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Gly3-MMAF is a drug-linker conjugate for ADC by using Monomethylauristatin F (MMAF,a potent tubulin polymerization inhibitor), linked via Gly3.
| Catalog Number | Size | Price | Quantity | |
|---|---|---|---|---|
| BADC-00768 | -- | $-- | Inquiry |
Gly3-MMAF is a potent cytotoxic conjugate used in the field of targeted cancer therapy, specifically in antibody-drug conjugates (ADCs). The compound consists of a glycine tripeptide (Gly3) linked to monomethyl auristatin F (MMAF), a highly effective microtubule-disrupting agent. The Gly3 peptide serves as a spacer to optimize the delivery and release of MMAF, enhancing the precision of cancer cell targeting when conjugated to monoclonal antibodies. The MMAF payload disrupts microtubule dynamics within the cancer cell, leading to cell cycle arrest and apoptosis. This makes Gly3-MMAF a key component in the development of ADCs aimed at treating various malignancies, including solid tumors and hematological cancers.
In addition to its role in ADCs, Gly3-MMAF is being explored for its potential in overcoming the limitations of traditional chemotherapy. MMAF, as a potent tubulin inhibitor, offers several advantages over conventional chemotherapeutic agents, including a lower likelihood of inducing multidrug resistance (MDR). The Gly3 peptide acts as a linker, enabling precise attachment to antibodies that specifically target tumor-associated antigens. This targeted delivery ensures that MMAF is primarily delivered to cancer cells, significantly reducing the off-target effects and systemic toxicity that are common with traditional chemotherapy. This makes Gly3-MMAF a promising candidate for developing more effective and less toxic cancer treatments.
Moreover, Gly3-MMAF is being investigated for use in combination therapies to enhance the effectiveness of other cancer treatments. Research has shown that when used in conjunction with immune checkpoint inhibitors or other targeted therapies, Gly3-MMAF can synergize to improve treatment outcomes. By providing direct cytotoxic effects while modulating the tumor microenvironment, this compound has the potential to increase the sensitivity of cancer cells to other therapies, ultimately leading to more successful treatment responses. This combination approach could be especially valuable for cancers with low immune response or resistance to conventional 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.
