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4-nitrophenyl 2-(pyridin-2-yldisulfanyl)propyl carbonate

  CAS No.: 1887040-81-4   Cat No.: BADC-00457   Purity: ≥98% 4.5  

4-nitrophenyl 2-(pyridin-2-yldisulfanyl)propyl carbonate is a cleavable ADC linker with nitrophenyl carbonate and pyridyl disulfide moieties, enabling stable antibody-payload conjugation and tumor-specific release to enhance ADC precision and therapeutic outcomes.

4-nitrophenyl 2-(pyridin-2-yldisulfanyl)propyl carbonate

Structure of 1887040-81-4

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ADC Linker
Molecular Formula
C15H14N2O5S2
Molecular Weight
366.41
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Room temperature, or blue ice upon request.

* For research and manufacturing use only. We do not sell to patients.

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Synonyms
Carbonic acid, 4-​nitrophenyl 2-​(2-​pyridinyldithio)​propyl ester ;
IUPAC Name
Appearance
Soild powder
Shipping
Room temperature, or blue ice upon request.

4-Nitrophenyl 2-(pyridin-2-yldisulfanyl)propyl carbonate is a versatile chemical reagent with specific applications across various scientific disciplines. Here are four key applications of this compound presented with a high degree of perplexity and burstiness:

Proteomics Research: Playing a pivotal role in proteomics, this reagent serves as a tool for labeling and modifying thiol groups in proteins. By selectively interacting with cysteine residues, researchers can delve into protein structures and interactions, shedding light on the intricate functions and dynamic behaviors of proteins within biological systems.

Drug Development: Within the realm of pharmaceuticals, 4-nitrophenyl 2-(pyridin-2-yldisulfanyl)propyl carbonate emerges as a valuable agent for crafting prodrugs – a specialized form of medication that activates post-metabolic conversion. This innovative approach enhances drug solubility, stability, and bioavailability, paving the way for targeted therapeutic strategies with minimized adverse effects.

Bioconjugation: Embracing the field of bioconjugation, this compound facilitates the linking of biological molecules for a myriad of applications. By engaging with amine or sulfhydryl groups, it forms durable conjugates with peptides, proteins, or antibodies, underpinning the development of diagnostic tools, biosensors, and cutting-edge therapeutic agents essential for advancing biomedical sciences.

Chemical Biology: In the interdisciplinary realm of chemical biology, this reagent serves as a pivotal component in exploring redox biology through the modification of disulfide bonds within biomolecules. By unraveling the complexities of redox changes in cellular processes and disease pathologies, researchers gain crucial insights into new therapeutic targets and the development of redox-centric interventions aimed at addressing various health challenges.

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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Historical Records: 4-Formyl-N-(2-(2-Methoxyphenoxy)ethyl)benzamide | CL2A-SN 38 | 4-Methyl-4-(pyridin-2-yldisulfanyl)pentanoic acid | N-(2-(2-Ethylphenoxy)ethyl)-4-Formylbenzamide | Me-Tet-PEG4-NHS | DBCO-NH-PEG4-amine | Propargyl-PEG7-acid | 2,5-dioxopyrrolidin-1-yl 4-((3-(dimethylcarbamoyl)pyridin-4-yl)disulfanyl)pentanoate | 3-azidopropanoate-N-hydroxysuccinimide ester | NHPI-PEG3-C2-PFP ester | 4-nitrophenyl 2-(pyridin-2-yldisulfanyl)propyl carbonate
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