies and offers renewed hope for patients prone to relapses. The versatility of DBM-MMAF in binding with different antibodies allows for customization and rapid iteration in drug development, accommodating evolving therapeutic strategies and the dynamic nature of cancer pathogenesis.
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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.
