GALK inhibitors for classic galactosemia

被引:0
|
作者
Lai, Kent [1 ]
Boxer, Matthew B. [2 ]
Marabotti, Anna [3 ]
机构
[1] Univ Utah, Dept Pediat, Div Med Genet, Salt Lake City, UT 84132 USA
[2] NIH, Natl Ctr Adv Translat Sci, Rockville, MD 20850 USA
[3] Univ Salerno, Dept Chem & Biol, I-84084 Fisciano, SA, Italy
关键词
DROSOPHILA-MELANOGASTER MODEL; GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DEFICIENCY; CHROMATOGRAPHY-MASS SPECTROMETRY; SMALL-MOLECULE INHIBITORS; HUMAN GALACTOKINASE; FLUOROMETRIC METHOD; VERBAL DYSPRAXIA; ACCURATE DOCKING; OXIDATIVE STRESS; OUTCOME SEVERITY;
D O I
10.4155/FMC.14.43
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Classic galactosemia is an inherited metabolic disease for which, at present, no therapy is available apart from galactose-restricted diet. However, the efficacy of the diet is questionable, since it is not able to prevent the insurgence of chronic complications later in life. In addition, it is possible that dietary restriction itself could induce negative side effects. Therefore, there is a need for an alternative therapeutic approach that can avert the manifestation of chronic complications in the patients. In this review, the authors describe the development of a novel class of pharmaceutical agents that target the production of a toxic metabolite, galactose-1-phosphate, considered as the main culprit for the cause of the complications, in the patients.
引用
收藏
页码:1003 / 1015
页数:13
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