Glycogen synthase kinase 3 (GSK-3) inhibitors as new promising drugs for diabetes, neurodegeneration, cancer, and inflammation

被引:282
作者
Martinez, A [1 ]
Castro, A [1 ]
Dorronsoro, I [1 ]
Alonso, M [1 ]
机构
[1] CSIC, Inst Quim Med, E-28006 Madrid, Spain
关键词
GSK-3; inhibitors; Alzheimer's disease; diabetes type II; cancer; inflammation;
D O I
10.1002/med.10011
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Glycogen synthase kinase 3 (GSK-3) was initially described as a key enzyme involved in glycogen metabolism, but is now known to regulate a diverse array of cell functions. Two forms of the enzyme, GSK-3alpha and GSK-3beta, have been previously identified. Small molecules inhibitors of GSK-3 may, therefore, have several therapeutic uses, including the treatment of neurodegenerative diseases, diabetes type II, bipolar disorders, stroke, cancer, and chronic inflammatory disease. As there is lot of recent literature dealing with the involvement of GSK-3 in the molecular pathways of different diseases, this review is mainly focused on the new GSK-3 inhibitors discovered or specifically developed for this enzyme, their chemical structure, synthesis, and structure-activity relationships, with the aim to provide some clues for the future optimization of these promising drugs. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:373 / 384
页数:12
相关论文
共 83 条
  • [1] Lithium protects cultured neurons against β-amyloid-induced neurodegeneration
    Alvarez, G
    Muñoz-Montaño, JR
    Satrústegui, J
    Avila, J
    Bogónez, E
    Díaz-Nido, J
    [J]. FEBS LETTERS, 1999, 453 (03) : 260 - 264
  • [2] The structure of phosphorylated GSK-3β complexed with a peptide, FRATtide, that inhibits β-catenin phosphorylation
    Bax, B
    Carter, PS
    Lewis, C
    Guy, AR
    Bridges, A
    Tanner, R
    Pettman, G
    Mannix, C
    Culbert, AA
    Brown, MJB
    Smith, DG
    Reith, AD
    [J]. STRUCTURE, 2001, 9 (12) : 1143 - 1152
  • [3] Bray A. M., 1998, [No title captured], Patent No. [9816528, WO9816528]
  • [4] Breton JJ, 1997, J PHARMACOL EXP THER, V282, P459
  • [5] Brion JP, 2001, BIOCHEM SOC SYMP, V67, P81
  • [6] Inhibition of tau phosphorylation: a new therapeutic strategy for the treatment of Alzheimer's disease and other neurodegenerative disorders
    Castro, A
    Martinez, A
    [J]. EXPERT OPINION ON THERAPEUTIC PATENTS, 2000, 10 (10) : 1519 - 1527
  • [7] Non-Cholinergic Pharmacotherapy Approaches to the Future Treatment of Alzheimer's Disease
    Castro, Ana
    Conde, Santiago
    Isabel Rodriguez-Franco, M.
    Martinez, Ana
    [J]. MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2002, 2 (01) : 37 - 50
  • [8] The mood-stabilizing agent valproate inhibits the activity of glycogen synthase kinase-3
    Chen, G
    Huang, LD
    Jiang, YM
    Manji, HK
    [J]. JOURNAL OF NEUROCHEMISTRY, 1999, 72 (03) : 1327 - 1330
  • [9] Selective small molecule inhibitors of glycogen synthase kinase-3 modulate glycogen metabolism and gene transcription
    Coghlan, MP
    Culbert, AA
    Cross, DAE
    Corcoran, SL
    Yates, JW
    Pearce, NJ
    Rausch, OL
    Murphy, GJ
    Carter, PS
    Cox, LR
    Mills, D
    Brown, MJ
    Haigh, D
    Ward, RW
    Smith, DG
    Murray, KJ
    Reith, AD
    Holder, JC
    [J]. CHEMISTRY & BIOLOGY, 2000, 7 (10): : 793 - 803
  • [10] The role of protein phosphorylation in human health and disease - Delivered on June 30th 2001 at the FEBS Meeting in Lisbon
    Cohen, P
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (19): : 5001 - 5010