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PMID: 12614874 Published · ppublish English Journal Article Review

Prodrugs of biologically active phosphate esters.

Bioorganic & medicinal chemistry ·Vol. 11 ·No. 6 ·2003-03-20 ·Pages 885-98

Schultz C

Abstract

Bioactivatable protecting groups represent an enormously powerful tool to increase bioavailability or to generally help deliver drugs to cells. This approach is particularly valuable in the case of biologically active phosphates because of the high intrinsic hydrophilicity and the multitude of biological functions phosphate esters exhibit inside cells. Here, the most prominent masking groups used so far are introduced. The stability and toxicology of the resulting prodrugs is discussed. Finally, this review tries to cover briefly some of the work that describes the usefulness and efficiency of the approach in various application areas.

MeSH Terms
Animals Esters/chemical synthesis,toxicity Humans Indicators and Reagents Inositol Phosphates/chemical synthesis,toxicity Oligonucleotides/chemistry Organophosphonates/chemical synthesis,toxicity Phosphates/chemical synthesis,toxicity Phosphatidylinositols/chemical synthesis,toxicity Phosphinic Acids/chemical synthesis,toxicity Prodrugs/chemical synthesis,toxicity
Chemicals
Esters Indicators and Reagents Inositol Phosphates Oligonucleotides Organophosphonates Phosphates Phosphatidylinositols Phosphinic Acids Prodrugs
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Schultz Carsten
European Molecular Biology Laboratory, Meyerhofstr. 1, 69117, Heidelberg, Germany. schultz@embl.de
Article Info
Journal
Bioorganic & medicinal chemistry
Abbr.
Bioorg Med Chem
ISSN
0968-0896
Published
2003-03-20
Pages
885-98
Language
English
Region
England
NLM ID
9413298
Subset
IM
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