메뉴 건너뛰기




Volumn 25, Issue 8, 2015, Pages 849-872

C-Jun N-terminal kinase inhibitors: A patent review (2010-2014)

Author keywords

Alzheimer's disease; C Jun N terminal kinase inhibitors; Cancer; Cardiovascular disorders; Chemical probes; Dual leucine zipper kinase; Huntington's disease; Inflammation; Isoform selectivity; JNK1; JNK2; JNK3; MAPK kinases; Metabolic disorders; Mitogen activated protein kinase kinase 4; Neurodegenerative disorders; P38 MAP kinase; Parkinson's disease; Stroke

Indexed keywords

ISOENZYME; STRESS ACTIVATED PROTEIN KINASE; STRESS ACTIVATED PROTEIN KINASE INHIBITOR; PROTEIN KINASE INHIBITOR;

EID: 84937208281     PISSN: 13543776     EISSN: 17447674     Source Type: Journal    
DOI: 10.1517/13543776.2015.1039984     Document Type: Review
Times cited : (50)

References (83)
  • 1
    • 63449112585 scopus 로고    scopus 로고
    • Therapeutic protein kinase inhibitors
    • Grant SK. Therapeutic Protein Kinase Inhibitors. Cell Mol Life Sci 2009;66(7):1163-77
    • (2009) Cell Mol Life Sci , vol.66 , Issue.7 , pp. 1163-1177
    • Grant, S.K.1
  • 2
    • 0037032817 scopus 로고    scopus 로고
    • Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases
    • (Washington, DC, U S)
    • Johnson GL, Lapadat R. Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases. Science (Washington, DC, U S) 2002;298(5600):1911-12
    • (2002) Science , vol.298 , Issue.5600 , pp. 1911-1912
    • Johnson, G.L.1    Lapadat, R.2
  • 3
    • 34247580832 scopus 로고    scopus 로고
    • JNK pathway: Diseases and therapeutic potential
    • Cui J, Zhang M, Zhang Y-Q, et al. JNK pathway: diseases and therapeutic potential. Acta Pharmacol Sin 2007;28(5):601-8
    • (2007) Acta Pharmacol Sin , vol.28 , Issue.5 , pp. 601-608
    • Cui, J.1    Zhang, M.2    Zhang, Y.-Q.3
  • 4
    • 0029885419 scopus 로고    scopus 로고
    • Selective interaction of JNK protein kinase isoforms with transcription factors
    • Gupta S, Barret T, Whitmarsh AJ, et al. Selective interaction of JNK protein kinase isoforms with transcription factors. EMBO J 1996;15(11):2760-70
    • (1996) EMBO J , vol.15 , Issue.11 , pp. 2760-2770
    • Gupta, S.1    Barret, T.2    Whitmarsh, A.J.3
  • 5
    • 67749117934 scopus 로고    scopus 로고
    • Signal integration by JNK and p38 MAPK pathways in cancer development
    • Wagner EF, Nebreda AR. Signal integration by JNK and p38 MAPK pathways in cancer development. Nat Rev Cancer 2009;9(8):537-49
    • (2009) Nat Rev Cancer , vol.9 , Issue.8 , pp. 537-549
    • Wagner, E.F.1    Nebreda, A.R.2
  • 6
    • 0032508714 scopus 로고    scopus 로고
    • A mammalian scaffold complex that selectively mediates MAP kinase activation
    • Whitmarsh AJ, Cavanagh J, Tournier C, et al. A mammalian scaffold complex that selectively mediates MAP kinase activation. Science (Washington, D C) 1998;281(5383):1671-4
    • (1998) Science (Washington, D C) , vol.281 , Issue.5383 , pp. 1671-1674
    • Whitmarsh, A.J.1    Cavanagh, J.2    Tournier, C.3
  • 7
    • 33845653234 scopus 로고    scopus 로고
    • Uses for JNK: The many and varied substrates of the c-Jun N-terminal kinases
    • Bogoyevitch MA, Kobe B. Uses for JNK: the many and varied substrates of the c-Jun N-terminal kinases. Microbiol Mol Biol Rev 2006;70(4):1061-95
    • (2006) Microbiol Mol Biol Rev , vol.70 , Issue.4 , pp. 1061-1095
    • Bogoyevitch, M.A.1    Kobe, B.2
  • 8
    • 84920964208 scopus 로고    scopus 로고
    • Inhibitors of c-jun N-terminal kinases: An update
    • Koch P, Gehringer M, Laufer SA. Inhibitors of c-jun N-terminal kinases: An update. J Med Chem 2015;58(1):72-95
    • (2015) J Med Chem , vol.58 , Issue.1 , pp. 72-95
    • Koch, P.1    Gehringer, M.2    Laufer, S.A.3
  • 9
    • 0037032835 scopus 로고    scopus 로고
    • The protein kinase complement of the human genome
    • (Washington, DC, U S); 33-34
    • Manning G, Whyte DB, Martinez R, et al. The protein kinase complement of the human genome. Science (Washington, DC, U S) 2002;298(5600):1912-16; 33-34
    • (2002) Science , vol.298 , Issue.5600 , pp. 1912-1916
    • Manning, G.1    Whyte, D.B.2    Martinez, R.3
  • 10
    • 84876139608 scopus 로고    scopus 로고
    • JNK inhibitors as antiinflammatory and neuroprotective agents
    • Graczyk PP. JNK inhibitors as antiinflammatory and neuroprotective agents. Future Med Chem 2013;5(5):539-51
    • (2013) Future Med Chem , vol.5 , Issue.5 , pp. 539-551
    • Graczyk, P.P.1
  • 11
    • 57449085907 scopus 로고    scopus 로고
    • Implication of the JNK pathway in a rat model of Huntington's disease
    • Perrin V, Dufour N, Raoul C, et al. Implication of the JNK pathway in a rat model of Huntington's disease. Exp Neurol 2009;215(1):191-200
    • (2009) Exp Neurol , vol.215 , Issue.1 , pp. 191-200
    • Perrin, V.1    Dufour, N.2    Raoul, C.3
  • 12
    • 0030881742 scopus 로고    scopus 로고
    • Jun N-terminal kinase/stress-activated protein kinase (JNK/SAPK) is required for lipopolysaccharide stimulation of tumor necrosis factor a (TNF-a) translation: Glucocorticoids inhibit TNF-a translation by blocking JNK/ SAPK
    • Swantek JL, Cobb MH, Geppert TD. Jun N-terminal kinase/stress-activated protein kinase (JNK/SAPK) is required for lipopolysaccharide stimulation of tumor necrosis factor a (TNF-a) translation: glucocorticoids inhibit TNF-a translation by blocking JNK/ SAPK. Mol Cell Biol 1997;17(11):6274-82
    • (1997) Mol Cell Biol , vol.17 , Issue.11 , pp. 6274-6282
    • Swantek, J.L.1    Cobb, M.H.2    Geppert, T.D.3
  • 13
    • 79958064088 scopus 로고    scopus 로고
    • JNK-1 deficiency limits macrophage-mediated antigen-induced arthritis
    • Guma M, Ronacher LM, Firestein GS, et al. JNK-1 deficiency limits macrophage-mediated antigen-induced arthritis. Arthritis Rheum 2011;63(6):1603-12
    • (2011) Arthritis Rheum , vol.63 , Issue.6 , pp. 1603-1612
    • Guma, M.1    Ronacher, L.M.2    Firestein, G.S.3
  • 14
    • 78649878876 scopus 로고    scopus 로고
    • The role of JNK proteins in metabolism
    • Vallerie SN, Hotamisligil GS. The role of JNK proteins in metabolism. Sci Transl Med 2010;2(60):60rv5
    • (2010) Sci Transl Med , vol.2 , Issue.60 , pp. 60rv5
    • Vallerie, S.N.1    Hotamisligil, G.S.2
  • 15
    • 84890284499 scopus 로고    scopus 로고
    • JNK signalling in cancer: In need of new, smarter therapeutic targets
    • Bubici C, Papa S. JNK signalling in cancer: in need of new, smarter therapeutic targets. Br J Pharmacol 2014;171(1):24-37
    • (2014) Br J Pharmacol , vol.171 , Issue.1 , pp. 24-37
    • Bubici, C.1    Papa, S.2
  • 16
    • 0035923665 scopus 로고    scopus 로고
    • SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase
    • Bennett BL, Sasaki DT, Murray BW, et al. SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase. Proc Natl Acad Sci USA 2001;98(24):13681-6
    • (2001) Proc Natl Acad Sci USA , vol.98 , Issue.24 , pp. 13681-13686
    • Bennett, B.L.1    Sasaki, D.T.2    Murray, B.W.3
  • 17
    • 19744365702 scopus 로고    scopus 로고
    • A small molecule-kinase interaction map for clinical kinase inhibitors
    • Fabian MA, Biggs WH, Treiber DK, et al. A small molecule-kinase interaction map for clinical kinase inhibitors. Nat Biotechnol 2005;23(3):329-36
    • (2005) Nat Biotechnol , vol.23 , Issue.3 , pp. 329-336
    • Fabian, M.A.1    Biggs, W.H.2    Treiber, D.K.3
  • 18
    • 77951136174 scopus 로고    scopus 로고
    • Small molecule JNK (c-Jun N-terminal kinase) inhibitors
    • Siddiqui MA, Reddy PA. Small molecule JNK (c-Jun N-terminal kinase) inhibitors. J Med Chem 2010;53(8):3005-12
    • (2010) J Med Chem , vol.53 , Issue.8 , pp. 3005-3012
    • Siddiqui, M.A.1    Reddy, P.A.2
  • 19
    • 80052815074 scopus 로고    scopus 로고
    • Design and characterization of a potent and selective dual ATP-and substratecompetitive subnanomolar bidentate c-Jun N-terminal kinase (JNK) inhibitor
    • Stebbins JL, De SK, Pavlickova P, et al. Design and characterization of a potent and selective dual ATP-and substratecompetitive subnanomolar bidentate c-Jun N-terminal kinase (JNK) inhibitor. J Med Chem 2011;54(18):6206-14
    • (2011) J Med Chem , vol.54 , Issue.18 , pp. 6206-6214
    • Stebbins, J.L.1    De, S.K.2    Pavlickova, P.3
  • 20
    • 84863056297 scopus 로고    scopus 로고
    • Discovery of potent and selective covalent inhibitors of JNK
    • Zhang T, Inesta-Vaquera F, Niepel M, et al. Discovery of potent and selective covalent inhibitors of JNK. Chem Biol (Oxford, U K) 2012;19(1):140-54
    • (2012) Chem Biol (Oxford, U K) , vol.19 , Issue.1 , pp. 140-154
    • Zhang, T.1    Inesta-Vaquera, F.2    Niepel, M.3
  • 21
    • 84856233549 scopus 로고    scopus 로고
    • Aminopurine based JNK inhibitors for the prevention of ischemia reperfusion injury
    • Krenitsky VP, Delgado M, Nadolny L, et al. Aminopurine based JNK inhibitors for the prevention of ischemia reperfusion injury. Bioorg Med Chem Lett 2012;22(3):1427-32
    • (2012) Bioorg Med Chem Lett , vol.22 , Issue.3 , pp. 1427-1432
    • Krenitsky, V.P.1    Delgado, M.2    Nadolny, L.3
  • 22
    • 84866398396 scopus 로고    scopus 로고
    • Identification of an adamantyl azaquinolone JNK selective inhibitor
    • Haynes N-E, Scott NR, Chen LC, et al. Identification of an adamantyl azaquinolone JNK selective inhibitor. ACS Med Chem Lett 2012;3(9):764-8
    • (2012) ACS Med Chem Lett , vol.3 , Issue.9 , pp. 764-768
    • Haynes, N.-E.1    Scott, N.R.2    Chen, L.C.3
  • 23
    • 22244479745 scopus 로고    scopus 로고
    • Design and synthesis of the first generation of novel potent, selective, and in vivo active (benzothiazol-2-yl)acetonitrile inhibitors of the c-Jun N-terminal kinase
    • Gaillard P, Jeanclaude-Etter I, Ardissone V, et al. Design and synthesis of the first generation of novel potent, selective, and in vivo active (benzothiazol-2-yl)acetonitrile inhibitors of the c-Jun N-terminal kinase. J Med Chem 2005;48(14):4596-607
    • (2005) J Med Chem , vol.48 , Issue.14 , pp. 4596-4607
    • Gaillard, P.1    Jeanclaude-Etter, I.2    Ardissone, V.3
  • 27
    • 75349096996 scopus 로고    scopus 로고
    • C-Jun N-terminal kinase (JNK) signaling: Recent advances and challenges
    • Bogoyevitch MA, Ngoei KRW, Zhao TT, et al. c-Jun N-terminal kinase (JNK) signaling: recent advances and challenges. Biochim Biophys Acta 2010;1804(3):463-75
    • (2010) Biochim Biophys Acta , vol.1804 , Issue.3 , pp. 463-475
    • Bogoyevitch, M.A.1    Ngoei, K.R.W.2    Zhao, T.T.3
  • 33
    • 84873709116 scopus 로고    scopus 로고
    • Development of amino-pyrimidine inhibitors of c-Jun N-terminal kinase (JNK:Kinase profiling guided optimization of a 1, 2, 3-benzotriazole lead
    • Palmer WS, Alam M, Arzeno HB, et al. Development of amino-pyrimidine inhibitors of c-Jun N-terminal kinase (JNK): Kinase profiling guided optimization of a 1, 2, 3-benzotriazole lead. Bioorg Med Chem Lett 2013;23(5):1486-92
    • (2013) Bioorg Med Chem Lett , vol.23 , Issue.5 , pp. 1486-1492
    • Palmer, W.S.1    Alam, M.2    Arzeno, H.B.3
  • 35
    • 84878115112 scopus 로고    scopus 로고
    • Development of indole/indazoleaminopyrimidines as inhibitors of c-Jun N-terminal kinase (JNK:Optimization for JNK potency and physicochemical properties
    • Gong L, Han X, Silva T, et al. Development of indole/indazoleaminopyrimidines as inhibitors of c-Jun N-terminal kinase (JNK): Optimization for JNK potency and physicochemical properties. Bioorg Med Chem Lett 2013;23(12):3565-9
    • (2013) Bioorg Med Chem Lett , vol.23 , Issue.12 , pp. 3565-3569
    • Gong, L.1    Han, X.2    Silva, T.3
  • 38
    • 84870255764 scopus 로고    scopus 로고
    • Discovery of a novel series of 4-quinolone JNK inhibitors
    • Gong L, Tan Y-C, Boice G, et al. Discovery of a novel series of 4-quinolone JNK inhibitors. Bioorg Med Chem Lett 2012;22(24):7381-7
    • (2012) Bioorg Med Chem Lett , vol.22 , Issue.24 , pp. 7381-7387
    • Gong, L.1    Tan, Y.-C.2    Boice, G.3
  • 45
    • 84862776641 scopus 로고    scopus 로고
    • Discovery of CC-930, an orally active anti-fibrotic JNK inhibitor
    • Plantevin Krenitsky V, Nadolny L, Delgado M, et al. Discovery of CC-930, an orally active anti-fibrotic JNK inhibitor. Bioorg Med Chem Lett 2012;22(3):1433-8
    • (2012) Bioorg Med Chem Lett , vol.22 , Issue.3 , pp. 1433-1438
    • Plantevin Krenitsky, V.1    Nadolny, L.2    Delgado, M.3
  • 50
    • 84921023407 scopus 로고    scopus 로고
    • Novel hinge-binding motifs for janus kinase 3 inhibitors:A comprehensive structure-activity relationship study on tofacitinib bioisosteres
    • Gehringer M, Forster M, Pfaffenrot E, et al. Novel hinge-binding motifs for janus kinase 3 inhibitors: A comprehensive structure-activity relationship study on tofacitinib bioisosteres. ChemMedChem 2014;9(11):2516-27
    • (2014) ChemMedChem , vol.9 , Issue.11 , pp. 2516-2527
    • Gehringer, M.1    Forster, M.2    Pfaffenrot, E.3
  • 52
    • 84871312669 scopus 로고    scopus 로고
    • A public-private partnership to unlock the untargeted kinome
    • Knapp S, Arruda P, Blagg J, et al. A public-private partnership to unlock the untargeted kinome. Nat Chem Biol 2013;9(1):3-6
    • (2013) Nat Chem Biol , vol.9 , Issue.1 , pp. 3-6
    • Knapp, S.1    Arruda, P.2    Blagg, J.3
  • 53
    • 74849136062 scopus 로고    scopus 로고
    • Synthesis, biological evaluation, X-ray structure, and pharmacokinetics of aminopyrimidine c-jun-N-terminal Kinase (JNK) inhibitors
    • Kamenecka T, Jiang R, Song X, et al. Synthesis, biological evaluation, X-ray structure, and pharmacokinetics of aminopyrimidine c-jun-N-terminal Kinase (JNK) inhibitors. J Med Chem 2010;53(1):419-31
    • (2010) J Med Chem , vol.53 , Issue.1 , pp. 419-431
    • Kamenecka, T.1    Jiang, R.2    Song, X.3
  • 57
    • 3042689209 scopus 로고    scopus 로고
    • Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125
    • Heo Y-S, Kim S-K, Seo CI, et al. Structural basis for the selective inhibition of JNK1 by the scaffolding protein JIP1 and SP600125. EMBO J 2004;23(11):2185-95
    • (2004) EMBO J , vol.23 , Issue.11 , pp. 2185-2195
    • Heo, Y.-S.1    Kim, S.-K.2    Seo, C.I.3
  • 59
    • 79954420335 scopus 로고    scopus 로고
    • Design, synthesis, and structure-activity relationship studies of thiophene-3-carboxamide derivatives as dual inhibitors of the c-Jun N-terminal kinase
    • De SK, Barile E, Chen V, et al. Design, synthesis, and structure-activity relationship studies of thiophene-3-carboxamide derivatives as dual inhibitors of the c-Jun N-terminal kinase. Bioorg Med Chem 2011;19(8):2582-8
    • (2011) Bioorg Med Chem , vol.19 , Issue.8 , pp. 2582-2588
    • De, S.K.1    Barile, E.2    Chen, V.3
  • 63
    • 0035152487 scopus 로고    scopus 로고
    • Cell-permeable peptide inhibitors of JNK. Novel blockers of b-cell death
    • Bonny C, Oberson A, Negri S, et al. Cell-permeable peptide inhibitors of JNK: novel blockers of b-cell death. Diabetes 2001;50(1):77-82
    • (2001) Diabetes , vol.50 , Issue.1 , pp. 77-82
    • Bonny, C.1    Oberson, A.2    Negri, S.3
  • 66
    • 79958100824 scopus 로고    scopus 로고
    • Development of JNK2-selective peptide inhibitors that inhibit breast cancer cell migration
    • Kaoud TS, Mitra S, Lee S, et al. Development of JNK2-selective peptide inhibitors that inhibit breast cancer cell migration. ACS Chem Biol 2011;6(6):658-66
    • (2011) ACS Chem Biol , vol.6 , Issue.6 , pp. 658-666
    • Kaoud, T.S.1    Mitra, S.2    Lee, S.3
  • 70
    • 78449267492 scopus 로고    scopus 로고
    • Design and synthesis of disubstituted thiophene and thiazole based inhibitors of JNK
    • Hom RK, Bowers S, Sealy JM, et al. Design and synthesis of disubstituted thiophene and thiazole based inhibitors of JNK. Bioorg Med Chem Lett 2010;20(24):7303-7
    • (2010) Bioorg Med Chem Lett , vol.20 , Issue.24 , pp. 7303-7307
    • Hom, R.K.1    Bowers, S.2    Sealy, J.M.3
  • 71
    • 79952363889 scopus 로고    scopus 로고
    • Design and synthesis of a novel, orally active, brain penetrant, TRI-substituted thiophene based JNK inhibitor
    • Bowers S, Truong AP, Neitz RJ, et al. Design and synthesis of a novel, orally active, brain penetrant, TRI-substituted thiophene based JNK inhibitor. Bioorg Med Chem Lett 2011;21(6):1838-43
    • (2011) Bioorg Med Chem Lett , vol.21 , Issue.6 , pp. 1838-1843
    • Bowers, S.1    Truong, A.P.2    Neitz, R.J.3
  • 72
    • 80051924264 scopus 로고    scopus 로고
    • Design and synthesis of brain penetrant selective JNK inhibitors with improved pharmacokinetic properties for the prevention of neurodegeneration
    • Bowers S, Truong AP, Jeffrey Neitz R, et al. Design and synthesis of brain penetrant selective JNK inhibitors with improved pharmacokinetic properties for the prevention of neurodegeneration. Bioorg Med Chem Lett 2011;21(18):5521-7
    • (2011) Bioorg Med Chem Lett , vol.21 , Issue.18 , pp. 5521-5527
    • Bowers, S.1    Truong, A.P.2    Jeffrey Neitz, R.3
  • 73
    • 84902117987 scopus 로고    scopus 로고
    • Halogen-enriched fragment libraries as chemical probes for harnessing halogen bonding in fragment-based lead discovery
    • Zimmermann MO, Lange A, Wilcken R, et al. Halogen-enriched fragment libraries as chemical probes for harnessing halogen bonding in fragment-based lead discovery. Future Med Chem 2014;6(6):617-39
    • (2014) Future Med Chem , vol.6 , Issue.6 , pp. 617-639
    • Zimmermann, M.O.1    Lange, A.2    Wilcken, R.3
  • 75
    • 84855841424 scopus 로고    scopus 로고
    • Potent galloyl-based selective modulators targeting multidrug resistance associated protein 1 and P-glycoprotein
    • Pellicani RZ, Stefanachi A, Niso M, et al. Potent galloyl-based selective modulators targeting multidrug resistance associated protein 1 and P-glycoprotein. J Med Chem 2012;55(1):424-36
    • (2012) J Med Chem , vol.55 , Issue.1 , pp. 424-436
    • Pellicani, R.Z.1    Stefanachi, A.2    Niso, M.3
  • 77
    • 84859845948 scopus 로고    scopus 로고
    • Reversible targeting of noncatalytic cysteines with chemically tuned electrophiles
    • Serafimova IM, Pufall MA, Krishnan S, et al. Reversible targeting of noncatalytic cysteines with chemically tuned electrophiles. Nat Chem Biol 2012;8(5):471-6
    • (2012) Nat Chem Biol , vol.8 , Issue.5 , pp. 471-476
    • Serafimova, I.M.1    Pufall, M.A.2    Krishnan, S.3
  • 78
    • 58049211592 scopus 로고    scopus 로고
    • Small-molecule inhibitors binding to protein kinase. Part II: The novel pharmacophore approach of type II and type III inhibition
    • Backes AC, Zech B, Felber B, et al. Small-molecule inhibitors binding to protein kinase. Part II: the novel pharmacophore approach of type II and type III inhibition. Expert Opin Drug Discov 2008;3(12):1427-49
    • (2008) Expert Opin Drug Discov , vol.3 , Issue.12 , pp. 1427-1449
    • Backes, A.C.1    Zech, B.2    Felber, B.3
  • 79
    • 77955664248 scopus 로고    scopus 로고
    • X-ray crystal structure of JNK2 complexed with the p38a inhibitor BIRB 796: Insights into the rational design of DFG-out binding MAP kinase inhibitors
    • Kuglstatter A, Ghate M, Tsing S, et al. X-ray crystal structure of JNK2 complexed with the p38a inhibitor BIRB 796: Insights into the rational design of DFG-out binding MAP kinase inhibitors. Bioorg Med Chem Lett 2010;20(17):5217-20
    • (2010) Bioorg Med Chem Lett , vol.20 , Issue.17 , pp. 5217-5220
    • Kuglstatter, A.1    Ghate, M.2    Tsing, S.3
  • 80
    • 79551594605 scopus 로고    scopus 로고
    • Protein kinases: Evolution of dynamic regulatory proteins
    • Taylor SS, Kornev AP. Protein kinases: evolution of dynamic regulatory proteins. Trends Biochem Sci 2011;36(2):65-77
    • (2011) Trends Biochem Sci , vol.36 , Issue.2 , pp. 65-77
    • Taylor, S.S.1    Kornev, A.P.2
  • 81
    • 84873298611 scopus 로고    scopus 로고
    • MAP kinase phosphatase 1 (MKP-1/ DUSP1) is neuroprotective in Huntington's disease via additive effects of JNK and p38 inhibition
    • Taylor DM, Moser R, Regulier E, et al. MAP kinase phosphatase 1 (MKP-1/ DUSP1) is neuroprotective in Huntington's disease via additive effects of JNK and p38 inhibition. J Neurosci 2013;33(6):2313-25
    • (2013) J Neurosci , vol.33 , Issue.6 , pp. 2313-2325
    • Taylor, D.M.1    Moser, R.2    Regulier, E.3
  • 82
    • 84928429443 scopus 로고    scopus 로고
    • Tetra-substituted pyridinylimidazoles as dual inhibitors of p38a mitogenactivated protein kinase and c-Jun N-terminal kinase 3 for potential treatment of neurodegenerative diseases
    • Muth F, Günther M, Bauer SM, et al. Tetra-substituted pyridinylimidazoles as dual inhibitors of p38a mitogenactivated protein kinase and c-Jun N-terminal kinase 3 for potential treatment of neurodegenerative diseases. J Med Chem 2015;58(1):443-56
    • (2015) J Med Chem , vol.58 , Issue.1 , pp. 443-456
    • Muth, F.1    Günther, M.2    Bauer, S.M.3
  • 83
    • 84879696121 scopus 로고    scopus 로고
    • The DLK signalling pathway - A double-edged sword in neural development and regeneration
    • Tedeschi A, Bradke F. The DLK signalling pathway-a double-edged sword in neural development and regeneration. EMBO Rep 2013;14(7):605-14
    • (2013) EMBO Rep , vol.14 , Issue.7 , pp. 605-614
    • Tedeschi, A.1    Bradke, F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.