58047-86-2

Usage

General Description

2,5-Pyrrolidinedione, 1-[(1-oxodocosyl)oxy]- is a chemical compound that belongs to the class of pyrrolidinediones, which are five-membered heterocyclic compounds. The compound contains a long chain of 22 carbon atoms (docosyl group) attached to an oxo group, and the whole structure is attached to the pyrrolidinedione ring. 2,5-Pyrrolidinedione, 1-[(1-oxodocosyl)oxy]- has potential applications in various fields, including as a building block for the synthesis of other organic compounds and in the field of materials science. The specific properties and potential uses of 2,5-Pyrrolidinedione, 1-[(1-oxodocosyl)oxy]- can vary depending on the specific application and the context in which it is being used.

Upstream product

• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 112-85-6 n-docosanoic acid 

Relevant academic research and scientific papers

Reactive Langmuir-Blodgett membrane for biosensor applications. Use of succinimidyl behenoate-based membranes as support for covalently immobilizing α-chymotrypsin

Succinimidyl behenoate was synthesized to prepare Langmuir-Blodgett (LB) membranes which possess reactive groups on the surface. The surface of the succinimidyl behenoate-based LB membrane could be covalently modified with α-chymotrypsin, for the purpose of biosensor applications.

DNA micelles as nanoreactors: Efficient DNA functionalization with hydrophobic organic molecules

We report a micelle-templated method to enhance the reactivity of DNA with highly hydrophobic molecules. Lipids, chromophores and polymers can be conjugated to DNA in high yield and under mild conditions. This method expands the range of DNA-templated reactions for DNA-encoded libraries, oligonucleotide and drug delivery, nanopore mimetics and DNA nanotechnology.

Synthesis and Biological Activities of N-Acetylglucosaminyl-&β(1->4)-N-Acetylmuramyl Tri- and Tetrapeptide Derivatives

The acylated, amidated and esterified derivatives of N-acetylglucosaminyl-β(1->4)-N-acetylmuramyl tri- and tetrapeptide were synthesized and examined as to their protective effect on pseudomonal infection in the mouse and pyrogenicity in the rabbit.Modifications of the terminal end function of the peptide moieties in their molecules caused enhancement of resistance to pseudomonal infection and reduction of pyrogenicity.Among the compounds tested, sodium N-acetylglucosaminyl-β(1->4)-N-acetylmuramyl-L-alanyl-D-isoglutaminyl-(L)-stearoyl-(D)-meso-2,6-diaminopimelic acid-(D)-amide and sodium N-acetylglucosaminyl-β(1->4)-N-acetylmuramyl-L-alanyl-D-isoglutaminyl-(L)-stearoyl-(D)-meso-2,6-diaminopimelic acid-(D)-amide-(L)-D-alanine were found to be advantageous and conceivably worthwhile for further investigation as immunobiologically active compounds.

Acylation of amino acids

N-mono-substituted derivatives of diamino acids are prepared by the reaction of succinimidyl esters of carboxylic acids or substituted carbonic acids with the unprotected diamino acid. The acylation preferentially occurs at the side chain or terminal amino group of the diamino acid. For example, selective acylation of the terminal amino group of lysine occurs without first having protected the 2-amino group. Such acylation has application in the preparation of inter alia N6 -palmitoyl-lysine.