14354-86-0Relevant articles and documents
The Synthesis of N-Hydroxy-N'-phenyloctanediamide and Its Inhibitory Effect on Proliferation of AXC Rat Prostate Cancer Cells
Stowell, John C.,Huot, Rachel I.,Voast, Lainie Van
, p. 1411 - 1413 (1995)
We have developed a practical synthesis of N-hydroxy-N'-phenyloctanediamide from the methyl ester of suberanilic acid.It provides the product in high yield and purity with a simple purification process.We have found that at 10-5 M it has a dramatic effect on T/5 AXC/SSh rat prostate cancer cells in vitro.It is a potent inhibitor of cell proliferation and it changes the cell morphology to resemble nonmalignant cells.
Synthesis of N,N′-diarylalkanediamides and their antimycobacterial and antialgal activity
Kubicova, Lenka,Waisser, Karel,Kunes, Jiri,Kralova, Katarina,Odlerova, Zelmira,Slosarek, Milan,Janota, Jiri,Svoboda, Zbynek
, p. 714 - 726 (2007/10/03)
A set of N,N′-diarylalkanediamides was synthesized. The compounds were tested for their antimycobacterial and antialgal activity. The antimycobacterial activity of N,N′-diarylalkanediamides depends on the lipophilicity of the respective acid. Antimycobacteri-ally active substances were found only in the series of N,N′-diarylethanediamides and N,N′-diarylbutanediamides. Other compounds (derivatives of pentane-, hexane-, octane- and nonanediamide) were inactive against various strains of mycobacteria. The compounds inhibited growth and chlorophyll production in Chlorella vulgaris. Their relatively low antial-gal activity is probably connected with their lowered aqueous solubility, and hence by a restricted passage of the inhibitor through the hydrophilic regions of thylakoid membranes.
