(2S,2'S)-Bis(2,5-Dioxopyrrolidin-1-yl) 4,4'-Disulfanediylbis(2-Acetamidobutanoate) - CAS 102814-00-6

(2S,2'S)-Bis(2,5-Dioxopyrrolidin-1-yl) 4,4'-Disulfanediylbis(2-Acetamidobutanoate) - CAS 102814-00-6 Catalog number: BADC-00513

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(2S, 2'S)-Bis(2, 5-dioxopyrrolidin-1-yl)4, 4'-disulfanediylbis(2-acetamidobutanoate) is a linker for antibody-drug-conjugation (ADC).

Category
ADCs Linker
Product Name
(2S,2'S)-Bis(2,5-Dioxopyrrolidin-1-yl) 4,4'-Disulfanediylbis(2-Acetamidobutanoate)
CAS
102814-00-6
Catalog Number
BADC-00513
Molecular Formula
C20H26N4O10S2
Molecular Weight
546.57
(2S,2'S)-Bis(2,5-Dioxopyrrolidin-1-yl) 4,4'-Disulfanediylbis(2-Acetamidobutanoate)

Ordering Information

Catalog Number Size Price Quantity
BADC-00513 -- $-- Inquiry
Description
(2S, 2'S)-Bis(2, 5-dioxopyrrolidin-1-yl)4, 4'-disulfanediylbis(2-acetamidobutanoate) is a linker for antibody-drug-conjugation (ADC).
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.

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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