Catalog Number | Size | Price | Quantity |
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BADC-00470 | -- | $-- |
One key application of 2,5-dioxopyrrolidin-1-yl 4-((3-(dimethylcarbamoyl)pyridin-4-yl)disulfanyl)pentanoate is in biochemical research as a cross-linking reagent. Cross-linking reagents are pivotal in studying protein-protein interactions, providing insights into the spatial arrangement and functional connectivity within protein complexes. This compound can be particularly useful in stabilizing transient protein interactions, which are often difficult to study using conventional techniques. By creating stable covalent bonds between interacting proteins, researchers can more easily isolate and identify the components of complex biochemical pathways. This application is especially valuable in understanding diseases at the molecular level, enabling the development of targeted therapeutic strategies.
Another significant application of 2,5-dioxopyrrolidin-1-yl 4-((3-(dimethylcarbamoyl)pyridin-4-yl)disulfanyl)pentanoate is in the synthesis of antibody-drug conjugates (ADCs). ADCs are an innovative class of biopharmaceutical drugs designed to selectively target and kill cancer cells while minimizing damage to normal tissues. The compound serves as a linker that connects cytotoxic drugs to monoclonal antibodies, which specifically bind to cancer cell antigens. The disulfide bond within the structure is particularly advantageous as it offers a controlled release mechanism—once inside the target cell, the bond can be cleaved, releasing the cytotoxic agent to exert its therapeutic effect. This precise targeting capability enhances the efficacy and safety profile of cancer treatments.
The compound also finds application in the field of targeted protein degradation, specifically in the development of proteolysis-targeting chimeras (PROTACs). PROTACs are molecules designed to selectively degrade specific proteins by harnessing the cell’s ubiquitin-proteasome system. In this context, 2,5-dioxopyrrolidin-1-yl 4-((3-(dimethylcarbamoyl)pyridin-4-yl)disulfanyl)pentanoate can be used as a linker that joins a ligand capable of binding the target protein with another ligand that recruits an E3 ubiquitin ligase. This bifunctional molecule brings the target protein into proximity with the ubiquitin-proteasome machinery, resulting in its degradation. This approach offers a novel therapeutic strategy, especially for treating diseases caused by aberrant protein function, such as cancer and neurodegenerative disorders.
Additionally, this compound can be employed in the realm of redox biology as a disulfide exchange reagents. Disulfide exchange reactions are crucial in the formation and isomerization of disulfide bonds, which play a vital role in protein folding and stability. The presence of a disulfide bond in 2,5-dioxopyrrolidin-1-yl 4-((3-(dimethylcarbamoyl)pyridin-4-yl)disulfanyl)pentanoate allows it to act as a modulator of thiol-disulfide balance within cells. This capability can be exploited to probe cellular redox states and to study the mechanisms of diseases related to oxidative stress. Furthermore, manipulating disulfide bonds in peptides and proteins using this reagent can lead to the development of novel biopharmaceuticals with improved stability and activity profiles.
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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.