Heparin/heparan sulphate-based drugs

被引:87
作者
Gandhi, Neha S. [1 ]
Mancera, Ricardo L. [1 ,2 ]
机构
[1] Curtin Univ Technol, Sch Biomed Sci, Western Australian Biomed Res Inst, Curtin Hlth Innovat Res Inst, Perth, WA 6845, Australia
[2] Curtin Univ Technol, Sch Pharm, Perth, WA 6845, Australia
关键词
MOLECULAR-WEIGHT HEPARIN; FACTOR-XA INHIBITOR; PHASE-I; VENOUS THROMBOEMBOLISM; SANORG; 34006; UNFRACTIONATED HEPARIN; ALZHEIMERS-DISEASE; BETA-ANTITHROMBIN; HIGH-AFFINITY; AMYLOID-BETA;
D O I
10.1016/j.drudis.2010.10.009
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Glycosaminoglycans (GAGs) are an untapped source of novel chemical entities and, therefore, offer exciting new opportunities for the development of novel drug molecules because of their unique physical and biological properties. Advances in the functional understanding of GAG-protein interactions are enabling the development of GAG mimetics for use as anti-angiogenic, anti-metastatic, anti-inflammatory, anticoagulant and anti-thrombotic agents. Many anti-thrombotic molecules, such as Fondaparinux and Idraparinux, have been successful in clinical trials, and a new generation of heparin mimetic oligosaccharides and small molecules are currently in different stages of clinical development. In particular, the recent increased activity in the development of new mimetics by altering the composition of sulphated GAGs is very encouraging. This article reviews structurally defined heparin-mimetic oligosaccharides and small molecules currently in development or clinical trials.
引用
收藏
页码:1058 / 1069
页数:12
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