Phosphonate prodrugs: an overview and recent advances

被引:72
|
作者
Heidel, Kenneth M. [1 ]
Dowd, Cynthia S. [1 ]
机构
[1] George Washington Univ, Dept Chem, Washington, DC 20052 USA
关键词
drug discovery; medicinal chemistry; phosphonate; prodrug activation; prodrugs; ACYCLIC NUCLEOSIDE PHOSPHONATES; TENOFOVIR DISOPROXIL FUMARATE; IN-VITRO EVALUATION; IMMUNODEFICIENCY-VIRUS TYPE-1; ADENYLATE-CYCLASE TOXIN; ETHER LIPID ESTERS; HEPATITIS-B; ANTIVIRAL ACTIVITY; CYCLIC CIDOFOVIR; DOUBLE-BLIND;
D O I
10.4155/fmc-2018-0591
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Phosphonates, often used as isosteric replacements for phosphates, can provide important interactions with an enzyme. Due to their high charge at physiological pH, however, permeation into cells can be a challenge. Protecting phosphonates as prodrugs has shown promise in drug delivery. Thus, a variety of structures and cleavage/activation mechanisms exist, enabling release of the active compound. This review describes the structural diversity of these pro-moieties, relevant cleavage mechanisms and recent advances in the design of phosphonate prodrugs.
引用
收藏
页码:1625 / 1643
页数:19
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