-
2
-
-
0036732019
-
The role of prostaglandin E2 receptors in the pathogenesis of rheumatoid arthritis
-
J.M. McCoy, J.R. Wicks, and L.P. Audoly The role of prostaglandin E2 receptors in the pathogenesis of rheumatoid arthritis The Journal of Clinical Investigation 110 2002 651 658
-
(2002)
The Journal of Clinical Investigation
, vol.110
, pp. 651-658
-
-
McCoy, J.M.1
Wicks, J.R.2
Audoly, L.P.3
-
6
-
-
0043261465
-
Impaired inflammatory and pain responses in mice lacking an inducible prostaglandin e synthase
-
C.E. Trebino, J.L. Stock, C.P. Gibbons, B.M. Naiman, T.S. Watchmann, J.P. Umland, K. Pandher, J.M. Lapointe, S. Saha, M.L. Roach, D. Carter, N.A. Thomas, B.A. Durtschi, J.D. McNeish, J.E. Hambor, P.J. Jakobsson, T.J. Carty, J.R. Perez, and L.P. Audoly Impaired inflammatory and pain responses in mice lacking an inducible prostaglandin E synthase Proceedings of the National Academy of Sciences of the United States of America 100 2003 9044 9049
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, pp. 9044-9049
-
-
Trebino, C.E.1
Stock, J.L.2
Gibbons, C.P.3
Naiman, B.M.4
Watchmann, T.S.5
Umland, J.P.6
Pandher, K.7
Lapointe, J.M.8
Saha, S.9
Roach, M.L.10
Carter, D.11
Thomas, N.A.12
Durtschi, B.A.13
McNeish, J.D.14
Hambor, J.E.15
Jakobsson, P.J.16
Carty, T.J.17
Perez, J.R.18
Audoly, L.P.19
-
7
-
-
0033594963
-
Identification of human prostaglandin e synthase: A microsomal, glutathione-dependent, inducible enzyme, constituting a potential novel drug target
-
P.J. Jakobsson, S. Thoren, R. Morgenstern, and B. Samuelsson Identification of human prostaglandin E synthase: a microsomal, glutathione-dependent, inducible enzyme, constituting a potential novel drug target Proceedings of the National Academy of Sciences of the United States of America 96 1999 7220 7225
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, pp. 7220-7225
-
-
Jakobsson, P.J.1
Thoren, S.2
Morgenstern, R.3
Samuelsson, B.4
-
8
-
-
49649104307
-
Structural basis for induced formation of the inflammatory mediator prostaglandin E2
-
C. Jegerschöld, S. Pawelzik, P. Purhonen, P. Bhakat, K.R. Gheorghe, N. Gyobu, K. Mitsuoka, R. Morgenstern, P. Jakobsson, and H. Hebert Structural basis for induced formation of the inflammatory mediator prostaglandin E2 Proceedings of the National Academy of Sciences of the United States of America 105 2008 11110 11115
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, pp. 11110-11115
-
-
Jegerschöld, C.1
Pawelzik, S.2
Purhonen, P.3
Bhakat, P.4
Gheorghe, K.R.5
Gyobu, N.6
Mitsuoka, K.7
Morgenstern, R.8
Jakobsson, P.9
Hebert, H.10
-
9
-
-
84874608767
-
Crystal structure of microsomal prostaglandin E2 synthase provides insight into diversity in the MAPEG superfamily
-
T. Sjögren, J. Nord, M. Ek, P. Johansson, G. Liu, and S. Geschwindner Crystal structure of microsomal prostaglandin E2 synthase provides insight into diversity in the MAPEG superfamily Proceedings of the National Academy of Sciences of the United States of America 110 2013 3806 3811
-
(2013)
Proceedings of the National Academy of Sciences of the United States of America
, vol.110
, pp. 3806-3811
-
-
Sjögren, T.1
Nord, J.2
Ek, M.3
Johansson, P.4
Liu, G.5
Geschwindner, S.6
-
10
-
-
80054891699
-
Microsomal prostaglandin e synthase-1 exhibits one-Third-Of-The-Sites reactivity
-
S. He, Y. Wu, D. Yu, and L. Lai Microsomal prostaglandin E synthase-1 exhibits one-third-of-the-sites reactivity The Biochemical Journal 440 2011 13 21
-
(2011)
The Biochemical Journal
, vol.440
, pp. 13-21
-
-
He, S.1
Wu, Y.2
Yu, D.3
Lai, L.4
-
11
-
-
34247583280
-
Synthesis and pharmacological evaluation of a selected library of new potential anti-inflammatory agents bearing the gamma-hydroxybutenolide Scaffold: A new class of inhibitors of prostanoid production through the selective modulation of microsomal prostaglandin e synthase-1 expression (mPGES-1)
-
M.D. Guerrero, M. Aquino, I. Bruno, M.C. Terencio, M. Paya, R. Riccio, and L. Gomez-Paloma Synthesis and pharmacological evaluation of a selected library of new potential anti-inflammatory agents bearing the gamma-hydroxybutenolide Scaffold: a new class of inhibitors of prostanoid production through the selective modulation of microsomal prostaglandin E synthase-1 expression (mPGES-1) Journal of Medicinal Chemistry 50 2007 2176 2184
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, pp. 2176-2184
-
-
Guerrero, M.D.1
Aquino, M.2
Bruno, I.3
Terencio, M.C.4
Paya, M.5
Riccio, R.6
Gomez-Paloma, L.7
-
12
-
-
52949144554
-
Development of a second generation of inhibitors of microsomal prostaglandin e synthase 1 expression bearing the gamma-hydroxybutenolide scaffold
-
M. Aquino, M.D. Guerrero, I. Bruno, M.C. Terencio, M. Paya, and R. Riccio Development of a second generation of inhibitors of microsomal prostaglandin E synthase 1 expression bearing the gamma-hydroxybutenolide scaffold Bioorganic & Medicinal Chemistry 16 2008 9056 9064
-
(2008)
Bioorganic & Medicinal Chemistry
, vol.16
, pp. 9056-9064
-
-
Aquino, M.1
Guerrero, M.D.2
Bruno, I.3
Terencio, M.C.4
Paya, M.5
Riccio, R.6
-
13
-
-
70349101232
-
Anti-inflammatory and analgesic activity of a novel inhibitor of microsomal prostaglandin e synthase-1 expression
-
M.D. Guerrero, M. Aquino, I. Bruno, R. Riccio, M.C. Terencio, and M. Payá Anti-inflammatory and analgesic activity of a novel inhibitor of microsomal prostaglandin E synthase-1 expression European Journal of Pharmacology 620 2009 112 119
-
(2009)
European Journal of Pharmacology
, vol.620
, pp. 112-119
-
-
Guerrero, M.D.1
Aquino, M.2
Bruno, I.3
Riccio, R.4
Terencio, M.C.5
Payá, M.6
-
14
-
-
77952961509
-
Toward the discovery of new agents able to inhibit the expression of microsomal prostaglandin e synthase-1 enzyme as promising tools in drug development
-
R. De Simone, R.M. Andres, M. Aquino, I. Bruno, M.D. Guerrero, M.C. Terencio, M. Paya, and R. Riccio Toward the discovery of new agents able to inhibit the expression of microsomal prostaglandin E synthase-1 enzyme as promising tools in drug development Chemical Biology & Drug Design 76 2010 17 24
-
(2010)
Chemical Biology & Drug Design
, vol.76
, pp. 17-24
-
-
De Simone, R.1
Andres, R.M.2
Aquino, M.3
Bruno, I.4
Guerrero, M.D.5
Terencio, M.C.6
Paya, M.7
Riccio, R.8
-
15
-
-
79952788439
-
Structure-based discovery of inhibitors of microsomal prostaglandin E2 synthase-1, 5-lipoxygenase and 5-lipoxygenase-activating protein: Promising hits for the development of new anti-inflammatory agents
-
R. De Simone, M.G. Chini, I. Bruno, R. Riccio, D. Mueller, O. Werz, and G. Bifulco Structure-based discovery of inhibitors of microsomal prostaglandin E2 synthase-1, 5-lipoxygenase and 5-lipoxygenase-activating protein: promising hits for the development of new anti-inflammatory agents Journal of Medicinal Chemistry 54 2011 1565 1575
-
(2011)
Journal of Medicinal Chemistry
, vol.54
, pp. 1565-1575
-
-
De Simone, R.1
Chini, M.G.2
Bruno, I.3
Riccio, R.4
Mueller, D.5
Werz, O.6
Bifulco, G.7
-
16
-
-
84864443266
-
Identification of new γ-hydroxybutenolides that preferentially inhibit the activity of mPGES-1
-
R. De Simone, I. Bruno, R. Riccio, K. Stadler, J. Bauer, A.M. Schaible, S. Laufer, and O. Werz Identification of new γ-hydroxybutenolides that preferentially inhibit the activity of mPGES-1 Bioorganic & Medicinal Chemistry 20 2012 5012 5016
-
(2012)
Bioorganic & Medicinal Chemistry
, vol.20
, pp. 5012-5016
-
-
De Simone, R.1
Bruno, I.2
Riccio, R.3
Stadler, K.4
Bauer, J.5
Schaible, A.M.6
Laufer, S.7
Werz, O.8
-
17
-
-
84864408638
-
Design and synthesis of a second series of triazole-based compounds as potent dual mPGES-1 and 5-lipoxygenase inhibitors
-
M.G. Chini, R. De Simone, I. Bruno, R. Riccio, F. Dehm, C. Weinigel, D. Barz, O. Werz, and G. Bifulco Design and synthesis of a second series of triazole-based compounds as potent dual mPGES-1 and 5-lipoxygenase inhibitors European Journal of Medicinal Chemistry 54 2012 311 323
-
(2012)
European Journal of Medicinal Chemistry
, vol.54
, pp. 311-323
-
-
Chini, M.G.1
De Simone, R.2
Bruno, I.3
Riccio, R.4
Dehm, F.5
Weinigel, C.6
Barz, D.7
Werz, O.8
Bifulco, G.9
-
18
-
-
14644388180
-
Creating chemical diversity space by scaffold decoration of dihydropyrimidines
-
D. Dallinger, and C.O. Kappe Creating chemical diversity space by scaffold decoration of dihydropyrimidines Pure and Applied Chemistry 77 2005 155 161
-
(2005)
Pure and Applied Chemistry
, vol.77
, pp. 155-161
-
-
Dallinger, D.1
Kappe, C.O.2
-
19
-
-
0034519777
-
Biologically active dihydropyrimidones of the Biginelli - Type-A literature survey
-
C.O. Kappe Biologically active dihydropyrimidones of the Biginelli - type-a literature survey European Journal of Medicinal Chemistry 35 2000 1043 1052
-
(2000)
European Journal of Medicinal Chemistry
, vol.35
, pp. 1043-1052
-
-
Kappe, C.O.1
-
20
-
-
84555169343
-
Molecular docking and competitive binding study discovered different binding modes of microsomal prostaglandin e synthase-1 inhibitors
-
S. He, and L. Lai Molecular docking and competitive binding study discovered different binding modes of microsomal prostaglandin E synthase-1 inhibitors Journal of Chemical Information and Modeling 51 2011 3254 3261
-
(2011)
Journal of Chemical Information and Modeling
, vol.51
, pp. 3254-3261
-
-
He, S.1
Lai, L.2
-
21
-
-
34249932286
-
5-Aroyl-3,4-dihydropyrimidin-2-one library generation via automated sequential and parallel microwave-assisted synthesis techniques
-
L. Pisani, H. Prokopcovà, J.M. Kremsner, and C.O. Kappe 5-Aroyl-3,4-dihydropyrimidin-2-one library generation via automated sequential and parallel microwave-assisted synthesis techniques Journal of Combinatorial Chemistry 9 2007 415 421
-
(2007)
Journal of Combinatorial Chemistry
, vol.9
, pp. 415-421
-
-
Pisani, L.1
Prokopcovà, H.2
Kremsner, J.M.3
Kappe, C.O.4
-
22
-
-
0001260317
-
Automated library generation using sequential microwave-assisted chemistry. Application toward the Biginelli multicomponent condensation
-
A. Stadler, and C.O. Kappe Automated library generation using sequential microwave-assisted chemistry. Application toward the Biginelli multicomponent condensation Journal of Combinatorial Chemistry 3 2001 624 630
-
(2001)
Journal of Combinatorial Chemistry
, vol.3
, pp. 624-630
-
-
Stadler, A.1
Kappe, C.O.2
-
23
-
-
52649119793
-
Licofelone suppresses prostaglandin E2 formation by interference with the inducible microsomal prostaglandin E2 synthase-1
-
A. Koeberle, U. Siemoneit, U. Buehring, H. Northoff, S. Laufer, W. Albrecht, and O. Werz Licofelone suppresses prostaglandin E2 formation by interference with the inducible microsomal prostaglandin E2 synthase-1 The Journal of Pharmacology and Experimental Therapeutics 326 2008 975 982
-
(2008)
The Journal of Pharmacology and Experimental Therapeutics
, vol.326
, pp. 975-982
-
-
Koeberle, A.1
Siemoneit, U.2
Buehring, U.3
Northoff, H.4
Laufer, S.5
Albrecht, W.6
Werz, O.7
-
24
-
-
84899880603
-
-
LLC, New York, NY
-
Schroedinger, LLC, New York, NY, 2013.
-
(2013)
Schroedinger
-
-
-
25
-
-
80053512597
-
Open Babel: An open chemical toolbox
-
N.M. O'Boyle, M. Banck, C.A. James, C. Morley, T. Vandermeersch, and G.R. Hutchison Open Babel: an open chemical toolbox Journal of Cheminformatics 3 2011 33
-
(2011)
Journal of Cheminformatics
, vol.3
, pp. 33
-
-
O'Boyle, N.M.1
Banck, M.2
James, C.A.3
Morley, C.4
Vandermeersch, T.5
Hutchison, G.R.6
-
26
-
-
76149120388
-
AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization and multithreading
-
O. Trott, and A.J. Olson AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization and multithreading Journal of Computational Chemistry 31 2010 455 461
-
(2010)
Journal of Computational Chemistry
, vol.31
, pp. 455-461
-
-
Trott, O.1
Olson, A.J.2
-
28
-
-
58149097590
-
Pirinixic acid derivatives as novel dual inhibitors of microsomal prostaglandin E2 synthase-1 and 5-lipoxygenase
-
A. Koeberle, H. Zettl, C. Greiner, M. Wurglics, M. Schubert-Zsilavecz, and O. Werz Pirinixic acid derivatives as novel dual inhibitors of microsomal prostaglandin E2 synthase-1 and 5-lipoxygenase Journal of Medicinal Chemistry 51 2008 8068 8076
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, pp. 8068-8076
-
-
Koeberle, A.1
Zettl, H.2
Greiner, C.3
Wurglics, M.4
Schubert-Zsilavecz, M.5
Werz, O.6
|