A series of eight novel nitropyrazines has been prepared by oxidation of sulfoximine intermediates. The partition coefficient, one-electron reduction potential, sensitizer enhancement ratio, and chronic and acute aerobic cytotoxicity have been measured for each. Two representatives of this series were tested in the Ames test and were not found to be mutagenic.
![N-[5-chloro-6-(4-methylpiperazin-1-yl)-3-nitropyrazin-2-yl]acetamide Structure](https://image.chemsrc.com/caspic/261/89083-22-7.png)
![3-[(6-amino-3-chloro-5-nitropyrazin-2-yl)amino]propane-1,2-diol Structure](https://image.chemsrc.com/caspic/289/88793-46-8.png)
![3-[(5-nitropyrazin-2-yl)amino]butane-1,2,4-triol Structure](https://image.chemsrc.com/caspic/205/89690-76-6.png)