Name: (2S,2'S)-Bis(2,5-Dioxopyrrolidin-1-yl) 4,4'-Disulfanediylbis(2-Acetamidobutanoate)
Brand: BOC Sciences
Rating: 5 (1 reviews)

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Synonyms

(2,5-dioxopyrrolidin-1-yl) 2-acetamido-4-[[3-acetamido-4-(2,5-dioxopyrrolidin-1-yl)oxy-4-oxobutyl]disulfanyl]butanoate

IUPAC Name

(2,5-dioxopyrrolidin-1-yl) (2S)-2-acetamido-4-[[(3S)-3-acetamido-4-(2,5-dioxopyrrolidin-1-yl)oxy-4-oxobutyl]disulfanyl]butanoate

Canonical SMILES

CC(=O)NC(CCSSCCC(C(=O)ON1C(=O)CCC1=O)NC(=O)C)C(=O)ON2C(=O)CCC2=O

InChI

InChI=1S/C20H26N4O10S2/c1-11(25)21-13(19(31)33-23-15(27)3-4-16(23)28)7-9-35-36-10-8-14(22-12(2)26)20(32)34-24-17(29)5-6-18(24)30/h13-14H,3-10H2,1-2H3,(H,21,25)(H,22,26)

InChIKey

GEFQVWRCWUXPLJ-UHFFFAOYSA-N

Shipping

Room temperature, or blue ice upon request.

(2S,2'S)-Bis(2,5-Dioxopyrrolidin-1-yl) 4,4'-Disulfanediylbis(2-Acetamidobutanoate) is a specialized chemical compound with diverse applications in biochemical research and biotechnology. Here are four key applications presented with high perplexity and burstiness:

Protein Cross-Linking: This compound serves as a pivotal protein cross-linking reagent, facilitating the exploration of intricate protein-protein interactions. By forging enduring covalent bonds among proteins, scientists delve into complex protein architectures and functionalities. This is indispensable for unraveling enzyme mechanisms and advancing the realm of protein-based therapeutics.

Bioconjugation: In the realm of bioconjugation protocols, (2S,2'S)-Bis(2,5-Dioxopyrrolidin-1-yl) 4,4'-Disulfanediylbis(2-Acetamidobutanoate) plays a crucial role in linking biomolecules like antibodies, peptides, or nucleic acids to diverse tags or carriers. This process enables the creation of targeted drug delivery systems, diagnostic assays, and imaging agents. The formation of stable conjugates elevates the specificity and efficacy of biomedical applications, revolutionizing targeted therapeutics.

Surface Modification: Employed in surface modification, this compound imparts specific biochemical properties to diverse surfaces. By tethering biologically active molecules to surfaces such as biosensors, medical implants, or cell culture materials, it enhances their operational capabilities. This application plays a pivotal role in the advancement of sophisticated biomedical devices and the creation of tissue engineering scaffolds, embodying the forefront of biomedical innovations.

Peptide Synthesis: In the realm of peptide chemistry, (2S,2'S)-Bis(2,5-Dioxopyrrolidin-1-yl) 4,4'-Disulfanediylbis(2-Acetamidobutanoate) acts as a potent coupling reagent, streamlining the formation of peptide bonds. By driving efficient coupling reactions, it facilitates the synthesis of intricate peptides and proteins. This process is indispensable for delving into protein structure, functionality, and propelling the development of peptide-based pharmaceuticals, thereby heralding a new era in therapeutic interventions.