53417-18-8Relevant articles and documents
Evaluation of biological properties of 3,3′,4,4′-benzophenonetetracarboxylic dianhydride derivatives and their ability to inhibit hexokinase activity
Kochel, Krzysztof,Tomczyk, Mateusz D.,Sim?es, Rui F.,Fr?czek, Tomasz,Soboń, Adrian,Oliveira, Paulo J.,Walczak, Krzysztof Z.,Koceva-Chy?a, Aneta
, p. 427 - 431 (2017)
This investigation has explored the properties of 3,3′,4,4′-benzophenonetetracarboxylic dianhydride (BDTA) derivatives with regard to their being prospective inhibitors of hexokinase II (HKII). A pluripotent embryonic carcinoma cell line P19 (ECC), was used as the biological target for newly generated potential inhibitors of HKII. The results obtained from Virtual High-Throughput Screening (VHTS), molecular modeling and biological activity studies showed BDTA to be a promising leading structure with a good binding score and simplest functionalization. The inhibitory effect was measured after 72?h incubation. Of selected BDTA derivatives, the most active was compound 3b, containing 3-hydroxyphenyl moiety in the para position, being able at 100?μM to decrease the mass of differentiated P19dCs cells by 30%, changing both the mitochondrial transmembrane potential and reactive oxygen species level. Under these conditions, only compound 3b had the ability to decrease hexokinase activity in a dose-dependent manner.
New copoly(ether-imide-sulfone) oligomers having pendant ionic groups
Ciobanu, Manuela,Brunchi, Cristina-Eliza,Perju, Elena,Cozan, Vasile,Bruma, Maria
experimental part, p. 685 - 692 (2010/07/02)
New copoly(ether-imide-sulfone) oligomers have been synthesized by solution polycondensation reaction of bis(pchlorophenyl)sulfone with various imide bisphenols and 2,2-bis(4-hydroxyphenyl)-propane (Bisphenol A). The Williamson polyetherification procedur