-
1
-
-
0015237292
-
Inhibition of Prostaglandin Synthesis as a Mechanism of Action for Aspirin-Like Drugs
-
(a) Vane, J. R. Inhibition of Prostaglandin Synthesis as a Mechanism of Action for Aspirin-Like Drugs. Nature (New Biol.) 1971, 231, 232-235.
-
(1971)
Nature (New Biol.)
, vol.231
, pp. 232-235
-
-
Vane, J.R.1
-
2
-
-
0015237275
-
Aspirin Selectivity Inhibits Prostaglandin Production in Human Platelets
-
(b) Smith, J. B.; Willis, A. L. Aspirin Selectivity Inhibits Prostaglandin Production in Human Platelets. Nature (New Biol.) 1971, 231, 235-237.
-
(1971)
Nature (New Biol.)
, vol.231
, pp. 235-237
-
-
Smith, J.B.1
Willis, A.L.2
-
3
-
-
0026788165
-
Gastrointestinal Damage Associated wiith the Use of Nonsteroidal Antiinflammatory Drugs
-
(a) Allison, M. C.; Howatson, A. G.; Torrence, C. J.; Lee, F. D.; Russel, R. I. Gastrointestinal Damage Associated wiith the Use of Nonsteroidal Antiinflammatory Drugs. N. Engl. J. Med. 1992, 327, 749-754.
-
(1992)
N. Engl. J. Med.
, vol.327
, pp. 749-754
-
-
Allison, M.C.1
Howatson, A.G.2
Torrence, C.J.3
Lee, F.D.4
Russel, R.I.5
-
4
-
-
0023031955
-
Prostaglandins in Peptic Ulcer Disease. An Overview of Current Status and Future Directions
-
(b) Sontag, S. J. Prostaglandins in Peptic Ulcer Disease. An Overview of Current Status and Future Directions. Drugs 1986, 32, 445-457.
-
(1986)
Drugs
, vol.32
, pp. 445-457
-
-
Sontag, S.J.1
-
5
-
-
0023178776
-
The Clinical Significance of Inhibition of Renal Prostaglandin Synthesis
-
(c) Patrono, C.; Dunn, M. J. The Clinical Significance of Inhibition of Renal Prostaglandin Synthesis. Kidney Int. 1987, 32, 1-12.
-
(1987)
Kidney Int.
, vol.32
, pp. 1-12
-
-
Patrono, C.1
Dunn, M.J.2
-
7
-
-
0025754779
-
Expression of a Mitogen-Response Gene Encoding Prostaglandin Synthase is Regulated by mRNA Splicing
-
Xie, W.; Chipman, J. G.; Robertson, D. L.; Erikson, R. L.; Simmons, D. L. Expression of a Mitogen-Response Gene Encoding Prostaglandin Synthase is Regulated by mRNA Splicing. Proc. Natl. Acad. Sci. U.S.A. 1991, 88, 2692-2696.
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, pp. 2692-2696
-
-
Xie, W.1
Chipman, J.G.2
Robertson, D.L.3
Erikson, R.L.4
Simmons, D.L.5
-
8
-
-
0025871150
-
TIS10, a Phorbol Ester Tumor Promoter-Inducible mRNA from Swiss 3T3 Cells, Encodes a Novel Prostaglandin Synthase/Cyclooxygenase Homologue
-
Kujubu, D. A.; Fletcher, B. S.; Varnum, B. C.; Lim, R. W.; Herschman, H. R. TIS10, a Phorbol Ester Tumor Promoter-Inducible mRNA From Swiss 3T3 Cells, Encodes a Novel Prostaglandin Synthase/Cyclooxygenase Homologue. J. Biol. Chem. 1991, 266, 12866-12872.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 12866-12872
-
-
Kujubu, D.A.1
Fletcher, B.S.2
Varnum, B.C.3
Lim, R.W.4
Herschman, H.R.5
-
9
-
-
0028322893
-
Selective Inhibition of Inducible Cyclooxygenase-2 in Vivo is Antiinflammatory and Nonulcerogenic
-
(a) Masferrer, J. L.; Zweifel, B. S.; Manning, P. T.; Hauser, S. D.; Leahey, K. M.; Smith, W. G.; Isakson, P. C.; Seibert, K. Selective Inhibition of Inducible Cyclooxygenase-2 In Vivo is Antiinflammatory and Nonulcerogenic. Proc. Natl. Acad. Sci. U.S.A. 1994, 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
Leahey, K.M.5
Smith, W.G.6
Isakson, P.C.7
Seibert, K.8
-
10
-
-
0028399309
-
Role of Inducuble Cyclooxygenase (COX-2) in Inflammation
-
(b) Seibert, K.; Masferrer, J. L. Role of Inducuble Cyclooxygenase (COX-2) in Inflammation. Receptor 1994, 4, 17-23.
-
(1994)
Receptor
, vol.4
, pp. 17-23
-
-
Seibert, K.1
Masferrer, J.L.2
-
11
-
-
0027480087
-
Differential Inhibition of Prostaglandin Endoperoxide Synthase (Cyclooxygenase) Isozymes by Aspirin and Other Nonsteroidal Antiinflammatory Drugs
-
(a) Meade, E. A.; Smith, W. L.; DeWitt, D. L. Differential Inhibition of Prostaglandin Endoperoxide Synthase (Cyclooxygenase) Isozymes by Aspirin and Other Nonsteroidal Antiinflammatory Drugs. J. Biol. Chem. 1993, 268, 6610-6614.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 6610-6614
-
-
Meade, E.A.1
Smith, W.L.2
DeWitt, D.L.3
-
12
-
-
0027146692
-
Selectivity of Nonsteroidal Antiinflammatory Drugs as Inhibitors of Constitutive and Inducible Cyclooxygenase
-
(b) Mitchell, J. A.; Akarasereemont, P.; Thiemerman, C.; Flower, R. J.; Vane, J. R. Selectivity of Nonsteroidal Antiinflammatory Drugs as Inhibitors of Constitutive and Inducible Cyclooxygenase. Proc. Natl. Acad. Sci. U.S.A. 1993, 90, 11693-11697.
-
(1993)
Proc. Natl. Acad. Sci. U.S.A.
, vol.90
, pp. 11693-11697
-
-
Mitchell, J.A.1
Akarasereemont, P.2
Thiemerman, C.3
Flower, R.J.4
Vane, J.R.5
-
13
-
-
0028323295
-
Inducible Isoforms of Cyclooxygenase and Nitric-Oxide Synthase in Inflammation
-
(c) Vane, J. R.; Mitchell, J. A.; Appleton, I.; Tomlinson, A.; Bishop-Bailey, D.; Croxtail, J.; Willoughby, D. A. Inducible Isoforms of Cyclooxygenase and Nitric-Oxide Synthase in Inflammation. Proc. Natl. Acad. Sci. U.S.A. 1994, 91, 2046-2050.
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 2046-2050
-
-
Vane, J.R.1
Mitchell, J.A.2
Appleton, I.3
Tomlinson, A.4
Bishop-Bailey, D.5
Croxtail, J.6
Willoughby, D.A.7
-
14
-
-
0028278018
-
Detection of Inducible Prostaglandin H Synthase-2 in cells in the Exudate of Rat Carrageenan Induced Pleurisy
-
Harada, Y.; Hatanaka, K.; Saito, M.; Majima, M.; Ogina, M.; Kawamura, M.; Ohno, T.; Yang, Q.; Katori, M.; Yamamoto, S. Detection of Inducible Prostaglandin H Synthase-2 in cells in the Exudate of Rat Carrageenan Induced Pleurisy. Biomed. Res. 1994, 15, 127-130.
-
(1994)
Biomed. Res.
, vol.15
, pp. 127-130
-
-
Harada, Y.1
Hatanaka, K.2
Saito, M.3
Majima, M.4
Ogina, M.5
Kawamura, M.6
Ohno, T.7
Yang, Q.8
Katori, M.9
Yamamoto, S.10
-
15
-
-
0025160887
-
Antiinflammatory 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.; Hewews, W. E.; Ackerman, N. R. Antiinflammatory and Safety Profile of DuP 697, A Novel Orally Effective Prostaglandin Synthesis Inhibitor. J. Pharmacol. Exp. Ther. 1990, 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
Hewews, W.E.8
Ackerman, N.R.9
-
16
-
-
26844542187
-
Synthesis and Biological Evaluation of 1,5-Diarylpyrazole Class of Cyclooxygenase-2 Inhibitors: Identification of SC-58635 (Celecoxib)
-
Submitted
-
Penning, T. D.; Talley, J. J.; Bertenshaw, S. R.; Carter, J. S.; Collins, P. W.; Docter, S.; Graneto, M. J.; Lee, L. F.; Malecha, J. W.; Miyashiro, J. M.; Rogers, R. S.; Rogier, D. J.; Yu, S. S.; Anderson, G. D.; Cogburn, J. N.; Gregory, S. A.; Koboldt, C. M.; Perkins, W. E.; Seibert, K.; Veenhuizen, A. W.; Zhang, Y. Y.; Isakson, P. C. Synthesis and Biological Evaluation of 1,5-Diarylpyrazole Class of Cyclooxygenase-2 Inhibitors: Identification of SC-58635 (Celecoxib). Submitted to Chem.
-
Chem.
-
-
Penning, T.D.1
Talley, J.J.2
Bertenshaw, S.R.3
Carter, J.S.4
Collins, P.W.5
Docter, S.6
Graneto, M.J.7
Lee, L.F.8
Malecha, J.W.9
Miyashiro, J.M.10
Rogers, R.S.11
Rogier, D.J.12
Yu, S.S.13
Anderson, G.D.14
Cogburn, J.N.15
Gregory, S.A.16
Koboldt, C.M.17
Perkins, W.E.18
Seibert, K.19
Veenhuizen, A.W.20
Zhang, Y.Y.21
Isakson, P.C.22
more..
-
17
-
-
0027944191
-
Selective Cyclooxygenase Inhibitors: Novel 1,2-Diarylcyclopentenes are Potent and Orally Active COX-2 Inhibitors
-
(a) Reitz, D. B.; Li, J J.; Norton, M. B.; Reinhard, E. J.; Collins, J. T.; Anderson, G. D.; Gregory, S.; Koboldt, C. M.; Perkins, W. E.; Seibert, K.; Isakson, P. C. Selective Cyclooxygenase Inhibitors: Novel 1,2-Diarylcyclopentenes are Potent and Orally Active COX-2 Inhibitors. J. Med. Chem. 1994, 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.7
Koboldt, C.M.8
Perkins, W.E.9
Seibert, K.10
Isakson, P.C.11
-
18
-
-
0028952998
-
Selective Cyclooxygenase Inhibitors: Novel 4-Spiro 1,2-Diarylcyclopentenes are Potent and Orally Active COX-2 Inhibitors
-
(b) Reitz, D. B.; Huang, H.-C.; Li, J. J.; Garland, D. J.; Manning, R. E.; Anderson, G. D.; Gregory, S.; Koboldt, C. M.; Perkins, W. E.; Seibert, K.; Isakson, P. C. Selective Cyclooxygenase Inhibitors: Novel 4-Spiro 1,2-Diarylcyclopentenes are Potent and Orally Active COX-2 Inhibitors. Biorg. Med. Chem. Lett. 1995, 5, 867-872.
-
(1995)
Biorg. 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.7
Koboldt, C.M.8
Perkins, W.E.9
Seibert, K.10
Isakson, P.C.11
-
19
-
-
0000375266
-
Novel 1,2-Diarylcyclopentenes are Selective, Potent and Orally Active Cyclooxygenase Inhibitors
-
(c) Reitz, D. B.; Li, J. J.; Norton, M. B.; Reinhard, E. J.; Huang, H.-C.; Penick, M. A.; Collins, J. T.; Garland, D. J.; Seibert, K.; Koboldt, C. M.; Gregory, S.; Veenhuizen, A.; Zhang, Y.; Isakson, P. C. Novel 1,2-Diarylcyclopentenes are Selective, Potent and Orally Active Cyclooxygenase Inhibitors. Med. Chem. Res. 1995, 5, 351-363.
-
(1995)
Med. Chem. Res.
, vol.5
, pp. 351-363
-
-
Reitz, D.B.1
Li, J.J.2
Norton, M.B.3
Reinhard, E.J.4
Huang, H.-C.5
Penick, M.A.6
Collins, J.T.7
Garland, D.J.8
Seibert, K.9
Koboldt, C.M.10
Gregory, S.11
Veenhuizen, A.12
Zhang, Y.13
Isakson, P.C.14
-
20
-
-
13344261416
-
1,2-Diarylspiro[2,4]heptenes as Orally Active, Highly Selective Cyclooxygenase-2 Inhibitors: Synthesis and Structure-Activity relationships
-
(d) Huang, H.-C.; Li, J. J.; Garland, D. J.; Chamberlain, T. S.; Reinhard, E. J.; Manning, R. E.; Seibert, K.; Koboldt, C. M.; Gregory, S. A.; Anderson, G. D.; Veenhuizen, A. W.; Zhang, Y.; Perkins, W. E.; Burton, E. G.; Cogburn, J. N.; Isakson, P. C.; Reitz, D. B. 1,2-Diarylspiro[2,4]heptenes as Orally Active, Highly Selective Cyclooxygenase-2 Inhibitors: Synthesis and Structure-Activity relationships. J. Med. Chem. 1996, 39, 253-266.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 253-266
-
-
Huang, H.-C.1
Li, J.J.2
Garland, D.J.3
Chamberlain, T.S.4
Reinhard, E.J.5
Manning, R.E.6
Seibert, K.7
Koboldt, C.M.8
Gregory, S.A.9
Anderson, G.D.10
Veenhuizen, A.W.11
Zhang, Y.12
Perkins, W.E.13
Burton, E.G.14
Cogburn, J.N.15
Isakson, P.C.16
Reitz, D.B.17
-
21
-
-
0028889567
-
1,2-Diarylcyclopentenes as Selective Cyclooxygenase-2 Inhibitors and Orally Active Anti-inflammatory Agents
-
(e) Li, J. J.; Anderson, G. D.; Burton, E. G.; Cogburn, J. N.; Collins, J. T.; Garland, D. J.; Gregory, S. A.; Huang, H.-C.; Isakson, P. C.; Koboldt, C. M.; Logusch, E. W.; Norton, M. B.; Perkins, W. E.; Reinhard, E. J.; Seibert, K.; Veenhuizen, A. W.; Zhang, Y.; Reitz, D. B. 1,2-Diarylcyclopentenes as Selective Cyclooxygenase-2 Inhibitors and Orally Active Anti-inflammatory Agents. J. Med. Chem. 1995, 38, 4570-4578.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4570-4578
-
-
Li, J.J.1
Anderson, G.D.2
Burton, E.G.3
Cogburn, J.N.4
Collins, J.T.5
Garland, D.J.6
Gregory, S.A.7
Huang, H.-C.8
Isakson, P.C.9
Koboldt, C.M.10
Logusch, E.W.11
Norton, M.B.12
Perkins, W.E.13
Reinhard, E.J.14
Seibert, K.15
Veenhuizen, A.W.16
Zhang, Y.17
Reitz, D.B.18
-
22
-
-
0030029368
-
Synthesis and Biological Evaluation of 2,3-Diarylthiophenes as Selective COX-2 Inhibitors. Part II: Replacing the Heterocycle
-
(a) Gauthier, J. Y.; Leblanc, Y.; Black, W. C.; Chan, C. C.; Cromlish, W. A.; Gordon, R.; Kennedey, B. P.; Lau, C. K.; Leger, S.; Wang, Z.; Ethier, D.; Guay, J.; Mancini, J.; Riendeau, D.; Tagari, P.; Vickers, P.; Wong, E.; Xu, L.; Prasit, P. Synthesis and Biological Evaluation of 2,3-Diarylthiophenes as Selective COX-2 Inhibitors. Part II: Replacing The Heterocycle. Bioorg. Med. Chem. Lett. 1996, 6, 87-92.
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 87-92
-
-
Gauthier, J.Y.1
Leblanc, Y.2
Black, W.C.3
Chan, C.C.4
Cromlish, W.A.5
Gordon, R.6
Kennedey, B.P.7
Lau, C.K.8
Leger, S.9
Wang, Z.10
Ethier, D.11
Guay, J.12
Mancini, J.13
Riendeau, D.14
Tagari, P.15
Vickers, P.16
Wong, E.17
Xu, L.18
Prasit, P.19
-
23
-
-
0028825848
-
Diaryl Indenes and Benzofurans: Novel Classes of Potent and Selective Cyclooxygenase-2 Inhibitors
-
(b) Huang, H.-C.; Chamberlain, T. S. Diaryl Indenes and Benzofurans: Novel Classes of Potent and Selective Cyclooxygenase-2 Inhibitors. Bioorg. Med. Chem. Lett. 1995, 5, 2377-2380.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 2377-2380
-
-
Huang, H.-C.1
Chamberlain, T.S.2
-
24
-
-
0028858633
-
3,4-Diarylthiophenes are Selective COX-2 Inhibitors
-
(c) Bertenshaw, S. R.; Talley, J. J.; Rogier, D. J.; Graneto, M. J.; Rogers, R. S.; Kramer, S. W.; Penning, T. D.; Koboldt, C. M.; Veenhuizen, A. W.; Zhang, Y.; Perkins, W. E. 3,4-Diarylthiophenes are Selective COX-2 Inhibitors. Bioorg. Med. Chem. Lett. 1995, 5, 2919-2922.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 2919-2922
-
-
Bertenshaw, S.R.1
Talley, J.J.2
Rogier, D.J.3
Graneto, M.J.4
Rogers, R.S.5
Kramer, S.W.6
Penning, T.D.7
Koboldt, C.M.8
Veenhuizen, A.W.9
Zhang, Y.10
Perkins, W.E.11
-
25
-
-
0029151693
-
Synthesis and Biological Evaluation of 2,3-Diarylthiophenes as Selective COX-2 and COX-1 Inhibitors
-
(d) Leblanc, Y.; Gauthier, J. Y.; Ethier, D.; Guay, J.; Mancini, J.; Reindeau, D.; Tagari, P.; Vickers, P.; Wong, E.; Prasit, P. Synthesis and Biological Evaluation of 2,3-Diarylthiophenes as Selective COX-2 and COX-1 Inhibitors. Bioorg. Med. Chem. Lett. 1995, 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
Reindeau, D.6
Tagari, P.7
Vickers, P.8
Wong, E.9
Prasit, P.10
-
26
-
-
0002511399
-
Selective Time Dependent Inhibition of Cyclooxygenase-2
-
(e) Copeland, R. A.; Williaks, J. M.; Rider, N. L.; Van Dyk, D. E.; Giannaras, J.; Nurnberg, S.; Covington, M.; Pinto, D.; Magolda, R.-L.; Trzaskos, J. M. Selective Time Dependent Inhibition of Cyclooxygenase-2. Med. Chem. Res. 1995, 5, 384-393.
-
(1995)
Med. Chem. Res.
, vol.5
, pp. 384-393
-
-
Copeland, R.A.1
Williaks, J.M.2
Rider, N.L.3
Van Dyk, D.E.4
Giannaras, J.5
Nurnberg, S.6
Covington, M.7
Pinto, D.8
Magolda, R.-L.9
Trzaskos, J.M.10
-
27
-
-
0000291842
-
Selective Inhibition of Cyclooxygenase-2: Diaryl Heterocycles vs Classical NSAIDS
-
(f) Pinto, D. J.; Pitts, W. J.; Copeland, R. A.; Covington, M. B.; Trzaskos, J.; Magolda, R. Selective Inhibition of Cyclooxygenase-2: Diaryl Heterocycles vs Classical NSAIDS. Med. Chem. Res. 1995, 5, 394-398.
-
(1995)
Med. Chem. Res.
, vol.5
, pp. 394-398
-
-
Pinto, D.J.1
Pitts, W.J.2
Copeland, R.A.3
Covington, M.B.4
Trzaskos, J.5
Magolda, R.6
-
28
-
-
0015510175
-
Diaryl Pyrroles: A New Series of Anti-inflammatory Agents
-
(a) Tanaka, K.; Yoshida, I. N.; Tomita, K.; Masuda, H. Diaryl Pyrroles: A New Series of Anti-inflammatory Agents. Experientia 1972, 28, 937-938.
-
(1972)
Experientia
, vol.28
, pp. 937-938
-
-
Tanaka, K.1
Yoshida, I.N.2
Tomita, K.3
Masuda, H.4
-
29
-
-
0028853738
-
Antiinflammatory 4,5-Diarylpyrroles. 2. Activity as a Function of Cyclooxygenase-2 Inhibition
-
(b) Wilkerson, W. W.; Copeland, R. A.; Covington, M.; Trzaskos, J. M. Antiinflammatory 4,5-Diarylpyrroles. 2. Activity as a Function of Cyclooxygenase-2 Inhibition. J. Med. Chem. 1995, 38, 3895-3901.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3895-3901
-
-
Wilkerson, W.W.1
Copeland, R.A.2
Covington, M.3
Trzaskos, J.M.4
-
30
-
-
0000647033
-
Cyclooxygenase-2 Inhibitory 2-Substituted 4,5-Diarylpyrroles
-
(c) Wilkerson, W. W.; Copeland, R. A.; Covington, M.; Grubb, M. F.; Hewes, W. E.; Kerr, J. S.; Trzaskos, J. M. Cyclooxygenase-2 Inhibitory 2-Substituted 4,5-Diarylpyrroles. Med. Chem. Res. 1995, 5, 399-408.
-
(1995)
Med. Chem. Res.
, vol.5
, pp. 399-408
-
-
Wilkerson, W.W.1
Copeland, R.A.2
Covington, M.3
Grubb, M.F.4
Hewes, W.E.5
Kerr, J.S.6
Trzaskos, J.M.7
-
31
-
-
0028218012
-
Antiinflammatory 4,5-Diarylpyrroles: Synthesis and QSAR
-
(d) Wilkerson, W. W.; Galbraith, W.; Gans-Brangs, K.; Grubb, M.; Hewes, W. E.; Jaffee, B.; Kenney, J. P.; Kerr, J.; Wong, N. Antiinflammatory 4,5-Diarylpyrroles: Synthesis and QSAR. J. Med. Chem. 1994, 37, 988-998.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 988-998
-
-
Wilkerson, W.W.1
Galbraith, W.2
Gans-Brangs, K.3
Grubb, M.4
Hewes, W.E.5
Jaffee, B.6
Kenney, J.P.7
Kerr, J.8
Wong, N.9
-
32
-
-
26844515308
-
-
These results are consistent with the first observation made by Len Lee in 1,5-diarylpyrazole series, unpublished results
-
These results are consistent with the first observation made by Len Lee in 1,5-diarylpyrazole series, unpublished results.
-
-
-
-
33
-
-
0006225524
-
The X-Ray Structures of Cyclooxygenase-1 and Inhibitors
-
Garavito, R. M.; Picot, D.; Loll, P. J. The X-Ray Structures of Cyclooxygenase-1 And Inhibitors. Med. Chem. Res. 1995, 5, 375-383.
-
(1995)
Med. Chem. Res.
, vol.5
, pp. 375-383
-
-
Garavito, R.M.1
Picot, D.2
Loll, P.J.3
-
34
-
-
84982417601
-
Catalyzed Addition of Aldehydes to Activated Double Bonds-A New Synthetic Approach
-
For a review on Stetter reaction, see: Stetter, H. Catalyzed Addition of Aldehydes to Activated Double Bonds-A New Synthetic Approach. Angew. Chem., Int. Ed. Engl. 1976, 15, 639-712.
-
(1976)
Angew. Chem., Int. Ed. Engl.
, vol.15
, pp. 639-712
-
-
Stetter, H.1
-
35
-
-
0342293600
-
A Facile Procedure for Producing γ-Halo Butyraldehyde Acetals
-
Stowell, J. C.; Polito, M. A. A Facile Procedure for Producing γ-Halo Butyraldehyde Acetals. J. Org. Chem. 1992, 57, 2195-2196.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 2195-2196
-
-
Stowell, J.C.1
Polito, M.A.2
-
36
-
-
0027229656
-
Synthesis of Perfluoroalkylpyrroles by Homolytic Substitution with Perfluoroalkyl Radicals
-
Baciocchi, E.; Muraglia, E. Synthesis of Perfluoroalkylpyrroles by Homolytic Substitution with Perfluoroalkyl Radicals. Tetrahedron Lett. 1993, 34, 3799-3800.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 3799-3800
-
-
Baciocchi, E.1
Muraglia, E.2
-
37
-
-
26844431988
-
-
note
-
3 group is at either the C-3 or C-5 position of the pyrrole nucleus. Further irradiation of the pyrrole proton signal at δ 5 6.52 gave 12.2% enhancements of the adjacent pyrrole proton at δ 6.80 and 8.8% signal enhancements of the protons at C-3′ and C-5′ on the aryl sulfone ring (see structure 27), suugesting that the position C-3 on pyrrole ring must be unoccupied.
-
-
-
-
38
-
-
33751554339
-
N-(Triisopropylsilyl)pyrrole. A Progenator "Par Excellence" of 3-Substituted Pyrroles
-
For chemistry on electrophilic substitutions in pyrroles, see: (a) Bray, B. L.; Mathies, P. H.; Naef, R.; Solas, D. R.; Tidwell, T. T.; Artis, D. R.; Muchowski, J. M. N-(Triisopropylsilyl)pyrrole. A Progenator "Par Excellence" of 3-Substituted Pyrroles. J. Org. Chem. 1990, 55, 6317-6328. (b) Cerreto, R; Villa, A.; Retico, A.; Scalzo, M. Studies on Anti-Candida Agents With a Pyrrole Moiety. Synthesis and Microbiological Activity of Some 3-Aminomethyl-1,5-Diaryl-2-Methyl-Pyrrole Derivatives. Eur. J. Med. Chem. 1992, 27, 701-708. (c) Gilow, H. M.; Burton, D. E. Bromination and Chlorination of Pyrrole and Some Reactive 1-Substituted Pyrroles. J. Org. Chem. 1981, 46, 2221-2225. (d) Chang, M. N.; Biftu, T.; Boulton, D. A.; Finke, P. E.; Hammond, M. I.; Pessolano, A. A.; Zambias, R. A.; Bailey, P.; Goldenberg, M.; Rackham, A. Syntheses and Analgesic/Antiinflammatory Activities of Novel 2-(5-Aroyl-Pyrrolo)Alkanoic Acids. Eur. J. Med. Chem. 1986, 21, 363-369.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 6317-6328
-
-
Bray, B.L.1
Mathies, P.H.2
Naef, R.3
Solas, D.R.4
Tidwell, T.T.5
Artis, D.R.6
Muchowski, J.M.7
-
39
-
-
0026439431
-
Studies on Anti-Candida Agents with a Pyrrole Moiety. Synthesis and Microbiological Activity of Some 3-Aminomethyl-1,5-Diaryl-2-Methyl-Pyrrole Derivatives
-
For chemistry on electrophilic substitutions in pyrroles, see: (a) Bray, B. L.; Mathies, P. H.; Naef, R.; Solas, D. R.; Tidwell, T. T.; Artis, D. R.; Muchowski, J. M. N-(Triisopropylsilyl)pyrrole. A Progenator "Par Excellence" of 3-Substituted Pyrroles. J. Org. Chem. 1990, 55, 6317-6328. (b) Cerreto, R; Villa, A.; Retico, A.; Scalzo, M. Studies on Anti-Candida Agents With a Pyrrole Moiety. Synthesis and Microbiological Activity of Some 3-Aminomethyl-1,5-Diaryl-2-Methyl-Pyrrole Derivatives. Eur. J. Med. Chem. 1992, 27, 701-708. (c) Gilow, H. M.; Burton, D. E. Bromination and Chlorination of Pyrrole and Some Reactive 1-Substituted Pyrroles. J. Org. Chem. 1981, 46, 2221-2225. (d) Chang, M. N.; Biftu, T.; Boulton, D. A.; Finke, P. E.; Hammond, M. I.; Pessolano, A. A.; Zambias, R. A.; Bailey, P.; Goldenberg, M.; Rackham, A. Syntheses and Analgesic/Antiinflammatory Activities of Novel 2-(5-Aroyl-Pyrrolo)Alkanoic Acids. Eur. J. Med. Chem. 1986, 21, 363-369.
-
(1992)
Eur. J. Med. Chem.
, vol.27
, pp. 701-708
-
-
Cerreto, R.1
Villa, A.2
Retico, A.3
Scalzo, M.4
-
40
-
-
0000113044
-
Bromination and Chlorination of Pyrrole and Some Reactive 1-Substituted Pyrroles
-
For chemistry on electrophilic substitutions in pyrroles, see: (a) Bray, B. L.; Mathies, P. H.; Naef, R.; Solas, D. R.; Tidwell, T. T.; Artis, D. R.; Muchowski, J. M. N-(Triisopropylsilyl)pyrrole. A Progenator "Par Excellence" of 3-Substituted Pyrroles. J. Org. Chem. 1990, 55, 6317-6328. (b) Cerreto, R; Villa, A.; Retico, A.; Scalzo, M. Studies on Anti-Candida Agents With a Pyrrole Moiety. Synthesis and Microbiological Activity of Some 3-Aminomethyl-1,5-Diaryl-2-Methyl-Pyrrole Derivatives. Eur. J. Med. Chem. 1992, 27, 701-708. (c) Gilow, H. M.; Burton, D. E. Bromination and Chlorination of Pyrrole and Some Reactive 1-Substituted Pyrroles. J. Org. Chem. 1981, 46, 2221-2225. (d) Chang, M. N.; Biftu, T.; Boulton, D. A.; Finke, P. E.; Hammond, M. I.; Pessolano, A. A.; Zambias, R. A.; Bailey, P.; Goldenberg, M.; Rackham, A. Syntheses and Analgesic/Antiinflammatory Activities of Novel 2-(5-Aroyl-Pyrrolo)Alkanoic Acids. Eur. J. Med. Chem. 1986, 21, 363-369.
-
(1981)
J. Org. Chem.
, vol.46
, pp. 2221-2225
-
-
Gilow, H.M.1
Burton, D.E.2
-
41
-
-
0023024932
-
Syntheses and Analgesic/Antiinflammatory Activities of Novel 2-(5-Aroyl-Pyrrolo)Alkanoic Acids
-
For chemistry on electrophilic substitutions in pyrroles, see: (a) Bray, B. L.; Mathies, P. H.; Naef, R.; Solas, D. R.; Tidwell, T. T.; Artis, D. R.; Muchowski, J. M. N-(Triisopropylsilyl)pyrrole. A Progenator "Par Excellence" of 3-Substituted Pyrroles. J. Org. Chem. 1990, 55, 6317-6328. (b) Cerreto, R; Villa, A.; Retico, A.; Scalzo, M. Studies on Anti-Candida Agents With a Pyrrole Moiety. Synthesis and Microbiological Activity of Some 3-Aminomethyl-1,5-Diaryl-2-Methyl-Pyrrole Derivatives. Eur. J. Med. Chem. 1992, 27, 701-708. (c) Gilow, H. M.; Burton, D. E. Bromination and Chlorination of Pyrrole and Some Reactive 1-Substituted Pyrroles. J. Org. Chem. 1981, 46, 2221-2225. (d) Chang, M. N.; Biftu, T.; Boulton, D. A.; Finke, P. E.; Hammond, M. I.; Pessolano, A. A.; Zambias, R. A.; Bailey, P.; Goldenberg, M.; Rackham, A. Syntheses and Analgesic/Antiinflammatory Activities of Novel 2-(5-Aroyl-Pyrrolo)Alkanoic Acids. Eur. J. Med. Chem. 1986, 21, 363-369.
-
(1986)
Eur. J. Med. Chem.
, vol.21
, pp. 363-369
-
-
Chang, M.N.1
Biftu, T.2
Boulton, D.A.3
Finke, P.E.4
Hammond, M.I.5
Pessolano, A.A.6
Zambias, R.A.7
Bailey, P.8
Goldenberg, M.9
Rackham, A.10
-
42
-
-
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.; Seibert, IC Expression and Selective Inhibition of the Constitutive and Inducible Forms of Human Cyclooxygenase. Biochem. J. 1995, 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, I.C.7
-
43
-
-
0027940487
-
Biochemical and Pharmacological Characterization of the Cyclooxygenase Activity of Human Blood Prostaglandin Endoperoxide Synthases
-
(a) Patrignani, P.; Panara, M. R.; Greco, A.; Fusco, O.; Natoli, C.; Iacobelli, S.; Cipollone, F.; Ganci, A.; Creminon, C.; Maclouf, J.; Patrono, C. Biochemical and Pharmacological Characterization of the Cyclooxygenase Activity of Human Blood Prostaglandin Endoperoxide Synthases. J. Pharmacol. Exp. Ther. 1994, 277, 1705-1712.
-
(1994)
J. Pharmacol. Exp. Ther.
, vol.277
, pp. 1705-1712
-
-
Patrignani, P.1
Panara, M.R.2
Greco, A.3
Fusco, O.4
Natoli, C.5
Iacobelli, S.6
Cipollone, F.7
Ganci, A.8
Creminon, C.9
Maclouf, J.10
Patrono, C.11
-
44
-
-
0030022032
-
A Human Whole Blood Assay for Clinical Evaluation of Biochemical Efficay of Cyclooxygenase Inhibitors
-
(b) Brideau, C.; Kargman, S.; Liu, S.; Dallob, A. L.; Ehrich, E. W.; Rodger, I. W.; Chan, C.-C. A Human Whole Blood Assay for Clinical Evaluation of Biochemical Efficay of Cyclooxygenase Inhibitors. Inflamm. Res. 1996, 45, 68-74.
-
(1996)
Inflamm. Res.
, vol.45
, pp. 68-74
-
-
Brideau, C.1
Kargman, S.2
Liu, S.3
Dallob, A.L.4
Ehrich, E.W.5
Rodger, I.W.6
Chan, C.-C.7
-
45
-
-
0027944075
-
Pharmacological and Biochemical Demonstration of the Role of Cyclooxygenase-2 in Inflammation and Pain
-
(a) Seibert, K.; Zhang, Y.; Leahy, K.; Hauser, S.; Masferrer, J.; Perkins, W.; Lee, L.; Isakson, P. Pharmacological and Biochemical Demonstration of the Role of Cyclooxygenase-2 in Inflammation and Pain. Proc. Natl. Acad. Sci. U.S.A. 1994, 91, 12013-12017.
-
(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
-
46
-
-
67249094291
-
Carrageenan Induced Edema in Hind Paw of the Rat as an Assay for Antiinflammatory Drugs
-
(b) Winter, C. A.; Risley, E. A.; Nuss, G. W. Carrageenan Induced Edema in Hind Paw of the Rat as an Assay for Antiinflammatory Drugs. Proc. Soc. Exp. Biol. Med. 1962, 111, 544-547.
-
(1962)
Proc. Soc. Exp. Biol. Med.
, vol.111
, pp. 544-547
-
-
Winter, C.A.1
Risley, E.A.2
Nuss, G.W.3
-
47
-
-
0023854087
-
Regulation of Fibroblast Cyclooxygenase Synthesis by Interleukin-1
-
(a) Raz, A.; Wyche, A.; Siegel, N.; Needleman, P. Regulation of Fibroblast Cyclooxygenase Synthesis by Interleukin-1. J. Biol. Chem. 1988, 263, 3022-3028.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 3022-3028
-
-
Raz, A.1
Wyche, A.2
Siegel, N.3
Needleman, P.4
-
48
-
-
0026050107
-
The Biochemical and Pharmacological Manipulation of Cellular Cyclooxygenase Activity
-
(b) Seibert, K.; Masferrer, J. L.; Honda, A.; Raz, A.; Needleman, P. The Biochemical and Pharmacological Manipulation of Cellular Cyclooxygenase Activity. Adv. Prostaglandin, Thromboxane, Leukotriene Res. 1990, 21, 45-51.
-
(1990)
Adv. Prostaglandin, Thromboxane, Leukotriene Res.
, vol.21
, pp. 45-51
-
-
Seibert, K.1
Masferrer, J.L.2
Honda, A.3
Raz, A.4
Needleman, P.5
|