Glycogen phosphorylase inhibitors: a patent review (2008-2012)

被引:31
|
作者
Gaboriaud-Kolar, Nicolas [1 ]
Skaltsounis, Alexios-Leandros [1 ]
机构
[1] Univ Athens, Dept Pharm & Nat Prod Chem, GR-15771 Athens, Greece
关键词
allosteric inhibitors; cancer; glycogen phosphorylase; patents; regulation; type; 2; diabetes; POTENTIAL INHIBITORS; PHARMACOLOGICAL EVALUATION; ALLOSTERIC INHIBITION; BIOLOGICAL EVALUATION; TARGETING SUBUNIT; CATALYTIC SITE; BINDING-SITE; RAT-LIVER; DERIVATIVES; ACID;
D O I
10.1517/13543776.2013.794790
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Introduction: Glycogen phosphorylase (GP) is the enzyme responsible for the synthesis of glucose-1-phosphate, the source of energy for muscles and the rest of the body. The binding of different ligands in catalytic or allosteric sites assures activation and deactivation of the enzyme. A description of the regulation mechanism and the implications in glycogen metabolism are given. Areas covered: Deregulation of GP has been observed in diseases such as diabetes mellitus or cancers. Therefore, it appears as an attractive therapeutic target for the treatment of such pathologies. Numbers of inhibitors have been published in academic literature or patented in the last two decades. This review presents the main patent claims published between 2008 and 2012. Expert opinion: Good inhibitors with interesting IC50 and in vivo results are presented. However, such therapeutic strategy raises questions and some answers are proposed to bring new insights in the field.
引用
收藏
页码:1017 / 1032
页数:16
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