-
1
-
-
0034513614
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
26
-
-
3142677902
-
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
-
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
-
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
-
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
-
-
LEO PHARMACEUTICALS: Press release (April)
-
LEO PHARMACEUTICALS: Press release (April 2002).
-
(2002)
-
-
-
31
-
-
2942560873
-
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
-
-
VERTEX PHARMACEUTICALS, INC.: Press release (September)
-
VERTEX PHARMACEUTICALS, INC.: Press release (September 2001).
-
(2001)
-
-
-
33
-
-
22744434492
-
-
VERTEX PHARMACEUTICALS, INC.: Press release (May 2003 and April)
-
VERTEX PHARMACEUTICALS, INC.: Press release (May 2003 and April 2004).
-
(2004)
-
-
-
34
-
-
10744219935
-
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
-
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
-
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
-
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
-
-
Annual Press Conference 2003: Boehringer Ingelheim Company Presentation. (8 April)
-
Annual Press Conference 2003: Boehringer Ingelheim Company Presentation. (8 April 2003).
-
(2003)
-
-
-
40
-
-
0037019275
-
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
-
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
|