메뉴 건너뛰기




Volumn 15, Issue 10, 2005, Pages 1315-1331

GSK-3 inhibitors and their potential in the treatment of Alzheimer's disease

Author keywords

Alzheimer's disease; Glycogen synthase kinase 3 (GSK 3) inhibitor

Indexed keywords

2 (2,4 DICHLOROPHENYL) 3 (1 METHYL 3 INDOLYL)MALEIMIDE; 2 (3 CHLORO 4 HYDROXYANILINO) 3 (2 NITROPHENYL)MALEIMIDE; 2 [1 (3 AMIDINOTHIOPROPYL) 1H INDOL 3 YL] 3 (1 METHYL 1H INDOL 3 YL)MALEIMIDE; 2 [1 (3 DIMETHYLAMINOPROPYL) 3 INDOLYL] 3 (3 INDOLYL)MALEIMIDE; 2 [2 (2,6 DIMETHOXYPHENYL)MORPHOLIN 4 YL] 3 METHYL 6 (PYRIMIDIN 4 YL) 3H PYRIMIDIN 4 ONE; 2 HYDROXY 3 [4[(4 METHYLPIPERAZIN 1 YL)CARBONYL]PYRIDIN 2YL] 1H INDOLE 5 CARBONITRILE; 3 (1,2,3,4 TETRAHYDRO[1,4]DIAZEPINO[6,7,1 HI]INDOL 7 YL) 4 (5 FLUOROBENZOFURAN 7 YL) 2,5 DIOXOPYRROLE; 3 BROMO 5 PHENYL 1H PYRAZOLO[3,4 B]PYRIDINE; 4 (2,1,3 BENZOXADIAZOL 4 YL) 5 CYANO 4,7 DIHYDRO 6 (1 METHYLPIPERIDIN 4 YL) 2H PYRAZOLO[3,4 B]PYRIDINE; 5 METHYL 4 OXO 6 PHENYL 3,4 DIHYDROPYRROLO[3,2 D]PYRIMIDINE 7 CARBONITRILE; 7,7 DIMETHYL 9 (2 METHYL 6,7 DIHYDRO 5H CYCLOPENTAL[B]PYRIDIN 6 YLMETHYL) 2 (PYRIDIN 4 YL) 6,7,8,9 TETRAHYDRO PYRIMIDO[1,2 A]PYRIMIDIN 4 ONE; ALSTERPAULLONE; AMINOPYRIDINE DERIVATIVE; ANILINOARYLMALEIMIDE; AR AO 14418; BISINDOLYLMALEIMIDE; CARBAZOLE DERIVATIVE; CHIR 025; CHIR 98014; CHIR 99021; GLYCOGEN SYNTHASE KINASE 3; GLYCOGEN SYNTHASE KINASE 3 INHIBITOR; INDOLE DERIVATIVE; LITHIUM CHLORIDE; MALEIMIDE DERIVATIVE; N (4 METHOXYBENZYL) N' (5 NITRO 1,3 THIAZOL 2 YL)UREA; N [6 (4 CHLOROPHENYL) 1H PYRAZOLO[3,4 B] PYRIDIN 3 YL]ACETAMIDE; PAULLONE DERIVATIVE; PYRAZINE DERIVATIVE; PYRIDINE DERIVATIVE; PYRIMIDINE DERIVATIVE; PYRIMIDINONE DERIVATIVE; PYRROLE DERIVATIVE; PYRROLOPYRIMIDINE DERIVATIVE; ROSCOVITINE; TWS 119; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 27744574179     PISSN: 13543776     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543776.15.10.1315     Document Type: Review
Times cited : (31)

References (77)
  • 1
    • 0037383322 scopus 로고    scopus 로고
    • GSK3: Tricks of the trade for a multi-tasking kinase
    • DOBLE BW, WOODGETT JR: GSK3: tricks of the trade for a multi-tasking kinase. J. Cell Sci. (2003) 116(Pt.7):1175-1186.
    • (2003) J. Cell Sci. , vol.116 , Issue.PART 7 , pp. 1175-1186
    • Doble, B.W.1    Woodgett, J.R.2
  • 2
    • 0035863188 scopus 로고    scopus 로고
    • Decreased nuclear β-catenin, tau hyperphosphorylation and neurodegeneration in GSK-3β conditional transgenic mice
    • LUCAS JJ, HERNANDEZ F, GOMEZ-RAMOS P et al.: Decreased nuclear β-catenin, tau hyperphosphorylation and neurodegeneration in GSK-3β conditional transgenic mice. EMBO J. (2001) 20(1-2):27-39.
    • (2001) EMBO J. , vol.20 , Issue.1-2 , pp. 27-39
    • Lucas, J.J.1    Hernandez, F.2    Gomez-Ramos, P.3
  • 3
    • 1642363745 scopus 로고    scopus 로고
    • Spatial learning deficit in transgenic mice that conditionally overexpress GSK-3β in the brain but do not form tau filaments
    • HERNANDEZ F, BORRELL J, GUAZA C, AVILA J, LUCAS JJ: Spatial learning deficit in transgenic mice that conditionally overexpress GSK-3β in the brain but do not form tau filaments. J. Neurochem. (2002) 83(6):1529-1533.
    • (2002) J. Neurochem. , vol.83 , Issue.6 , pp. 1529-1533
    • Hernandez, F.1    Borrell, J.2    Guaza, C.3    Avila, J.4    Lucas, J.J.5
  • 4
    • 0036441486 scopus 로고    scopus 로고
    • A cell biological perspective on Alzheimer's disease
    • ANNAERT W, DE STROOPER B: A cell biological perspective on Alzheimer's disease. Annu. Rev. Cell Dev. Biol. (2002) 18:25-51.
    • (2002) Annu. Rev. Cell Dev. Biol. , vol.18 , pp. 25-51
    • Annaert, W.1    De Strooper, B.2
  • 5
    • 3042558276 scopus 로고    scopus 로고
    • Glycogen synthase kinase 3: A drug target for CNS therapies
    • BHAT RV, BUDD HAEBERLEIN SL, AVILA J: Glycogen synthase kinase 3: a drug target for CNS therapies. J. Neurochem. (2004) 89(6):1313-1317.
    • (2004) J. Neurochem. , vol.89 , Issue.6 , pp. 1313-1317
    • Bhat, R.V.1    Budd Haeberlein, S.L.2    Avila, J.3
  • 6
    • 0242720372 scopus 로고    scopus 로고
    • Chronic lithium treatment decreases mutant tau protein aggregation in a transgenic mouse model
    • PEREZ M, HERNANDEZ F, LIM F, DIAZ-NIDO J, AVILA J: Chronic lithium treatment decreases mutant tau protein aggregation in a transgenic mouse model. J. Alzheimers Dis. (2003) 5(4):301-308.
    • (2003) J. Alzheimers Dis. , vol.5 , Issue.4 , pp. 301-308
    • Perez, M.1    Hernandez, F.2    Lim, F.3    Diaz-Nido, J.4    Avila, J.5
  • 7
    • 21044449225 scopus 로고    scopus 로고
    • Inhibition of glycogen synthase kinase-3 by lithium correlates with reduced tauopathy and degeneration in vivo
    • NOBLE W, PLANEL E, ZEHR C et al.: Inhibition of glycogen synthase kinase-3 by lithium correlates with reduced tauopathy and degeneration in vivo. Proc. Natl. Acad. Sci. USA (2005) 102(19):6990-6995.
    • (2005) Proc. Natl. Acad. Sci. USA , vol.102 , Issue.19 , pp. 6990-6995
    • Noble, W.1    Planel, E.2    Zehr, C.3
  • 8
    • 22344438508 scopus 로고    scopus 로고
    • Tau suppression in a neurodegenerative mouse model improves memory function
    • SANTACRUZ K, LEWIS J, SPIRES T et al.: Tau suppression in a neurodegenerative mouse model improves memory function. Science (2005) 309(5733):476-481.
    • (2005) Science , vol.309 , Issue.5733 , pp. 476-481
    • Santacruz, K.1    Lewis, J.2    Spires, T.3
  • 9
    • 0037087220 scopus 로고    scopus 로고
    • Lithium inhibits amyloid secretion in COS7 cells transfected with amyloid precursor protein C100
    • SUN X, SATO S, MURAYAMA O et al.: Lithium inhibits amyloid secretion in COS7 cells transfected with amyloid precursor protein C100. Neurosci. Lett. (2002) 321(1-2):61-64.
    • (2002) Neurosci. Lett. , vol.321 , Issue.1-2 , pp. 61-64
    • Sun, X.1    Sato, S.2    Murayama, O.3
  • 10
    • 0038187674 scopus 로고    scopus 로고
    • GSK-3α regulates production of Alzheimer's disease amyloid-β peptides
    • PHIEL CJ, WILSON CA, LEE VM, KLEIN PS: GSK-3α regulates production of Alzheimer's disease amyloid-β peptides. Nature (2003) 423(6938):435-439.
    • (2003) Nature , vol.423 , Issue.6938 , pp. 435-439
    • Phiel, C.J.1    Wilson, C.A.2    Lee, V.M.3    Klein, P.S.4
  • 11
    • 0142123260 scopus 로고    scopus 로고
    • APP processing is regulated by cytoplasmic phosphorylation
    • LEE MS, KAO SC, LEMERE CA et al.: APP processing is regulated by cytoplasmic phosphorylation. J. Cell Biol. (2003) 163(1):83-95.
    • (2003) J. Cell Biol. , vol.163 , Issue.1 , pp. 83-95
    • Lee, M.S.1    Kao, S.C.2    Lemere, C.A.3
  • 12
    • 0344926464 scopus 로고    scopus 로고
    • Divergent roles of GSK3 and CDK5 in APP processing
    • RYDER J, SU Y, LIU F et al.: Divergent roles of GSK3 and CDK5 in APP processing. Biochem. Biophys. Res. Commun. (2003) 312(4):922-929.
    • (2003) Biochem. Biophys. Res. Commun. , vol.312 , Issue.4 , pp. 922-929
    • Ryder, J.1    Su, Y.2    Liu, F.3
  • 13
    • 2642552331 scopus 로고    scopus 로고
    • Lithium, a common drug for bipolar disorder treatment, regulates amyloid-β precursor protein processing
    • SU Y, RYDER J, LI B et al.: Lithium, a common drug for bipolar disorder treatment, regulates amyloid-β precursor protein processing. Biochemistry (2004) 43(22):6899-6908.
    • (2004) Biochemistry , vol.43 , Issue.22 , pp. 6899-6908
    • Su, Y.1    Ryder, J.2    Li, B.3
  • 14
    • 3343005434 scopus 로고    scopus 로고
    • PS1 activates PI3K thus inhibiting GSK3 activity and tau overphosphorylation: Effects of FAD mutations
    • BAKI L, SHIOI J, WEN P et al.: PS1 activates PI3K thus inhibiting GSK3 activity and tau overphosphorylation: effects of FAD mutations. EMBO J. (2004) 23(13):2586-2596.
    • (2004) EMBO J. , vol.23 , Issue.13 , pp. 2586-2596
    • Baki, L.1    Shioi, J.2    Wen, P.3
  • 15
    • 13144265717 scopus 로고    scopus 로고
    • Presenilin 1 associates with glycogen synthase kinase-3β and its substrate tau
    • TAKASHIMA A, MURAYAMA M, MURAYAMA O et al.: Presenilin 1 associates with glycogen synthase kinase-3β and its substrate tau. Proc. Natl. Acad. Sci. USA (1998) 95(16):9637-9641.
    • (1998) Proc. Natl. Acad. Sci. USA , vol.95 , Issue.16 , pp. 9637-9641
    • Takashima, A.1    Murayama, M.2    Murayama, O.3
  • 16
    • 0242656408 scopus 로고    scopus 로고
    • Akt/GSK3β serine/threonine kinases: Evidence for a signalling pathway mediated by familial Alzheimer's disease mutations
    • RYDER J, SU Y,NI B: Akt/GSK3β serine/threonine kinases: evidence for a signalling pathway mediated by familial Alzheimer's disease mutations. Cell. Signal. (2004) 16(2):187-200.
    • (2004) Cell. Signal , vol.16 , Issue.2 , pp. 187-200
    • Ryder, J.1    Su, Y.2    Ni, B.3
  • 17
    • 4344619713 scopus 로고    scopus 로고
    • Pharmacological inhibitors of glycogen synthase kinase 3
    • MEIJER L, FLAJOLET M, GREENGARD P: Pharmacological inhibitors of glycogen synthase kinase 3. Trends Pharmacol. Sci. (2004) 25(9):471-480.
    • (2004) Trends Pharmacol. Sci. , vol.25 , Issue.9 , pp. 471-480
    • Meijer, L.1    Flajolet, M.2    Greengard, P.3
  • 18
    • 3042635178 scopus 로고    scopus 로고
    • GSK3 inhibitors: Development and therapeutic potential
    • COHEN P, GOEDERT M: GSK3 inhibitors: development and therapeutic potential. Nat. Rev. Drug Discov. (2004) 3(6):479-487.
    • (2004) Nat. Rev. Drug Discov. , vol.3 , Issue.6 , pp. 479-487
    • Cohen, P.1    Goedert, M.2
  • 19
    • 1842588303 scopus 로고    scopus 로고
    • Discovery and development of GSK3 inhibitors for the treatment of Type 2 diabetes
    • WAGMAN AS, JOHNSON KW, BUSSIERE DE: Discovery and development of GSK3 inhibitors for the treatment of Type 2 diabetes. Curr. Pharm. Des. (2004) 10(10):1105-1137.
    • (2004) Curr. Pharm. Des. , vol.10 , Issue.10 , pp. 1105-1137
    • Wagman, A.S.1    Johnson, K.W.2    Bussiere, D.E.3
  • 20
    • 0033776383 scopus 로고    scopus 로고
    • Selective small molecule inhibitors of glycogen synthase kinase-3 modulate glycogen metabolism and gene transcription
    • COGHLAN MP, CULBERT AA, CROSS DA et al.: Selective small molecule inhibitors of glycogen synthase kinase-3 modulate glycogen metabolism and gene transcription. Chem. Biol. (2000) 7(10):793-803.
    • (2000) Chem. Biol. , vol.7 , Issue.10 , pp. 793-803
    • Coghlan, M.P.1    Culbert, A.A.2    Cross, D.A.3
  • 21
    • 0035087123 scopus 로고    scopus 로고
    • Selective small-molecule inhibitors of glycogen synthase kinase-3 activity protect primary neurones from death
    • CROSS DA, CULBERT AA, CHALMERS KA et al.: Selective small-molecule inhibitors of glycogen synthase kinase-3 activity protect primary neurones from death. J. Neurochem. (2001) 77(1):94-102.
    • (2001) J. Neurochem. , vol.77 , Issue.1 , pp. 94-102
    • Cross, D.A.1    Culbert, A.A.2    Chalmers, K.A.3
  • 22
    • 0041831195 scopus 로고    scopus 로고
    • Glycogen synthase kinase-3 inhibitors protect central neurons against excitotoxicity
    • FACCI L, STEVENS DA, SKAPER SD: Glycogen synthase kinase-3 inhibitors protect central neurons against excitotoxicity. Neuroreport (2003) 14(11):1467-1470.
    • (2003) Neuroreport , vol.14 , Issue.11 , pp. 1467-1470
    • Facci, L.1    Stevens, D.A.2    Skaper, S.D.3
  • 23
    • 0141645621 scopus 로고    scopus 로고
    • Structural characterization of the GSK-3β active site using selective and non-selective ATP-mimetic inhibitors
    • BERTRAND JA, THIEFFINE S, VULPETTI A et al.: Structural characterization of the GSK-3β active site using selective and non-selective ATP-mimetic inhibitors. J. Mol. Biol. (2003) 333(2):393-407.
    • (2003) J. Mol. Biol. , vol.333 , Issue.2 , pp. 393-407
    • Bertrand, J.A.1    Thieffine, S.2    Vulpetti, A.3
  • 24
    • 0035848403 scopus 로고    scopus 로고
    • 3-Amino-4-arylmaleimides: Potent and selective inhibitors of glycogen synthase kinase-3 (GSK3)
    • SMITH DG, BUFFET M, FENWICK AE et al.: 3-Amino-4-arylmaleimides: potent and selective inhibitors of glycogen synthase kinase-3 (GSK3). Bioorg. Med. Chem. Lett. (2001) 11(5):635-639.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , Issue.5 , pp. 635-639
    • Smith, D.G.1    Buffet, M.2    Fenwick, A.E.3
  • 25
    • 3242766018 scopus 로고    scopus 로고
    • Substituted 3-imidazo[1,2-a]pyridin-3-yl- 4-(1,2,3,4-tenahydro-[1,4]diazepino-[6,7, 1-hi]indol-7-yl)pyrrole-2,5-diones as highly selective and potent inhibitors of glycogen synthase kinase-3
    • ENGLER TA, HENRY JR, MALHOTRA S et al.: Substituted 3-imidazo[1,2-a]pyridin-3-yl- 4-(1,2,3,4-tenahydro-[1,4]diazepino-[6,7, 1-hi]indol-7-yl)pyrrole-2,5-diones as highly selective and potent inhibitors of glycogen synthase kinase-3. J. Med. Chem. (2004) 47(16):3934-3937.
    • (2004) J. Med. Chem. , vol.47 , Issue.16 , pp. 3934-3937
    • Engler, T.A.1    Henry, J.R.2    Malhotra, S.3
  • 26
    • 20144388396 scopus 로고    scopus 로고
    • The development of potent and selective bisarylmaleimide GSK3 inhibitors
    • ENGLER TA, MALHOTRA S, BURKHOLDER TP et al.: The development of potent and selective bisarylmaleimide GSK3 inhibitors. Bioorg. Med. Chem. Lett. (2005) 15(4):899-903.
    • (2005) Bioorg. Med. Chem. Lett. , vol.15 , Issue.4 , pp. 899-903
    • Engler, T.A.1    Malhotra, S.2    Burkholder, T.P.3
  • 27
    • 12444300117 scopus 로고    scopus 로고
    • Macrocyclic bisindolylmaleimides as inhibitors of protein kinase C and glycogen synthase kinase-3
    • ZHANG HC, WHITE KB, YE H et al.: Macrocyclic bisindolylmaleimides as inhibitors of protein kinase C and glycogen synthase kinase-3. Bioorg. Med. Chem. Lett. (2003) 13(18):3049-3053.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , Issue.18 , pp. 3049-3053
    • Zhang, H.C.1    White, K.B.2    Ye, H.3
  • 28
    • 0032705583 scopus 로고    scopus 로고
    • The protein kinase C inhibitors bisindolylmaleimide I (GF 109203x) and IX (Ro 31-8220) are potent inhibitors of glycogen synthase kinase-3 activity
    • HERS I, TAVARE JM, DENTON RM: The protein kinase C inhibitors bisindolylmaleimide I (GF 109203x) and IX (Ro 31-8220) are potent inhibitors of glycogen synthase kinase-3 activity. FEBS Lett. (1999) 460(3):433-436.
    • (1999) FEBS Lett. , vol.460 , Issue.3 , pp. 433-436
    • Hers, I.1    Tavare, J.M.2    Denton, R.M.3
  • 29
    • 0141567462 scopus 로고    scopus 로고
    • Synthesis and discovery of macrocyclic polyoxygenated bis-7-azaindolylmaleimides as a novel series of potent and highly selective glycogen synthase kinase-3β inhibitors
    • KUO GH, PROUTY C, DEANGELIS A et al.: Synthesis and discovery of macrocyclic polyoxygenated bis-7-azaindolylmaleimides as a novel series of potent and highly selective glycogen synthase kinase-3β inhibitors. J. Med. Chem. (2003) 46(19):4021-4031.
    • (2003) J. Med. Chem. , vol.46 , Issue.19 , pp. 4021-4031
    • Kuo, G.H.1    Prouty, C.2    Deangelis, A.3
  • 30
    • 10744228214 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of novel macrocyclic bis-7-azaindolylmaleimides as potent and highly selective glycogen synthase kinase-3β (GSK-3β) inhibitors
    • SHEN L, PROUTY C, CONWAY BR et al.: Synthesis and biological evaluation of novel macrocyclic bis-7-azaindolylmaleimides as potent and highly selective glycogen synthase kinase-3β (GSK-3β) inhibitors. Bioorg. Med. Chem. (2004) 12(5):1239-1255.
    • (2004) Bioorg. Med. Chem. , vol.12 , Issue.5 , pp. 1239-1255
    • Shen, L.1    Prouty, C.2    Conway, B.R.3
  • 31
    • 2442564369 scopus 로고    scopus 로고
    • 3-(7-Azaindolyl)-4-arylmaleimides as potent, selective inhibitors of glycogen synthase kinase-3
    • ZHANG HC, YE H, CONWAY BR et al.: 3-(7-Azaindolyl)-4-arylmaleimides as potent, selective inhibitors of glycogen synthase kinase-3. Bioorg. Med. Chem. Lett. (2004) 14(12):3245-3250.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , Issue.12 , pp. 3245-3250
    • Zhang, H.C.1    Ye, H.2    Conway, B.R.3
  • 32
    • 2542434120 scopus 로고    scopus 로고
    • Design, synthesis, and biological evaluation of novel 7-azaindolyl-heteroaryl-maleimides as potent and selective glycogen synthase kinase-3β (GSK-3β) inhibitors
    • O'NEILL DJ, SHEN L, PROUTY C et al.: Design, synthesis, and biological evaluation of novel 7-azaindolyl-heteroaryl-maleimides as potent and selective glycogen synthase kinase-3β (GSK-3β) inhibitors. Bioorg. Med. Chem. (2004) 12(12):3167-3185.
    • (2004) Bioorg. Med. Chem. , vol.12 , Issue.12 , pp. 3167-3185
    • O'Neill, D.J.1    Shen, L.2    Prouty, C.3
  • 33
    • 0037339766 scopus 로고    scopus 로고
    • Selective glycogen synthase kinase 3 inhibitors potentiate insulin activation of glucose transport and utilization in vitro and in vivo
    • RING DB, JOHNSON KW, HENRIKSEN EJ et al.: Selective glycogen synthase kinase 3 inhibitors potentiate insulin activation of glucose transport and utilization in vitro and in vivo. Diabetes (2003) 52(3):588-595.
    • (2003) Diabetes , vol.52 , Issue.3 , pp. 588-595
    • Ring, D.B.1    Johnson, K.W.2    Henriksen, E.J.3
  • 34
    • 3042749593 scopus 로고    scopus 로고
    • Glycogen synthase kinase 3β inhibitor Chir025 reduces neuronal death resulting from oxygen-glucose deprivation, glutamate excitotoxicity, and cerebral ischemia
    • KELLY S, ZHAO H, HUA SUN G et al.: Glycogen synthase kinase 3β inhibitor Chir025 reduces neuronal death resulting from oxygen-glucose deprivation, glutamate excitotoxicity, and cerebral ischemia. Exp. Neurol. (2004) 188(2):378-386.
    • (2004) Exp. Neurol. , vol.188 , Issue.2 , pp. 378-386
    • Kelly, S.1    Zhao, H.2    Hua Sun, G.3
  • 35
    • 11144356458 scopus 로고    scopus 로고
    • Novel pyrazolopyrimidine derivatives as GSK3 inhibitors
    • PEAT AJ, BOUCHERON JA, DICKERSON SH et al.: Novel pyrazolopyrimidine derivatives as GSK3 inhibitors. Bioorg. Med. Chem. Lett. (2004) 14(9):2121-2125.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , Issue.9 , pp. 2121-2125
    • Peat, A.J.1    Boucheron, J.A.2    Dickerson, S.H.3
  • 36
    • 1842740894 scopus 로고    scopus 로고
    • Novel GSK3 inhibitors with improved cellular activity
    • PEAT AJ, GARRIDO D, BOUCHERON JA et al.: Novel GSK3 inhibitors with improved cellular activity. Bioorg. Med. Chem. Lett. (2004) 14(9):2127-2130.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , Issue.9 , pp. 2127-2130
    • Peat, A.J.1    Garrido, D.2    Boucheron, J.A.3
  • 37
    • 3042640438 scopus 로고    scopus 로고
    • 4-Acylamino-6-arylfuro[2,3-d]pyrimidines: Potent and selective glycogen synthase kinase-3 inhibitors
    • MAEDA Y, NAKANO M, SATO H et al.: 4-Acylamino-6-arylfuro[2,3-d]pyrimidines: potent and selective glycogen synthase kinase-3 inhibitors. Bioorg. Med. Chem. Lett. (2004) 14(15):3907-3911.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , Issue.15 , pp. 3907-3911
    • Maeda, Y.1    Nakano, M.2    Sato, H.3
  • 38
    • 0037596751 scopus 로고    scopus 로고
    • Synthetic small molecules that control stem cell fate
    • DING S, WU TY, BRINKER A et al.: Synthetic small molecules that control stem cell fate. Proc. Natl Acad. Sci. USA (2003) 100(13):7632-7637.
    • (2003) Proc. Natl. Acad. Sci. USA , vol.100 , Issue.13 , pp. 7632-7637
    • Ding, S.1    Wu, T.Y.2    Brinker, A.3
  • 39
    • 12444280004 scopus 로고    scopus 로고
    • 6-aryl-pyrazolo[3,4-b]pyridines: Potent inhibitors of glycogen synthase kinase-3 (GSK3)
    • WITHERINGTON J, BORDAS V, GAIBA A et al.: 6-aryl-pyrazolo[3,4-b]pyridines: potent inhibitors of glycogen synthase kinase-3 (GSK3). Bioorg. Med. Chem. Lett. (2003) 13(18):3055-3057.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , Issue.18 , pp. 3055-3057
    • Witherington, J.1    Bordas, V.2    Gaiba, A.3
  • 40
    • 0043022153 scopus 로고    scopus 로고
    • 6-heteroaryl-pyrazolo[3,4-b]pyridines: Potent and selective inhibitors of glycogen synthase kinase-3 (GSK3)
    • WITHERINGTON J, BORDAS V, GAIBA A et al.: 6-heteroaryl-pyrazolo[3,4-b]pyridines: potent and selective inhibitors of glycogen synthase kinase-3 (GSK3). Bioorg. Med. Chem. Lett. (2003) 13(18):3059-3062.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , Issue.18 , pp. 3059-3062
    • Witherington, J.1    Bordas, V.2    Gaiba, A.3
  • 41
    • 0037420819 scopus 로고    scopus 로고
    • 5-aryl-pyrazolo[3,4-blpyridines: Potent inhibitors of glycogen synthase kinase-3 (GSK3)
    • WITHERINGTON J, BORDAS V, GARLAND SL et al.: 5-aryl-pyrazolo[3,4-blpyridines: potent inhibitors of glycogen synthase kinase-3 (GSK3). Bioorg. Med. Chem. Lett. (2003) 13(9):1577-1580.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , Issue.9 , pp. 1577-1580
    • Witherington, J.1    Bordas, V.2    Garland, S.L.3
  • 42
    • 0037420819 scopus 로고    scopus 로고
    • 5-Aryl-pyrazolo[3,4-b]pyridazines: Potent inhibitors of glycogen synthase kinase-3 (GSK3)
    • WITHERINGTON J, BORDAS V, HAIGH D et al.: 5-Aryl-pyrazolo[3,4-b]pyridazines: potent inhibitors of glycogen synthase kinase-3 (GSK3). Bioorg. Med. Chem. Lett. (2003) 13(9):1581-1584.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , Issue.9 , pp. 1581-1584
    • Witherington, J.1    Bordas, V.2    Haigh, D.3
  • 43
    • 4444288154 scopus 로고    scopus 로고
    • N-Phenyl-4-pyrazolo[1,5-b] pyridazin-3-ylpyrimidin-2-amines as potent and selective inhibitors of glycogen synthase kinase 3 with good cellular efficacy
    • TAVARES FX, BOUCHERON JA, DICKERSON SH et al.: N-Phenyl-4-pyrazolo[1,5-b] pyridazin-3-ylpyrimidin-2-amines as potent and selective inhibitors of glycogen synthase kinase 3 with good cellular efficacy. J. Med. Chem. (2004) 47(19):4716-4730.
    • (2004) J. Med. Chem. , vol.47 , Issue.19 , pp. 4716-4730
    • Tavares, F.X.1    Boucheron, J.A.2    Dickerson, S.H.3
  • 44
    • 0242664588 scopus 로고    scopus 로고
    • Structural insights and biological effects of glycogen synthase kinase 3-specific inhibitor AR-A014418
    • BHAT R, XUE Y, BERG S et al.: Structural insights and biological effects of glycogen synthase kinase 3-specific inhibitor AR-A014418. J. Biol. Chem. (2003) 278(46):45937-45945.
    • (2003) J. Biol. Chem. , vol.278 , Issue.46 , pp. 45937-45945
    • Bhat, R.1    Xue, Y.2    Berg, S.3
  • 45
    • 10644255687 scopus 로고    scopus 로고
    • AR-A014418, a selective GSK-3 inhibitor, produces antidepressant-like effects in the forced swim test
    • GOULD TD, EINAT H, BHAT R, MANJI HK: AR-A014418, a selective GSK-3 inhibitor, produces antidepressant-like effects in the forced swim test. Int. J. Neuropsychopharmacol. (2004) 7(4):387-390.
    • (2004) Int. J. Neuropsychopharmacol. , vol.7 , Issue.4 , pp. 387-390
    • Gould, T.D.1    Einat, H.2    Bhat, R.3    Manji, H.K.4
  • 46
    • 0037817456 scopus 로고    scopus 로고
    • Synthesis and in vitro characterization of 1-(4-aminofurazan-3-yl)-5-dialkylaminomethyl- 1H-[1,2,3]triazole-4-carboxylic acid derivatives. A new class of selective GSK3 inhibitors
    • OLESEN PH, SORENSEN AR, URSO B et al.: Synthesis and in vitro characterization of 1-(4-aminofurazan-3-yl)-5-dialkylaminomethyl- 1H-[1,2,3]triazole-4-carboxylic acid derivatives. A new class of selective GSK3 inhibitors. J. Med. Chem. (2003) 46(15):3333-3341.
    • (2003) J. Med. Chem. , vol.46 , Issue.15 , pp. 3333-3341
    • Olesen, P.H.1    Sorensen, A.R.2    Urso, B.3
  • 47
    • 0035808457 scopus 로고    scopus 로고
    • Indirubins inhibit glycogen synthase kinase-3β and CDK5/p25, two protein kinases involved in abnormal tau phosphorylation in Alzheimer's disease. A property common to most cyclin-dependent kinase inhibitors?
    • LECLERC S, GARNIER M, HOESSEL R et al.: Indirubins inhibit glycogen synthase kinase-3β and CDK5/p25, two protein kinases involved in abnormal tau phosphorylation in Alzheimer's disease. A property common to most cyclin-dependent kinase inhibitors? J. Biol. Chem. (2001) 276(1):251-260.
    • (2001) J. Biol. Chem. , vol.276 , Issue.1 , pp. 251-260
    • Leclerc, S.1    Garnier, M.2    Hoessel, R.3
  • 48
    • 0346875916 scopus 로고    scopus 로고
    • GSK3-selective inhibitors derived from Tyrian purple indirubins
    • MEIJER L, SKALTSOUNIS AL, MAGIATIS P et al.: GSK3-selective inhibitors derived from Tyrian purple indirubins. Chem. Biol. (2003) 10(12):1255-1266.
    • (2003) Chem. Biol. , vol.10 , Issue.12 , pp. 1255-1266
    • Meijer, L.1    Skaltsounis, A.L.2    Magiatis, P.3
  • 49
    • 2442589341 scopus 로고    scopus 로고
    • Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinases
    • POLYCHRONOPOULOS P, MAGIATIS P, SKALTSOUNIS AL et al.: Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinases. J. Med. Chem. (2004) 47(4):935-946.
    • (2004) J. Med. Chem. , vol.47 , Issue.4 , pp. 935-946
    • Polychronopoulos, P.1    Magiatis, P.2    Skaltsounis, A.L.3
  • 50
    • 0033798031 scopus 로고    scopus 로고
    • Paullones are potent inhibitors of glycogen synthase kinase-3β and cyclin-dependent kinase 5/p25
    • LEOST M, SCHULTZ C, LINK A et al.: Paullones are potent inhibitors of glycogen synthase kinase-3β and cyclin-dependent kinase 5/p25. Eur. J. Biochem. (2000) 267(19):5983-5994.
    • (2000) Eur. J. Biochem. , vol.267 , Issue.19 , pp. 5983-5994
    • Leost, M.1    Schultz, C.2    Link, A.3
  • 51
    • 0037067733 scopus 로고    scopus 로고
    • Intracellular targets of paullones. Identification following affinity purification on immobilized inhibitor
    • KNOCKAERT M, WIEKING K, SCHMITT S et al.: Intracellular targets of paullones. Identification following affinity purification on immobilized inhibitor. J. Biol. Chem. (2002) 277(28):25493-25501.
    • (2002) J. Biol. Chem. , vol.277 , Issue.28 , pp. 25493-25501
    • Knockaert, M.1    Wieking, K.2    Schmitt, S.3
  • 52
  • 53
    • 0037448375 scopus 로고    scopus 로고
    • Aloisines, a new family of CDK/GSK3 inhibitors. SAR study, crystal structure in complex with CDK2, enzyme selectivity, and cellular effects
    • METTEY Y, GOMPEL M, THOMAS V et al.: Aloisines, a new family of CDK/GSK3 inhibitors. SAR study, crystal structure in complex with CDK2, enzyme selectivity, and cellular effects. J. Med. Chem. (2003) 46(2):222-236.
    • (2003) J. Med. Chem. , vol.46 , Issue.2 , pp. 222-236
    • Mettey, Y.1    Gompel, M.2    Thomas, V.3
  • 54
    • 0037013685 scopus 로고    scopus 로고
    • Scaffold hopping and optimization towards libraries of glycogen synthase kinase-3 inhibitors
    • NAERUM L, NORSKOV-LAURITSEN L, OLESEN PH: Scaffold hopping and optimization towards libraries of glycogen synthase kinase-3 inhibitors. Bioorg. Med. Chem. Lett. (2002) 12(11):1525-1528.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , Issue.11 , pp. 525-1528
    • Naerum, L.1    Norskov-Lauritsen, L.2    Olesen, P.H.3
  • 55
    • 0034010742 scopus 로고    scopus 로고
    • Inhibition of cyclin-dependent kinases, GSK-3β and CK1 by hymenialdisine, a marine sponge constituent
    • MEIJER L, THUNNISSEN AM, WHITE AW et al.: Inhibition of cyclin-dependent kinases, GSK-3β and CK1 by hymenialdisine, a marine sponge constituent. Chem. Biol. (2000) 7(1):51-63.
    • (2000) Chem. Biol. , vol.7 , Issue.1 , pp. 51-63
    • Meijer, L.1    Thunnissen, A.M.2    White, A.W.3
  • 56
    • 0037075791 scopus 로고    scopus 로고
    • First non-ATP competitive glycogen synthase kinase 3β (GSK-3β) inhibitors: Thiadiazolidinones (TDZD) as potential drugs for the treatment of Alzheimer's disease
    • MARTINEZ A, ALONSO M, CASTRO A, PEREZ C, MORENO FJ: First non-ATP competitive glycogen synthase kinase 3β (GSK-3β) inhibitors: thiadiazolidinones (TDZD) as potential drugs for the treatment of Alzheimer's disease. J. Med. Chem. (2002) 45(6):1292-1299.
    • (2002) J. Med. Chem. , vol.45 , Issue.6 , pp. 1292-1299
    • Martinez, A.1    Alonso, M.2    Castro, A.3    Perez, C.4    Moreno, F.J.5
  • 57
    • 20444398490 scopus 로고    scopus 로고
    • Regulation of inflammatory response in neural cells in vitro by thiadiazolidinones derivatives through peroxisome proliferator-activated receptor γ activation
    • LUNA-MEDINA R, CORTES-CANTELI M, ALONSO M et al.: Regulation of inflammatory response in neural cells in vitro by thiadiazolidinones derivatives through peroxisome proliferator-activated receptor γ activation. J. Biol. Chem. (2005) 280(22):21453-21462.
    • (2005) J. Biol. Chem. , vol.280 , Issue.22 , pp. 21453-21462
    • Luna-Medina, R.1    Cortes-Canteli, M.2    Alonso, M.3
  • 58
    • 0142060928 scopus 로고    scopus 로고
    • Thienyl and phenyl α-halomethyl ketones: New inhibitors of glycogen synthase kinase (GSK-3β) from a library of compound searching
    • CONDE S, PEREZ DI, MARTINEZ A, PEREZ C, MORENO FJ: Thienyl and phenyl α-halomethyl ketones: new inhibitors of glycogen synthase kinase (GSK-3β) from a library of compound searching. J. Med. Chem. (2003) 46(22):4631-4633.
    • (2003) J. Med. Chem. , vol.46 , Issue.22 , pp. 4631-4633
    • Conde, S.1    Perez, D.I.2    Martinez, A.3    Perez, C.4    Moreno, F.J.5
  • 59
    • 0032821768 scopus 로고    scopus 로고
    • A GSK3-binding peptide from FRAT1 selectively inhibits the GSK3-catalysed phosphorylation of axin and β-catenin
    • THOMAS GM, FRAME S, GOEDERT M et al.: A GSK3-binding peptide from FRAT1 selectively inhibits the GSK3-catalysed phosphorylation of axin and β-catenin. FEBS Lett. (1999) 458(2):247-251.
    • (1999) FEBS Lett. , vol.458 , Issue.2 , pp. 247-251
    • Thomas, G.M.1    Frame, S.2    Goedert, M.3
  • 60
    • 0035798069 scopus 로고    scopus 로고
    • GSK-3 inhibition by adenoviral FRAT1 overexpression is neuroprotective and induces Tau dephosphorylation and β-catenin stabilisation without elevation of glycogen synthase activity
    • CULBERT AA, BROWN MJ, FRAME S et al.: GSK-3 inhibition by adenoviral FRAT1 overexpression is neuroprotective and induces Tau dephosphorylation and β-catenin stabilisation without elevation of glycogen synthase activity. FEBS Lett. (2001) 507(3):288-294.
    • (2001) FEBS Lett. , vol.507 , Issue.3 , pp. 288-294
    • Culbert, A.A.1    Brown, M.J.2    Frame, S.3
  • 61
    • 0142231434 scopus 로고    scopus 로고
    • FRAT1 peptide decreases Aβ production in swAPP(751) cells
    • LI B, RYDER J, SU Y et al.: FRAT1 peptide decreases Aβ production in swAPP(751) cells. FEBS Lett. (2003) 553(3):347-350.
    • (2003) FEBS Lett. , vol.553 , Issue.3 , pp. 347-350
    • Li, B.1    Ryder, J.2    Su, Y.3
  • 62
    • 0032849085 scopus 로고    scopus 로고
    • Regulation of glycogen synthase kinase 3β and downstream Wnt signaling by axin
    • HEDGEPETH CM, DEARDORFF MA, RANKIN K, KLEIN PS: Regulation of glycogen synthase kinase 3β and downstream Wnt signaling by axin. Mol. Cell. Biol. (1999) 19(10):7147-7157.
    • (1999) Mol. Cell. Biol. , vol.19 , Issue.10 , pp. 7147-7157
    • Hedgepeth, C.M.1    Deardorff, M.A.2    Rankin, K.3    Klein, P.S.4
  • 63
    • 0037348372 scopus 로고    scopus 로고
    • A novel viral mechanism for dysregulation of β-catenin in Kaposi's sarcoma-associated herpesvirus latency
    • FUJIMURO M, WU FY, APRHYS C et al.: A novel viral mechanism for dysregulation of β-catenin in Kaposi's sarcoma-associated herpesvirus latency. Nat. Med. (2003) 9(3):300-306.
    • (2003) Nat. Med. , vol.9 , Issue.3 , pp. 300-306
    • Fujimuro, M.1    Wu, F.Y.2    Aprhys, C.3
  • 64
    • 0038811796 scopus 로고    scopus 로고
    • Insulin mimetic action of synthetic phosphorylated peptide inhibitors of glycogen synthase kinase-3
    • PLOTKIN B, KAIDANOVICH O, TALIOR I, ELDAR-FINKELMAN H: Insulin mimetic action of synthetic phosphorylated peptide inhibitors of glycogen synthase kinase-3. J. Pharmacol. Exp. Ther. (2003) 305(3):974-980.
    • (2003) J. Pharmacol. Exp. Ther. , vol.305 , Issue.3 , pp. 974-980
    • Plotkin, B.1    Kaidanovich, O.2    Talior, I.3    Eldar-Finkelman, H.4
  • 65
    • 1842420631 scopus 로고    scopus 로고
    • Rapid antidepressive-like activity of specific glycogen synthase kinase-3 inhibitor and its effect on β-catenin in mouse hippocampus
    • KAIDANOVICH-BEILIN O, MILMAN A, WEIZMAN A, PICK CG, ELDAR-FINKELMAN H: Rapid antidepressive-like activity of specific glycogen synthase kinase-3 inhibitor and its effect on β-catenin in mouse hippocampus. Biol. Psychiatry (2004) 55(8):781-784.
    • (2004) Biol. Psychiatry , vol.55 , Issue.8 , pp. 781-784
    • Kaidanovich-Beilin, O.1    Milman, A.2    Weizman, A.3    Pick, C.G.4    Eldar-Finkelman, H.5
  • 66
    • 0037303455 scopus 로고    scopus 로고
    • Simultaneous inhibition of GSK-3α and GSK-3β using hairpin siRNA expression vectors
    • YU JY, TAYLOR J, DERUITER SL, VOJTEK AB, TURNER DL: Simultaneous inhibition of GSK-3α and GSK-3β using hairpin siRNA expression vectors. Mol. Ther. (2003) 7(2):228-236.
    • (2003) Mol. Ther. , vol.7 , Issue.2 , pp. 228-236
    • Yu, J.Y.1    Taylor, J.2    Deruiter, S.L.3    Vojtek, A.B.4    Turner, D.L.5
  • 67
    • 0346156074 scopus 로고    scopus 로고
    • Conditional protein alleles using knockin mice and a chemical inducer of dimerization
    • STANKUNAS K, BAYLE JH, GESTWICKI JE et al.: Conditional protein alleles using knockin mice and a chemical inducer of dimerization. Mol. Cell (2003) 12(6):1615-1624.
    • (2003) Mol. Cell , vol.12 , Issue.6 , pp. 1615-1624
    • Stankunas, K.1    Bayle, J.H.2    Gestwicki, J.E.3
  • 68
    • 0034612636 scopus 로고    scopus 로고
    • Requirement for glycogen synthase kinase-3β in cell survival and NF-κB activation
    • HOEFLICH KP, LUO J, RUBIE EA et al.: Requirement for glycogen synthase kinase-3β in cell survival and NF-κB activation. Nature (2000) 406(6791):86-90.
    • (2000) Nature , vol.406 , Issue.6791 , pp. 86-90
    • Hoeflich, K.P.1    Luo, J.2    Rubie, E.A.3
  • 69
    • 3342955475 scopus 로고    scopus 로고
    • Glycogen synthase kinase-3β haploinsufficiency mimics the behavioral and molecular effects of lithium
    • O'BRIEN WT, HARPER AD, JOVE F et al.: Glycogen synthase kinase-3β haploinsufficiency mimics the behavioral and molecular effects of lithium. J. Neurosci. (2004) 24(30):6791-6798.
    • (2004) J. Neurosci. , vol.24 , Issue.30 , pp. 6791-6798
    • O'Brien, W.T.1    Harper, A.D.2    Jove, F.3
  • 71
    • 9644275641 scopus 로고    scopus 로고
    • Signal transduction during amyloid-β-peptide neurotoxicity: Role in Alzheimer's disease
    • FUENTEALBA RA, FARIAS G, SCHEU J et al.: Signal transduction during amyloid-β-peptide neurotoxicity: role in Alzheimer's disease. Brain Res. Brain Res. Rev. (2004) 47(1-3):275-289.
    • (2004) Brain Res. Brain Res. Rev. , vol.47 , Issue.1-3 , pp. 275-289
    • Fuentealba, R.A.1    Farias, G.2    Scheu, J.3
  • 72
    • 15944363787 scopus 로고    scopus 로고
    • Unraveling signalling cascades for the Snail family of transcription factors
    • DE CRAENE B, VAN ROY F, BERX G: Unraveling signalling cascades for the Snail family of transcription factors. Cell. Signal. (2005) 17(5):535-547.
    • (2005) Cell. Signal , vol.17 , Issue.5 , pp. 535-547
    • De Craene, B.1    Van Roy, F.2    Berx, G.3
  • 73
    • 5444259864 scopus 로고    scopus 로고
    • GSK-3β sets Snail's pace
    • SCHLESSINGER K, HALL A: GSK-3β sets Snail's pace. Nat. Cell Biol. (2004) 6(10):913-915.
    • (2004) Nat. Cell Biol. , vol.6 , Issue.10 , pp. 913-915
    • Schlessinger, K.1    Hall, A.2
  • 74
    • 0031809141 scopus 로고    scopus 로고
    • Cancer morbidity in psychiatric patients: Influence of lithium carbonate treatment
    • COHEN Y, CHETRIT A, COHEN Y, SIROTA P, MODAN B: Cancer morbidity in psychiatric patients: influence of lithium carbonate treatment. Med. Oncol. (1998) 15(1):32-36.
    • (1998) Med. Oncol. , vol.15 , Issue.1 , pp. 32-36
    • Cohen, Y.1    Chetrit, A.2    Cohen, Y.3    Sirota, P.4    Modan, B.5
  • 75
    • 7644220896 scopus 로고    scopus 로고
    • Inhibition of glycogen synthase kinase-3 represses androgen receptor activity and prostate cancer cell growth
    • MAZOR M, KAWANO Y, ZHU H, WAXMAN J, KYPTA RM: Inhibition of glycogen synthase kinase-3 represses androgen receptor activity and prostate cancer cell growth. Oncogene (2004) 23(47):7882-7892.
    • (2004) Oncogene , vol.23 , Issue.47 , pp. 7882-7892
    • Mazor, M.1    Kawano, Y.2    Zhu, H.3    Waxman, J.4    Kypta, R.M.5
  • 76
    • 16844374033 scopus 로고    scopus 로고
    • Glycogen synthase kinase-3β participates in nuclear factor κB-mediated gene transcription and cell survival in pancreatic cancer cells
    • OUGOLKOV AV, FERNANDEZ-ZAPICO ME, SAVOY DN, URRUTIA RA, BILLADEAU DD: Glycogen synthase kinase-3β participates in nuclear factor κB-mediated gene transcription and cell survival in pancreatic cancer cells. Cancer Res. (2005) 65(6):2076-2081.
    • (2005) Cancer Res. , vol.65 , Issue.6 , pp. 2076-2081
    • Ougolkov, A.V.1    Fernandez-Zapico, M.E.2    Savoy, D.N.3    Urrutia, R.A.4    Billadeau, D.D.5
  • 77
    • 23044444841 scopus 로고    scopus 로고
    • Deregulated GSK-3β activity in colorectal cancer: Its association with tumor cell survival and proliferation
    • SHAKOORI A, OUGOLKOV A, YU ZW et al.: Deregulated GSK-3β activity in colorectal cancer: its association with tumor cell survival and proliferation. Biochem. Biophys. Res. Commun. (2005) 334(4):1365-1373.
    • (2005) Biochem. Biophys. Res. Commun. , vol.334 , Issue.4 , pp. 1365-1373
    • Shakoori, A.1    Ougolkov, A.2    Yu, Z.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.