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Volumn 15, Issue 7, 2005, Pages 801-816

p38 inhibitors: Beyond pyridinylimidazoles

Author keywords

Cytokine biosynthesis inhibitor; Cytokine mediated disease; IL 1 ; Inflammation; p38 kinase inhibitor; p38 mitogen activated protein kinase (MAPK); TNF

Indexed keywords

4 (4 FLUOROPHENYL) 2 (4 METHYLSULFINYLPHENYL) 5 (4 PYRIDYL)IMIDAZOLE; 5 (2,6 DICHLOROPHENYL) 2 (2,4 DIFLUOROPHENYLTHIO)PYRIMIDO[1,6 B]PYRIDAZIN 6 ONE; BENZAMIDE DERIVATIVE; BENZOPHENONE DERIVATIVE; CYTOKINE; DORAMAPIMOD; EO 1428; EO 1606; IMIDAZOLE DERIVATIVE; IMIDAZOPYRIDINE DERIVATIVE; INTERLEUKIN 1BETA; MITOGEN ACTIVATED PROTEIN KINASE INHIBITOR; MITOGEN ACTIVATED PROTEIN KINASE P38; MITOGEN ACTIVATED PROTEIN KINASE P38 INHIBITOR; PYRAZINE DERIVATIVE; PYRAZOLE DERIVATIVE; PYRIDINE DERIVATIVE; RO 3201195; SB 242235; SCIO 469; SX 011; TRIAZINE DERIVATIVE; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG; VX 702;

EID: 22744454243     PISSN: 13543776     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543776.15.7.801     Document Type: Review
Times cited : (30)

References (41)
  • 1
    • 0034513614 scopus 로고    scopus 로고
    • Potential of p38 inhibitors in the treatment of rheumatoid arthritis
    • FOSTER ML, HALLEY F, SOUNESS JE: Potential of p38 inhibitors in the treatment of rheumatoid arthritis. Drug News Perspect. (2000) 13:488-497.
    • (2000) Drug News Perspect. , vol.13 , pp. 488-497
    • Foster, M.L.1    Halley, F.2    Souness, J.E.3
  • 2
    • 0032833517 scopus 로고    scopus 로고
    • Efficacy and safety of retreatment with anti-tumor necrosis factor antibody (infliximab) to maintain remission in Crohn's disease
    • RUTGEERTS P, D'HAENS G, TARGAN S et al.: Efficacy and safety of retreatment with anti-tumor necrosis factor antibody (infliximab) to maintain remission in Crohn's disease. Gastroenterology (1999) 117:761-769.
    • (1999) Gastroenterology , vol.117 , pp. 761-769
    • Rutgeerts, P.1    D'haens, G.2    Targan, S.3
  • 3
    • 0033574147 scopus 로고    scopus 로고
    • Etanercept therapy in rheumatoid arthritis: A randomized, controlled trial
    • MORELAND LW, SCHIFF MH, BAUMGARTNER SW et al.: Etanercept therapy in rheumatoid arthritis: a randomized, controlled trial. Ann. Intern. Med. (1999) 130:478-486.
    • (1999) Ann. Intern. Med. , vol.130 , pp. 478-486
    • Moreland, L.W.1    Schiff, M.H.2    Baumgartner, S.W.3
  • 4
    • 0028143211 scopus 로고
    • Randomized double-blind comparison of chimeric monoclonal antibody to tumor necrosis factor-α (cA2) versus placebo in rheumatoid arthritis
    • ELLIOT MJ, MAINI RN, FELDMANN M et al.: Randomized double-blind comparison of chimeric monoclonal antibody to tumor necrosis factor-α (cA2) versus placebo in rheumatoid arthritis. Lancet (1994) 344:1105-1110.
    • (1994) Lancet , vol.344 , pp. 1105-1110
    • Elliot, M.J.1    Maini, R.N.2    Feldmann, M.3
  • 5
    • 0000697234 scopus 로고    scopus 로고
    • Efficacy of the fully human anti-TNF antibody D2E7 in rheumatoid arthritis
    • VAN DE PUTTE LB, RAU R, BREEDVELD FC et al.: Efficacy of the fully human anti-TNF antibody D2E7 in rheumatoid arthritis. Arthritis Rheum. (1999) 42:S400.
    • (1999) Arthritis Rheum. , vol.42
    • Van De Putte, L.B.1    Rau, R.2    Breedveld, F.C.3
  • 6
    • 0037309790 scopus 로고    scopus 로고
    • Interleukin 1 receptor antagonist Anakinra improves functional status in patients with rheumatoid arthritis
    • COHEN SB: WOOLLEY JM, CHAN WW: Interleukin 1 receptor antagonist Anakinra improves functional status in patients with rheumatoid arthritis. J. Rheumatol. (2003) 30:225-231.
    • (2003) J. Rheumatol. , vol.30 , pp. 225-231
    • Cohen, S.B.1    Woolley, J.M.2    Chan, W.W.3
  • 7
    • 0344926414 scopus 로고    scopus 로고
    • Etanercept as monotherapy in patients with psoriasis
    • LEONARDI CL, POWERS JL, MATHESON RE et al.: Etanercept as monotherapy in patients with psoriasis. N. Engl. J. Med. (2003) 349:2014-2022.
    • (2003) N. Engl. J. Med. , vol.349 , pp. 2014-2022
    • Leonardi, C.L.1    Powers, J.L.2    Matheson, R.E.3
  • 8
    • 4644327125 scopus 로고    scopus 로고
    • Infliximab induction therapy for patients with severe plaque-type psoriasis: A randomized, double-blind, placebo-controlled trial
    • GOTTLIEB AB, EVANS R, LI S et al.: Infliximab induction therapy for patients with severe plaque-type psoriasis: A randomized, double-blind, placebo-controlled trial. J. Am. Acad. Dermatol. (2004) 51:534-542.
    • (2004) J. Am. Acad. Dermatol. , vol.51 , pp. 534-542
    • Gottlieb, A.B.1    Evans, R.2    Li, S.3
  • 9
    • 0030765077 scopus 로고    scopus 로고
    • Stress activated protein kinases: Activation, regulation and function
    • PAUL A, WILSON S, BELHAM CM et al.: Stress activated protein kinases: activation, regulation and function. Cell. Signal. (1997) 9:403-410.
    • (1997) Cell Signal , vol.9 , pp. 403-410
    • Paul, A.1    Wilson, S.2    Belham, C.M.3
  • 10
    • 0037255931 scopus 로고    scopus 로고
    • Inhibitors of p38 mitogen activated protein kinase potential as anti-inflammatory agents in asthma?
    • NEWTON R, HOLDEN N: Inhibitors of p38 mitogen activated protein kinase potential as anti-inflammatory agents in asthma? Biodrugs (2003) 17:113-129.
    • (2003) Biodrugs , vol.17 , pp. 113-129
    • Newton, R.1    Holden, N.2
  • 11
    • 0030044182 scopus 로고    scopus 로고
    • Characterization of the structure and function of a novel MAP kinase kinase (MKK6)
    • HAN J, LEE JD, JIANG Y, LI Z, FENG L, ULEVITCH RJ: Characterization of the structure and function of a novel MAP kinase kinase (MKK6). J. Biol. Chem. (1996) 271:2886-2891.
    • (1996) J. Biol. Chem. , vol.271 , pp. 2886-2891
    • Han, J.1    Lee, J.D.2    Jiang, Y.3    Li, Z.4    Feng, L.5    Ulevitch, R.J.6
  • 12
    • 0028605318 scopus 로고
    • A protein kinase involved in the regulation of inflammatory cytokine biosynthesis
    • LEE JC, LAYDON JT, McDONNELL PC et al.: A protein kinase involved in the regulation of inflammatory cytokine biosynthesis. Nature (1994) 372:739-746.
    • (1994) Nature , vol.372 , pp. 739-746
    • Lee, J.C.1    Laydon, J.T.2    Mcdonnell, P.C.3
  • 13
    • 22744438578 scopus 로고    scopus 로고
    • Vertex has suspended development of VX 745, a p38 MAP kinase inhibitor, which was in Phase II trials in the: USA and Europe as potential treatment for rheumatoid arthritis
    • VERTEX USA: Vertex Inc, Press release (September)
    • VERTEX USA: Vertex has suspended development of VX 745, a p38 MAP kinase inhibitor, which was in Phase II trials in the: USA and Europe as potential treatment for rheumatoid arthritis. Vertex Inc, Press release (September 2001).
    • (2001)
  • 14
    • 22744451660 scopus 로고    scopus 로고
    • This product was in Phase I clinical studies in the UK (SmithKline Beechman, March 1999) and was being investigated as a potential treatment for rheumatoid arthritis
    • SmithKline Beechman (now GlaxoSmithKline) has discontinued development of SB 242235, a cytokine suppressor (SmithKline Beechman, April 1999). (SmithKline Beechman, April 1999) R&D Focus Report March 27
    • SmithKline Beechman (now GlaxoSmithKline) has discontinued development of SB 242235, a cytokine suppressor (SmithKline Beechman, April 1999). This product was in Phase I clinical studies in the UK (SmithKline Beechman, March 1999) and was being investigated as a potential treatment for rheumatoid arthritis (SmithKline Beechman, April 1999) R&D Focus Report March 27 2001.
    • (2001)
  • 16
    • 0036715931 scopus 로고    scopus 로고
    • Pyridinylimidazole based p38 MAP kinase inhibitors
    • JACKSON PF, BULLINGTON JL: Pyridinylimidazole based p38 MAP kinase inhibitors. Curr. Top. Med. Chem. (2002) 2:1011-1020.
    • (2002) Curr. Top. Med. Chem. , vol.2 , pp. 1011-1020
    • Jackson, P.F.1    Bullington, J.L.2
  • 17
    • 0032541986 scopus 로고    scopus 로고
    • Pyrimidinylimidazole inhibitors of CSBP/p38 kinase demonstrating decreased inhibition of hepatic cytochrome P450 enzymes
    • ADAMS JL, BOEHM JC, KASSIS S et al.: Pyrimidinylimidazole inhibitors of CSBP/p38 kinase demonstrating decreased inhibition of hepatic cytochrome P450 enzymes. Bioorg. Med. Chem. Lett. (1998) 8:3111-3118.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 3111-3118
    • Adams, J.L.1    Boehm, J.C.2    Kassis, S.3
  • 18
    • 18044405088 scopus 로고    scopus 로고
    • Pyrimidinyimidazole inhibitors of p38: Cyclic N-imidazole subsdtuents enhance p38 kinase inhibition and oral activity
    • ADAMS JL, BOEHM JC, GALLAGHER TF et al.: Pyrimidinyimidazole inhibitors of p38: cyclic N-imidazole subsdtuents enhance p38 kinase inhibition and oral activity: Bioorg. Med. Chem. Lett. (2001) 11:2867-2870.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 2867-2870
    • Adams, J.L.1    Boehm, J.C.2    Gallagher, T.F.3
  • 19
    • 0000458458 scopus 로고    scopus 로고
    • Suppression of ex vivo cytokine production by SB-242235, a selective inhibitor of p38 MAP kinase
    • FULLERTON T, SHARMA A, PRABHAKAR U et al.: Suppression of ex vivo cytokine production by SB-242235, a selective inhibitor of p38 MAP kinase. Clin. Pharmacol. Ther. (2000) 67:114.
    • (2000) Clin. Pharmacol. Ther. , vol.67 , pp. 114
    • Fullerton, T.1    Sharma, A.2    Prabhakar, U.3
  • 20
    • 2942560875 scopus 로고    scopus 로고
    • Novel p38 inhibitors with potent oral efficacy in several models of rheumatoid arthritis
    • REVESZ L, BLUM E, DIPADOVA FE et al.: Novel p38 inhibitors with potent oral efficacy in several models of rheumatoid arthritis. Bioorg. Med. Chem. Lett. (2004) 14:3595-3599.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 3595-3599
    • Revesz, L.1    Blum, E.2    Dipadova, F.E.3
  • 21
    • 0034608331 scopus 로고    scopus 로고
    • SAR of 4-hydroxypiperidine and hydroxyalkyl substituted heterocycles as novel p38 map kinase inhibitors
    • REVESZ L, DIPADOVA FE, BUHL T et al.: SAR of 4-hydroxypiperidine and hydroxyalkyl substituted heterocycles as novel p38 map kinase inhibitors. Bioorg. Med. Chem. Lett. (2000) 10:1261-1264.
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 1261-1264
    • Revesz, L.1    Dipadova, F.E.2    Buhl, T.3
  • 22
    • 0037136006 scopus 로고    scopus 로고
    • SAR of 2,6-diamino-3,5-difluoropyridinyl substituted heterocycles as novel p38 MAP kinase inhibitors
    • REVESZ L, DIPADOVA FE, BUHL T et al.: SAR of 2,6-diamino-3,5-difluoropyridinyl substituted heterocycles as novel p38 MAP kinase inhibitors. Bioorg. Med. Chem. Lett. (2002) 12:2109-2112.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 2109-2112
    • Revesz, L.1    Dipadova, F.E.2    Buhl, T.3
  • 25
    • 0037330356 scopus 로고    scopus 로고
    • Imidazopyrimidines, potent inhibitors of p38 MAP kinase
    • RUPERT KC, HENRY JR, DODD JH et al.: Imidazopyrimidines, potent inhibitors of p38 MAP kinase. Bioorg. Med. Chem. Lett. (2003) 13:347-350.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 347-350
    • Rupert, K.C.1    Henry, J.R.2    Dodd, J.H.3
  • 26
    • 3142677902 scopus 로고    scopus 로고
    • The development of novel inhibitors of tumor necrosis factor-α (TNF-α) production based on substituted [5,5]-bicyclic pyrazolones
    • LAUFERSWEILER MJ, BRUGEL TA, CLARK MP et al.: The development of novel inhibitors of tumor necrosis factor-α (TNF-α) production based on substituted [5,5]-bicyclic pyrazolones. Bioorg. Med. Chem. Lett. (2004) 14:4267-4272.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 4267-4272
    • Laufersweiler, M.J.1    Brugel, T.A.2    Clark, M.P.3
  • 27
    • 4444346777 scopus 로고    scopus 로고
    • The development of new bicyclic pyrazole-based cytokine synthesis inhibitors
    • TOWNES JA, GOLEBIOWSKI A, CLARK MP et al.: The development of new bicyclic pyrazole-based cytokine synthesis inhibitors. Bioorg. Med. Chem. Lett. (2004) 14:4945-4948.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 4945-4948
    • Townes, J.A.1    Golebiowski, A.2    Clark, M.P.3
  • 28
    • 9144219693 scopus 로고    scopus 로고
    • An efficient proteomics method to identify the cellular targets of protein kinase inhibitors
    • GODL K, WISSING J, KURTENBACH A et al.: An efficient proteomics method to identify the cellular targets of protein kinase inhibitors. Proc. Natl. Acad. Sci. USA (2003) 100:15434-15439.
    • (2003) Proc. Natl. Acad. Sci. USA , vol.100 , pp. 15434-15439
    • Godl, K.1    Wissing, J.2    Kurtenbach, A.3
  • 29
    • 0347627154 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationship of aminobenzophenones. A novel class of p38 MAP kinase inhibitors with high antiinflammatory activity
    • OTTOSEN ER, SORENSEN MD, BJORKLING F et al.: Synthesis and structure-activity relationship of aminobenzophenones. A novel class of p38 MAP kinase inhibitors with high antiinflammatory activity. J. Med. Chem. (2003) 46:5651-5662.
    • (2003) J. Med. Chem. , vol.46 , pp. 5651-5662
    • Ottosen, E.R.1    Sorensen, M.D.2    Bjorkling, F.3
  • 30
    • 22744441392 scopus 로고    scopus 로고
    • LEO PHARMACEUTICALS: Press release (April)
    • LEO PHARMACEUTICALS: Press release (April 2002).
    • (2002)
  • 31
    • 2942560873 scopus 로고    scopus 로고
    • SAR of benzoylpyridines and benzophenones as p38 MAP kinase inhibitors with oral activity
    • REVESZ L, BLUM E, DIPADOVA FE et al.: SAR of benzoylpyridines and benzophenones as p38 MAP kinase inhibitors with oral activity. Bioorg. Med. Chem. Lett. (2004) 14:3601-3605.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 3601-3605
    • Revesz, L.1    Blum, E.2    Dipadova, F.E.3
  • 32
    • 22744442294 scopus 로고    scopus 로고
    • VERTEX PHARMACEUTICALS, INC.: Press release (September)
    • VERTEX PHARMACEUTICALS, INC.: Press release (September 2001).
    • (2001)
  • 33
    • 22744434492 scopus 로고    scopus 로고
    • VERTEX PHARMACEUTICALS, INC.: Press release (May 2003 and April)
    • VERTEX PHARMACEUTICALS, INC.: Press release (May 2003 and April 2004).
    • (2004)
  • 34
    • 10744219935 scopus 로고    scopus 로고
    • SAR of 3,4-dihydropyrido[3,2-d]pyrimidone p38 inhibitors
    • LIU L, STELMACH JE, NATARAJAN SR et al.: SAR of 3,4-dihydropyrido[3,2-d]pyrimidone p38 inhibitors. Bioorg. Med. Chem. Lett. (2003) 13:3979-3982.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 3979-3982
    • Liu, L.1    Stelmach, J.E.2    Natarajan, S.R.3
  • 35
    • 0041318841 scopus 로고    scopus 로고
    • Structural basis for p38α MAP kinase quinazolinone and pyridol-pyrimidine inhibitor specificity
    • FITZGERALD CE, PATEL SB, BECKER JW et al.: Structural basis for p38α MAP kinase quinazolinone and pyridol-pyrimidine inhibitor specificity. Nat. Struc. Biol. (2003) 10:764-769.
    • (2003) Nat. Struc. Biol. , vol.10 , pp. 764-769
    • Fitzgerald, C.E.1    Patel, S.B.2    Becker, J.W.3
  • 36
    • 12444323524 scopus 로고    scopus 로고
    • Indole-based heterocyclic inhibitors of p38α MAP kinase: Designing a conformationally restricted analogue
    • MAVUNKEL BJ, CHAKRAVARTY S, PERUMATTAM JJ et al.: Indole-based heterocyclic inhibitors of p38α MAP kinase: designing a conformationally restricted analogue. Bioorg. Med. Chem. Lett. (2003) 13:3087-3090.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 3087-3090
    • Mavunkel, B.J.1    Chakravarty, S.2    Perumattam, J.J.3
  • 37
    • 21544433855 scopus 로고    scopus 로고
    • SCIO 469, a novel p38α MAPK inhibitor, provides efficacy in acute post-surgical dental pain
    • TONG SE, DANIELS SE, CHANG S et al.: SCIO 469, a novel p38α MAPK inhibitor, provides efficacy in acute post-surgical dental pain. Clin. Pharm. Ther. (2004) 75(2):3.
    • (2004) Clin. Pharm. Ther. , vol.75 , Issue.2 , pp. 3
    • Tong, S.E.1    Daniels, S.E.2    Chang, S.3
  • 39
    • 22744456013 scopus 로고    scopus 로고
    • Annual Press Conference 2003: Boehringer Ingelheim Company Presentation. (8 April)
    • Annual Press Conference 2003: Boehringer Ingelheim Company Presentation. (8 April 2003).
    • (2003)
  • 40
    • 0037019275 scopus 로고    scopus 로고
    • Pyrazole urea-base inhibitors of p38 MAP kinase: From lead compound to clinical candidate
    • REGAN J, BREITFELDER S, CIRILLO P et al.: Pyrazole urea-base inhibitors of p38 MAP kinase: From lead compound to clinical candidate. J. Med. Chem. (2002) 45:2994-3008.
    • (2002) J. Med. Chem. , vol.45 , pp. 2994-3008
    • Regan, J.1    Breitfelder, S.2    Cirillo, P.3
  • 41
    • 5444244504 scopus 로고    scopus 로고
    • Novel, potent and selective anilinoquinazoline and anilinopyrimidine inhibitors of p38 MAP kinase
    • CUMMING JC, McKENZIE CL, BOWDEN SG et al.: Novel, potent and selective anilinoquinazoline and anilinopyrimidine inhibitors of p38 MAP kinase. Bioorg. Med. Chem. Lett. (2004) 14:5389-5394.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 5389-5394
    • Cumming, J.C.1    Mckenzie, C.L.2    Bowden, S.G.3


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