EC089 is a cleavable linker used in conjugates of tubulysins and folates, and extracted from patent WO2011069116A1.
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BADC-00684 | -- | $-- | Inquiry |
EC089 is recognized as a cleavable linker, playing a significant role in the conjugation of tubulysins and folates. This compound enables targeted drug delivery systems by linking potent cytotoxic tubulysins to molecules like folate for receptor-mediated endocytosis. Such a system allows drugs to be released specifically within tumor cells, thereby minimizing effects on healthy cells and enhancing the therapeutic index of the drugs. EC089’s role as a linker lies in its ability to undergo cleavage under physiological conditions, which is crucial in releasing the drug once inside the target cell.
One of the unique features of EC089 is its design, which incorporates both a spacer and a releasable linker. This design ensures that the conjugate remains stable during circulation in the bloodstream but becomes activated upon reaching the acidic environment within specific cellular targets like cancer cells. The cleavable bond is typically susceptible to the intracellular environment, promoting selective cytotoxicity towards tumor cells, thus decreasing systemic toxicity. The utilization of folate as the targeting moiety leverages the overexpression of folate receptors in many cancerous cells, employing a well-understood mechanism to facilitate the cellular uptake of therapeutic agents.
The pharmaceutical applications of EC089, particularly in the formulation of drug conjugates, underscore its importance in modern oncology therapeutics. Drug conjugates utilizing EC089 are formulated to exploit receptor-mediated mechanisms for targeted therapy, thereby improving the pharmacokinetics and biodistribution of molecules like tubulysins. This conjugation strategy not only enhances the potency of tubulysins by concentrating them at the tumor site but also permits a higher therapeutic drug index than conventional chemotherapy, setting a new paradigm in cancer treatment modalities. These advances offer a substantial reduction in non-specific toxicity, which has historically been a significant drawback in cytotoxic chemotherapy.
Moreover, the development of EC089 and its subsequent applications highlight the intersection of synthetic chemistry and therapeutics—a convergence that epitomizes the innovation driving the future of drug discovery and development. By facilitating the targeted release of drugs within designated cellular environments, EC089 contributes to the burgeoning field of precision medicine, where treatment regimens are tailored according to the molecular and cellular characteristics of individual patients’ conditions. As such, EC089 not only represents a technical advancement in chemical design but also a promising tool in the quest for more effective and less harmful cancer 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.