D-Galactose as a Vector for Prodrug Design

Author(s): Daniela Melisi, Annalisa Curcio, Elvira Luongo, Elena Morelli, Maria Grazia Rimoli.

Journal Name: Current Topics in Medicinal Chemistry

Volume 11 , Issue 18 , 2011

Become EABM
Become Reviewer


D-galactose is a simple and natural compound that has mainly been exploited in prodrug strategies. Galactosyl prodrugs can be considered a good approach to reach different goals in clinical drug application, especially when traditional drugs are likely to fail therapeutically owing to reasons such as the lack of site specificity, toxicity, and chemical instability. Indeed, of paramount importance is their ability to increase the selectivity of the parent compound, a phenomenon that helps to reduce the incidence of adverse effects, while preserving intact the pharmacodynamic features of the parent drug. Study results have varied according to the type of linkage between the drug and the hydroxyl group exploited. By working with these parameters, researchers have been able not only to generate selective pharmacological targeting of brain, liver, and cancerous cells, but also to improve cellular permeability as well as the pharmacokinetic profile of parent drugs. This review describes the broad spectrum of possibilities for exploiting D-galactose as a vector for prodrug design and the synthetic strategies that allow its realization.

Keywords: Galactosyl prodrugs, drug targeting, cell permeability, pharmacokinetic improvement, toxicity, and chemical instability, pharmacodynamic, cancerous cells, synthetic strategies, potential moieties, prodrug synthesis, mesencephalon, electrochemical detector, antioxidant enzyme, carboxylic group, synthesizing galactos

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2011
Page: [2288 - 2298]
Pages: 11
DOI: 10.2174/156802611797183258
Price: $65

Article Metrics

PDF: 33