32564-25-3

Usage

InChI:InChI=1/C18H16N2O8/c21-17(27-15-9-5-13(6-10-15)19(23)24)3-1-2-4-18(22)28-16-11-7-14(8-12-16)20(25)26/h5-12H,1-4H2

Upstream product

• 100-02-7 4-nitro-phenol 
• 111-50-2 Adipic acid dichloride 
• 2035-75-8 adipic anhydride 

Downstream Products

• 100-02-7 4-nitro-phenol 
• 87876-26-4 N^δ-<5-<(4-Nitrophenyl)oxycarbonyl>pentanoyl>-δ-aminophalloin 
• 87892-74-8 N^δ,N^δ'-Adipoylbis<δ-aminophalloin> 
• 124-04-9 Adipic acid 
• 865179-82-4 7-aza-8,13-dioxo-13-(4-nitrophenoxy)-4-thiatridecanyl (β-D-mannopyranosyl)-(1->2)-β-D-mannopyranoside 
• 1044500-07-3 7-aza-8,13-dioxo-13-(4-nitrophenoxy)-4-thiatridecanyl (β-D-mannopyranosyl)-(1->2)-(β-D-mannopyranosyl)-(1->2)-2-deoxy-2-thio-β-D-mannopyranoside 
• 1044500-06-2 7-aza-8,13-dioxo-13-(4-nitrophenoxy)-4-thiatridecanyl (β-D-mannopyranosyl)-(1->2)-(2-deoxy-2-thio-β-D-mannopyranosyl)-(1->2)-β-D-mannopyranoside 
• 1459246-71-9 6-[[2-[[8-(β-D-galactopyranosyl(1→4)-[α-L-fucopyranosyl(1→3)]-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→3)-β-D-galactopyranosyl(1→4)-β-D-glucopyranosyloxy)octyl]thiol]ethyl]amino]-6-oxo-hexanoic acid p-nitrophenyl ester 

Relevant academic research and scientific papers

REDUCTION SENSITIVE BIODEGRADABLE POLYESTERAMIDES

The present invention relates to biodegradable polyesteramides (PEAs) comprising hydrophobic alpha -amino acids, diols, aliphatic dicarboxylic acids and optionally diamines whereby at least one of the dicarboxylic acids, diols or diamines comprises disulp

Bioerodable poly(etheresteramides) and medical article uses

Bioerodable poly(etheresteramides) and matrices formed therefrom, such as medical device coatings, are described. The matrices show desirable erosion properties desirable for therapeutic use. The matrices can include a bioactive agent which can be used to

From macro to micro to nano: The development of a novel lysine based hydrogel platform and enzyme triggered self-assembly of macro hydrogel into nanogel

A novel L-lysine based multifunctional crosslinker family was developed and utilized to fabricate a 100% pure poly(ester amide) (PEA) hydrogel with unique structure via a novel gelation strategy in a single and rapid step. Enzyme triggered biodegradation

CATIONIC MATERIALS AND FORMULATIONS FOR DRUG DELIVERY

Cationic polymers are provided for delivering anionic active agents, preferably in the form or nanoparticles and other nanostructures. The polymer can be a polycation homopolymer or a copolymer containing a polycation block. The polycations and polycation

Water insoluble cationic poly(ester amide)s: Synthesis, characterization and applications

We reported a new family of water insoluble, biocompatible and biodegradable cationic arginine and phenylalanine based poly(ester amide)s (Arg-Phe-PEAs) for potential biomedical applications. The Arg-Phe-PEA consists of 3 building blocks: amino acids, dio

Implantable medical devices comprising semi-crystalline poly(easter-amide)

The current invention relates to an implantable medical device made of semi-crystalline poly(ester amide) (PEA) polymer.

BIODEGRADABLE WATER SOLUBLE POLYMERS

The invention provides biodegradable, water soluble PEA, PEUR and PEU carrier polymers, which can be used to conjugate, and thereby stabilize and/or solublize, bioactive agents via polar uncharged or charged groups and activated ester or amino groups cont

A new homobifunctional p-nitro phenyl ester coupling reagent for the preparation of neoglycoproteins

(Chemical equation presented) A new linker system has been designed and applied to neoglycoprotein synthesis. Reaction of oligosaccharide ω-aminoalkyl glycosides with homobifunctional adipic acid p-nitrophenyl diesters in dry DMF gave the corresponding am

Activated polycondensation in synthesis of polyamidobenzimidazoles

Formation of polyaminoimides by activated copolycondensation of bis-p-nitrophenyl esters of aliphatic and aromatic dicarboxylic acids with aromatic tetraamines and ε-caprolactam in N-methylpyrrolidone was studied. The optimal synthesis conditions were det