-
1
-
-
0026788165
-
Gastrointestinal damage associated with the use of nonsteroidal antiinflammatory drugs
-
Allison, M.C., Howatson, A.G., Torrance, C.J., Lee, F.D., and Russell, R.I. 1992. Gastrointestinal damage associated with the use of nonsteroidal antiinflammatory drugs. New Engl. J. Med. 327: 749-754.
-
(1992)
New Engl. J. Med.
, vol.327
, pp. 749-754
-
-
Allison, M.C.1
Howatson, A.G.2
Torrance, C.J.3
Lee, F.D.4
Russell, R.I.5
-
2
-
-
0030045189
-
Tumor necrosis factor mediation of NSAID-induced gastric damage: Role of leucocyte adherence
-
Appleyard, C.B., McCafferty, D.-M., Tigley, A.W., Swain, M.G., and Wallace, J.L. 1996. Tumor necrosis factor mediation of NSAID-induced gastric damage: role of leucocyte adherence. Am. J. Physiol. 270: G42-G48.
-
(1996)
Am. J. Physiol.
, vol.270
-
-
Appleyard, C.B.1
McCafferty, D.-M.2
Tigley, A.W.3
Swain, M.G.4
Wallace, J.L.5
-
3
-
-
0028170934
-
Tepoxalin: A dual cyclooxygenase/5-lipoxygenase inhibitor of arachidonic acid metabolism with potent anti-inflammatory activity and a favorable gastrointestinal profile
-
Argentieri, D.C., Ritchie, D.M., Ferro, M.P., Kirchner, T., Wachter, M.P., Anderson, D.W., Rosenthale, M.E., and Capetola, R.J. 1994. Tepoxalin: a dual cyclooxygenase/5-lipoxygenase inhibitor of arachidonic acid metabolism with potent anti-inflammatory activity and a favorable gastrointestinal profile. J. Pharmacol. Exp. Ther. 271: 1399-1408.
-
(1994)
J. Pharmacol. Exp. Ther.
, vol.271
, pp. 1399-1408
-
-
Argentieri, D.C.1
Ritchie, D.M.2
Ferro, M.P.3
Kirchner, T.4
Wachter, M.P.5
Anderson, D.W.6
Rosenthale, M.E.7
Capetola, R.J.8
-
4
-
-
0029904828
-
Cyclooxygenase-2 and its regulation in inflammation
-
Bakhle, Y.S., and Botting, R.M. 1996. Cyclooxygenase-2 and its regulation in inflammation. Mediators Inflammation, 5: 305-323.
-
(1996)
Mediators Inflammation
, vol.5
, pp. 305-323
-
-
Bakhle, Y.S.1
Botting, R.M.2
-
5
-
-
34547393346
-
-
Eur. Patent-714895
-
Barnett, J.W., Dunn, J.P., Kertesz, D.J., Miller, A.B., Morgans, D.J., Ramesha, C.S., Sigal, C.E., Sjogren, E.B., Smith, D.B., Talamas, F.X., Sigal, E.C., and Morgans, D. 1996. Eur. Patent-714895.
-
(1996)
-
-
Barnett, J.W.1
Dunn, J.P.2
Kertesz, D.J.3
Miller, A.B.4
Morgans, D.J.5
Ramesha, C.S.6
Sigal, C.E.7
Sjogren, E.B.8
Smith, D.B.9
Talamas, F.X.10
Sigal, E.C.11
Morgans, D.12
-
6
-
-
0028032723
-
COX-1 and COX-2: Toward the development of more selective NSAIDs
-
Battistini, B., Botting, R., and Bakhle, Y.S. 1994. COX-1 and COX-2: toward the development of more selective NSAIDs. Drug News Perspect. 7: 501-512.
-
(1994)
Drug News Perspect.
, vol.7
, pp. 501-512
-
-
Battistini, B.1
Botting, R.2
Bakhle, Y.S.3
-
7
-
-
0029650018
-
NSAIDs, COX-2 inhibitors, and the gut
-
Bennett, A., and Tavares, I.A. 1995. NSAIDs, COX-2 inhibitors, and the gut. Lancet, 346: 1105.
-
(1995)
Lancet
, vol.346
, pp. 1105
-
-
Bennett, A.1
Tavares, I.A.2
-
8
-
-
0026487129
-
The unique pharmacologic profile of nabumetone
-
Blower, P.R. 1992. The unique pharmacologic profile of nabumetone. J. Rheumatol. 19(Suppl. 36): 13-19.
-
(1992)
J. Rheumatol.
, vol.19
, Issue.36 SUPPL.
, pp. 13-19
-
-
Blower, P.R.1
-
9
-
-
0020696959
-
Stimulation and inhibition of prostacyclin formation in the gastric mucosa and ileum in vitro by anti-inflammatory agents
-
Boughton-Smith, N.K., and Whittle, B.J.R. 1983. Stimulation and inhibition of prostacyclin formation in the gastric mucosa and ileum in vitro by anti-inflammatory agents. Br. J. Pharmacol. 78: 173-180.
-
(1983)
Br. J. Pharmacol.
, vol.78
, pp. 173-180
-
-
Boughton-Smith, N.K.1
Whittle, B.J.R.2
-
10
-
-
0344798192
-
NSAID-induced gastrointestinal damage
-
Champion, G.D., Feng, P.H., Azuma, T., Caughey, D.E., Chan, K.H., Kashiwazaki, S., Liu, H.-C., Nasution, A.R., Nobunaga, M., Prichanond, S., Torralba, T.P., Udom, V., Utis, D., Wang, S.R., Wong, W.S., Yang, D.-J., and Yoo, M.C. 1997. NSAID-induced gastrointestinal damage. Drugs, 53: 6-19.
-
(1997)
Drugs
, vol.53
, pp. 6-19
-
-
Champion, G.D.1
Feng, P.H.2
Azuma, T.3
Caughey, D.E.4
Chan, K.H.5
Kashiwazaki, S.6
Liu, H.-C.7
Nasution, A.R.8
Nobunaga, M.9
Prichanond, S.10
Torralba, T.P.11
Udom, V.12
Utis, D.13
Wang, S.R.14
Wong, W.S.15
Yang, D.-J.16
Yoo, M.C.17
-
11
-
-
0029033219
-
Pharmacology of a selective cyclooxygenase-2 inhibitor, L-745,337: A novel nonsteroidal anti-inflammatory agent with an ulcerogenic sparing effect in rat and nonhuman primate stomach
-
Chan, C.-C., Boyce, S., Brideau, C., Ford-Hutchinson, A.W., Gordon, R., Guay, D., Hill, R.G., Li, C.-S., Mancini, J., Penneton, M., Prasit, P., Rasori, R., Riendeau, D., Roy, P., Tagari, P., Vickers, P., Wong, E., and Rodger, I.W. 1995. Pharmacology of a selective cyclooxygenase-2 inhibitor, L-745,337: a novel nonsteroidal anti-inflammatory agent with an ulcerogenic sparing effect in rat and nonhuman primate stomach. J. Pharmacol. Exp. Ther. 274: 1531-1537.
-
(1995)
J. Pharmacol. Exp. Ther.
, vol.274
, pp. 1531-1537
-
-
Chan, C.-C.1
Boyce, S.2
Brideau, C.3
Ford-Hutchinson, A.W.4
Gordon, R.5
Guay, D.6
Hill, R.G.7
Li, C.-S.8
Mancini, J.9
Penneton, M.10
Prasit, P.11
Rasori, R.12
Riendeau, D.13
Roy, P.14
Tagari, P.15
Vickers, P.16
Wong, E.17
Rodger, I.W.18
-
12
-
-
0028139275
-
Mechanism of selective inhibition of the inducible isoform of prostaglandin G/H synthase
-
Copeland, R.A., Williams, J.M., Giannaras, J., Nurnberg, S., Covington, M., Pinto, D., Pick, S., and Trzaskos, J.M. 1994. Mechanism of selective inhibition of the inducible isoform of prostaglandin G/H synthase. Proc. Natl. Acad. Sci. U.S.A. 91: 11 202-11 206.
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 11202-11206
-
-
Copeland, R.A.1
Williams, J.M.2
Giannaras, J.3
Nurnberg, S.4
Covington, M.5
Pinto, D.6
Pick, S.7
Trzaskos, J.M.8
-
13
-
-
0024388452
-
In vivo assessment of precursor induced prostaglandin release within the rat gastric lumen
-
Doyle, M.J., Nemeth, P.R., Skoglund, M.L., and Mandel, K.G. 1989. In vivo assessment of precursor induced prostaglandin release within the rat gastric lumen. Prostaglandins, 38: 581-597.
-
(1989)
Prostaglandins
, vol.38
, pp. 581-597
-
-
Doyle, M.J.1
Nemeth, P.R.2
Skoglund, M.L.3
Mandel, K.G.4
-
14
-
-
0001867832
-
Efficacy of MK-966, a highly selective inhibitor of COX-2, in the treatment of postoperative dental pain
-
Ehrich, E., Mehlisch, D., Perkins, S., Brown, P., Wittreich, J., Lipschutz, K., and Gertz, B. 1996. Efficacy of MK-966, a highly selective inhibitor of COX-2, in the treatment of postoperative dental pain. Arthritis Rheum. 39(Suppl. 9): S81.
-
(1996)
Arthritis Rheum.
, vol.39
, Issue.9 SUPPL.
-
-
Ehrich, E.1
Mehlisch, D.2
Perkins, S.3
Brown, P.4
Wittreich, J.5
Lipschutz, K.6
Gertz, B.7
-
15
-
-
0028860983
-
Anti-inflammatory, analgesic, antipyretic and related properties of meloxicam, a new non-steroidal anti-inflammatory agent with favourable gastrointestinal tolerance
-
Engelhardt, G., Homma, D., Schlegel, K., Utzmann, R., and Schnitzler, C. 1995. Anti-inflammatory, analgesic, antipyretic and related properties of meloxicam, a new non-steroidal anti-inflammatory agent with favourable gastrointestinal tolerance. Inflamm. Res. 44: 423-433.
-
(1995)
Inflamm. Res.
, vol.44
, pp. 423-433
-
-
Engelhardt, G.1
Homma, D.2
Schlegel, K.3
Utzmann, R.4
Schnitzler, C.5
-
16
-
-
0030030129
-
Meloxicam: Influence on arachidonic acid metabolism. Part 1. In Vitro findings
-
Engelhardt, G., Bogel, R., Schnitzer, C., and Utzmann, R. 1996. Meloxicam: influence on arachidonic acid metabolism. Part 1. In Vitro findings. Biochem. Pharmacol. 51: 21-28.
-
(1996)
Biochem. Pharmacol.
, vol.51
, pp. 21-28
-
-
Engelhardt, G.1
Bogel, R.2
Schnitzer, C.3
Utzmann, R.4
-
18
-
-
0028089109
-
NS-398, a new anti-inflammatory agent, selectively inhibits prostaglandin G/H synthase/cyclooxygenase (COX-2) activity in vitro
-
Futaki, N., Takahashi, S., Yokoyama, M., Arai, I., Higuchi, S., and Otomo, S. 1994. NS-398, a new anti-inflammatory agent, selectively inhibits prostaglandin G/H synthase/cyclooxygenase (COX-2) activity in vitro. Prostaglandins, 47: 55-59.
-
(1994)
Prostaglandins
, vol.47
, pp. 55-59
-
-
Futaki, N.1
Takahashi, S.2
Yokoyama, M.3
Arai, I.4
Higuchi, S.5
Otomo, S.6
-
19
-
-
0025160887
-
Anti-inflammatory and safety profile of DuP 697, a novel orally effective prostaglandin synthesis inhibitor
-
Gans, K.R., Galbraith, W., Roman, R.J., Haber, S.B., Kerr, J.S., Schmidt, W.K., Smith, C., Hewes, W.E., and Ackerman, N.R. 1990. Anti-inflammatory and safety profile of DuP 697, a novel orally effective prostaglandin synthesis inhibitor. J. Pharmacol. Exp. Ther. 254: 180-187.
-
(1990)
J. Pharmacol. Exp. Ther.
, vol.254
, pp. 180-187
-
-
Gans, K.R.1
Galbraith, W.2
Roman, R.J.3
Haber, S.B.4
Kerr, J.S.5
Schmidt, W.K.6
Smith, C.7
Hewes, W.E.8
Ackerman, N.R.9
-
20
-
-
0028830109
-
Expression and selective inhibition of the constitutive and inducible forms of human cyclooxygenase
-
Gierse, J.K., Hauser, S.D., Creely, D.P., Koboldt, C., Rangwala, S.H., Isakson, P.C., and Seibert, K. 1995. Expression and selective inhibition of the constitutive and inducible forms of human cyclooxygenase. Biochem. J. 305: 479-484.
-
(1995)
Biochem. J.
, vol.305
, pp. 479-484
-
-
Gierse, J.K.1
Hauser, S.D.2
Creely, D.P.3
Koboldt, C.4
Rangwala, S.H.5
Isakson, P.C.6
Seibert, K.7
-
21
-
-
0029983843
-
Constitutive cyclooxygenase (COX-1) and inducible cyclooxygenase (COX-2): Rationale for selective inhibition and progress to date
-
Griswold, D.E., and Adams, J.L. 1996. Constitutive cyclooxygenase (COX-1) and inducible cyclooxygenase (COX-2): rationale for selective inhibition and progress to date. Med. Res. Rev. 16: 181-206.
-
(1996)
Med. Res. Rev.
, vol.16
, pp. 181-206
-
-
Griswold, D.E.1
Adams, J.L.2
-
22
-
-
0029029296
-
Inhibition of constitutive and inducible cyclooxygenase activity in human platelets and mononuclear cells by NSAIDs and COX 2 inhibitors
-
Grossmann, C.J., Wiseman, J., Lucas, F.S., Trevethick, M.A., and Birch, P.J. 1995. Inhibition of constitutive and inducible cyclooxygenase activity in human platelets and mononuclear cells by NSAIDs and COX 2 inhibitors. Inflamm. Res. 44: 253-257.
-
(1995)
Inflamm. Res.
, vol.44
, pp. 253-257
-
-
Grossmann, C.J.1
Wiseman, J.2
Lucas, F.S.3
Trevethick, M.A.4
Birch, P.J.5
-
23
-
-
0029145880
-
NSAIDs, COX-2 inhibitors, and the gut
-
Hayllar, J., and Bjarnason, I. 1995. NSAIDs, COX-2 inhibitors, and the gut. Lancet, 346: 1629.
-
(1995)
Lancet
, vol.346
, pp. 1629
-
-
Hayllar, J.1
Bjarnason, I.2
-
24
-
-
0030049390
-
Prostaglandin synthase 2
-
Herschman, H.R. 1996. Prostaglandin synthase 2. Biochim. Biophys. Acta, 1299: 125-140.
-
(1996)
Biochim. Biophys. Acta
, vol.1299
, pp. 125-140
-
-
Herschman, H.R.1
-
25
-
-
0000263466
-
SC-58635 (Celecoxib), a novel COX-2 selective inhibitor, is effective as a treatment for osteoarthritis (OA) in a short-term pilot study
-
Hubbard, R.C., Koepp, R.J., Yu, S., Talwalker, S., Geis, G.S., Wiesenhutter, C.W., Makarowski, W.S., and Paulus, H.A. 1996. SC-58635 (Celecoxib), a novel COX-2 selective inhibitor, is effective as a treatment for osteoarthritis (OA) in a short-term pilot study. Arthritis Rheum. 39 (Suppl. 9): S226.
-
(1996)
Arthritis Rheum.
, vol.39
, Issue.9 SUPPL.
-
-
Hubbard, R.C.1
Koepp, R.J.2
Yu, S.3
Talwalker, S.4
Geis, G.S.5
Wiesenhutter, C.W.6
Makarowski, W.S.7
Paulus, H.A.8
-
26
-
-
0026551623
-
Mechanisms of gastric and duodenal damage and protection
-
Hudson, N., Hawthorne, A.B., Cole, A.T., Jones, P.D.E., and Hawkey, C.J. 1992. Mechanisms of gastric and duodenal damage and protection. Hepatogastroenterol. 39(Suppl. 1): 31-36.
-
(1992)
Hepatogastroenterol.
, vol.39
, Issue.1 SUPPL.
, pp. 31-36
-
-
Hudson, N.1
Hawthorne, A.B.2
Cole, A.T.3
Jones, P.D.E.4
Hawkey, C.J.5
-
27
-
-
0030017042
-
Characterization of prostaglandin G/H synthase 1 and 2 in rat, dog, monkey, and human gastrointestinal tracts
-
Kargman, S., Charleson, S., Cartwright, M., Frank, J., Riendeau, D., Mancini, J., Evans, J., and O'Neill, G. 1996a. Characterization of prostaglandin G/H synthase 1 and 2 in rat, dog, monkey, and human gastrointestinal tracts. Gastroenterology, 111: 445-454.
-
(1996)
Gastroenterology
, vol.111
, pp. 445-454
-
-
Kargman, S.1
Charleson, S.2
Cartwright, M.3
Frank, J.4
Riendeau, D.5
Mancini, J.6
Evans, J.7
O'Neill, G.8
-
28
-
-
0030580035
-
Mechanism of selective inhibition of human prostaglandin G/H synthase-1 and -2 in intact cells
-
Kargman, S., Wong, E., Greig, G.M., Falgueyret, J.-P., Cromlish, W., Ethier, D., Yergey, J.A., Riendeau, D., Evans, J.F., Kennedy, B., Tagari, P., Francis, D.A., and O'Neill, G.P. 19966. Mechanism of selective inhibition of human prostaglandin G/H synthase-1 and -2 in intact cells. Biochem. Pharmacol. 52: 1113-1125.
-
(1996)
Biochem. Pharmacol.
, vol.52
, pp. 1113-1125
-
-
Kargman, S.1
Wong, E.2
Greig, G.M.3
Falgueyret, J.-P.4
Cromlish, W.5
Ethier, D.6
Yergey, J.A.7
Riendeau, D.8
Evans, J.F.9
Kennedy, B.10
Tagari, P.11
Francis, D.A.12
O'Neill, G.P.13
-
29
-
-
0027988173
-
Selective inhibition of cyclooxygenase 2
-
Klein, T., Nusing, R.M., Pfeilschifter, J., and Ullrich, V. 1994. Selective inhibition of cyclooxygenase 2. Biochem. Pharmacol. 48: 1605-1610.
-
(1994)
Biochem. Pharmacol.
, vol.48
, pp. 1605-1610
-
-
Klein, T.1
Nusing, R.M.2
Pfeilschifter, J.3
Ullrich, V.4
-
30
-
-
0027986841
-
Differential inhibition of human prostaglandin endoperoxide H synthases-1 and -2 by nonsteroidal anti-inflammatory drugs
-
Laneuville, O., Breuer, D.K., DeWitt, D.L., Hla, T., Funk, C.D., and Smith, W.L. 1995. Differential inhibition of human prostaglandin endoperoxide H synthases-1 and -2 by nonsteroidal anti-inflammatory drugs. J. Pharmacol. Exp. Ther. 271: 927-934.
-
(1995)
J. Pharmacol. Exp. Ther.
, vol.271
, pp. 927-934
-
-
Laneuville, O.1
Breuer, D.K.2
DeWitt, D.L.3
Hla, T.4
Funk, C.D.5
Smith, W.L.6
-
31
-
-
0028843881
-
Prostaglandin synthase 1 gene disruption in mice reduces arachidonic acid-induced inflammation and indomethacin-induced gastric ulceration
-
Langenbach, R., Morham, S.G., Tiano, H.F., Loftin, C.D., Ghanayem, B.I., Chulada, P.C., Mahler, J.F., Lee, C.A., Goulding, E.H., Kluckman, K.D., Kim, H.S., and Smities, O. 1995. Prostaglandin synthase 1 gene disruption in mice reduces arachidonic acid-induced inflammation and indomethacin-induced gastric ulceration. Cell, 83: 483-492.
-
(1995)
Cell
, vol.83
, pp. 483-492
-
-
Langenbach, R.1
Morham, S.G.2
Tiano, H.F.3
Loftin, C.D.4
Ghanayem, B.I.5
Chulada, P.C.6
Mahler, J.F.7
Lee, C.A.8
Goulding, E.H.9
Kluckman, K.D.10
Kim, H.S.11
Smities, O.12
-
32
-
-
0028353941
-
Risks of bleeding peptic ulcer associated with individual non-steroidal anti-inflammatory drugs
-
Langman, M.J.S., Weil, J., Wainwright, P., Lawson, D.H., Rawlins, M.D., Logan, R.F.A., Murphy, M., Vessey, M.P., and Colin-Jones, D.G. 1994. Risks of bleeding peptic ulcer associated with individual non-steroidal anti-inflammatory drugs. Lancet, 343: 1075-1078.
-
(1994)
Lancet
, vol.343
, pp. 1075-1078
-
-
Langman, M.J.S.1
Weil, J.2
Wainwright, P.3
Lawson, D.H.4
Rawlins, M.D.5
Logan, R.F.A.6
Murphy, M.7
Vessey, M.P.8
Colin-Jones, D.G.9
-
33
-
-
0026097522
-
Upper gastrointestinal bleeding in relation to previous use of analgesics and non-steroidal anti-inflammatory drugs
-
Laporte, J.-R., Carne, X., Vidal, X., Moreno, V., and Juan, J. 1991. Upper gastrointestinal bleeding in relation to previous use of analgesics and non-steroidal anti-inflammatory drugs. Lancet, 337: 85-89.
-
(1991)
Lancet
, vol.337
, pp. 85-89
-
-
Laporte, J.-R.1
Carne, X.2
Vidal, X.3
Moreno, V.4
Juan, J.5
-
34
-
-
0029151693
-
Synthesis and biological evaluation of 2,3-diarylthiophenes as selective COX-2 and COX-1 inhibitors
-
Leblanc, Y., Gauthier, J.Y., Ethier, D., Guay, J., Mancini, J., Riendeau, D., Tagari, P., Vickers, P., Wong, E., and Prasit, P. 1995. Synthesis and biological evaluation of 2,3-diarylthiophenes as selective COX-2 and COX-1 inhibitors. Bioorg. Med. Chem. Lett. 5: 2123-2128.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 2123-2128
-
-
Leblanc, Y.1
Gauthier, J.Y.2
Ethier, D.3
Guay, J.4
Mancini, J.5
Riendeau, D.6
Tagari, P.7
Vickers, P.8
Wong, E.9
Prasit, P.10
-
35
-
-
0028322893
-
Selective inhibition of inducible cyclooxygenase 2 in vivo is antiinflammatory and nonulcerogenic
-
Masferrer, J.L., Zweifel, B.S., Manning, P.T., Hauser, S.D., Leahy, K.M., Smith, W.G., Isakson, P.C., and Seibert, K. 1994. Selective inhibition of inducible cyclooxygenase 2 in vivo is antiinflammatory and nonulcerogenic. Proc. Natl. Acad. Sci. U.S.A. 91:3228-3232.
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 3228-3232
-
-
Masferrer, J.L.1
Zweifel, B.S.2
Manning, P.T.3
Hauser, S.D.4
Leahy, K.M.5
Smith, W.G.6
Isakson, P.C.7
Seibert, K.8
-
36
-
-
0029021264
-
Nabumetone, in contrast to etodolac, lacks gastrointestinal irritancy in the rat: Assessment by the inflammatory marker, haptoglobin, and blood loss
-
Melarange, R., Gentry, C., Blower, P.R., Toseland, C.D.N., and Spangler, R. 1995. Nabumetone, in contrast to etodolac, lacks gastrointestinal irritancy in the rat: assessment by the inflammatory marker, haptoglobin, and blood loss. Inflammopharmacology, 3: 259-270.
-
(1995)
Inflammopharmacology
, vol.3
, pp. 259-270
-
-
Melarange, R.1
Gentry, C.2
Blower, P.R.3
Toseland, C.D.N.4
Spangler, R.5
-
37
-
-
9044253709
-
Tenidap, a structurally novel drug for the treatment of arthritis: Antiinfiammatory and analgesic properties
-
Moore, P.F., Larson, D.L., Otterness, I.G., Weissman, A., Kadin, S.B., Sweeney, F.J., Eskra, J.D., Nagahisa, A., Sakakibara, M., and Carty, T.J. 1996. Tenidap, a structurally novel drug for the treatment of arthritis: antiinfiammatory and analgesic properties. Inflamm. Res. 45: 54-61.
-
(1996)
Inflamm. Res.
, vol.45
, pp. 54-61
-
-
Moore, P.F.1
Larson, D.L.2
Otterness, I.G.3
Weissman, A.4
Kadin, S.B.5
Sweeney, F.J.6
Eskra, J.D.7
Nagahisa, A.8
Sakakibara, M.9
Carty, T.J.10
-
38
-
-
0028123502
-
Overexpression of human prostaglandin G/H synthase-1 and -2 by recombinant vaccinia virus: Inhibition by nonsteroidal anti-inflammatory drugs and biosynthesis of 15-hydroxyeicosatetraenoic acid
-
O'Neill, G.P., Mancini, J.A., Kargman, S., Yergey, J., Kwan, M.Y., Falgueyret, J.-P., Abramovitz, M., Kennedy, B.P., Ouellet, M., Cromlish, W., Culp, S., Evans, J.F., Ford-Hutchinson, A.W., and Vickers, P.J. 1994. Overexpression of human prostaglandin G/H synthase-1 and -2 by recombinant vaccinia virus: inhibition by nonsteroidal anti-inflammatory drugs and biosynthesis of 15-hydroxyeicosatetraenoic acid. Mol. Pharmacol. 45: 245-254.
-
(1994)
Mol. Pharmacol.
, vol.45
, pp. 245-254
-
-
O'Neill, G.P.1
Mancini, J.A.2
Kargman, S.3
Yergey, J.4
Kwan, M.Y.5
Falgueyret, J.-P.6
Abramovitz, M.7
Kennedy, B.P.8
Ouellet, M.9
Cromlish, W.10
Culp, S.11
Evans, J.F.12
Ford-Hutchinson, A.W.13
Vickers, P.J.14
-
39
-
-
0028831977
-
Effect of inhibitor time-dependency on selectivity towards cyclooxygenase isoforms
-
Ouellet, M., and Percival, M.D. 1995. Effect of inhibitor time-dependency on selectivity towards cyclooxygenase isoforms. Biochem. J. 306: 247-251.
-
(1995)
Biochem. J.
, vol.306
, pp. 247-251
-
-
Ouellet, M.1
Percival, M.D.2
-
40
-
-
0029993460
-
Nonsteroidal anti-inflammatory drugs: Practical and theoretical considerations in their selection
-
Polisson, R. 1996. Nonsteroidal anti-inflammatory drugs: practical and theoretical considerations in their selection. Am. J. Med. 100: 31S-36S.
-
(1996)
Am. J. Med.
, vol.100
-
-
Polisson, R.1
-
41
-
-
0026712152
-
Limited utilization of exogenous arachidonic acid by the prostaglandin cyclooxygenase in gastric mucosa: The role of protein binding, glutathione peroxidase, and hydrogen peroxides
-
Preclik, G., Stange, E.F., and Ditschuneit, H. 1992. Limited utilization of exogenous arachidonic acid by the prostaglandin cyclooxygenase in gastric mucosa: the role of protein binding, glutathione peroxidase, and hydrogen peroxides. Prostaglandins, 44: 177-197.
-
(1992)
Prostaglandins
, vol.44
, pp. 177-197
-
-
Preclik, G.1
Stange, E.F.2
Ditschuneit, H.3
-
42
-
-
0027008091
-
Mechanisms of NSAID-induced ulcerogenesis: Structural properties of drugs, focus on the micro vascular factors, and novel approaches for gastro-intestinal protection
-
Rainsford, K.D. 1992. Mechanisms of NSAID-induced ulcerogenesis: structural properties of drugs, focus on the micro vascular factors, and novel approaches for gastro-intestinal protection. Acta Physiol. Hungarica, 80: 23-38.
-
(1992)
Acta Physiol. Hungarica
, vol.80
, pp. 23-38
-
-
Rainsford, K.D.1
-
43
-
-
0027944191
-
Selective cyclooxygenase inhibitors: Novel 1,2-diarylcyclopentenes are potent and orally active COX-2 inhibitors
-
Reitz, D.B., Li, J.J., Norton, M.B., Reinhard, E.J., Collins, J.T., Anderson, G.D., Gregory, S.A., Koboldt, C.M., Perkins, W.E., Seibert, K., and Isakson, P.C. 1994. Selective cyclooxygenase inhibitors: novel 1,2-diarylcyclopentenes are potent and orally active COX-2 inhibitors. J. Med. Chem. 37: 3878-3881.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3878-3881
-
-
Reitz, D.B.1
Li, J.J.2
Norton, M.B.3
Reinhard, E.J.4
Collins, J.T.5
Anderson, G.D.6
Gregory, S.A.7
Koboldt, C.M.8
Perkins, W.E.9
Seibert, K.10
Isakson, P.C.11
-
44
-
-
0028952998
-
Selective cyclooxygenase inhibitors: Novel 4-spiro 1,2-diarylcyclopentenes are potent and orally active COX-2 inhibitors
-
Reitz, D.B., Huang, H.-C., Li, J.J., Garland, D.J., Manning, R.E., Anderson, G.D., Gregory, S.A., Kobolt, C.M., Perkins, W.E., Seibert, K., and Isakson, P.C. 1995. Selective cyclooxygenase inhibitors: novel 4-spiro 1,2-diarylcyclopentenes are potent and orally active COX-2 inhibitors. Bioorg. Med. Chem. Lett. 5: 867-872.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 867-872
-
-
Reitz, D.B.1
Huang, H.-C.2
Li, J.J.3
Garland, D.J.4
Manning, R.E.5
Anderson, G.D.6
Gregory, S.A.7
Kobolt, C.M.8
Perkins, W.E.9
Seibert, K.10
Isakson, P.C.11
-
45
-
-
8244255009
-
Biochemical and pharmacological profile of a tetrasubstituted furanone as a highly selective COX-2 inhibitor
-
Riendeau, D., Percival, M.D., Boyce, S., Brideau, C., Charleson, S., Cromlish, W., Ethier, D., Evans, J., Falgueyret, J.-P., Ford-Hutchinson, A.W., Gordon, R., Greig, G., Gresser, M., Guay, J., Kargman, S., Leger, S., Mancini, J.A., O'Neill, G., Ouellet, M., Rodger, I.W., Therien, M., Wang, Z., Webb, J.K., Wong, E., Xu, L., Young, R.N., Zamboni, R., Prasit, P., and Chan, C.-C. 1997. Biochemical and pharmacological profile of a tetrasubstituted furanone as a highly selective COX-2 inhibitor. Br. J. Pharmacol. 121: 105-117.
-
(1997)
Br. J. Pharmacol.
, vol.121
, pp. 105-117
-
-
Riendeau, D.1
Percival, M.D.2
Boyce, S.3
Brideau, C.4
Charleson, S.5
Cromlish, W.6
Ethier, D.7
Evans, J.8
Falgueyret, J.-P.9
Ford-Hutchinson, A.W.10
Gordon, R.11
Greig, G.12
Gresser, M.13
Guay, J.14
Kargman, S.15
Leger, S.16
Mancini, J.A.17
O'Neill, G.18
Ouellet, M.19
Rodger, I.W.20
Therien, M.21
Wang, Z.22
Webb, J.K.23
Wong, E.24
Xu, L.25
Young, R.N.26
Zamboni, R.27
Prasit, P.28
Chan, C.-C.29
more..
-
46
-
-
0027944075
-
Pharmacological and biochemical demonstration of the role of cyclooxygenase 2 in inflammation and pain
-
Seibert, K., Zhang, Y., Leahy, K., Hauser, S., Masferrer, J., Perkins, W., Lee, L., and Isakson, P. 1994. Pharmacological and biochemical demonstration of the role of cyclooxygenase 2 in inflammation and pain. Proc. Natl. Acad. Sci. U.S.A. 91: 12 013-12 017.
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 12013-12017
-
-
Seibert, K.1
Zhang, Y.2
Leahy, K.3
Hauser, S.4
Masferrer, J.5
Perkins, W.6
Lee, L.7
Isakson, P.8
-
47
-
-
0029016804
-
T-614, a novel antirheumatic drug, inhibits both the activity and induction of cyclooxygenase-2 (COX-2) in cultured fibroblasts
-
Tanaka, K., Kawasaki, H., Kurata, K., Aikawa, Y., Tsukamoto, Y., and Inaba, T. 1995. T-614, a novel antirheumatic drug, inhibits both the activity and induction of cyclooxygenase-2 (COX-2) in cultured fibroblasts. Jpn. J. Pharmacol. 67: 305-314.
-
(1995)
Jpn. J. Pharmacol.
, vol.67
, pp. 305-314
-
-
Tanaka, K.1
Kawasaki, H.2
Kurata, K.3
Aikawa, Y.4
Tsukamoto, Y.5
Inaba, T.6
-
48
-
-
0028878713
-
Gastroduodenal toxicity of different nonsteroidal antiinflammatory drugs
-
Traversa, G., Walker, A.M., Ippolito, F.M., Caffari, B., Capurso, L., Dezi, A., Koch, M., Maggini, M., Alegiani, S.S., and Raschetti, R. 1995. Gastroduodenal toxicity of different nonsteroidal antiinflammatory drugs. Epidemiology, 6: 49-54.
-
(1995)
Epidemiology
, vol.6
, pp. 49-54
-
-
Traversa, G.1
Walker, A.M.2
Ippolito, F.M.3
Caffari, B.4
Capurso, L.5
Dezi, A.6
Koch, M.7
Maggini, M.8
Alegiani, S.S.9
Raschetti, R.10
-
49
-
-
0028926813
-
New insights into the mode of action of anti-inflammatory drugs
-
Vane, J.R., and Botting, R.M. 1995. New insights into the mode of action of anti-inflammatory drugs. Inflamm. Res. 44: 1-10.
-
(1995)
Inflamm. Res.
, vol.44
, pp. 1-10
-
-
Vane, J.R.1
Botting, R.M.2
-
50
-
-
0028641257
-
The 1994 Merck Frosst Award. Mechanisms of nonsteroidal anti-inflammatory drug (NSAID) induced gastrointestinal damage - Potential for development of gastrointestinal tract safe NSAIDs
-
Wallace, J.L. 1994. The 1994 Merck Frosst Award. Mechanisms of nonsteroidal anti-inflammatory drug (NSAID) induced gastrointestinal damage - potential for development of gastrointestinal tract safe NSAIDs. Can. J. Physiol. Pharmacol. 72: 1493-1498.
-
(1994)
Can. J. Physiol. Pharmacol.
, vol.72
, pp. 1493-1498
-
-
Wallace, J.L.1
-
51
-
-
0002663215
-
Unwanted effects of aspirin and related agents on the gastrointestinal tract
-
Edited by J.R. Vane and R.M. Botting. Chapman and Hall Medical, London
-
Whittle, B.J.R. 1992. Unwanted effects of aspirin and related agents on the gastrointestinal tract. In Aspirin and other salicylates. Edited by J.R. Vane and R.M. Botting. Chapman and Hall Medical, London, pp. 465-509.
-
(1992)
Aspirin and Other Salicylates
, pp. 465-509
-
-
Whittle, B.J.R.1
-
52
-
-
0024569690
-
The pharmacological profile of CGP 28238, a highly potent anti-inflammatory compound
-
Wiesenberg-Bottcher, I., Schweizer, A., Green, J.R., Seltenmeyer, Y., and Muller, K. 1989. The pharmacological profile of CGP 28238, a highly potent anti-inflammatory compound. Agents Actions, 26: 240-242.
-
(1989)
Agents Actions
, vol.26
, pp. 240-242
-
-
Wiesenberg-Bottcher, I.1
Schweizer, A.2
Green, J.R.3
Seltenmeyer, Y.4
Muller, K.5
-
53
-
-
8044259636
-
Characterization of autocrine inducible prostaglandin H synthase-2 (PGHS-2) in human osteosarcoma cells
-
Wong, E., DeLuca, C., Boily, C., Charleson, S., Cromlish, W., Denis, D., Kargman, S., Kennedy, B.P., Ouellet, M., Skorey, K., O'Neill, G.P., Vickers, P.J., and Riendeau, D. 1997. Characterization of autocrine inducible prostaglandin H synthase-2 (PGHS-2) in human osteosarcoma cells. Inflamm. Res. 46: 51-59.
-
(1997)
Inflamm. Res.
, vol.46
, pp. 51-59
-
-
Wong, E.1
DeLuca, C.2
Boily, C.3
Charleson, S.4
Cromlish, W.5
Denis, D.6
Kargman, S.7
Kennedy, B.P.8
Ouellet, M.9
Skorey, K.10
O'Neill, G.P.11
Vickers, P.J.12
Riendeau, D.13
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