Synthesis and biological evaluation of novel cyanuric acid-tethered tris-pyridinium derivatives
Novel tris(4-alkylaminopyridin-1-ium) trichlorides with alkylcyanuric spacer were synthesized by quaternization of 4-alkylaminopyridines with tris(2-chloroethyl) cyanurate. The obtained compounds were evaluated for microbiological activity against five pathogenic bacterial strains (Escherichia coli, Klebsiella pneumoniae, Staphylococcus aureus, Acinobacter baumannii, Pseudomonas aeruginosa). The results indicate the presence of pronounced antibacterial properties in this group of compounds.
Derkach, Yana V.,Detusheva, Elena V.,Egorov, Mikhail P.,Frolov, Nikita A.,Minaeva, Alexandra P.,Vereshchagin, Anatoly N.
THE DESIGN AND SYNTHESIS OF MACROBICYCLIC HOSTS FEATURING CONVERGENT FUNCTIONAL GROUPS.
Macrobicyclic structures in which carboxylate derivatives converge on a central cavity have been prepared.This report details the synthesis of the first of a series of such hosts and discusses their ability to complex amino acids in aqueous solutions.
Askew, Benny C.
p. 4245 - 4248
(2007/10/02)
More Articles about upstream products of 6299-37-2