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Volumn 69, Issue 1, 2007, Pages 23-30

Synthesis and biological activity of a focused library of mitogen-activated protein kinase phosphatase inhibitors

Author keywords

Dual specificity phosphatase; Inhibitor synthesis; Library synthesis; Mitogen activated protein kinase phosphatase 1; Molecular Libraries Screening Center Network; PubChem; Quinolines; Uracils

Indexed keywords

MITOGEN ACTIVATED PROTEIN KINASE; MITOGEN ACTIVATED PROTEIN KINASE INHIBITOR; MITOGEN ACTIVATED PROTEIN KINASE P38; MITOGEN ACTIVATED PROTEIN KINASE PHOSPHATASE 1; STRESS ACTIVATED PROTEIN KINASE;

EID: 33847138939     PISSN: 17470277     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1747-0285.2007.00474.x     Document Type: Article
Times cited : (16)

References (16)
  • 1
    • 13844312725 scopus 로고    scopus 로고
    • Dual specificity protein phosphatases: Therapeutic targets for cancer and Alzheimer's disease
    • Ducruet A.P., Vogt A., Wipf P., Lazo J.S. (2005) Dual specificity protein phosphatases: therapeutic targets for cancer and Alzheimer's disease. Annu Rev Pharmacol Toxicol;45:725-750.
    • (2005) Annu Rev Pharmacol Toxicol , vol.45 , pp. 725-750
    • Ducruet, A.P.1    Vogt, A.2    Wipf, P.3    Lazo, J.S.4
  • 2
    • 33646416743 scopus 로고    scopus 로고
    • The role of mitogen-activated protein kinase phosphatase-1 in oxidative damage-induced cell death
    • Zhou J.-Y., Liu Y., Wu G.S. (2006) The role of mitogen-activated protein kinase phosphatase-1 in oxidative damage-induced cell death. Cancer Res;66:4888-4894.
    • (2006) Cancer Res , vol.66 , pp. 4888-4894
    • Zhou, J.-Y.1    Liu, Y.2    Wu, G.S.3
  • 4
    • 0036884693 scopus 로고    scopus 로고
    • Dual specificity phosphatases as targets for antineoplastic agents
    • Lyon M.A., Ducruet A.P., Wipf P., Lazo J.S. (2002) Dual specificity phosphatases as targets for antineoplastic agents. Nat Rev Drug Discov;1:961-976.
    • (2002) Nat Rev Drug Discov , vol.1 , pp. 961-976
    • Lyon, M.A.1    Ducruet, A.P.2    Wipf, P.3    Lazo, J.S.4
  • 5
    • 33748536137 scopus 로고    scopus 로고
    • MAPK-specific tyrosine phosphatases: New targets for drug discovery?
    • Barr A.J., Knapp S. (2006) MAPK-specific tyrosine phosphatases: new targets for drug discovery? Trends Pharmacol Sci;27:525-530.
    • (2006) Trends Pharmacol Sci , vol.27 , pp. 525-530
    • Barr, A.J.1    Knapp, S.2
  • 6
    • 0035282334 scopus 로고    scopus 로고
    • Mammalian MAP kinase signalling cascades
    • Chang L., Karin M. (2001) Mammalian MAP kinase signalling cascades. Nature;410:37-40.
    • (2001) Nature , vol.410 , pp. 37-40
    • Chang, L.1    Karin, M.2
  • 7
    • 0041913991 scopus 로고    scopus 로고
    • Cell-active dual specificity phosphatase inhibitors identified by high-content screening
    • Vogt A., Cooley K.A., Brisson M., Tarpley M.G., Wipf P., Lazo J.S. (2003) Cell-active dual specificity phosphatase inhibitors identified by high-content screening. Chem Biol;10:733-742.
    • (2003) Chem Biol , vol.10 , pp. 733-742
    • Vogt, A.1    Cooley, K.A.2    Brisson, M.3    Tarpley, M.G.4    Wipf, P.5    Lazo, J.S.6
  • 8
    • 21344451886 scopus 로고    scopus 로고
    • The benzo[c]phenanthridine alkaloid, sanguinarine, is a selective, cell-active inhibitor of mitogen-activated protein kinase phosphatase-1
    • Vogt A., Tamewitz A., Skoko J., Sikorski R.P., Giuliano K.A., Lazo J.S. (2005) The benzo[c]phenanthridine alkaloid, sanguinarine, is a selective, cell-active inhibitor of mitogen-activated protein kinase phosphatase-1. J Biol Chem;280:19078-19086.
    • (2005) J Biol Chem , vol.280 , pp. 19078-19086
    • Vogt, A.1    Tamewitz, A.2    Skoko, J.3    Sikorski, R.P.4    Giuliano, K.A.5    Lazo, J.S.6
  • 9
    • 33745610883 scopus 로고    scopus 로고
    • Novel benzofuran inhibitors of human mitogen-activated protein kinase phosphatase-1
    • Lazo J.S., Nunes R., Skoko J.J., de Oliveira P.E.Q., Vogt A., Wipf P. (2006) Novel benzofuran inhibitors of human mitogen-activated protein kinase phosphatase-1. Bioorg Med Chem;14:5643-5650.
    • (2006) Bioorg Med Chem , vol.14 , pp. 5643-5650
    • Lazo, J.S.1    Nunes, R.2    Skoko, J.J.3    de Oliveira, P.E.Q.4    Vogt, A.5    Wipf, P.6
  • 10
    • 0036729435 scopus 로고    scopus 로고
    • Glucocorticoids inhibit lung cancer cell growth through both the extracellular signal-related kinase pathway and cell cycle regulators
    • Greenberg A.K., Hu J., Basu S., Hay J., Reibman J., Yie T.-A. et al. (2002) Glucocorticoids inhibit lung cancer cell growth through both the extracellular signal-related kinase pathway and cell cycle regulators. Am J Respir Cell Mol Biol;27:320-328.
    • (2002) Am J Respir Cell Mol Biol , vol.27 , pp. 320-328
    • Greenberg, A.K.1    Hu, J.2    Basu, S.3    Hay, J.4    Reibman, J.5    Yie, T.-A.6
  • 11
    • 0036303150 scopus 로고    scopus 로고
    • The carboxyl-terminal domain of MKP-1 and MKP-2 have inhibitory effects on their phosphatase activity
    • Hutter D., Chen P., Li J., Barnes J., Liu Y. (2002) The carboxyl-terminal domain of MKP-1 and MKP-2 have inhibitory effects on their phosphatase activity. Mol Cell Biochem;233:107-117.
    • (2002) Mol Cell Biochem , vol.233 , pp. 107-117
    • Hutter, D.1    Chen, P.2    Li, J.3    Barnes, J.4    Liu, Y.5
  • 12
    • 0032910476 scopus 로고    scopus 로고
    • Crystal structure of the MAPK phosphatase Pyst1 catalytic domain and implications for regulated activation
    • Stewart A.E., Dowd S., Keyse S.M., McDonald N.Q. (1999) Crystal structure of the MAPK phosphatase Pyst1 catalytic domain and implications for regulated activation. Nat Struct Biol;6:174-181.
    • (1999) Nat Struct Biol , vol.6 , pp. 174-181
    • Stewart, A.E.1    Dowd, S.2    Keyse, S.M.3    McDonald, N.Q.4
  • 13
    • 0037317607 scopus 로고    scopus 로고
    • Solution structure of the MAPK phosphatase PAC-1 catalytic domain. Insights into substrate-induced enzymatic activation of MKP
    • Farooq A., Plotnikova O., Chaturvedi G., Yan S., Zeng L., Zhang Q. et al. (2003) Solution structure of the MAPK phosphatase PAC-1 catalytic domain. Insights into substrate-induced enzymatic activation of MKP. Structure;11:155-164.
    • (2003) Structure , vol.11 , pp. 155-164
    • Farooq, A.1    Plotnikova, O.2    Chaturvedi, G.3    Yan, S.4    Zeng, L.5    Zhang, Q.6
  • 14
    • 33745968271 scopus 로고    scopus 로고
    • Crystal structure of the catalytic domain of human MAP kinase phosphatase 5: Structural insight into constitutively active phosphatase
    • Jeong D.G., Yoon T.-S., Kim J.H., Shim M.Y., Jung S.-K., Son J.H. et al. (2006) Crystal structure of the catalytic domain of human MAP kinase phosphatase 5: structural insight into constitutively active phosphatase. J Mol Biol;360:946-955.
    • (2006) J Mol Biol , vol.360 , pp. 946-955
    • Jeong, D.G.1    Yoon, T.-S.2    Kim, J.H.3    Shim, M.Y.4    Jung, S.-K.5    Son, J.H.6
  • 15
    • 0342368828 scopus 로고    scopus 로고
    • Synthesis and preliminary evaluation of new 5-pyrazolinone derivatives as analgesic agents
    • Gursoy A., Demirayak S., Capan G., Erol K., Vural K. (2000) Synthesis and preliminary evaluation of new 5-pyrazolinone derivatives as analgesic agents. Eur J Med Chem;35:359-364.
    • (2000) Eur J Med Chem , vol.35 , pp. 359-364
    • Gursoy, A.1    Demirayak, S.2    Capan, G.3    Erol, K.4    Vural, K.5
  • 16
    • 0028930769 scopus 로고
    • Picornavirus inhibitors: Trifluoromethyl substitution provides a global protective effect against hepatic metabolism
    • Diana G.D., Rudewicz P., Pevear D.C., Nitz T.J., Aldous S.C., Aldous D.J. et al. (1995) Picornavirus inhibitors: trifluoromethyl substitution provides a global protective effect against hepatic metabolism. J Med Chem;38:1355-1371.
    • (1995) J Med Chem , vol.38 , pp. 1355-1371
    • Diana, G.D.1    Rudewicz, P.2    Pevear, D.C.3    Nitz, T.J.4    Aldous, S.C.5    Aldous, D.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.