64026-31-9Relevant academic research and scientific papers
Rational design of nanofibers and nanorings through complementary hydrogen-bonding interactions of functional π systems
Yagai, Shiki,Aonuma, Hiroaki,Kikkawa, Yoshihiro,Kubota, Shun,Karatsu, Takashi,Kitamura, Akihide,Mahesh, Sankarapillai,Ajayaghosh, Ayyappanpillai
, p. 8652 - 8661 (2010)
A simple protocol to create nanofibers and -rings through a rational self-assembly approach is described. Whereas the melamine-oligo(p- phenylenevinylene) conjugate la self-aggregates to form ill-defined nanostructures, conjugate 1b, which possesses an am
OXAZOLIDINONE DERIVATIVES AS PPAR LIGANDS
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Paragraph 0150; 0171, (2016/06/28)
The present invention relates to a family of differently substituted oxazolidinones and to the pharmaceutically acceptable salts, esters, prodrugs, tautomers, solvates and hydrates thereof, which show affinity for the alpha and gamma subtypes of the perox
Novel Oxazolidinone-Based Peroxisome Proliferator Activated Receptor Agonists: Molecular Modeling, Synthesis, and Biological Evaluation
Fresno,Macías-González,Torres-Zaguirre,Romero-Cuevas,Sanz-Camacho,Elguero,Pavón,Rodríguez De Fonseca,Goya,Pérez-Fernández
, p. 6639 - 6652 (2015/09/07)
(Figure Presented). A series of new peroxisome proliferator activated receptors (PPARs) chiral ligands have been designed following the accepted three-module structure comprising a polar head, linker, and hydrophobic tail. The majority of the ligands inco
N-(acyl)-p-amino-N'-(monosubstituted)-benzamide anti-ulcer agents
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, (2008/06/13)
The preparation of novel N-(acyl)-p-amino-N'-(monosubstituted) benzamides by modified Schotten-Baumann reaction of the corresponding p-aminobenzamides is described. These compounds are effective anti-ulcer agents.
