Synthesis and antiviral activity of conformational analogues of leucamide A.

In order to study the effect of heterocyclic core conformational state of leucamide A on its anti-influenza virus A activity, five conformational analogues were prepared by replacing the Pro-Leu dipeptide in the molecule with various amino acids. The amino acids used were of 2 to 6 carbons. The results showed that these replacements not only changed the conformational relationship between the 4,2-bisheterocycle tandem pair and the third heterocycle, but also had dramatic effect on its activity against influenza virus A.

[Biocathode denitrification in a two-columnar microbial fuel cell].

The biocathode of the two-columnar microbial fuel cell was used to denitrify. Factors influencing denitrification performance and power production were studied. When the external resistance decreased from 50 omega to 5 omega, the nitrate removal rate increased from 0.26 mg/(L x h) to 0.76 mg/(L x h). The nitrite accumulated to 55 mg/L with the external resistance decreasing to 5 omega. The nitrate degradation followed the zero order reaction model when the initial nitrate concentration was 20-120 mg/L. The power generation was not affected by the nitrate concentration distinctly. The nitrite concentration increased with the initial nitrate concentration. The nitrite removal could be enhanced by adding organic matter, without significant influence on the power generation.

Synthesis and biological evaluation of novel bisheterocycle-containing compounds as potential anti-influenza virus agents.

A series of novel 4,2-bisheterocycle tandem derivatives consisting of a methyloxazole and thiazole subunit were synthesized. Many compounds were found to inhibit human influenza A virus. Several analogues exhibited moderate biological activity and could serve as leads for further optimizations for antivirus research.