2,5-dioxopyrrolidin-1-yl 4-((5-(dimethylcarbamoyl)pyridin-2-yl)disulfanyl)butanoate - CAS 663599-05-1

2,5-dioxopyrrolidin-1-yl 4-((5-(dimethylcarbamoyl)pyridin-2-yl)disulfanyl)butanoate - CAS 663599-05-1 Catalog number: BADC-00483

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DMAC-SPDB is a bioactive compound. It blocks signaling pathways associated with cancer and inflammation, exerting its influence as a targeted enzyme inhibitor. Furthermore, it shows decent proficiency in regulating the harmonious balance of enzymatic reactions associated with metabolic dysfunction.

Category
ADCs Linker
Product Name
2,5-dioxopyrrolidin-1-yl 4-((5-(dimethylcarbamoyl)pyridin-2-yl)disulfanyl)butanoate
CAS
663599-05-1
Catalog Number
BADC-00483
Molecular Formula
C16H19N3O5S2
Molecular Weight
397.47
2,5-dioxopyrrolidin-1-yl 4-((5-(dimethylcarbamoyl)pyridin-2-yl)disulfanyl)butanoate

Ordering Information

Catalog Number Size Price Quantity
BADC-00483 -- $--
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Description
DMAC-SPDB is a bioactive compound. It blocks signaling pathways associated with cancer and inflammation, exerting its influence as a targeted enzyme inhibitor. Furthermore, it shows decent proficiency in regulating the harmonious balance of enzymatic reactions associated with metabolic dysfunction.
Synonyms
(2,5-dioxopyrrolidin-1-yl) 4-[[5-(dimethylcarbamoyl)pyridin-2-yl]disulfanyl]butanoate;
Canonical SMILES
CN(C)C(=O)C1=CN=C(C=C1)SSCCCC(=O)ON2C(=O)CCC2=O
InChI
InChI=1S/C16H19N3O5S2/c1-18(2)16(23)11-5-6-12(17-10-11)26-25-9-3-4-15(22)24-19-13(20)7-8-14(19)21/h5-6,10H,3-4,7-9H2,1-2H3
InChIKey
XDZYHHAHYBOELZ-UHFFFAOYSA-N
Appearance
Soild powder
Purity
≥98%
Shipping
Room temperature, or blue ice upon request.

2,5-Dioxopyrrolidin-1-yl 4-((5-(dimethylcarbamoyl)pyridin-2-yl)disulfanyl)butanoate, often abbreviated as DSPB, is a compound with significant applications in biochemical research. One of its primary uses is in protein bioconjugation. In this process, DSPB serves as a critical linker molecule that facilitates the attachment of proteins to various surfaces or other molecules. Its disulfide bond is particularly effective for creating stable connections that can later be cleaved under reducing conditions, making it ideal for applications where reversible linkages are needed. This ability to form and break bonds under specific conditions makes DSPB invaluable in the study of protein interactions and dynamics.

Another important application of DSPB is in drug delivery systems. Due to its unique chemical structure, DSPB can be used to attach therapeutic agents to nanoparticles or other delivery vehicles. The disulfide bond in DSPB is stable under normal physiological conditions but can be selectively broken in the presence of high concentrations of reducing agents, such as those found in tumor tissues. This property allows for targeted release of drugs at the site of interest, minimizing systemic side effects and improving the efficacy of the treatment. Hence, DSPB is increasingly being explored in the development of targeted cancer therapies and other precision medicine applications.

DSPB also finds application in the field of biosensors. The compound can be used to immobilize enzymes, antibodies, or other bioreceptive elements on sensor surfaces, thereby enhancing the sensitivity and specificity of the sensors. The reversible nature of its disulfide bond allows for easy regeneration of the biosensor surface, extending the lifespan and usability of these devices. This makes DSPB a valuable tool in the creation of highly efficient and reusable biosensors for medical diagnostics, environmental monitoring, and biodefense applications.

Lastly, DSPB is utilized in the synthesis of advanced biomaterials. Its ability to form strong, yet reversible linkages makes it an ideal candidate for creating dynamic, stimuli-responsive materials. These materials can change their properties in response to environmental changes such as pH, temperature, or redox conditions. This adaptability is useful in the design of smart materials for tissue engineering, drug delivery, and responsive coatings. The versatility and functionality brought by DSPB’s unique chemistry facilitate the development of innovative materials that can meet the demands of various biomedical applications.

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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