2,5-dioxo-1-(4-(pyridin-2-yldisulfanyl)pentanoyloxy)pyrrolidine-3-sulfonic acid - CAS 452072-27-4

2,5-dioxo-1-(4-(pyridin-2-yldisulfanyl)pentanoyloxy)pyrrolidine-3-sulfonic acid - CAS 452072-27-4 Catalog number: BADC-00474

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Category
ADCs Linker
Product Name
2,5-dioxo-1-(4-(pyridin-2-yldisulfanyl)pentanoyloxy)pyrrolidine-3-sulfonic acid
CAS
452072-27-4
Catalog Number
BADC-00474
Molecular Formula
C14H16N2O7S3
Molecular Weight
420.48
2,5-dioxo-1-(4-(pyridin-2-yldisulfanyl)pentanoyloxy)pyrrolidine-3-sulfonic acid

Ordering Information

Catalog Number Size Price Quantity
BADC-00474 -- $--
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Synonyms
2,5-dioxo-1-[4-(pyridin-2-yldisulfanyl)pentanoyloxy]pyrrolidine-3-sulfonic acid;
Canonical SMILES
CC(CCC(=O)ON1C(=O)CC(C1=O)S(=O)(=O)O)SSC2=CC=CC=N2
InChI
InChI=1S/C14H16N2O7S3/c1-9(24-25-11-4-2-3-7-15-11)5-6-13(18)23-16-12(17)8-10(14(16)19)26(20,21)22/h2-4,7,9-10H,5-6,8H2,1H3,(H,20,21,22)
InChIKey
ORKSBKSSOSUJOY-UHFFFAOYSA-N
Appearance
Soild powder
Purity
≥98%
Shipping
Room temperature

2,5-dioxo-1-(4-(pyridin-2-yldisulfanyl)pentanoyloxy)pyrrolidine-3-sulfonic acid, a complex compound with diverse applications in bioscience research and industry, showcases its versatility in multiple key areas presented with high perplexity and burstiness:

Drug Design and Development: Serving as a foundational scaffold in medicinal chemistry, this compound offers a platform for the creation of innovative pharmaceutical agents. Its intricate structure enables the attachment of diverse functional groups, potentially leading to the emergence of novel drugs with enhanced biological activity and specificity for targeted diseases. Researchers leverage its properties to synthesize molecules that push the boundaries of therapeutic possibilities.

Biochemical Research: Within the realm of biochemical studies, this compound plays a pivotal role in exploring enzyme-substrate interactions and protein-ligand binding dynamics. Its disulfide bond can be selectively cleaved or formed to delve into the realms of redox biology and intracellular signaling pathways. As a valuable tool in unraveling complex biochemical processes and deciphering protein functions, it offers insights into the intricate mechanisms governing biological systems.

Cell Signaling Studies: Acting as a versatile modulator in the landscape of cell signaling research, this molecule facilitates investigations into oxidative stress and redox regulation. By introducing it into cellular systems, scientists can dissect the impacts of oxidative modifications on signaling pathways, shedding light on the intricate roles of redox states in cellular communication and the progression of diseases. This exploration unveils the underlying mechanisms driving cellular responses to external stimuli.

Synthetic Chemistry: In the domain of synthetic organic chemistry, this compound emerges as a dynamic intermediate for constructing intricate molecular structures. Its reactive sites provide a canvas for the introduction of a wide array of substituents, empowering chemists to craft diverse derivatives with tailored properties. This application holds significant implications for the advancement of new materials, catalysts, and bioactive molecules, paving the way for innovative developments in multiple fields of science and industry.

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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