2-methyl-2-(pyridin-2-yldisulfanyl)propyl 4-nitrophenyl carbonate - CAS 1956318-90-3

2-methyl-2-(pyridin-2-yldisulfanyl)propyl 4-nitrophenyl carbonate - CAS 1956318-90-3 Catalog number: BADC-00456

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Category
ADCs Linker
Product Name
2-methyl-2-(pyridin-2-yldisulfanyl)propyl 4-nitrophenyl carbonate
CAS
1956318-90-3
Catalog Number
BADC-00456
Molecular Formula
C16H16N2O5S2
Molecular Weight
380.44
2-methyl-2-(pyridin-2-yldisulfanyl)propyl 4-nitrophenyl carbonate

Ordering Information

Catalog Number Size Price Quantity
BADC-00456 -- $--
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Synonyms
Carbonic acid, 2-​methyl-​2-​(2-​pyridinyldithio)​propyl 4-​nitrophenyl ester ;
Canonical SMILES
CC(C)(COC(=O)OC1=CC=C(C=C1)[N+](=O)[O-])SSC2=CC=CC=N2
InChI
InChI=1S/C16H16N2O5S2/c1-16(2,25-24-14-5-3-4-10-17-14)11-22-15(19)23-13-8-6-12(7-9-13)18(20)21/h3-10H,11H2,1-2H3
InChIKey
WQCUUTNIMCNOHP-UHFFFAOYSA-N
Appearance
Soild powder
Purity
≥98%
Shipping
Room temperature

2-methyl-2-(pyridin-2-yldisulfanyl)propyl 4-nitrophenyl carbonate, a specialized chemical compound with diverse applications in biosciences and medicinal chemistry. Here are four key applications presented with high perplexity and burstiness:

Protein Modification: This compound enables the selective modification of protein thiols, allowing for in-depth investigations into protein function and structure. By introducing disulfide linkages, researchers can craft stable protein conjugates tailored for a myriad of biochemical assays. Its utility shines in the realm of protein-based therapeutics and diagnostic tools, pushing the boundaries of protein science.

Drug Delivery Systems: At the forefront of pharmaceutical innovation, 2-methyl-2-(pyridin-2-yldisulfanyl)propyl 4-nitrophenyl carbonate plays a pivotal role in designing sophisticated drug delivery systems. Acting as a prodrug linker, it orchestrates the controlled release of active pharmaceutical ingredients under precise conditions. This precision delivery mechanism enables targeted drug administration, minimizing side effects and amplifying therapeutic efficacy, heralding a new era in drug delivery technology.

Chemical Probes: Serving as a versatile chemical probe, this compound stands as a stalwart ally in unraveling intricate biological pathways and deciphering enzyme activities. By engaging with specific amino acid residues, it sheds light on the functions of enzymes and proteins within cellular processes. These probes are indispensable in identifying novel drug targets and advancing the development of therapeutic agents, propelling the field of chemical biology forward.

Bioconjugation: Within the domain of bioconjugation, this compound emerges as a linchpin for securing biomolecules to surfaces or other biomolecules, forming robust conjugates essential for various applications. This process is indispensable in crafting biosensors, immunoassays, and other diagnostic tools. By linking antigens, antibodies, or proteins, it facilitates the sensitive detection of biological markers, empowering diagnostic advancements and bioanalytical research.

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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