Substituent effects on the kinetics of reductively-initiated fragmentation of nitrobenzyl carbamates designed as triggers for bioreductive prodrugs
…, BM Sykes, WA Denny, CJ O'Connor
文献索引:Hay, Michael P.; Sykes, Bridget M.; Denny, William A.; O'Connor, Charmian J. Journal of the Chemical Society - Perkin Transactions 1, 1999 , # 19 p. 2759 - 2770
4-Nitrobenzyl carbamates are of interest as triggers for bioreductive drugs, particularly in conjunction with the E. coli B nitroreductase, which efficiently reduces them to the corresponding hydroxylamines. These then fragment to release highly toxic amine-based toxins. While many 4-nitrobenzyl carbamate derivatives have been evaluated as bioreductive drugs, there has been no systematic study of substituent effects on the rate of ...