Abstract
A recent study challenges the oft-held notion that ester bonds in prodrug molecules are cleaved rapidly and completely inside cells by endogenous, nonspecific esterases. Structure-activity relationship studies on acylated sugars reveal that regioisomeric compounds display disparate biological activity, suggesting that ester bonds can persist in a cellular context. © 2008 American Chemical Society.
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CITATION STYLE
APA
Lavis, L. D. (2008, April 18). Ester bonds in prodrugs. ACS Chemical Biology. https://doi.org/10.1021/cb800065s
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