1-(4-((5-(dimethylcarbamoyl)pyridin-2-yl)disulfanyl)butanoyloxy)-2,5-dioxopyrrolidine-3-sulfonic acid - CAS 663599-07-3

1-(4-((5-(dimethylcarbamoyl)pyridin-2-yl)disulfanyl)butanoyloxy)-2,5-dioxopyrrolidine-3-sulfonic acid - CAS 663599-07-3 Catalog number: BADC-00478

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DMAC-SPDB-sulfo is an effective small molecule reagent. Its efficacy is primarily due to its selective mediation of key enzyme cascades and receptor signaling pathways, which are critical for targeted disease progression. This breakthrough bioactive compound has great potential to intervene in specific diseases.

Category
ADCs Linker
Product Name
1-(4-((5-(dimethylcarbamoyl)pyridin-2-yl)disulfanyl)butanoyloxy)-2,5-dioxopyrrolidine-3-sulfonic acid
CAS
663599-07-3
Catalog Number
BADC-00478
Molecular Formula
C16H19N3O8S3
Molecular Weight
477.53
1-(4-((5-(dimethylcarbamoyl)pyridin-2-yl)disulfanyl)butanoyloxy)-2,5-dioxopyrrolidine-3-sulfonic acid

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Catalog Number Size Price Quantity
BADC-00478 -- $--
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Description
DMAC-SPDB-sulfo is an effective small molecule reagent. Its efficacy is primarily due to its selective mediation of key enzyme cascades and receptor signaling pathways, which are critical for targeted disease progression. This breakthrough bioactive compound has great potential to intervene in specific diseases.
Synonyms
1-[4-[[5-(dimethylcarbamoyl)pyridin-2-yl]disulfanyl]butanoyloxy]-2,5-dioxopyrrolidine-3-sulfonic acid;
Canonical SMILES
CN(C)C(=O)C1=CN=C(C=C1)SSCCCC(=O)ON2C(=O)CC(C2=O)S(=O)(=O)O
InChI
InChI=1S/C16H19N3O8S3/c1-18(2)15(22)10-5-6-12(17-9-10)29-28-7-3-4-14(21)27-19-13(20)8-11(16(19)23)30(24,25)26/h5-6,9,11H,3-4,7-8H2,1-2H3,(H,24,25,26)
InChIKey
KMRAQLKAJPMTOK-UHFFFAOYSA-N
Appearance
Soild powder
Purity
≥98%
Shipping
Room temperature

1-(4-((5-(dimethylcarbamoyl)pyridin-2-yl)disulfanyl)butanoyloxy)-2,5-dioxopyrrolidine-3-sulfonic acid is a synthetic compound with potential applications in various areas of biochemistry and pharmacology. Here are some key applications of this compound:

Protein Modification: This compound can be used in the selective modification of cysteine residues in proteins. By forming disulfide bonds with cysteine, it allows for the targeted alteration of protein structure and function. This application is crucial for studying protein interactions and developing novel protein-based therapeutics.

Chemical Biology: In chemical biology, this compound serves as a useful tool for probing and manipulating biological systems. It can be used to label proteins or small molecules, facilitating the study of their localization, dynamics, and interactions within cells. Such insights are valuable for understanding complex biological processes and disease mechanisms.

Drug Development: The compound's unique structure makes it a potential candidate for drug development, particularly in the design of enzyme inhibitors or activators. Its ability to target specific amino acid residues can lead to the discovery of new therapeutic agents with high specificity and efficacy. This can be especially useful in developing treatments for diseases with known protein targets.

Bioconjugation: The compound can be utilized in bioconjugation techniques to attach various biomolecules, such as peptides, antibodies, or nucleic acids, to surfaces or other molecules. This capability is essential for the development of biosensors, targeted drug delivery systems, and diagnostic tools. It enables the creation of multifunctional biomaterials with tailored properties for specific 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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