(2,5-dioxopyrrolidin-1-yl) 5-[[3-(2,5-dioxopyrrolidin-1-yl)oxycarbonyl-4-nitrocyclohexyl]disulfanyl]-2-nitrobenzoate is a linker for antibody-drug-conjugation (ADC).
Structure of 924898-35-1
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Capabilities & Facilities
(2,5-dioxopyrrolidin-1-yl) 5-[[3-(2,5-dioxopyrrolidin-1-yl)oxycarbonyl-4-nitrocyclohexyl]disulfanyl]-2-nitrobenzoate, with its intricate structure, finds applications in specialized fields of biochemistry and molecular biology. Here are four key applications presented with high perplexity and burstiness:
Drug Delivery Systems: Acting as a pivotal linker, this compound facilitates the precise attachment of drugs to targeted delivery systems. By conjugating therapeutic molecules to this linker, medications can be delivered with pinpoint accuracy to specific tissues or cells, thereby enhancing their effectiveness and reducing potential side effects. This targeted approach is particularly advantageous in the realm of precision cancer therapy, where accuracy is paramount.
Protein Labeling: Within the realm of biochemical research, this compound serves as a valuable tool for protein labeling, enabling scientists to delve into protein dynamics and interactions. Through its interaction with specific amino acid residues in proteins, this compound acts as a visual marker for tracking and imaging studies, providing crucial insights into protein functionality and cellular processes.
Synthetic Chemistry: The versatility of (2,5-dioxopyrrolidin-1-yl) 5-[[3-(2,5-dioxopyrrolidin-1-yl)oxycarbonyl-4-nitrocyclohexyl]disulfanyl]-2-nitrobenzoate shines in the realm of synthetic chemistry, serving as a key player in the synthesis of complex molecules. Its functional groups can undergo diverse chemical reactions, making it a versatile intermediate in organic synthesis. This property enables the creation of novel compounds for both research and industrial applications, fueling advancements in chemistry.
Bioconjugation: Widely employed in the field of bioconjugation, this molecule facilitates the formation of stable linkages between biological molecules and synthetic compounds. By establishing disulfide bonds, it can connect antibodies or other proteins to fluorescent dyes, drugs, or other molecules, enabling a range of applications in drug development, diagnostic assays, and imaging studies. This technique lies at the core of interdisciplinary research at the intersection of biology and chemistry.
Catalog | Product Name | CAS | Inquiry |
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BADC-00663 | (2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propanoate | 216145-65-2 | |
BADC-00689 | (2,5-dioxopyrrolidin-1-yl) 4-methyl-4-(methyldisulfanyl)pentanoate | 796073-56-8 | |
BADC-00690 | (2,5-dioxopyrrolidin-1-yl) 4-(methyldisulfanyl)pentanoate | 796073-59-1 | |
BADC-00691 | (2,5-dioxopyrrolidin-1-yl) 3-(2,3-dihydrothieno[3,4-b][1,4]dioxin-3-ylmethoxy)propanoate | 853799-72-1 | |
BADC-00705 | (2,5-dioxopyrrolidin-1-yl) 4-(methyldisulfanyl)butanoate | 905449-92-5 |
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