-
1
-
-
0015237263
-
Indomethacin and aspirin abolish prostaglandin release from the spleen
-
Ferreira, S.H., Moncada, S., and Vane, J.R. (1971) Indomethacin and aspirin abolish prostaglandin release from the spleen. Nat. New. Biol. 231, 237-239
-
(1971)
Nat. New. Biol.
, vol.231
, pp. 237-239
-
-
Ferreira, S.H.1
Moncada, S.2
Vane, J.R.3
-
2
-
-
0015150481
-
Stimulation and blockade of prostaglandin biosynthesis
-
Smith, W.L. and Lands, W.E. (1971) Stimulation and blockade of prostaglandin biosynthesis. J. Biol. Chem. 246, 6700-6702
-
(1971)
J. Biol. Chem.
, vol.246
, pp. 6700-6702
-
-
Smith, W.L.1
Lands, W.E.2
-
4
-
-
0035829592
-
A subset of NSAIDs lower amyloidogenic Aβ42 independently of cyclooxygenase activity
-
Weggen, S., Eriksen, J.L., Das, P., Sagi, S.A., Wang, R., Pietrzik, C.U., Findlay, K.A., Smith, T.E., Murphy, M.P., Bulter, T., Kang, D.E., Marquez-Sterling, N., Golde, T.E., and Koo, E.H. (2001) A subset of NSAIDs lower amyloidogenic Aβ42 independently of cyclooxygenase activity. Nature 414, 212-216
-
(2001)
Nature
, vol.414
, pp. 212-216
-
-
Weggen, S.1
Eriksen, J.L.2
Das, P.3
Sagi, S.A.4
Wang, R.5
Pietrzik, C.U.6
Findlay, K.A.7
Smith, T.E.8
Murphy, M.P.9
Bulter, T.10
Kang, D.E.11
Marquez-Sterling, N.12
Golde, T.E.13
Koo, E.H.14
-
5
-
-
0031013395
-
Peroxisome proliferator-activated receptors α and γ are activated by indomethacin and other non-steroidal anti-inflammatory drugs
-
Lehmann, J.M., Lenhard, J.M., Oliver, B.B., Ringold, G.M., and Kliewer, S.A. (1997) Peroxisome proliferator-activated receptors α and γ are activated by indomethacin and other non-steroidal anti-inflammatory drugs. J. Biol. Chem. 272, 3406-3410
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 3406-3410
-
-
Lehmann, J.M.1
Lenhard, J.M.2
Oliver, B.B.3
Ringold, G.M.4
Kliewer, S.A.5
-
6
-
-
0035060429
-
Cyclooxygenase inhibitors regulate the expression of a TGF-β superfamily member that has proapoptotic and antitumorigenic activities
-
Baek, S.J., Kim, K.S., Nixon, J.B., Wilson, L.C., and Eling, T.E. (2001) Cyclooxygenase inhibitors regulate the expression of a TGF-β superfamily member that has proapoptotic and antitumorigenic activities. Mol. Pharmacol. 59, 901-908
-
(2001)
Mol. Pharmacol.
, vol.59
, pp. 901-908
-
-
Baek, S.J.1
Kim, K.S.2
Nixon, J.B.3
Wilson, L.C.4
Eling, T.E.5
-
8
-
-
0031759084
-
2 11-ketoreductase activity
-
2 11-ketoreductase activity. J. Biochem. 124, 940-946
-
(1998)
J. Biochem.
, vol.124
, pp. 940-946
-
-
Matsuura, K.1
Shiraishi, H.2
Hara, A.3
Sato, K.4
Deyashiki, Y.5
Ninomiya, M.6
Sakai, S.7
-
9
-
-
18044367744
-
Crystal structure and possible catalytic mechanism of microsomal prostaglandin E synthase type 2 (mPGES-2)
-
Yamada, T., Komoto, J., Watanabe, K., Ohmiya, Y., and Takusagawa, F. (2005) Crystal structure and possible catalytic mechanism of microsomal prostaglandin E synthase type 2 (mPGES-2). J. Mol. Biol. 348, 1163-1176
-
(2005)
J. Mol. Biol.
, vol.348
, pp. 1163-1176
-
-
Yamada, T.1
Komoto, J.2
Watanabe, K.3
Ohmiya, Y.4
Takusagawa, F.5
-
10
-
-
0028802627
-
Differential activation of peroxisome proliferator-activated receptors by eicosanoids
-
Yu, K., Bayona, W., Kallen, C.B., Harding, H.P., Ravera, C.P., McMahon, G., Brown, M., and Lazar, M.A. (1995) Differential activation of peroxisome proliferator-activated receptors by eicosanoids. J. Biol. Chem. 270, 23975-23983
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 23975-23983
-
-
Yu, K.1
Bayona, W.2
Kallen, C.B.3
Harding, H.P.4
Ravera, C.P.5
McMahon, G.6
Brown, M.7
Lazar, M.A.8
-
11
-
-
0036467346
-
2 receptor, CRTH2
-
2 receptor, CRTH2. J. Immunol. 168, 981-985
-
(2002)
J. Immunol.
, vol.168
, pp. 981-985
-
-
Hirai, H.1
Tanaka, K.2
Takano, S.3
Ichimasa, M.4
Nakamura, M.5
Nagata, K.6
-
14
-
-
0027198335
-
4 by a novel enzyme found in the porcine kidney
-
4 by a novel enzyme found in the porcine kidney. J. Biol. Chem. 268, 18128-18135
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 18128-18135
-
-
Yokomizo, T.1
Izumi, T.2
Takahashi, T.3
Kasama, T.4
Kobayashi, Y.5
Sato, F.6
Taketani, Y.7
Shimizu, T.8
-
15
-
-
0032519441
-
Purification, cDNA cloning and expression of 15-oxoprostaglandin 13-reductase from pig lung
-
Ensor, C.M., Zhang, H., and Tai, H.H. (1998) Purification, cDNA cloning and expression of 15-oxoprostaglandin 13-reductase from pig lung. Biochem. J. 330, 103-108
-
(1998)
Biochem. J.
, vol.330
, pp. 103-108
-
-
Ensor, C.M.1
Zhang, H.2
Tai, H.H.3
-
17
-
-
2542479700
-
4 12-hydroxydehydrogenase/15- oxo-prostaglandin 13-reductase catalytic mechanism and a possible Src homology 3 domain binding loop
-
4 12-hydroxydehydrogenase/15-oxo-prostaglandin 13-reductase catalytic mechanism and a possible Src homology 3 domain binding loop. J. Biol. Chem. 279, 22615-22623
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 22615-22623
-
-
Hori, T.1
Yokomizo, T.2
Ago, H.3
Sugahara, M.4
Ueno, G.5
Yamamoto, M.6
Kumasaka, T.7
Shimizu, T.8
Miyano, M.9
-
18
-
-
0036779617
-
Anti-inflammatory lipid mediators and insights into the resolution of inflammation
-
Lawrence, T., Willoughby, D.A., and Gilroy, D.W. (2002) Anti-inflammatory lipid mediators and insights into the resolution of inflammation. Nat. Rev. Immunol. 2, 787-795
-
(2002)
Nat. Rev. Immunol.
, vol.2
, pp. 787-795
-
-
Lawrence, T.1
Willoughby, D.A.2
Gilroy, D.W.3
-
20
-
-
0042574211
-
Dual inhibition of cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX) as a new strategy to provide safer non-steroidal anti-inflammatory drugs
-
Charlier, C. and Michaux, C. (2003) Dual inhibition of cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX) as a new strategy to provide safer non-steroidal anti-inflammatory drugs. Eur. J. Med. Chem. 38, 645-659
-
(2003)
Eur. J. Med. Chem.
, vol.38
, pp. 645-659
-
-
Charlier, C.1
Michaux, C.2
-
21
-
-
0034916569
-
Lipid mediator class switching during acute inflammation: Signals in resolution
-
Levy, B.D., Clish, C.B., Schmidt, B., Gronert, K., and Serhan, C.N. (2001) Lipid mediator class switching during acute inflammation: signals in resolution. Nat. Immunol. 2, 612-619
-
(2001)
Nat. Immunol.
, vol.2
, pp. 612-619
-
-
Levy, B.D.1
Clish, C.B.2
Schmidt, B.3
Gronert, K.4
Serhan, C.N.5
-
22
-
-
1842866520
-
Trichromatic concept optimizes MAD experiments in synchrotron X-ray crystallography
-
Kumasaka, T., Yamamoto, M., Yamashita, E., Moriyama, H., and Ueki, T. (2002) Trichromatic concept optimizes MAD experiments in synchrotron X-ray crystallography. Structure 10, 1205-1210
-
(2002)
Structure
, vol.10
, pp. 1205-1210
-
-
Kumasaka, T.1
Yamamoto, M.2
Yamashita, E.3
Moriyama, H.4
Ueki, T.5
-
23
-
-
0031059866
-
Processing of x-ray diffraction data collected in oscillation mode
-
Otwinowski, Z. and Minor, W. (1997) Processing of x-ray diffraction data collected in oscillation mode. Methods Enzymol. 276, 307-326
-
(1997)
Methods Enzymol.
, vol.276
, pp. 307-326
-
-
Otwinowski, Z.1
Minor, W.2
-
24
-
-
3543012707
-
Crystallography & NMR system: A new software suite for macromolecular structure determination
-
Brunger, A.T., Adams, P.D., Clore, G.M., DeLano, W.L., Gros, P., Grosse-Kunstleve, R.W., Jiang, J.S., Kuszewski, J., Nilges, M., Pannu, N.S., Read, R.J., Rice, L.M., Simonson, T., and Warren, G.L. (1998) Crystallography & NMR system: A new software suite for macromolecular structure determination. Acta Crystallogr. Sect. D 54, 905-921
-
(1998)
Acta Crystallogr. Sect. D
, vol.54
, pp. 905-921
-
-
Brunger, A.T.1
Adams, P.D.2
Clore, G.M.3
DeLano, W.L.4
Gros, P.5
Grosse-Kunstleve, R.W.6
Jiang, J.S.7
Kuszewski, J.8
Nilges, M.9
Pannu, N.S.10
Read, R.J.11
Rice, L.M.12
Simonson, T.13
Warren, G.L.14
-
25
-
-
0003630244
-
1-(4-iodobenzoyl)-5-methoxy-2-methyl-3-indoleacetic acid, an iodinated indomethacin analog
-
Loll, P.J., Garavito, R.M., Carrell, C.J., and Carrell, H.L. (1996) 1-(4-iodobenzoyl)-5-methoxy-2-methyl-3-indoleacetic acid, an iodinated indomethacin analog. Acta. Crystallogr. Sect. C 52, 455-157
-
(1996)
Acta. Crystallogr. Sect. C
, vol.52
, pp. 455-1157
-
-
Loll, P.J.1
Garavito, R.M.2
Carrell, C.J.3
Carrell, H.L.4
-
26
-
-
84889120137
-
Improved methods for building protein models in electron density maps and the location of errors in these models
-
Jones, T.A., Zou, J.Y., Cowan, S.W., and Kjeldgaard, M. (1991) Improved methods for building protein models in electron density maps and the location of errors in these models. Acta Crystallogr. Sect. A 47, 110-119
-
(1991)
Acta Crystallogr. Sect. A
, vol.47
, pp. 110-119
-
-
Jones, T.A.1
Zou, J.Y.2
Cowan, S.W.3
Kjeldgaard, M.4
-
27
-
-
0030924992
-
Refinement of macromolecular structures by the maximum-likelihood method
-
Murshudov, G.N., Vagin, A.A., and Dodson, E.J. (1997) Refinement of macromolecular structures by the maximum-likelihood method. Acta Crystallogr. Sect. D 53, 240-255
-
(1997)
Acta Crystallogr. Sect. D
, vol.53
, pp. 240-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Dodson, E.J.3
-
28
-
-
0026244229
-
MOLSCRIPT: A program to produce both detailed and schematic plots of protein structures
-
Kraulis, P.J. (1991) MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures. J. Appl. Crystallogr. 24, 946-950
-
(1991)
J. Appl. Crystallogr.
, vol.24
, pp. 946-950
-
-
Kraulis, P.J.1
-
29
-
-
0030729838
-
An extensively modified version of MolScript that includes greatly enhanced coloring capabilities
-
Esnouf, R.M. (1997) An extensively modified version of MolScript that includes greatly enhanced coloring capabilities. J. Mol. Graph. 15, 132-134
-
(1997)
J. Mol. Graph.
, vol.15
, pp. 132-134
-
-
Esnouf, R.M.1
-
30
-
-
0030815133
-
Raster 3D: Photorealistic molecular graphics
-
Merrit, E.A. and Bacon, D.J. (1997) Raster 3D: Photorealistic molecular graphics. Methods Enzymol. 277, 505-524
-
(1997)
Methods Enzymol.
, vol.277
, pp. 505-524
-
-
Merrit, E.A.1
Bacon, D.J.2
-
31
-
-
11744374008
-
Dimerization energetics of benzene and aromatic amino acid side chains
-
Burley, S.K. and Petsko, G.A. (1986) Dimerization energetics of benzene and aromatic amino acid side chains. J. Am. Chem. Soc. 108, 7995-8001
-
(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 7995-8001
-
-
Burley, S.K.1
Petsko, G.A.2
-
32
-
-
1842763826
-
Unrolling the hydrogen bond properties of C-H⋯O interactions
-
Steiner, T. (1997) Unrolling the hydrogen bond properties of C-H⋯O interactions. Chem. Commun. 727-734
-
(1997)
Chem. Commun.
, pp. 727-734
-
-
Steiner, T.1
-
33
-
-
0030461132
-
Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents
-
Kurumbail, R.G., Stevens, A.M., Gierse, J.K., McDonald, J.J., Stegeman, R.A., Pak, J.Y., Gildehaus, D., Miyashiro, J.M., Penning, T.D., Seibert, K., Isakson, P.C., and Stallings, W.C. (1996) Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents. Nature 384, 644-648
-
(1996)
Nature
, vol.384
, pp. 644-648
-
-
Kurumbail, R.G.1
Stevens, A.M.2
Gierse, J.K.3
McDonald, J.J.4
Stegeman, R.A.5
Pak, J.Y.6
Gildehaus, D.7
Miyashiro, J.M.8
Penning, T.D.9
Seibert, K.10
Isakson, P.C.11
Stallings, W.C.12
-
35
-
-
16744369033
-
Structural insights into the stereochemistry of the cyclooxygenase reaction
-
Kiefer, J.R., Pawlitz, J.L., Moreland, K.T., Stegeman, R.A., Hood, W.F., Gierse, J.K., Stevens, A.M., Goodwin, D.C., Rowlinson, S.W., Marnett, L.J., Stallings, W.O., and Kurumbail, R.G. (2000) Structural insights into the stereochemistry of the cyclooxygenase reaction. Nature 405, 97-101
-
(2000)
Nature
, vol.405
, pp. 97-101
-
-
Kiefer, J.R.1
Pawlitz, J.L.2
Moreland, K.T.3
Stegeman, R.A.4
Hood, W.F.5
Gierse, J.K.6
Stevens, A.M.7
Goodwin, D.C.8
Rowlinson, S.W.9
Marnett, L.J.10
Stallings, W.O.11
Kurumbail, R.G.12
-
36
-
-
0030063502
-
The kinetic factors that determine the affinity and selectivity for slow binding inhibition of human prostaglandin H synthase 1 and 2 by indomethacin and flurbiprofen
-
Callan, O.K., So, O.Y., and Swinney, D.C. (1996) The kinetic factors that determine the affinity and selectivity for slow binding inhibition of human prostaglandin H synthase 1 and 2 by indomethacin and flurbiprofen. J. Biol. Chem. 271, 3548-3554
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 3548-3554
-
-
Callan, O.K.1
So, O.Y.2
Swinney, D.C.3
-
37
-
-
0028783912
-
Arginine 120 of prostaglandin G/H synthase-1 is required for the inhibition by nonsteroidal antiinflammatory drugs containing a carboxylic acid moiety
-
Mancini, J.A., Riendeau, D., Falgueyret, J.P., Vickers, P.J., and O'Neill, G.P. (1995) Arginine 120 of prostaglandin G/H synthase-1 is required for the inhibition by nonsteroidal antiinflammatory drugs containing a carboxylic acid moiety. J. Biol. Chem. 270, 29372-29377
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 29372-29377
-
-
Mancini, J.A.1
Riendeau, D.2
Falgueyret, J.P.3
Vickers, P.J.4
O'Neill, G.P.5
-
38
-
-
0242580725
-
A novel mechanism of cyclooxygenase-2 inhibition involving interactions with Ser-530 and Tyr-385
-
Rowlinson, S.W., Kiefer, J.R., Prusakiewicz, J.J., Pawlitz, J.L., Kozak, K.R., Kalgutkar, A.S., Stallings, W.C., Kurumbail, R.G., and Marnett, L.J. (2003) A novel mechanism of cyclooxygenase-2 inhibition involving interactions with Ser-530 and Tyr-385. J. Biol. Chem. 278, 45763-45769
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 45763-45769
-
-
Rowlinson, S.W.1
Kiefer, J.R.2
Prusakiewicz, J.J.3
Pawlitz, J.L.4
Kozak, K.R.5
Kalgutkar, A.S.6
Stallings, W.C.7
Kurumbail, R.G.8
Marnett, L.J.9
-
39
-
-
0034681109
-
Biochemically based design of cyclooxygenase-2 (COX-2) inhibitors: Facile conversion of nonsteroidal antiinflammatory drugs to potent and highly selective COX-2 inhibitors
-
Kalgutkar, A.S., Crews, B.C., Rowlinson, S.W., Marnett, A.B., Kozak, K.R., Remmel, R.P., and Marnett, L.J. (2000) Biochemically based design of cyclooxygenase-2 (COX-2) inhibitors: facile conversion of nonsteroidal antiinflammatory drugs to potent and highly selective COX-2 inhibitors. Proc. Natl. Acad. Sci. USA 97, 925-930
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 925-930
-
-
Kalgutkar, A.S.1
Crews, B.C.2
Rowlinson, S.W.3
Marnett, A.B.4
Kozak, K.R.5
Remmel, R.P.6
Marnett, L.J.7
-
40
-
-
1442276491
-
Crystal structure of human prostaglandin F synthase (AKR1C3)
-
Komoto, J., Yamada, T., Watanabe, K., and Takusagawa, F. (2004) Crystal structure of human prostaglandin F synthase (AKR1C3). Biochemistry 43, 2188-2198
-
(2004)
Biochemistry
, vol.43
, pp. 2188-2198
-
-
Komoto, J.1
Yamada, T.2
Watanabe, K.3
Takusagawa, F.4
-
41
-
-
1642540579
-
Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: New pharmacological opportunities due to related binding site recognition
-
Weber, A., Casini, A., Heine, A., Kuhn, D., Supuran, C.T., Scozzafava, A., and Klebe, G. (2004) Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: new pharmacological opportunities due to related binding site recognition. J. Med. Chem. 47, 550-557
-
(2004)
J. Med. Chem.
, vol.47
, pp. 550-557
-
-
Weber, A.1
Casini, A.2
Heine, A.3
Kuhn, D.4
Supuran, C.T.5
Scozzafava, A.6
Klebe, G.7
-
42
-
-
0037132622
-
Reactivity differences of indomethacin solid forms with ammonia gas
-
Chen, X., Morris, K.R., Griesser, U.J., Byrn, S.R., and Stowell, J.G. (2002) Reactivity differences of indomethacin solid forms with ammonia gas. J. Am. Chem. Soc. 124, 15012-15019
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 15012-15019
-
-
Chen, X.1
Morris, K.R.2
Griesser, U.J.3
Byrn, S.R.4
Stowell, J.G.5
|