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Inhibitors of protein tyrosine phosphatases: Next-generation drugs?
被引:389
作者
:
Bialy, L
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Mol Physiol, Abt Chem Biol, D-44227 Dortmund, Germany
Bialy, L
Waldmann, H
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Mol Physiol, Abt Chem Biol, D-44227 Dortmund, Germany
Waldmann, H
机构
:
[1]
Max Planck Inst Mol Physiol, Abt Chem Biol, D-44227 Dortmund, Germany
[2]
Univ Dortmund, Fachbereich Org Chem 3, D-44221 Dortmund, Germany
来源
:
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
|
2005年
/ 44卷
/ 25期
关键词
:
inhibitors;
medicinal chemistry;
phosphatases;
phosphorylation;
signal transduction;
D O I
:
10.1002/anie.200461517
中图分类号
:
O6 [化学];
学科分类号
:
0703
[化学]
;
摘要
:
The protein tyrosine phosphatases (PTPs) constitute a family of closely related key regulatory enzymes that dephosphorylate phosphotyrosine residues in their protein substrates. Malfunctions in PTP activity are linked to various diseases, ranging from cancer to neurological disorders and diabetes. Consequently, PTPs have emerged as promising targets for therapeutic intervention in recent years. In this review, general aspects of PTPs and the development of small-molecule inhibitors of PTPs by both academic research groups and pharmaceutical companies are discussed. Different strategies have been successfully applied to identify potent and selective inhibitors. These studies constitute the basis for the future development of PTP inhibitors as drugs. © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:3814 / 3839
页数:26
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