메뉴 건너뛰기




Volumn 50, Issue 6, 2007, Pages 1213-1221

From five- to six-membered rings: 3,4-Diarylquinolinone as lead for novel p38MAP kinase inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

3 (4 FLUOROPHENYL) 4 PYRIDIN 4 YLQUINOLIN 2(1H) ONE; 4 [3 (4 FLUOROPHENYL) 5 ISOPROPYLISOXAZOL 4 YL]PYRIDINE; IMIDAZOLE DERIVATIVE; ISOXAZOLE DERIVATIVE; MITOGEN ACTIVATED PROTEIN KINASE 12; MITOGEN ACTIVATED PROTEIN KINASE P38; MITOGEN ACTIVATED PROTEIN KINASE P38 INHIBITOR; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33947626488     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm061097o     Document Type: Article
Times cited : (46)

References (40)
  • 1
    • 20344374894 scopus 로고    scopus 로고
    • Small-molecule kinase-inhibitor target assessment
    • Kung, C.; Shokat, K. M. Small-molecule kinase-inhibitor target assessment. ChemBioChem 2005, 6, 523-526.
    • (2005) ChemBioChem , vol.6 , pp. 523-526
    • Kung, C.1    Shokat, K.M.2
  • 4
    • 33947394888 scopus 로고    scopus 로고
    • Systematic analysis of human kinase genes: A large number of genes and alternative splicing events result in functional and structural diversity
    • Milanesi, L.; Petrillo, M.; Sepe, L.; Boccia, A.; D'Agostino, N.; Passamano, M.; Di Nardo, S.; Tasco, G.; Casadio, R.; Paolella, G. Systematic analysis of human kinase genes: a large number of genes and alternative splicing events result in functional and structural diversity. BMC Bioinformatics 2005, 6 Suppl 4, 20.
    • (2005) BMC Bioinformatics , vol.6 , Issue.SUPPL. 4 , pp. 20
    • Milanesi, L.1    Petrillo, M.2    Sepe, L.3    Boccia, A.4    D'Agostino, N.5    Passamano, M.6    Di Nardo, S.7    Tasco, G.8    Casadio, R.9    Paolella, G.10
  • 5
    • 29144453813 scopus 로고    scopus 로고
    • Characterization of kinase-selective inhibitors by chemical proteomics
    • Daub, H. Characterization of kinase-selective inhibitors by chemical proteomics. Biochim. Biophys. Acta 2005, 1754, 183-190.
    • (2005) Biochim. Biophys. Acta , vol.1754 , pp. 183-190
    • Daub, H.1
  • 6
    • 20344366516 scopus 로고    scopus 로고
    • Selectivity assessment of kinase inhibitors: Strategies and challenges
    • Luo, Y. Selectivity assessment of kinase inhibitors: Strategies and challenges. Curr. Opin. Mol. Ther. 2005, 7, 251-255.
    • (2005) Curr. Opin. Mol. Ther , vol.7 , pp. 251-255
    • Luo, Y.1
  • 8
    • 24944497371 scopus 로고    scopus 로고
    • Features of selective kinase inhibitors
    • Knight, Z. A.; Shokat, K. M. Features of selective kinase inhibitors. Chem. Biol. 2005, 12, 621-637.
    • (2005) Chem. Biol , vol.12 , pp. 621-637
    • Knight, Z.A.1    Shokat, K.M.2
  • 9
    • 33646188951 scopus 로고    scopus 로고
    • Richards, M. L. Hot topic: New approaches to the treatment of inflammatory disorders. Curr. Top. Med. Chem. 2006, 6, 75.
    • Richards, M. L. Hot topic: New approaches to the treatment of inflammatory disorders. Curr. Top. Med. Chem. 2006, 6, 75.
  • 10
    • 0037431421 scopus 로고    scopus 로고
    • Kinase inhibitors: Not just for kinases anymore
    • McGovern, S. L.; Shoichet, B. K. Kinase inhibitors: Not just for kinases anymore. J. Med. Chem. 2003, 46, 1478-1483.
    • (2003) J. Med. Chem , vol.46 , pp. 1478-1483
    • McGovern, S.L.1    Shoichet, B.K.2
  • 11
    • 2442469277 scopus 로고    scopus 로고
    • Targeting MAPK signalling: Prometheus' fire or pandora's box?
    • Boldt, S.; Kolch, W. Targeting MAPK signalling: Prometheus' fire or pandora's box? Curr. Pharm. Des. 2004, 10, 1885-1905.
    • (2004) Curr. Pharm. Des , vol.10 , pp. 1885-1905
    • Boldt, S.1    Kolch, W.2
  • 12
    • 0038004740 scopus 로고    scopus 로고
    • Targeting JNK for therapeutic benefit: From junk to gold?
    • Manning, A. M.; Davis, R. J. Targeting JNK for therapeutic benefit: From junk to gold? Nat. Rev. Drug Discovery 2003, 2, 554-565.
    • (2003) Nat. Rev. Drug Discovery , vol.2 , pp. 554-565
    • Manning, A.M.1    Davis, R.J.2
  • 13
    • 0037032817 scopus 로고    scopus 로고
    • Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases
    • Johnson, G. L.; Lapadat, R. Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases. Science 2002, 298, 1911-1912.
    • (2002) Science , vol.298 , pp. 1911-1912
    • Johnson, G.L.1    Lapadat, R.2
  • 14
    • 33646363800 scopus 로고    scopus 로고
    • TAK1-mediated stress signaling pathways are essential for TNF-α-promoted pulmonary metastasis of murine colon cancer cells
    • (a) Choo, M. K.; Sakurai, H.; Koizumi, K.; Saiki, I. TAK1-mediated stress signaling pathways are essential for TNF-α-promoted pulmonary metastasis of murine colon cancer cells. Int. J. Cancer 2006, 118, 2758-2764.
    • (2006) Int. J. Cancer , vol.118 , pp. 2758-2764
    • Choo, M.K.1    Sakurai, H.2    Koizumi, K.3    Saiki, I.4
  • 15
    • 14244262138 scopus 로고    scopus 로고
    • Inhibition of RIP2/RICK/CARDIAK activity by pyridinyl imidazole inhibitors of p38 MAPK
    • (b) Argast, G. M.; Fausto, N.; Campbell, J. S. Inhibition of RIP2/RICK/CARDIAK activity by pyridinyl imidazole inhibitors of p38 MAPK. Mol. Cell. Biochem. 2005, 268, 129-140.
    • (2005) Mol. Cell. Biochem , vol.268 , pp. 129-140
    • Argast, G.M.1    Fausto, N.2    Campbell, J.S.3
  • 16
    • 0035217119 scopus 로고    scopus 로고
    • Inhibitors of the JNK signaling pathway
    • (c) Harper, S. J.; LoGrasso, P. Inhibitors of the JNK signaling pathway. Drugs Future 2001, 26, 957-973.
    • (2001) Drugs Future , vol.26 , pp. 957-973
    • Harper, S.J.1    LoGrasso, P.2
  • 17
    • 27744582136 scopus 로고    scopus 로고
    • Pathway to the clinic: Inhibition of P38 MAP kinase. A review of ten chemotypes selected for development
    • Goldstein, D. M.; Gabriel, T. Pathway to the clinic: Inhibition of P38 MAP kinase. A review of ten chemotypes selected for development. Curr. Top. Med. Chem. 2005, 5, 1017-1029.
    • (2005) Curr. Top. Med. Chem , vol.5 , pp. 1017-1029
    • Goldstein, D.M.1    Gabriel, T.2
  • 18
    • 0021350020 scopus 로고
    • Antiinflammatory activity of 5,6-diaryl-2,3-dihydroimidazo[2,1-b]thiazoles. Isomeric 4-pyridyl and 4-substituted phenyl derivatives
    • (a) Lantos, I.; Bender, P. E.; Razgaitis, K. A.; Sutton, B. M.; DiMartino, M. J.; Griswold, D. E.; Walz, D. T. Antiinflammatory activity of 5,6-diaryl-2,3-dihydroimidazo[2,1-b]thiazoles. Isomeric 4-pyridyl and 4-substituted phenyl derivatives. J. Med. Chem. 1984, 27, 72-75.
    • (1984) J. Med. Chem , vol.27 , pp. 72-75
    • Lantos, I.1    Bender, P.E.2    Razgaitis, K.A.3    Sutton, B.M.4    DiMartino, M.J.5    Griswold, D.E.6    Walz, D.T.7
  • 20
    • 33644873660 scopus 로고    scopus 로고
    • Small molecular anti-cytokine agents
    • Wagner, G.; Laufer, S. Small molecular anti-cytokine agents. Med. Res. Rev. 2006, 26, 1-62.
    • (2006) Med. Res. Rev , vol.26 , pp. 1-62
    • Wagner, G.1    Laufer, S.2
  • 21
    • 33646165882 scopus 로고    scopus 로고
    • New approaches to the treatment of inflammatory disorders by small molecule inhibitors of p38 MAP kinase
    • Peifer, C.; Wagner, G.; Laufer, S. New approaches to the treatment of inflammatory disorders by small molecule inhibitors of p38 MAP kinase. Curr. Top. Med. Chem. 2006, 6, 113-149.
    • (2006) Curr. Top. Med. Chem , vol.6 , pp. 113-149
    • Peifer, C.1    Wagner, G.2    Laufer, S.3
  • 22
    • 20444387979 scopus 로고    scopus 로고
    • Substituting c-Jun N-terminal kinase-3 (JNK3) ATP-binding site amino acid residues with their p38 counterparts affects binding of JNK- and p38-selective inhibitors
    • Fricker, M.; LoGrasso, P.; Ellis, S.; Wilkie, N.; Hunt, P.; Pollack, S. J. Substituting c-Jun N-terminal kinase-3 (JNK3) ATP-binding site amino acid residues with their p38 counterparts affects binding of JNK- and p38-selective inhibitors. Arch. Biochem. Biophys. 2005, 438, 195-205.
    • (2005) Arch. Biochem. Biophys , vol.438 , pp. 195-205
    • Fricker, M.1    LoGrasso, P.2    Ellis, S.3    Wilkie, N.4    Hunt, P.5    Pollack, S.J.6
  • 23
    • 33744985984 scopus 로고    scopus 로고
    • Peifer, C.; Schollmeyer, D.; Laudage, S.; Laufer, S. 3-(4-Fluorophenyl)- 4-(4-pyridyl)quinolin-2(1H)-one. Acta Crystallogr., Sect. E: Struct. Rep. Online 2006, 62, 2475-2477.
    • Peifer, C.; Schollmeyer, D.; Laudage, S.; Laufer, S. 3-(4-Fluorophenyl)- 4-(4-pyridyl)quinolin-2(1H)-one. Acta Crystallogr., Sect. E: Struct. Rep. Online 2006, 62, 2475-2477.
  • 24
    • 33746030287 scopus 로고    scopus 로고
    • Peifer, C.; Schollmeyer, D.; Selig, R.; Lauter, S. 4-(4-Fluorophenyl)-3- (4-pyridyl)quinolin-2(1H)-one. Acta Crystallogr., Sect. E: Struct. Rep. Online 2006, 62, 2648-2650.
    • Peifer, C.; Schollmeyer, D.; Selig, R.; Lauter, S. 4-(4-Fluorophenyl)-3- (4-pyridyl)quinolin-2(1H)-one. Acta Crystallogr., Sect. E: Struct. Rep. Online 2006, 62, 2648-2650.
  • 27
    • 27644589566 scopus 로고    scopus 로고
    • An immunosorbent, nonradioactive p38 MAP kinase assay comparable to standard radioactive liquid-phase assays
    • Laufer, S.; Thuma, S.; Peifer, C.; Greim, C.; Herweh, Y.; Albrecht, A.; Dehner, F. An immunosorbent, nonradioactive p38 MAP kinase assay comparable to standard radioactive liquid-phase assays. Anal. Biochem. 2005, 135-137.
    • (2005) Anal. Biochem , pp. 135-137
    • Laufer, S.1    Thuma, S.2    Peifer, C.3    Greim, C.4    Herweh, Y.5    Albrecht, A.6    Dehner, F.7
  • 31
    • 4644316016 scopus 로고    scopus 로고
    • Synthesis of 2-quinolones via palladium-catalyzed carbonylative annulation of internal alkynes by N-substituted o-iodoanilines
    • Kadnikov, D. V.; Larock, R. C. Synthesis of 2-quinolones via palladium-catalyzed carbonylative annulation of internal alkynes by N-substituted o-iodoanilines. J. Org. Chem. 2004, 69, 6772-6780.
    • (2004) J. Org. Chem , vol.69 , pp. 6772-6780
    • Kadnikov, D.V.1    Larock, R.C.2
  • 32
    • 0000307431 scopus 로고
    • Carbonyl coupling reactions catalytic in titanium and the use of commercial titanium powder for organic synthesis
    • Fürstner, A.; Hupperts, A. Carbonyl coupling reactions catalytic in titanium and the use of commercial titanium powder for organic synthesis. J. Am. Chem. Soc. 1995, 117, 4468-4475.
    • (1995) J. Am. Chem. Soc , vol.117 , pp. 4468-4475
    • Fürstner, A.1    Hupperts, A.2
  • 33
    • 0026334290 scopus 로고
    • Synthesis of quinolines via ortho-lithiated N-acylanilines. A modified Friedlander synthesis
    • Cho, I. S.; Gong, L.; Muchowski, J. M. Synthesis of quinolines via ortho-lithiated N-acylanilines. A modified Friedlander synthesis. J. Org. Chem. 1991, 56, 7288-7291.
    • (1991) J. Org. Chem , vol.56 , pp. 7288-7291
    • Cho, I.S.1    Gong, L.2    Muchowski, J.M.3
  • 34
    • 0026546768 scopus 로고
    • A convenient and efficient three-step synthesis of α-chloro keto acids
    • Chai, K. B.; Sampson, P. A convenient and efficient three-step synthesis of α-chloro keto acids. Tetrahedron Lett. 1992, 33, 585-588.
    • (1992) Tetrahedron Lett , vol.33 , pp. 585-588
    • Chai, K.B.1    Sampson, P.2
  • 38
    • 0036591874 scopus 로고    scopus 로고
    • Structural biology in drug design: Selective protein kinase inhibitors
    • Scapin, G. Structural biology in drug design: Selective protein kinase inhibitors. Drug Discovery Today 2002, 7, 601-611.
    • (2002) Drug Discovery Today , vol.7 , pp. 601-611
    • Scapin, G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.