Abstract
A novel approach for developing prodrugs based on masked carboxylic acids is described. Rather than using conventional esterase-based activation, thiazolidinone protecting groups have been identified that can reveal carboxylic acid groups upon activation by hydrogen peroxide. This may prove valuable in the continuing development of prodrug strategies that rely on reactive oxygen species (ROS) as a trigger. This journal is
Cite
CITATION STYLE
Perez, C., Monserrat, J. P., Chen, Y., & Cohen, S. M. (2015). Exploring hydrogen peroxide responsive thiazolidinone-based prodrugs. Chemical Communications, 51(33), 7116–7119. https://doi.org/10.1039/c4cc09921d
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.