2,5-dioxopyrrolidin-1-yl 3-(2-(2-(1,3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)propanoate

2,5-dioxopyrrolidin-1-yl 3-(2-(2-(1,3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)propanoate Catalog number: BADC-00388

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Kaempferol 3-(2-(2-(1,3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)propanoate is a naturally occurring flavonoid compound that exhibits remarkable potential in biomedical research and development. Its multifaceted properties and chemical composition make it a promising candidate for various therapeutic applications. By precisely targeting specific receptors or pathways implicated in numerous diseases, it holds the key to unlocking novel treatment approaches

Category
ADCs Linker
Product Name
2,5-dioxopyrrolidin-1-yl 3-(2-(2-(1,3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)propanoate
Catalog Number
BADC-00388
Molecular Formula
C19H20N2O9
Molecular Weight
420.37
Purity
≥98%
2,5-dioxopyrrolidin-1-yl 3-(2-(2-(1,3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)propanoate

Ordering Information

Catalog Number Size Price Quantity
BADC-00388 -- $-- Inquiry
Description
Kaempferol 3-(2-(2-(1,3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)propanoate is a naturally occurring flavonoid compound that exhibits remarkable potential in biomedical research and development. Its multifaceted properties and chemical composition make it a promising candidate for various therapeutic applications. By precisely targeting specific receptors or pathways implicated in numerous diseases, it holds the key to unlocking novel treatment approaches
Synonyms
Phthalimidooxy-dPEG2-NHS ester;
Appearance
Soild powder

Application in Targeted Drug Delivery: 2,5-Dioxopyrrolidin-1-yl 3-(2-(2-(1,3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)propanoate can serve a vital role in targeted drug delivery systems. Its biocompatibility and capacity to form conjugates with a variety of therapeutic agents make it an excellent candidate for enhancing the precision of drug delivery. By attaching this compound to specific ligands that recognize and bind to certain cellular receptors or tissues, medications can be delivered more effectively to the targeted site, minimizing systemic toxicity and enhancing therapeutic outcomes.

Utility in Bioconjugation: The compound exhibits noteworthy potential in bioconjugation. Its functional groups allow it to form stable covalent bonds with biological molecules such as peptides, proteins, and antibodies. This property is particularly advantageous in the development of bioconjugates, which are essential in diagnostics and therapeutic applications. For instance, this molecule can be used to link diagnostic probes to antibodies, facilitating the specific detection of biomarkers and aiding in the early diagnosis of diseases.

Role in Polymer Science: 2,5-Dioxopyrrolidin-1-yl 3-(2-(2-(1,3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)propanoate is also significant in the field of polymer science. Its structural components can be utilized to synthesize novel polymers with unique properties, such as increased elasticity, enhanced thermal stability, or improved biocompatibility. These polymers can find applications in a variety of sectors, including medical devices, drug delivery systems, and biodegradable materials.

Applications in Chemical Synthesis: The compound has value in chemical synthesis, serving as a versatile intermediate. Its reactive sites make it suitable for various chemical reactions, enabling the synthesis of complex organic molecules. This can be particularly useful in medicinal chemistry for the synthesis of new pharmaceutical compounds, as well as in the development of advanced materials. Its ability to act as a bridging molecule between different chemical entities highlights its utility in the creation of novel compounds with desired properties.

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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