86970-12-9Relevant academic research and scientific papers
Syntheses, in vitro antibacterial and cytotoxic activities of a series of 3-substituted succinimides
Zentz, Frederic,Le Guillou, Regis,Labia, Roger,Sirot, Danielle,Linard, Boris,Valla, Alain
, p. 879 - 886 (2007/10/03)
We have synthesized a series of 3-substituted succinimides and their in vitro antibacterial activities have been tested towards Gram-positive and Gram-negative bacteria from the ATCC collection. Some of them possess significant antibacterial activity against Gram-positive organisms (Staphylococcus aureus ATCC 25923 and Enterococcus faecalis ATCC 29212) but all are poorly active or inactive against Gram-negative organisms (Escherichia coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853). The compounds with the lowest minimal inhibitory concentrations (esters of 3-hydroxy succinimides) are also the most cytotoxic against green monkey Vero cell line (ATCC CCL-81) and could explain that perhaps apoptosis should be implicated in eukaryotic cell cytotoxicity of succinimides.
Synthesis of Aminomethyl-Substituted Cyclic Imide Derivatives for Evaluation as Anticonvulsants
Stratford, Eugene S.,Curley, Robert W.
, p. 1463 - 1469 (2007/10/02)
A series of aminomethyl-substituted cyclic imides (II) based on the 2,5-pyrrolidinedione (X = CH2, succinimide) and 2,4-imidazolidinedione (X = NH, hydantoin) ring systems have been prepared.The compounds were designed on the basis of a potential interact
