2,5-dioxopyrrolidin-1-yl 4-methyl-4-((5-nitropyridin-2-yl)disulfanyl)pentanoate - CAS 663598-98-9

2,5-dioxopyrrolidin-1-yl 4-methyl-4-((5-nitropyridin-2-yl)disulfanyl)pentanoate - CAS 663598-98-9 Catalog number: BADC-00466

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NO2-SPDMV is a biomedical product used in the drug development of various diseases. With its unique chemical structure, it exhibits potential therapeutic properties to target specific receptors and enzymes involved in the progression of certain disorders. Its applications include drug research to treat cardiovascular disease, neurological diseases, and inflammatory diseases, among others.

Category
ADCs Linker
Product Name
2,5-dioxopyrrolidin-1-yl 4-methyl-4-((5-nitropyridin-2-yl)disulfanyl)pentanoate
CAS
663598-98-9
Catalog Number
BADC-00466
Molecular Formula
C15H17N3O6S2
Molecular Weight
399.44
2,5-dioxopyrrolidin-1-yl 4-methyl-4-((5-nitropyridin-2-yl)disulfanyl)pentanoate

Ordering Information

Catalog Number Size Price Quantity
BADC-00466 10 mg $729
BADC-00466 50 mg $999
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Description
NO2-SPDMV is a biomedical product used in the drug development of various diseases. With its unique chemical structure, it exhibits potential therapeutic properties to target specific receptors and enzymes involved in the progression of certain disorders. Its applications include drug research to treat cardiovascular disease, neurological diseases, and inflammatory diseases, among others.
Synonyms
NO2-SPDMV
Canonical SMILES
CC(C)(CCC(=O)ON1C(=O)CCC1=O)SSC2=NC=C(C=C2)[N+](=O)[O-]
InChI
InChI=1S/C15H17N3O6S2/c1-15(2,26-25-11-4-3-10(9-16-11)18(22)23)8-7-14(21)24-17-12(19)5-6-13(17)20/h3-4,9H,5-8H2,1-2H3
InChIKey
AQKHEWNNTCBJPY-UHFFFAOYSA-N
Appearance
Soild powder
Purity
≥98%
Shipping
Room temperature, or blue ice upon request.

2,5-Dioxopyrrolidin-1-yl 4-methyl-4-((5-nitropyridin-2-yl)disulfanyl)pentanoate is a potent chemical compound with a wide array of applications in various fields of science and industry. One of its critical uses is in drug development, particularly in the synthesis of novel pharmacological agents. Its unique molecular structure allows it to facilitate the creation of disulfide bonds, which are essential in the folding and stability of proteins and peptides. This characteristic makes it invaluable for designing drugs that require precise three-dimensional structures, such as enzyme inhibitors and receptor modulators. By leveraging its properties, researchers can develop more effective and targeted therapeutics to treat a range of diseases, from cancer to autoimmune disorders.

Another vital application of 2,5-Dioxopyrrolidin-1-yl 4-methyl-4-((5-nitropyridin-2-yl)disulfanyl)pentanoate is in biochemical research, especially in protein cross-linking studies. Cross-linking agents like this compound are crucial for probing protein-protein interactions and mapping out the functional relationships within complex biological systems. By forming stable disulfide bridges, this compound can help in stabilizing transient protein complexes, thereby enabling the detailed study of protein interaction networks. This application is particularly relevant in elucidating the mechanisms of signaling pathways and cellular responses, which can further our understanding of fundamental biological processes.

The compound also finds significant use in materials science, specifically in the development of advanced polymeric materials. Its ability to form strong and stable disulfide bonds allows it to act as a cross-linking agent in polymer chains, enhancing the mechanical strength, durability, and responsiveness of the resultant materials. Such polymers can be used in a variety of applications, including medical devices, industrial coatings, and smart materials that respond to environmental changes. The incorporation of this compound can lead to materials with superior properties, which are essential for the next generation of technological advancements.

Furthermore, 2,5-Dioxopyrrolidin-1-yl 4-methyl-4-((5-nitropyridin-2-yl)disulfanyl)pentanoate is employed in the development of diagnostic tools and biosensors. The high reactivity of its disulfide groups enables the covalent attachment of various biomolecules, making it an excellent candidate for the construction of bio-conjugates and molecular probes. These tools are crucial for detecting and quantifying biological entities, such as proteins, nucleic acids, and small molecules, with high specificity and sensitivity. This application is particularly vital in the fields of medical diagnostics, environmental monitoring, and biotechnology research, where accurate detection methods are paramount. By utilizing this compound, researchers can develop more reliable and efficient diagnostic devices that facilitate early disease detection and monitoring.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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