-
1
-
-
77954309291
-
Quinolines and structurally related heterocycles as antimalarials
-
Kaur, K.; Jain, M.; Reddy, R. P.; Jain, R. Quinolines and structurally related heterocycles as antimalarials. Eur. J. Med. Chem., 2010, 45(8), 3245-3264.
-
(2010)
Eur. J. Med. Chem.
, vol.45
, Issue.8
, pp. 3245-3264
-
-
Kaur, K.1
Jain, M.2
Reddy, R.P.3
Jain, R.4
-
2
-
-
0026680407
-
Quinolone antimicrobial agents
-
Neu, H. C. Quinolone antimicrobial agents. Annu. Rev. Med., 1992, 43, 465-486.
-
(1992)
Annu. Rev. Med.
, vol.43
, pp. 465-486
-
-
Neu, H.C.1
-
3
-
-
24344486053
-
Synthesis of novel 4-substituted-7-trifluoromethylquinoline derivatives with nitric oxide releasing properties and their evaluation as analgesic and antiinflammatory agents
-
Abadi, A. H.; Hegazy, G. H.; El-Zaher, A. A. Synthesis of novel 4-substituted-7-trifluoromethylquinoline derivatives with nitric oxide releasing properties and their evaluation as analgesic and antiinflammatory agents. Bioorg. Med. Chem., 2005, 13(20), 5759-5765.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, Issue.20
, pp. 5759-5765
-
-
Abadi, A.H.1
Hegazy, G.H.2
El-Zaher, A.A.3
-
4
-
-
35649019741
-
New 1,8-naphthyridine and quinoline derivatives as CB2 selective agonists
-
Manera, C.; Cascio, M. G.; Benetti, V.; Allará, M.; Tuccinardi, T.; Martinelli, A.; Saccomanni, G.; Vivoli, E.; Ghelardini, C.; Marzob, V. D.; Ferrarinia, P. L. New 1,8-naphthyridine and quinoline derivatives as CB2 selective agonists. Bioorg. Med. Chem. Lett., 2007, 17(23), 6505-6510.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, Issue.23
, pp. 6505-6510
-
-
Manera, C.1
Cascio, M.G.2
Benetti, V.3
Allará, M.4
Tuccinardi, T.5
Martinelli, A.6
Saccomanni, G.7
Vivoli, E.8
Ghelardini, C.9
Marzob, V.D.10
Ferrarinia, P.L.11
-
5
-
-
0028350652
-
Quinoline-4-carboxylic acids as angiotensin II receptor antagonists
-
Lloyd, J.; Ryono, D. E.; Bird, J. E.; Buote, J.; Delaney, C. L.; Dejneka, T.; Dickinson, K. E. J.; Moreland, S.; Normandin, D. E.; Skwish, S.; Spitzmiller, E. R.; Waldron, T. L. Quinoline-4-carboxylic acids as angiotensin II receptor antagonists. Bioorg. Med. Chem. Lett., 1994, 4(1), 195-200.
-
(1994)
Bioorg. Med. Chem. Lett.
, vol.4
, Issue.1
, pp. 195-200
-
-
Lloyd, J.1
Ryono, D.E.2
Bird, J.E.3
Buote, J.4
Delaney, C.L.5
Dejneka, T.6
Dickinson, K.E.J.7
Moreland, S.8
Normandin, D.E.9
Skwish, S.10
Spitzmiller, E.R.11
Waldron, T.L.12
-
6
-
-
60249100697
-
Biarylether amide quinolines as liver X receptor agonists
-
Bernotas, R. C.; Singhaus, R. R.; Kaufman, D. H.; Ullrich, J.; Fletcher III, H.; Quinet, E.; Nambi, P.; Unwalla, R.; Wilhelmsson, A.; Goos-Nilsson, A.; Farnegardh, M.; Wrobel, J. Biarylether amide quinolines as liver X receptor agonists. Bioorg. Med. Chem., 2009, 17(4), 1663-1670.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, Issue.4
, pp. 1663-1670
-
-
Bernotas, R.C.1
Singhaus, R.R.2
Kaufman, D.H.3
Ullrich, J.4
Fletcher III, H.5
Quinet, E.6
Nambi, P.7
Unwalla, R.8
Wilhelmsson, A.9
Goos-Nilsson, A.10
Farnegardh, M.11
Wrobel, J.12
-
7
-
-
79955004745
-
Quinoline as a privileged scaffold in cancer drug discovery
-
Solomon, V. R.; Lee, H. Quinoline as a privileged scaffold in cancer drug discovery. Curr. Med. Chem., 2011, 18(10), 1488-1508.
-
(2011)
Curr. Med. Chem.
, vol.18
, Issue.10
, pp. 1488-1508
-
-
Solomon, V.R.1
Lee, H.2
-
8
-
-
0034658440
-
Reversal of MRP-mediated doxorubicin resistance with quinoline-based drugs
-
Vezmar, M.; Georges, E. Reversal of MRP-Mediated Doxorubicin Resistance with Quinoline-Based Drugs. Biochem. Pharmacol., 2000, 59(10), 1245-1252.
-
(2000)
Biochem. Pharmacol.
, vol.59
, Issue.10
, pp. 1245-1252
-
-
Vezmar, M.1
Georges, E.2
-
9
-
-
0003527583
-
-
6th ed.; W. B. Saunders: Philadelphia, PA
-
Cotran, R. S., Kumar, V., Collins, T. Robbins Pathologic Basis of Disease, 6th ed.; W. B. Saunders: Philadelphia, PA, 1999.
-
(1999)
Robbins Pathologic Basis of Disease
-
-
Cotran, R.S.1
Kumar, V.2
Collins, T.3
-
10
-
-
0036566639
-
Atherosclerosis: The new view
-
Libby, P. Atherosclerosis: the new view. Sci. Am., 2002, 286(5), 46-55.
-
(2002)
Sci. Am.
, vol.286
, Issue.5
, pp. 46-55
-
-
Libby, P.1
-
11
-
-
33745571976
-
The immune response in atherosclerosis: A double-edged sword
-
Hansson, G. K.; Libby, P. The immune response in atherosclerosis: a double-edged sword. Nat. Rev. Immunol., 2006, 6(7), 508-519.
-
(2006)
Nat. Rev. Immunol.
, vol.6
, Issue.7
, pp. 508-519
-
-
Hansson, G.K.1
Libby, P.2
-
12
-
-
0031601339
-
The multienzyme PDE4 cyclic adenosine monophosphate-specific phosphodiesterase family: Intracellular targeting, regulation, and selective inhibition by compounds exerting anti-inflammatory and antidepressant actions
-
Houslay, M. D.; Sullivan, M.; Bolger, G. B. The multienzyme PDE4 cyclic adenosine monophosphate-specific phosphodiesterase family: intracellular targeting, regulation, and selective inhibition by compounds exerting anti-inflammatory and antidepressant actions. Adv. Pharmacol., 1998, 44, 225-342.
-
(1998)
Adv. Pharmacol.
, vol.44
, pp. 225-342
-
-
Houslay, M.D.1
Sullivan, M.2
Bolger, G.B.3
-
13
-
-
21144437565
-
Phosphodiesterase: Overview of protein structures, potential therapeutic applications and recent progress in drug development
-
Jeon, Y. H.; Heo, Y.-S.; Kim, C. M.; Hyun, Y.-L.; Lee, T. G.; Ro, S.; Cho, J. M. Phosphodiesterase: overview of protein structures, potential therapeutic applications and recent progress in drug development. Cell. Mol. Life Sci., 2005, 62(11), 1198-1220.
-
(2005)
Cell. Mol. Life Sci.
, vol.62
, Issue.11
, pp. 1198-1220
-
-
Jeon, Y.H.1
Heo, Y.-S.2
Kim, C.M.3
Hyun, Y.-L.4
Lee, T.G.5
Ro, S.6
Cho, J.M.7
-
14
-
-
15144351114
-
-
Hansch, C., Sammes, P. G., Taylor, J. B., Eds.; Pergamon Press: Oxford, U.K
-
Potter, B. V. L. In: Comprehensive Medicinal Chemistry; Hansch, C., Sammes, P. G., Taylor, J. B., Eds.; Pergamon Press: Oxford, U.K., 1990, pp. 102-128.
-
(1990)
Comprehensive Medicinal Chemistry
, pp. 102-128
-
-
Potter, B.V.L.1
-
15
-
-
52449115420
-
Recent advances on phosphodiesterase 4 inhibitors for the treatment of asthma and chronic obstructive pulmonary disease
-
Kodimuthali, A.; Jabaris, S. S. L.; Pal, M. Recent advances on phosphodiesterase 4 inhibitors for the treatment of asthma and chronic obstructive pulmonary disease. J. Med. Chem., 2008, 51(18), 5471-5489.
-
(2008)
J. Med. Chem.
, vol.51
, Issue.18
, pp. 5471-5489
-
-
Kodimuthali, A.1
Jabaris, S.S.L.2
Pal, M.3
-
17
-
-
0034687225
-
Hunting the emesis and efficacy targets of PDE4 inhibitors: Identification of the photoaffinity probe 8-(3-azidophenyl)-6-[(4-iodo-1H-1- imidazolyl)methyl] quinoline (APIIMQ)
-
Macdonald, D.; Perrier, H.; Liu, S.; Laliberté, F.; Rasori, R.; Robichaud, A.; Masson, P.; Huang, Z. Hunting the emesis and efficacy targets of PDE4 inhibitors: identification of the photoaffinity probe 8-(3-azidophenyl)-6- [(4-iodo-1H-1-imidazolyl)methyl] quinoline (APIIMQ). J. Med. Chem., 2000, 43(21), 3820-3823.
-
(2000)
J. Med. Chem.
, vol.43
, Issue.21
, pp. 3820-3823
-
-
Macdonald, D.1
Perrier, H.2
Liu, S.3
Laliberté, F.4
Rasori, R.5
Robichaud, A.6
Masson, P.7
Huang, Z.8
-
18
-
-
14444268769
-
1,4-Cyclohexanecarboxylates: Potent and selective inhibitors of phosophodiesterase 4 for the treatment of asthma
-
Christensen, S. B.; Guider, A.; Forster, C. J.; Gleason, J. G.; Bender, P. E.; Karpinski, J. M.; DeWolf, W. E. Jr.; Barnette, M. S.; Underwood, D. C.; Griswold, D. E.; Cieslinski, L. B.; Burman, M.; Bochnowicz, S.; Osborn, R. R.; Manning, C. D.; Grous, M.; Hillegas, L. M.; Bartus, J. O.; Ryan, M. D.; Eggleston, D. S.; Haltiwanger, R. C.; Torphy, T. J. 1,4-Cyclohexanecarboxylates: potent and selective inhibitors of phosophodiesterase 4 for the treatment of asthma. J. Med. Chem., 1998, 41(6), 821-835.
-
(1998)
J. Med. Chem.
, vol.41
, Issue.6
, pp. 821-835
-
-
Christensen, S.B.1
Guider, A.2
Forster, C.J.3
Gleason, J.G.4
Bender, P.E.5
Karpinski, J.M.6
DeWolf Jr., W.E.7
Barnette, M.S.8
Underwood, D.C.9
Griswold, D.E.10
Cieslinski, L.B.11
Burman, M.12
Bochnowicz, S.13
Osborn, R.R.14
Manning, C.D.15
Grous, M.16
Hillegas, L.M.17
Bartus, J.O.18
Ryan, M.D.19
Eggleston, D.S.20
Haltiwanger, R.C.21
Torphy, T.J.22
more..
-
19
-
-
8944247744
-
The inhibition of antigen-induced eosinophilia and bronchoconstriction by CDP840, a novel stereo-selective inhibitor of phosphodiesterase type 4
-
Hughes, B.; Howat, D.; Lisle, H.; Holbrook, M.; James, T.; Gozzard, N.; Blease, K.; Hughes, P.; Kingaby, R.; Warrellow, G.; Alexander, R.; Head, J.; Boyd, E.; Eaton, M.; Perry, M.; Wales, M.; Smith, B.; Owens, R.; Catterall, C.; Lumb, S.; Russell, A.; Allen, R.; Merriman, M.; Bloxham, D.; Higgs, G. The inhibition of antigen-induced eosinophilia and bronchoconstriction by CDP840, a novel stereo-selective inhibitor of phosphodiesterase type 4. Br. J. Pharmacol., 1996, 118(5), 1183-1191.
-
(1996)
Br. J. Pharmacol.
, vol.118
, Issue.5
, pp. 1183-1191
-
-
Hughes, B.1
Howat, D.2
Lisle, H.3
Holbrook, M.4
James, T.5
Gozzard, N.6
Blease, K.7
Hughes, P.8
Kingaby, R.9
Warrellow, G.10
Alexander, R.11
Head, J.12
Boyd, E.13
Eaton, M.14
Perry, M.15
Wales, M.16
Smith, B.17
Owens, R.18
Catterall, C.19
Lumb, S.20
Russell, A.21
Allen, R.22
Merriman, M.23
Bloxham, D.24
Higgs, G.25
more..
-
20
-
-
0031616075
-
CDP840: A novel inhibitor of PDE-4
-
Perry, M. J.; O'Connell, J.; Walker, C.; Crabbe, T.; Baldock, D.; Russell, A.; Lumb, S.; Huang, Z.; Howat, D.; Allen, R.; Merriman, M.; Walls, J.; Daniel, T.; Hughes, B.; Laliberte, F.; Higgs, G. A.; Owens, R. J. CDP840: a novel inhibitor of PDE-4. Cell Biochem. Biophys., 1998, 29(1-2), 113-132.
-
(1998)
Cell Biochem. Biophys.
, vol.29
, Issue.1-2
, pp. 113-132
-
-
Perry, M.J.1
O'Connell, J.2
Walker, C.3
Crabbe, T.4
Baldock, D.5
Russell, A.6
Lumb, S.7
Huang, Z.8
Howat, D.9
Allen, R.10
Merriman, M.11
Walls, J.12
Daniel, T.13
Hughes, B.14
Laliberte, F.15
Higgs, G.A.16
Owens, R.J.17
-
21
-
-
0036179542
-
The new phosphodiesterase 4 inhibitor roflumilast is efficacious in exercise-induced asthma and leads to suppression of LPS-stimulated TNF-alpha ex vivo
-
Timmer, W.; Leclerc, V.; Birraux, G.; Neuhauser, M.; Hatzelmann, A.; Bethke, T.; Wurst, W. The new phosphodiesterase 4 inhibitor roflumilast is efficacious in exercise-induced asthma and leads to suppression of LPS-stimulated TNF-alpha ex vivo. J. Clin. Pharmacol., 2002, 42(3), 297-303.
-
(2002)
J. Clin. Pharmacol.
, vol.42
, Issue.3
, pp. 297-303
-
-
Timmer, W.1
Leclerc, V.2
Birraux, G.3
Neuhauser, M.4
Hatzelmann, A.5
Bethke, T.6
Wurst, W.7
-
22
-
-
26844458998
-
Discovery of a substituted 8-arylquinoline series of PDE4 inhibitors: Structure-activity relationship, optimization, and identification of a highly potent, well tolerated, PDE4 inhibitor
-
Macdonald, D.; Mastracchio, A.; Perrier, H.; Dubé, D.; Gallant, M.; Lacombe, P.; Deschênes, D.; Roy, B.; Scheigetz, J.; Bateman, K.; Li, C.; Trimble, L. A.; Day, S.; Chauret, N.; Nicoll-Griffith, D. A.; Silva, J. M.; Huang, Z.; Laliberté, F.; Liu, S.; Ethier, D.; Pon, D.; Muise, E.; Boulet, L.; Chan, C. C.; Styhler, A.; Charleson, S.; Mancini, J.; Masson, P.; Claveau, D.; Nicholson, D.; Turner, M.; Young, R. N.; Girard, Y. Discovery of a substituted 8-arylquinoline series of PDE4 inhibitors: Structure-activity relationship, optimization, and identification of a highly potent, well tolerated, PDE4 inhibitor. Bioorg. Med. Chem. Lett., 2005, 15(23), 5241-5246.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, Issue.23
, pp. 5241-5246
-
-
Macdonald, D.1
Mastracchio, A.2
Perrier, H.3
Dubé, D.4
Gallant, M.5
Lacombe, P.6
Deschênes, D.7
Roy, B.8
Scheigetz, J.9
Bateman, K.10
Li, C.11
Trimble, L.A.12
Day, S.13
Chauret, N.14
Nicoll-Griffith, D.A.15
Silva, J.M.16
Huang, Z.17
Laliberté, F.18
Liu, S.19
Ethier, D.20
Pon, D.21
Muise, E.22
Boulet, L.23
Chan, C.C.24
Styhler, A.25
Charleson, S.26
Mancini, J.27
Masson, P.28
Claveau, D.29
Nicholson, D.30
Turner, M.31
Young, R.N.32
Girard, Y.33
more..
-
23
-
-
34247603063
-
L-454,560, a potent and selective PDE4 inhibitor with in vivo efficacy in animal models of asthma and cognition
-
Huang, Z.; Dias, R.; Jones, T.; Liu, S.; Styhler, A.; Claveau, D.; Otu, F.; Ng, K.; Laliberté, F.; Zhang, L.; Goetghebeur, P.; Abraham, W. M.; Macdonald, D.; Dubé, D.; Gallant, M.; Lacombe, P.; Girard, Y.; Young, R. N.; Turner, M. J.; Nicholson, D. W.; Mancini, J. A. L-454,560, a potent and selective PDE4 inhibitor with in vivo efficacy in animal models of asthma and cognition. Biochem. Pharmacol., 2007, 73(12), 1971-1981.
-
(2007)
Biochem. Pharmacol.
, vol.73
, Issue.12
, pp. 1971-1981
-
-
Huang, Z.1
Dias, R.2
Jones, T.3
Liu, S.4
Styhler, A.5
Claveau, D.6
Otu, F.7
Ng, K.8
Laliberté, F.9
Zhang, L.10
Goetghebeur, P.11
Abraham, W.M.12
Macdonald, D.13
Dubé, D.14
Gallant, M.15
Lacombe, P.16
Girard, Y.17
Young, R.N.18
Turner, M.J.19
Nicholson, D.W.20
Mancini, J.A.21
more..
-
24
-
-
38949088977
-
Design, synthesis, and biological evaluation of 8-biarylquinolines: A novel class of PDE4 inhibitors
-
Gallant, M.; Chauret, N.; Claveau, D.; Day, S.; Deschenes, D.; Dubé, D.; Huang, Z.; Lacombe, P.; Laliberté, F.; Lévesque, J. F.; Liu, S.; Macdonald, D.; Mancini, J.; Masson, P.; Mastracchio, A.; Nicholson, D.; Nicoll-Griffith, D. A.; Perrier, H.; Salem, M.; Styhler, A.; Young, R. N.; Girard, Y. Design, synthesis, and biological evaluation of 8-biarylquinolines: a novel class of PDE4 inhibitors. Bioorg. Med. Chem. Lett., 2008, 18(4), 1407-1412.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, Issue.4
, pp. 1407-1412
-
-
Gallant, M.1
Chauret, N.2
Claveau, D.3
Day, S.4
Deschenes, D.5
Dubé, D.6
Huang, Z.7
Lacombe, P.8
Laliberté, F.9
Lévesque, J.F.10
Liu, S.11
Macdonald, D.12
Mancini, J.13
Masson, P.14
Mastracchio, A.15
Nicholson, D.16
Nicoll-Griffith, D.A.17
Perrier, H.18
Salem, M.19
Styhler, A.20
Young, R.N.21
Girard, Y.22
more..
-
25
-
-
33645851018
-
Nitrogen-bridged substituted 8-arylquinolines as potent PDE IV inhibitors
-
Lacombe, P.; Deschênes, D.; Dubé, D.; Dubé, L.; Gallant, M.; Macdonald, D.; Mastracchio, A.; Perrier, H.; Charleson, S.; Huang, Z.; Laliberté, F.; Liu, S.; Mancini, J. A.; Masson, P.; Salem, M.; Styhler, A.; Girard, Y. Nitrogen-bridged substituted 8-arylquinolines as potent PDE IV inhibitors. Bioorg. Med. Chem. Lett., 2006, 16(10), 2608-2612.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, Issue.10
, pp. 2608-2612
-
-
Lacombe, P.1
Deschênes, D.2
Dubé, D.3
Dubé, L.4
Gallant, M.5
Macdonald, D.6
Mastracchio, A.7
Perrier, H.8
Charleson, S.9
Huang, Z.10
Laliberté, F.11
Liu, S.12
Mancini, J.A.13
Masson, P.14
Salem, M.15
Styhler, A.16
Girard, Y.17
-
26
-
-
0037124188
-
8-Methoxyquinoline-5-carboxamides as PDE4 Inhibitors: A Potential Treatment for Asthma
-
Buckley, G. M.; Cooper, N.; Dyke, H. J.; Galleway, F. P.; Gowers, L.; Haughan, A. F.; Kendall, H. J.; Lowe, C.; Maxey, R.; Montana, J. G. ; Naylor, R.; Oxford, J.; Peake, J. C.; Picken, C. L.; Runcie, K. A.; Sabin, V.; Sharpea, A.; Warneck, J. B. H. 8-Methoxyquinoline-5-carboxamides as PDE4 Inhibitors: A Potential Treatment for Asthma. Bioorg. Med. Chem. Lett., 2002, 12(12), 1613-1615.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, Issue.12
, pp. 1613-1615
-
-
Buckley, G.M.1
Cooper, N.2
Dyke, H.J.3
Galleway, F.P.4
Gowers, L.5
Haughan, A.F.6
Kendall, H.J.7
Lowe, C.8
Maxey, R.9
Montana, J.G.10
Naylor, R.11
Oxford, J.12
Peake, J.C.13
Picken, C.L.14
Runcie, K.A.15
Sabin, V.16
Sharpea, A.17
Warneck, J.B.H.18
-
27
-
-
0037124192
-
8-Methoxyquinolines as PDE4 inhibitors
-
Billah, M.; Buckley, G. M.; Cooper, N.; Dyke, H. J.; Egan, R.; Ganguly, A.; Gowers, L.; Haughan, A. F.; Kendall, H. J.; Lowe, C.; Minnicozzi, M.; Montana, J. G.; Oxford, J.; Peake, J. C.; Picken, C. L.; Piwinski, J. J.; Naylor, R.; Sabin, V.; Shih, N.-Y.; Warneck, J. B. H. 8-Methoxyquinolines as PDE4 inhibitors. Bioorg. Med. Chem. Lett., 2002, 12(12), 1617-1619.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, Issue.12
, pp. 1617-1619
-
-
Billah, M.1
Buckley, G.M.2
Cooper, N.3
Dyke, H.J.4
Egan, R.5
Ganguly, A.6
Gowers, L.7
Haughan, A.F.8
Kendall, H.J.9
Lowe, C.10
Minnicozzi, M.11
Montana, J.G.12
Oxford, J.13
Peake, J.C.14
Picken, C.L.15
Piwinski, J.J.16
Naylor, R.17
Sabin, V.18
Shih, N.-Y.19
Warneck, J.B.H.20
more..
-
28
-
-
0037124189
-
Synthesis and profile of SCH351591, a novel PDE4 inhibitor
-
Billah, M.; Cooper, N.; Cuss, F.; Davenport, R. J.; Dyke, H. J.; Egan, R.; Ganguly, A.; Gowers, L.; Hannah, D. R.; Haughan, A. F.; Kendall, H. J.; Lowe, C.; Minnicozzi, M.; Montana, J. G.; Naylor, R.; Oxford, J.; Peake, J. C.; Piwinski, J. J.; Runcie, K. A.; Sabin, V.; Sharpe, A.; Shih, N.-Y.; Warneck, J. B. H. Synthesis and profile of SCH351591, a novel PDE4 inhibitor. Bioorg. Med. Chem. Lett., 2002, 12(12), 1621-1623.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, Issue.12
, pp. 1621-1623
-
-
Billah, M.1
Cooper, N.2
Cuss, F.3
Davenport, R.J.4
Dyke, H.J.5
Egan, R.6
Ganguly, A.7
Gowers, L.8
Hannah, D.R.9
Haughan, A.F.10
Kendall, H.J.11
Lowe, C.12
Minnicozzi, M.13
Montana, J.G.14
Naylor, R.15
Oxford, J.16
Peake, J.C.17
Piwinski, J.J.18
Runcie, K.A.19
Sabin, V.20
Sharpe, A.21
Shih, N.-Y.22
Warneck, J.B.H.23
more..
-
29
-
-
34547854308
-
Discovery of a highly potent series of oxazole-based phosphodiesterase 4 inhibitors
-
Kuang, R.; Shue, H.-J.; Blythin, D. J.; Shih, N.-Y.; Gu, D.; Chen, X.; Schwerdt, J.; Lin, L.; Ting, P. C.; Zhu, X.; Aslanian, R.; Piwinski, J. J.; Xiao, L.; Prelusky, D.; Wu, P.; Zhang, J.; Zhang, X.; Celly, C. S.; Minnicozzi, M.; Billahd, M.; Wangd, P. Discovery of a highly potent series of oxazole-based phosphodiesterase 4 inhibitors. Bioorg. Med. Chem. Lett., 2007, 17(18), 5150-5154.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, Issue.18
, pp. 5150-5154
-
-
Kuang, R.1
Shue, H.-J.2
Blythin, D.J.3
Shih, N.-Y.4
Gu, D.5
Chen, X.6
Schwerdt, J.7
Lin, L.8
Ting, P.C.9
Zhu, X.10
Aslanian, R.11
Piwinski, J.J.12
Xiao, L.13
Prelusky, D.14
Wu, P.15
Zhang, J.16
Zhang, X.17
Celly, C.S.18
Minnicozzi, M.19
Billahd, M.20
Wangd, P.21
more..
-
30
-
-
84862779566
-
Discovery of oxazole-based PDE4 inhibitors with picomolar potency
-
Kuang, R.; Shue, H.-J.; Xiao, L.; Blythin, D. J.; Shih, N.-Y.; Chen, X.; Gu, D.; Schwerdt, J.; Lin, L.; Ting, P. C.; Cao, J.; Aslanian, R.; Piwinski, J. J.; Prelusky, D.; Wud, P.; Zhang, J.; Zhang, X.; Celly, C. S.; Billah, M.; Wang, P. Discovery of oxazole-based PDE4 inhibitors with picomolar potency. Bioorg. Med. Chem. Lett., 2012, 22(7), 2594-2597.
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, Issue.7
, pp. 2594-2597
-
-
Kuang, R.1
Shue, H.-J.2
Xiao, L.3
Blythin, D.J.4
Shih, N.-Y.5
Chen, X.6
Gu, D.7
Schwerdt, J.8
Lin, L.9
Ting, P.C.10
Cao, J.11
Aslanian, R.12
Piwinski, J.J.13
Prelusky, D.14
Wud, P.15
Zhang, J.16
Zhang, X.17
Celly, C.S.18
Billah, M.19
Wang, P.20
more..
-
31
-
-
60449108070
-
Quinolines as a novel structural class of potent and selective PDE4 inhibitors: Optimisation for oral administration
-
Lunniss, C. J.; Cooper, A. W. J.; Eldred, C. D.; Kranz, M.; Lindvall, M.; Lucas, F. S.; Neu, M.; Preston, A. G. S.; Ranshaw, L. E.; Redgrave, A. J.; Robinson, J. E.; Shipley, T. J. Solanke, Y. E.; Somers, D. O.; Wiseman, J. O. Quinolines as a novel structural class of potent and selective PDE4 inhibitors: Optimisation for oral administration. Bioorg. Med. Chem. Lett., 2009, 19(5), 1380-1385.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, Issue.5
, pp. 1380-1385
-
-
Lunniss, C.J.1
Cooper, A.W.J.2
Eldred, C.D.3
Kranz, M.4
Lindvall, M.5
Lucas, F.S.6
Neu, M.7
Preston, A.G.S.8
Ranshaw, L.E.9
Redgrave, A.J.10
Robinson, J.E.11
Shipley, T.J.12
Solanke, Y.E.13
Somers, D.O.14
Wiseman, J.O.15
-
32
-
-
68349150615
-
Quinolines as a novel structural class of potent and selective PDE4 inhibitors. Optimisation for inhaled administration
-
Woodrow, M. D.; Ballantine, S. P.; Barker, M. D.; Clarke, B. J.; Dawson, J.; Dean, T. W.; Delves, C. J.; Evans, B.; Gough, S. L. Guntrip, S. B.; Holman, S.; Holmes, D. S.; Kranz, M.; Lindvaal, M. K.; Lucas, F. S.; Neu, M.; Ranshaw, L. E.; Solanke, Y. E.; Somers, D. O.; Ward, P.; Wiseman, J.O. Quinolines as a novel structural class of potent and selective PDE4 inhibitors. Optimisation for inhaled administration. Bioorg. Med. Chem. Lett., 2009, 19(17), 5261-5265.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, Issue.17
, pp. 5261-5265
-
-
Woodrow, M.D.1
Ballantine, S.P.2
Barker, M.D.3
Clarke, B.J.4
Dawson, J.5
Dean, T.W.6
Delves, C.J.7
Evans, B.8
Gough, S.L.9
Guntrip, S.B.10
Holman, S.11
Holmes, D.S.12
Kranz, M.13
Lindvaal, M.K.14
Lucas, F.S.15
Neu, M.16
Ranshaw, L.E.17
Solanke, Y.E.18
Somers, D.O.19
Ward, P.20
Wiseman, J.O.21
more..
-
33
-
-
79953022070
-
GSK256066, an exceptionally high-affinity and selective inhibitor of phosphodiesterase 4 suitable for administration by inhalation: In vitro, kinetic, and in vivo characterization
-
Tralau-Stewart, C. J.; Williamson, R. A.; Nials, A. T.; Gascoigne, M.; Dawson, J.; Hart, G. J.; Angell, A. D. R.; Solanke, Y. E.; Lucas, F. S.; Wiseman, J.; Ward, P.; Ranshaw, L. E.; Knowles, R. G. GSK256066, an exceptionally high-affinity and selective inhibitor of phosphodiesterase 4 suitable for administration by inhalation: In vitro, kinetic, and in vivo characterization. J. Pharmacol. Exp. Ther., 2011, 337(1), 145-154.
-
(2011)
J. Pharmacol. Exp. Ther.
, vol.337
, Issue.1
, pp. 145-154
-
-
Tralau-Stewart, C.J.1
Williamson, R.A.2
Nials, A.T.3
Gascoigne, M.4
Dawson, J.5
Hart, G.J.6
Angell, A.D.R.7
Solanke, Y.E.8
Lucas, F.S.9
Wiseman, J.10
Ward, P.11
Ranshaw, L.E.12
Knowles, R.G.13
-
34
-
-
84858289520
-
C-C bond formation at C-2 of a quinoline ring: Synthesis of 2-(1H-indol-3-yl) quinoline-3-carbonitrile derivatives as a new class of PDE4 inhibitors
-
Kumar, K. S.; Kumar, S. K.; Yogi Sreenivas, B.; Gorja, D. R.; Kapavarapu, R.; Rambabu, D.; Krishna, G. R.; Reddy, C. M.; Rao, M. V. B.; Parsa, K. V. L.; Pal, M. C-C bond formation at C-2 of a quinoline ring: Synthesis of 2-(1H-indol-3-yl) quinoline-3-carbonitrile derivatives as a new class of PDE4 inhibitors. Bioorg. Med. Chem., 2012, 20(7), 2199-2207.
-
(2012)
Bioorg. Med. Chem.
, vol.20
, Issue.7
, pp. 2199-2207
-
-
Kumar, K.S.1
Kumar, S.K.2
Yogi Sreenivas, B.3
Gorja, D.R.4
Kapavarapu, R.5
Rambabu, D.6
Krishna, G.R.7
Reddy, C.M.8
Rao, M.V.B.9
Parsa, K.V.L.10
Pal, M.11
-
35
-
-
80054788578
-
Novel 1-alkynyl substituted 1,2-dihydroquinoline derivatives from nimesulide (and their 2-oxo analogues): A new strategy to identify inhibitors of PDE4B
-
Pal, S.; Durgadas, S.; Nallapati, S.; Mukkanti, K.; Kapavarapu, R.; Meda, C. L. T.; Parsa, K. V. L.; Pal, M. Novel 1-alkynyl substituted 1,2-dihydroquinoline derivatives from nimesulide (and their 2-oxo analogues): A new strategy to identify inhibitors of PDE4B. Bioorg. Med. Chem. Lett., 2011, 21(21), 6573-6576.
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, Issue.21
, pp. 6573-6576
-
-
Pal, S.1
Durgadas, S.2
Nallapati, S.3
Mukkanti, K.4
Kapavarapu, R.5
Meda, C.L.T.6
Parsa, K.V.L.7
Pal, M.8
-
36
-
-
77951490751
-
Ceric ammonium nitrate: An efficient catalyst for one-pot synthesis of 2,2,4-trimethyl-1,2-dihydroquinolines
-
Durgadas, S.; Chatare, V. K.; Mukkanti, K.; Pal, S. Ceric ammonium nitrate: An efficient catalyst for one-pot synthesis of 2,2,4-trimethyl-1,2- dihydroquinolines. Lett. Org. Chem. 2010, 7(4), 306-310.
-
(2010)
Lett. Org. Chem.
, vol.7
, Issue.4
, pp. 306-310
-
-
Durgadas, S.1
Chatare, V.K.2
Mukkanti, K.3
Pal, S.4
-
37
-
-
0034926291
-
The vanilloid receptor: A molecular gateway to the pain pathway
-
Caterina, M. J.; Julius, D. The vanilloid receptor: a molecular gateway to the pain pathway. Annu. Rev. Neurosci., 2001, 24, 487-517.
-
(2001)
Annu. Rev. Neurosci.
, vol.24
, pp. 487-517
-
-
Caterina, M.J.1
Julius, D.2
-
38
-
-
0034954583
-
VR1 protein expression increases in undamaged DRG neurons after partial nerve injury
-
Hudson, L. J.; Bevan, S.; Wotherspoon, G.; Gentry, C.; Fox, A.; Winter, J. VR1 protein expression increases in undamaged DRG neurons after partial nerve injury. Eur. J. Neurosci., 2001, 13(11), 2105-2114.
-
(2001)
Eur. J. Neurosci.
, vol.13
, Issue.11
, pp. 2105-2114
-
-
Hudson, L.J.1
Bevan, S.2
Wotherspoon, G.3
Gentry, C.4
Fox, A.5
Winter, J.6
-
39
-
-
0037179755
-
P38 MAPK activation by NGF in primary sensory neurons after inflammation increases TRPV1 levels and maintains heat hyperalgesia
-
Ji, R. R.; Samad, T. A.; Jin, S. X.; Schmoll, R.; Woolf, C. J. p38 MAPK activation by NGF in primary sensory neurons after inflammation increases TRPV1 levels and maintains heat hyperalgesia. Neuron, 2002, 36(1), 57-68.
-
(2002)
Neuron
, vol.36
, Issue.1
, pp. 57-68
-
-
Ji, R.R.1
Samad, T.A.2
Jin, S.X.3
Schmoll, R.4
Woolf, C.J.5
-
40
-
-
0034636441
-
Vanilloid receptor-1 is essential for inflammatory thermal hyperalgesia
-
Davis, J. B.; Gray, J.; Gunthorpe, M. J.; Hatcher, J. P.; Davey, P. T.; Overend, P.; Harries, M. H.; Latcham, J.; Clapham, C.; Atkinson, K.; Hughes, S.A.; Rance, K.; Grau, E.; Harper, A. J.; Pugh, P. L.; Rogers, D. C.; Bingham, S.; Randall, A.; Sheardown, S. A. Vanilloid receptor-1 is essential for inflammatory thermal hyperalgesia. Nature, 2000, 405(6783), 183-187.
-
(2000)
Nature
, vol.405
, Issue.6783
, pp. 183-187
-
-
Davis, J.B.1
Gray, J.2
Gunthorpe, M.J.3
Hatcher, J.P.4
Davey, P.T.5
Overend, P.6
Harries, M.H.7
Latcham, J.8
Clapham, C.9
Atkinson, K.10
Hughes, S.A.11
Rance, K.12
Grau, E.13
Harper, A.J.14
Pugh, P.L.15
Rogers, D.C.16
Bingham, S.17
Randall, A.18
Sheardown, S.A.19
-
41
-
-
0034646740
-
Impaired nociception and pain sensation in mice lacking the capsaicin receptor
-
Caterina, M. J.; Leffler, A.; Malmberg, A. B.; Martin, W. J.; Trafton, J., Petersen-Zeitz K. R.; Koltzenburg, M.; Basbaum, A. I.; Julius, D. Impaired nociception and pain sensation in mice lacking the capsaicin receptor. Science, 2000, 288(5464), 306-313.
-
(2000)
Science
, vol.288
, Issue.5464
, pp. 306-313
-
-
Caterina, M.J.1
Leffler, A.2
Malmberg, A.B.3
Martin, W.J.4
Trafton, J.5
Petersen-Zeitz, K.R.6
Koltzenburg, M.7
Basbaum, A.I.8
Julius, D.9
-
42
-
-
65549133355
-
Vanilloid receptor antagonists: Emerging class of novel anti-inflammatory agents for pain management
-
Pal, M.; Angaru, S.; Kodimuthali, A.; Dhingra, N. Vanilloid Receptor Antagonists: Emerging Class of Novel Anti-Inflammatory Agents for Pain Management. Curr. Pharm. Des., 2009, 15(9), 1008-1026.
-
(2009)
Curr. Pharm. Des.
, vol.15
, Issue.9
, pp. 1008-1026
-
-
Pal, M.1
Angaru, S.2
Kodimuthali, A.3
Dhingra, N.4
-
43
-
-
19944428963
-
Discovery of potent, orally available vanilloid receptor-1 antagonists. Structure-activity relationship of N-aryl cinnamides
-
Doherty, E. M.; Fotsch, C.; Bo, Y.; Chakrabarti, P. P.; Chen, N.; Gavva, N.; Han, N.; Kelly, M. G.; Kincaid, J.; Klionsky, L.; Liu, Q.; Ognyanov, V. I.; Tamir, R.; Wang, X.; Zhu, J.; Norman, M. H.; Treanor J. J. S. Discovery of Potent, Orally Available Vanilloid Receptor-1 Antagonists. Structure-Activity Relationship of N-Aryl Cinnamides. J. Med. Chem., 2005, 48(1), 71-90.
-
(2005)
J. Med. Chem.
, vol.48
, Issue.1
, pp. 71-90
-
-
Doherty, E.M.1
Fotsch, C.2
Bo, Y.3
Chakrabarti, P.P.4
Chen, N.5
Gavva, N.6
Han, N.7
Kelly, M.G.8
Kincaid, J.9
Klionsky, L.10
Liu, Q.11
Ognyanov, V.I.12
Tamir, R.13
Wang, X.14
Zhu, J.15
Norman, M.H.16
Treanor, J.J.S.17
-
44
-
-
34547573343
-
Novel vanilloid receptor-1 antagonists: 1. Conformationally restricted analogues of trans-cinnamides
-
Norman M. H.; Fotsch, C.; Doherty, E. M.; Bo, Y.; Chen, N.; Chakrabarti, P.; Doherty, E. M.; Gavva, N. R.; Nishimura, N.; Nixey, T.; Ognyanov, V. I.; Rzasa, R. M.; Stec, M.; Surapaneni, S.; Tamir, R.; Viswanadhan, V. N.; Treanor, J. J. Novel vanilloid receptor-1 antagonists: 1. Conformationally restricted analogues of trans-cinnamides. J. Med. Chem., 2007, 50(15), 3497-3514.
-
(2007)
J. Med. Chem.
, vol.50
, Issue.15
, pp. 3497-3514
-
-
Norman, M.H.1
Fotsch, C.2
Doherty, E.M.3
Bo, Y.4
Chen, N.5
Chakrabarti, P.6
Doherty, E.M.7
Gavva, N.R.8
Nishimura, N.9
Nixey, T.10
Ognyanov, V.I.11
Rzasa, R.M.12
Stec, M.13
Surapaneni, S.14
Tamir, R.15
Viswanadhan, V.N.16
Treanor, J.J.17
-
45
-
-
34547560453
-
Novel Vanilloid Receptor-1 Antagonists: 2. Structure-Activity Relationships of 4-oxopyrimidines leading to the selection of a clinical candidate
-
Doherty, E. M.; Fotsch, C.; Bannon, A. W.; Bo, Y.; Chen, N.; Dominguez, C.; Falsey, J.; Gavva, N. R.; Katon, J.; Nixey, T.; Ognyanov, V. I.; Pettus, L.; Rzasa, R. M.; Stec, M.; Surapaneni, S.; Tamir, R.; Zhu, J.; Treanor, J. J. S.; Norman, M. H. Novel Vanilloid Receptor-1 Antagonists: 2. Structure-Activity Relationships of 4-oxopyrimidines leading to the selection of a clinical candidate. J. Med. Chem., 2007, 50(15), 3515-3527.
-
(2007)
J. Med. Chem.
, vol.50
, Issue.15
, pp. 3515-3527
-
-
Doherty, E.M.1
Fotsch, C.2
Bannon, A.W.3
Bo, Y.4
Chen, N.5
Dominguez, C.6
Falsey, J.7
Gavva, N.R.8
Katon, J.9
Nixey, T.10
Ognyanov, V.I.11
Pettus, L.12
Rzasa, R.M.13
Stec, M.14
Surapaneni, S.15
Tamir, R.16
Zhu, J.17
Treanor, J.J.S.18
Norman, M.H.19
-
46
-
-
33746753399
-
Ntetrahydroquinolinyl, N-quinolinyl and N-isoquinolinyl biaryl carboxamides as antagonists of TRPV1
-
Westaway, S. M.; Chung, Y.-K.; Davis, J. B.; Holland, V.; Jerman, J. C.; Medhurst, S. J.; Rami, H. K.; Stemp, G.; Stevens, A. J.; Thompson, M.; Winbornb, K. Y.; Wright, J. Ntetrahydroquinolinyl, N-quinolinyl and N-isoquinolinyl biaryl carboxamides as antagonists of TRPV1. Bioorg. Med. Chem. Lett., 2006, 16(17), 4533-4536.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, Issue.17
, pp. 4533-4536
-
-
Westaway, S.M.1
Chung, Y.-K.2
Davis, J.B.3
Holland, V.4
Jerman, J.C.5
Medhurst, S.J.6
Rami, H.K.7
Stemp, G.8
Stevens, A.J.9
Thompson, M.10
Winbornb, K.Y.11
Wright, J.12
-
47
-
-
77951143988
-
Discovery of Novel 6,6-Heterocycles as Transient Receptor Potential Vanilloid (TRPV1) Antagonists
-
Blum, C. A.; Caldwell, T.; Zheng, X.; Bakthavatchalam, R.; Capitosti, S.; Brielmann, H. Lombaert, S. D.; Kershaw, M. T.; Matson, D.; Krause, J. E.; Cortright, D.; Crandall, M.; Martin, W. J.; Murphy, B. A.; Boyce, S.; Jones, A. B.; Mason, G.; Rycroft, W.; Perrett, H.; Conley, R.; Burnaby-Davies, N.; Chenard, B. L.; Hodgetts, K. J. Discovery of Novel 6,6-Heterocycles as Transient Receptor Potential Vanilloid (TRPV1) Antagonists. J. Med. Chem., 2010, 53(8), 3330-3348.
-
(2010)
J. Med. Chem.
, vol.53
, Issue.8
, pp. 3330-3348
-
-
Blum, C.A.1
Caldwell, T.2
Zheng, X.3
Bakthavatchalam, R.4
Capitosti, S.5
Brielmann, H.6
Lombaert, S.D.7
Kershaw, M.T.8
Matson, D.9
Krause, J.E.10
Cortright, D.11
Crandall, M.12
Martin, W.J.13
Murphy, B.A.14
Boyce, S.15
Jones, A.B.16
Mason, G.17
Rycroft, W.18
Perrett, H.19
Conley, R.20
Burnaby-Davies, N.21
Chenard, B.L.22
Hodgetts, K.J.23
more..
-
48
-
-
79951726098
-
Chroman and tetrahydroquinoline ureas as potent TRPV1 antagonists
-
Schmidt, R. G.; Bayburt, E. K.; Latshaw, S. P.; Koenig, J. R.; Daanen, J. F.; McDonald, H. A.; Bianchi, B. R.; Zhong, C.; Joshi, S.; Honore, P.; Marsh, K. C.; Lee, C.-H.; Faltynek, C. R.; Gomtsyan, A. Chroman and tetrahydroquinoline ureas as potent TRPV1 antagonists. Bioorg. Med. Chem. Lett., 2011, 21(5), 1338-1341.
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, Issue.5
, pp. 1338-1341
-
-
Schmidt, R.G.1
Bayburt, E.K.2
Latshaw, S.P.3
Koenig, J.R.4
Daanen, J.F.5
McDonald, H.A.6
Bianchi, B.R.7
Zhong, C.8
Joshi, S.9
Honore, P.10
Marsh, K.C.11
Lee, C.-H.12
Faltynek, C.R.13
Gomtsyan, A.14
-
49
-
-
84859805419
-
Discovery of novel 5,5-diarylpentadienamides as orally available transient receptor potential vanilloid 1 (TRPV1) antagonists
-
Saku, O.; Ishida, H.; Atsumi, E.; Sugimoto, Y.; Kodaira, H.; Kato, Y.; Shirakura, S.; Nakasato, Y. Discovery of novel 5,5-diarylpentadienamides as orally available transient receptor potential vanilloid 1 (TRPV1) antagonists. J. Med. Chem., 2012, 55(7), 3436-3451.
-
(2012)
J. Med. Chem.
, vol.55
, Issue.7
, pp. 3436-3451
-
-
Saku, O.1
Ishida, H.2
Atsumi, E.3
Sugimoto, Y.4
Kodaira, H.5
Kato, Y.6
Shirakura, S.7
Nakasato, Y.8
-
50
-
-
0028244816
-
Tumor necrosis factor: A pleiotropic cytokine and therapeutic target
-
Tracey, K. J.; Cerami, A. Tumor necrosis factor: a pleiotropic cytokine and therapeutic target. Annu. Rev. Med., 1994, 45, 491-503.
-
(1994)
Annu. Rev. Med.
, vol.45
, pp. 491-503
-
-
Tracey, K.J.1
Cerami, A.2
-
51
-
-
0025809325
-
Human tumor necrosis factor gene regulation in phorbol ester stimulated T and B cell lines
-
Goldfeld, A. E.; Strominger, J. L.; Doyle, C. Human Tumor Necrosis Factor Gene Regulation in Phorbol Ester Stimulated T and B Cell Lines. J. Exp. Med., 1991, 174(1), 73-81.
-
(1991)
J. Exp. Med.
, vol.174
, Issue.1
, pp. 73-81
-
-
Goldfeld, A.E.1
Strominger, J.L.2
Doyle, C.3
-
52
-
-
0032815883
-
Adamalysins. A family of metzincins including TNF-alpha converting enzyme (TACE)
-
Killar, L.; White, J.; Black, R.; Peschon, J. Adamalysins. A family of metzincins including TNF-alpha converting enzyme (TACE). Ann. NY Acad. Sci. 1999, 878, 442-452.
-
(1999)
Ann. NY Acad. Sci.
, vol.878
, pp. 442-452
-
-
Killar, L.1
White, J.2
Black, R.3
Peschon, J.4
-
53
-
-
0024281428
-
A novel form of TNF/cachectin is a cell surface cytotoxic transmembrane protein: Ramifications for the complex physiology of TNF
-
Kriegler, M.; Perez, C.; Defay, K.; Albert, I.; Lu, S. D. A novel form of TNF/cachectin is a cell surface cytotoxic transmembrane protein: Ramifications for the complex physiology of TNF. Cell, 1988, 53(1), 45-53.
-
(1988)
Cell
, vol.53
, Issue.1
, pp. 45-53
-
-
Kriegler, M.1
Perez, C.2
Defay, K.3
Albert, I.4
Lu, S.D.5
-
54
-
-
8044257704
-
A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells
-
Black, R. A.; Rauch, C. T.; Kozlosky, C. J.; Peschon, J. J.; Slack, J. L.; Wolfson, M. R.; Castner, B. J.; Stocking, K. L.; Reddy, P.; Srinivasan, S.; Melson, N.; Bioiani, N.; Schooley, K. A.; Gerhart, M.; Davis, R.; Fitzner, J. N.; Johnson, R. S.; Paxton, R. J.; March, C. J.; Cerretti, D. P. A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells. Nature, 1997, 385(6618), 729-733.
-
(1997)
Nature
, vol.385
, Issue.6618
, pp. 729-733
-
-
Black, R.A.1
Rauch, C.T.2
Kozlosky, C.J.3
Peschon, J.J.4
Slack, J.L.5
Wolfson, M.R.6
Castner, B.J.7
Stocking, K.L.8
Reddy, P.9
Srinivasan, S.10
Melson, N.11
Bioiani, N.12
Schooley, K.A.13
Gerhart, M.14
Davis, R.15
Fitzner, J.N.16
Johnson, R.S.17
Paxton, R.J.18
March, C.J.19
Cerretti, D.P.20
more..
-
55
-
-
8044250278
-
Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor-alpha
-
Moss, M. L.; Jin, S.-L.; Milla, M. E.; Bickett, D. M.; Burkhart, W.; Carter, H. L.; Chem, W. J.; Clay, W. C.; Didsbury, J. R.; Hassler, D.; Hoffman, C. R.; Kost, T. A.; Lambert, M. H.; Leesnitzer, M. A.; McCauley, P.; McGeehan, F.; Mitchell, J.; Moyer, M.; Pahel, G.; Rocque, W.; Overton, L. K.; Schoenen, R.; Seaton, T.; Su, J. L.; Becherer, J. D. Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor-alpha. Nature, 1997, 385(6618), 733-736.
-
(1997)
Nature
, vol.385
, Issue.6618
, pp. 733-736
-
-
Moss, M.L.1
Jin, S.-L.2
Milla, M.E.3
Bickett, D.M.4
Burkhart, W.5
Carter, H.L.6
Chem, W.J.7
Clay, W.C.8
Didsbury, J.R.9
Hassler, D.10
Hoffman, C.R.11
Kost, T.A.12
Lambert, M.H.13
Leesnitzer, M.A.14
McCauley, P.15
McGeehan, F.16
Mitchell, J.17
Moyer, M.18
Pahel, G.19
Rocque, W.20
Overton, L.K.21
Schoenen, R.22
Seaton, T.23
Su, J.L.24
Becherer, J.D.25
more..
-
56
-
-
0034775522
-
Biology of TACE inhibition
-
Newton, R. C.; Solomon, K. A.; Covington, M. B.; Deccico, C. P.; Haley, P. J.; Friedeman, S. M.; Vaddi, K. Biology of TACE inhibition. Ann. Rheum. Dis., 2001, 60, iii25-iii32.
-
(2001)
Ann. Rheum. Dis.
, vol.60
-
-
Newton, R.C.1
Solomon, K.A.2
Covington, M.B.3
Deccico, C.P.4
Haley, P.J.5
Friedeman, S.M.6
Vaddi, K.7
-
57
-
-
0033863530
-
Ongoing trials with matrix metalloproteinase inhibitors
-
Brown, P. D. Ongoing trials with matrix metalloproteinase inhibitors. Exp. Opin. Invest. Drugs, 2000, 9(9), 2167-2177.
-
(2000)
Exp. Opin. Invest. Drugs
, vol.9
, Issue.9
, pp. 2167-2177
-
-
Brown, P.D.1
-
58
-
-
0033946952
-
Metalloproteinase inhibitors: New opportunities for the treatment of rheumatoid arthritis and osteoarthritis
-
Shaw, T.; Nixon, J. S.; Bottomley, K. M. Metalloproteinase inhibitors: new opportunities for the treatment of rheumatoid arthritis and osteoarthritis. Exp. Opin. Invest. Drugs, 2000, 9(7), 1469-1478.
-
(2000)
Exp. Opin. Invest. Drugs
, vol.9
, Issue.7
, pp. 1469-1478
-
-
Shaw, T.1
Nixon, J.S.2
Bottomley, K.M.3
-
59
-
-
0035056510
-
The clinical potential of matrix metalloproteinase inhibitors in the rheumatic disorders
-
Elliot, S.; Cawston, T. The clinical potential of matrix metalloproteinase inhibitors in the rheumatic disorders. Drugs Aging, 2001, 18(2), 87-99.
-
(2001)
Drugs Aging
, vol.18
, Issue.2
, pp. 87-99
-
-
Elliot, S.1
Cawston, T.2
-
60
-
-
12444273714
-
Synthesis and structure-activity relationship of N-substituted 4-arylsulfonylpiperidine-4-hydroxamic acids as novel, orally active matrix metalloproteinase inhibitors for the treatment of osteoarthritis
-
Aranapakam, V.; Davis, J. M.; Grosu, G. T.; Baker, J.; Ellingboe, J.; Zask, A.; Levin, J. I.; Sandanayaka, V. P.; Du, M.; Skotnicki, J. S.; DiJoseph, J. F.; Sung, A.; Sharr, M. A.; Killar, L. M.; Walter, T.; Jin, G.; Cowling, R.; Tillett, J.; Zhao, W.; McDevitt, J.; Xu, Z. B. Synthesis and structure-activity relationship of N-substituted 4-arylsulfonylpiperidine-4-hydroxamic acids as novel, orally active matrix metalloproteinase inhibitors for the treatment of osteoarthritis. J. Med. Chem., 2003, 46(12), 2376-2396.
-
(2003)
J. Med. Chem.
, vol.46
, Issue.12
, pp. 2376-2396
-
-
Aranapakam, V.1
Davis, J.M.2
Grosu, G.T.3
Baker, J.4
Ellingboe, J.5
Zask, A.6
Levin, J.I.7
Sandanayaka, V.P.8
Du, M.9
Skotnicki, J.S.10
Dijoseph, J.F.11
Sung, A.12
Sharr, M.A.13
Killar, L.M.14
Walter, T.15
Jin, G.16
Cowling, R.17
Tillett, J.18
Zhao, W.19
McDevitt, J.20
Xu, Z.B.21
more..
-
61
-
-
0032816037
-
-
R. A., Zucker, S., Golub, L. M., Eds.; The New York Academy of Sciences: NY
-
Yocum, S. A.; Lopresti-Morrow, L. L.; Reeves, L. M.; Mitchell, P. G. In: Inhibition of Matrix Metalloproteinases: Therapeutic Applications; Greenwald, R. A., Zucker, S., Golub, L. M., Eds.; The New York Academy of Sciences: NY, 1999, pp. 583-586.
-
(1999)
Inhibition of Matrix Metalloproteinases: Therapeutic Applications; Greenwald
, pp. 583-586
-
-
Yocum, S.A.1
Lopresti-Morrow, L.L.2
Reeves, L.M.3
Mitchell, P.G.4
-
62
-
-
0035341741
-
TACE and other ADAM proteases as targets for drug discovery
-
Moss, M. L.; White, J. M.; Lambert, M. H.; Andrews, R. C. TACE and other ADAM proteases as targets for drug discovery. Drug Discov. Today, 2001, 6(8), 417-426.
-
(2001)
Drug Discov. Today
, vol.6
, Issue.8
, pp. 417-426
-
-
Moss, M.L.1
White, J.M.2
Lambert, M.H.3
Andrews, R.C.4
-
63
-
-
0037038311
-
Discovery of-Lactam Hydroxamic Acids as Selective Inhibitors of Tumor Necrosis Factor Converting Enzyme: Design, Synthesis, and Structure-Activity Relationships
-
Duan, J. J.-W.; Chen, L.; Wasserman, Z. R.; Lu, Z.; Liu, R.-Q.; Covington, M. B.; Qian, M.; Hardman, K. D.; Magolda, R. L.; Newton, R. C.; Christ, D.D.; Wexler, R. R.; Decicco, C. P. Discovery of-Lactam Hydroxamic Acids as Selective Inhibitors of Tumor Necrosis Factor Converting Enzyme: Design, Synthesis, and Structure-Activity Relationships. J. Med. Chem., 2002, 45(23), 4954-4957.
-
(2002)
J. Med. Chem.
, vol.45
, Issue.23
, pp. 4954-4957
-
-
Duan, J.J.-W.1
Chen, L.2
Wasserman, Z.R.3
Lu, Z.4
Liu, R.-Q.5
Covington, M.B.6
Qian, M.7
Hardman, K.D.8
Magolda, R.L.9
Newton, R.C.10
Christ, D.D.11
Wexler, R.R.12
Decicco, C.P.13
-
64
-
-
19944376150
-
Non-hydroxamate 5-phenylpyrimidine-2,4,6-trione derivatives as selective inhibitors of tumor necrosis factor-converting enzyme
-
Duan, J. J.-W.; Lu, Z.; Wasserman, Z. R.; Liu, R.-Q.; Covington, M. B.; Decicco, C. P. Non-hydroxamate 5-phenylpyrimidine-2,4,6-trione derivatives as selective inhibitors of tumor necrosis factor-converting enzyme. Bioorg. Med. Chem. Lett., 2005, 15(12), 2970-2973.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, Issue.12
, pp. 2970-2973
-
-
Duan, J.J.-W.1
Lu, Z.2
Wasserman, Z.R.3
Liu, R.-Q.4
Covington, M.B.5
Decicco, C.P.6
-
65
-
-
33845612218
-
Discovery of low nanomolar non-hydroxamate inhibitors of tumor necrosis factor-converting enzyme (TACE)
-
Duan, J. J.-W.; Chen, L.; Lu, Z.; Jiang, B.; Asakawa, N.; Sheppeck, J. E.; Liu, R.-Q.; Covington, M. B.; Pitts, W.; Kim, S.-H.; Decicco, C. P. Discovery of low nanomolar non-hydroxamate inhibitors of tumor necrosis factor-converting enzyme (TACE). Bioorg. Med. Chem. Lett., 2007, 17(1), 266-271.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, Issue.1
, pp. 266-271
-
-
Duan, J.J.-W.1
Chen, L.2
Lu, Z.3
Jiang, B.4
Asakawa, N.5
Sheppeck, J.E.6
Liu, R.-Q.7
Covington, M.B.8
Pitts, W.9
Kim, S.-H.10
Decicco, C.P.11
-
66
-
-
33645844249
-
Synthesis and structure-activity relationship of a novel, achiral series of TNF-converting enzyme inhibitors
-
Gilmore, J. L.; King, B. W.; Harris, C.; Maduskuie, T.; Mercer, S. E.; Liu, R.-Q.; Covington, M. B.; Qian, M.; Ribadeneria, M. D.; Vaddi, K.; Trzaskos, J. M.; Newton, R. C.; Decicco, C. P.; Duan, J. J.-W. Synthesis and structure-activity relationship of a novel, achiral series of TNF-converting enzyme inhibitors. Bioorg. Med. Chem. Lett., 2006, 16(10), 2699-2704.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, Issue.10
, pp. 2699-2704
-
-
Gilmore, J.L.1
King, B.W.2
Harris, C.3
Maduskuie, T.4
Mercer, S.E.5
Liu, R.-Q.6
Covington, M.B.7
Qian, M.8
Ribadeneria, M.D.9
Vaddi, K.10
Trzaskos, J.M.11
Newton, R.C.12
Decicco, C.P.13
Duan, J.J.-W.14
-
67
-
-
37549069911
-
Discovery of-benzamido hydroxamic acids as potent, selective, and orally bioavailable TACE inhibitors
-
Duan, J. J.-W.; Chen, L.; Lu, Z.; Xue, C.-B.; Liu, R.-Q.; Covington, M. B.; Qian, M.; Wasserman, Z. R.; Vaddi, K.; Christ, D. D.; Trzaskos, J. M.; Newton, R. C.; Decicco, C. P. Discovery of-benzamido hydroxamic acids as potent, selective, and orally bioavailable TACE inhibitors. Bioorg. Med. Chem. Lett., 2008, 18(1), 241-246.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, Issue.1
, pp. 241-246
-
-
Duan, J.J.-W.1
Chen, L.2
Lu, Z.3
Xue, C.-B.4
Liu, R.-Q.5
Covington, M.B.6
Qian, M.7
Wasserman, Z.R.8
Vaddi, K.9
Christ, D.D.10
Trzaskos, J.M.11
Newton, R.C.12
Decicco, C.P.13
-
68
-
-
38149000234
-
Cyclic-benzamido hydroxamic acids: Novel templates for the design, synthesis, and evaluation of selective inhibitors of TNF-converting enzyme (TACE)
-
Ott, G. R.; Asakawa, N.; Lu, Z.; Liu, R.-Q.; Covington, M. B.; Vaddi, K.; Qian, M.; Newton, R. C.; Christ, D. D.; Traskos, J.M.; Decicco, C. P.; Duan, J. J.-W. Cyclic-benzamido hydroxamic acids: Novel templates for the design, synthesis, and evaluation of selective inhibitors of TNF-converting enzyme (TACE). Bioorg. Med. Chem. Lett., 2008, 18(2), 694-699.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, Issue.2
, pp. 694-699
-
-
Ott, G.R.1
Asakawa, N.2
Lu, Z.3
Liu, R.-Q.4
Covington, M.B.5
Vaddi, K.6
Qian, M.7
Newton, R.C.8
Christ, D.D.9
Traskos, J.M.10
Decicco, C.P.11
Duan, J.J.-W.12
-
69
-
-
38949095681
-
Cyclic-benzamido hydroxamic acids: Novel oxaspiro[4. 4]nonane templates for the discovery of potent, selective, orally bioavailable inhibitors of tumor necrosis factor-converting enzyme (TACE)
-
Ott, G. R.; Asakawa, N.; Liu, R.-Q.; Covington, M. B.; Qian, M.; Vaddi, K.; Newton, R. C.; Trzaskos, J. M.; Christ, D. D.; Galya, L.; Scholz, T.; Marshall, W.; Duan, J. J.-W. Cyclic-benzamido hydroxamic acids: Novel oxaspiro[4.4]nonane templates for the discovery of potent, selective, orally bioavailable inhibitors of tumor necrosis factor-converting enzyme (TACE). Bioorg. Med. Chem. Lett., 2008, 18(4), 1288-1292.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, Issue.4
, pp. 1288-1292
-
-
Ott, G.R.1
Asakawa, N.2
Liu, R.-Q.3
Covington, M.B.4
Qian, M.5
Vaddi, K.6
Newton, R.C.7
Trzaskos, J.M.8
Christ, D.D.9
Galya, L.10
Scholz, T.11
Marshall, W.12
Duan, J.J.-W.13
-
70
-
-
34447322020
-
Synthesis and structure-activity relationship of a novel, nonhydroxamate series of TNF-converting enzyme inhibitors
-
Gilmore, J. L.; King, B. W.; Asakawa, N.; Harrison, K.; Tebben, A.; Sheppeck II, J. E.; Liu, R.-Q.; Covington, M.; Duan, J. J.-W. Synthesis and structure-activity relationship of a novel, nonhydroxamate series of TNF-converting enzyme inhibitors. Bioorg. Med. Chem. Lett., 2007, 17(16), 4678-4682.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, Issue.16
, pp. 4678-4682
-
-
Gilmore, J.L.1
King, B.W.2
Asakawa, N.3
Harrison, K.4
Tebben, A.5
Sheppeck, I.I.J.E.6
Liu, R.-Q.7
Covington, M.8
Duan, J.J.-W.9
-
71
-
-
53949085531
-
Discovery of novel hydroxamates as highly potent tumor necrosis factor-converting enzyme inhibitors. Part II: Optimization of the S3' pocket
-
Mazzola Jr. R. D.; Zhu, Z.; Sinning, L.; McKittrick, B.; Lavey, B.; Spitler, J.; Kozlowski, J.; Neng-Yang, S.; Zhou, G.; Guo, Z.; Orth, P.; Madison, V.; Sun, J.; Lundell, D.; Niu, X. Discovery of novel hydroxamates as highly potent tumor necrosis factor-converting enzyme inhibitors. Part II: Optimization of the S3' pocket. Bioorg. Med. Chem. Lett., 2008, 18(21), 5809-5814.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, Issue.21
, pp. 5809-5814
-
-
Mazzola Jr., R.D.1
Zhu, Z.2
Sinning, L.3
McKittrick, B.4
Lavey, B.5
Spitler, J.6
Kozlowski, J.7
Neng-Yang, S.8
Zhou, G.9
Guo, Z.10
Orth, P.11
Madison, V.12
Sun, J.13
Lundell, D.14
Niu, X.15
-
72
-
-
0033791318
-
Cyclooxygenases: Structural, cellular, and molecular biology
-
Smith, W. L.; DeWitt, D. L.; Garavito, R. M. Cyclooxygenases: structural, cellular, and molecular biology. Annu. Rev. Biochem., 2000, 69, 145-182.
-
(2000)
Annu. Rev. Biochem.
, vol.69
, pp. 145-182
-
-
Smith, W.L.1
Dewitt, D.L.2
Garavito, R.M.3
-
73
-
-
0033551847
-
Arachidonic acid oxygenation by COX-1 and COX-2
-
Marnett, L. J.; Rowlinson, S. W.; Goodwin, D. C.; Kalgutkar, A. S.; Lanzo, C. A. Arachidonic acid oxygenation by COX-1 and COX-2. Mechanisms of catalysis and inhibition. J. Biol. Chem., 1999, 274, 22903-22906.
-
(1999)
Mechanisms of Catalysis and Inhibition. J. Biol. Chem.
, vol.274
, pp. 22903-22906
-
-
Marnett, L.J.1
Rowlinson, S.W.2
Goodwin, D.C.3
Kalgutkar, A.S.4
Lanzo, C.A.5
-
74
-
-
34147119080
-
Structural and functional basis of cyclooxygenase inhibition
-
Blobaum, A. L.; Marnett, L. J. Structural and Functional Basis of Cyclooxygenase Inhibition. J. Med. Chem., 2007, 50(7), 1425-1441.
-
(2007)
J. Med. Chem.
, vol.50
, Issue.7
, pp. 1425-1441
-
-
Blobaum, A.L.1
Marnett, L.J.2
-
75
-
-
75149177657
-
Design, synthesis and biological evaluation of new 2,3-diarylquinoline derivatives as selective cyclooxygenase-2 inhibitors
-
Ghodsi, R.; Zarghi, A.; Daraei, B.; Hedayati, M. Design, synthesis and biological evaluation of new 2,3-diarylquinoline derivatives as selective cyclooxygenase-2 inhibitors. Bioorg. Med. Chem., 2010, 18(3), 1029-1033.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, Issue.3
, pp. 1029-1033
-
-
Ghodsi, R.1
Zarghi, A.2
Daraei, B.3
Hedayati, M.4
-
76
-
-
67650083504
-
Synthesis and biological evaluation of new 4-carboxyl quinoline derivatives as cyclooxygenase-2 inhibitors
-
Zarghi, A.; Ghodsi, R.; Azizi, E.; Daraie, B.; Hedayati, M.; Dadrass, O. G. Synthesis and biological evaluation of new 4-carboxyl quinoline derivatives as cyclooxygenase-2 inhibitors. Bioorg. Med. Chem., 2009, 17(14), 5312-5317.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, Issue.14
, pp. 5312-5317
-
-
Zarghi, A.1
Ghodsi, R.2
Azizi, E.3
Daraie, B.4
Hedayati, M.5
Dadrass, O.G.6
-
77
-
-
20944441781
-
Prostaglandinmediated control of rat brain kynurenic acid synthesis-opposite actions by COX-1 and COX-2 isoforms
-
Schwieler, L.; Erhardt, S.; Erhardt, C.; Engberg, G. Prostaglandinmediated control of rat brain kynurenic acid synthesis-opposite actions by COX-1 and COX-2 isoforms. J. Neural Transm., 2005, 112(7), 863-872.
-
(2005)
J. Neural Transm.
, vol.112
, Issue.7
, pp. 863-872
-
-
Schwieler, L.1
Erhardt, S.2
Erhardt, C.3
Engberg, G.4
-
78
-
-
0034047074
-
Glutamate and kynurenate in the rat central nervous system following treatments with tail ischaemia or diclofenac
-
Edwards, S. R.; Mather, L. E.; Lin, Y.; Power, I.; Cousins, M. J. Glutamate and kynurenate in the rat central nervous system following treatments with tail ischaemia or diclofenac. J. Pharm. Pharmacol., 2000, 52(1), 59-66.
-
(2000)
J. Pharm. Pharmacol.
, vol.52
, Issue.1
, pp. 59-66
-
-
Edwards, S.R.1
Mather, L.E.2
Lin, Y.3
Power, I.4
Cousins, M.J.5
-
79
-
-
78349258913
-
Synthesis and pharmacological evaluation of some 4-oxoquinoline-2- carboxylic acid derivatives as anti-inflammatory and analgesic agents
-
Mazzoni, O.; Esposito, G.; Diurno, M. V.; Brancaccio, D.; Carotenuto, A.; Grieco, P.; Novellino, E.; Filippelli, W. Synthesis and pharmacological evaluation of some 4-oxoquinoline-2-carboxylic acid derivatives as anti-inflammatory and analgesic agents. Arch. Pharm. Chem. Life Sci., 2010, 10, 561-569.
-
(2010)
Arch. Pharm. Chem. Life Sci.
, vol.10
, pp. 561-569
-
-
Mazzoni, O.1
Esposito, G.2
Diurno, M.V.3
Brancaccio, D.4
Carotenuto, A.5
Grieco, P.6
Novellino, E.7
Filippelli, W.8
-
80
-
-
0347990509
-
1,2-Diaryl-1-ethanone and pyrazolo[4,3-c]quinoline-4-one as novel selective cyclooxygenase-2 inhibitors
-
Baruah, B.; Dasu, K.; Vaitilingam, B.; Vanguri, A.; Casturi, S. R.; Yeleswarapu, K. R. 1,2-Diaryl-1-ethanone and pyrazolo[4,3-c]quinoline-4-one as novel selective cyclooxygenase-2 inhibitors. Bioorg. Med. Chem. Lett., 2004, 14(2), 445-448.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, Issue.2
, pp. 445-448
-
-
Baruah, B.1
Dasu, K.2
Vaitilingam, B.3
Vanguri, A.4
Casturi, S.R.5
Yeleswarapu, K.R.6
-
81
-
-
33846217395
-
Synthesis and biological evaluation of quinoline salicylic acids as P-Selectin antagonists
-
Kaila, N.; Janz, K.; DeBernardo, S.; Bedard, P. W.; Camphausen, R. T.; Tam, S.; Tsao, D.H. H.; Keith Jr., J. C.; Nickerson-Nutter, C.; Shilling, A.; Young-Sciame, R.; Wang, Q. Synthesis and biological evaluation of quinoline salicylic acids as P-Selectin antagonists. J. Med. Chem., 2007, 50(1), 21-39.
-
(2007)
J. Med. Chem.
, vol.50
, Issue.1
, pp. 21-39
-
-
Kaila, N.1
Janz, K.2
Debernardo, S.3
Bedard, P.W.4
Camphausen, R.T.5
Tam, S.6
Tsao, D.H.H.7
Keith Jr., J.C.8
Nickerson-Nutter, C.9
Shilling, A.10
Young-Sciame, R.11
Wang, Q.12
-
82
-
-
0033613168
-
Multiple, targeted deficiencies in selectins reveal a predominant role for Pselectin in leukocyte recruitment
-
Robinson, S. D.; Frenette, P. S.; Rayburn, H.; Cummiskey, M.; Ullman-Culleré, M.; Wagner, D. D.; Hynes, R. O. Multiple, targeted deficiencies in selectins reveal a predominant role for Pselectin in leukocyte recruitment. Proc. Natl. Acad. Sci. U.S.A. 1999, 96(20), 11452-11457.
-
(1999)
Proc. Natl. Acad. Sci. U.S.A.
, vol.96
, Issue.20
, pp. 11452-11457
-
-
Robinson, S.D.1
Frenette, P.S.2
Rayburn, H.3
Cummiskey, M.4
Ullman-Culleré, M.5
Wagner, D.D.6
Hynes, R.O.7
-
84
-
-
0346059512
-
Synthesis and anti-inflammatory evaluation of 4-anilinofuro[2,3-b] quinoline and 4-phenoxyfuro[2,3-b]quinoline derivatives
-
Chen, Y.-L.; Chen, I.-L.; Lu, C.-M.; Tzeng, C.-C.; Tsao, L.-T.; Wang, J.-P. Synthesis and anti-inflammatory evaluation of 4-anilinofuro[2,3-b] quinoline and 4-phenoxyfuro[2,3-b]quinoline derivatives. Part 3. Bioorg. Med. Chem., 2004, 12(2), 387-392.
-
(2004)
Part 3. Bioorg. Med. Chem.
, vol.12
, Issue.2
, pp. 387-392
-
-
Chen, Y.-L.1
Chen, I.-L.2
Lu, C.-M.3
Tzeng, C.-C.4
Tsao, L.-T.5
Wang, J.-P.6
-
85
-
-
46449106774
-
Synthesis and anti-inflammatory activity evaluation of novel 7-alkoxy 1-amino-4,5-dihydro[1,2,4]triazole[4,3-A]quinolines
-
Sun, X.-Y.; Wei, C.-X.; Chai, K.-Y.; Piao, H.-R.; Quan, Z.-S. Synthesis and anti-inflammatory activity evaluation of novel 7-alkoxy 1-amino-4,5- dihydro[1,2,4]triazole[4,3-a]quinolines. Arch. Pharm. Chem. Life Sci., 2008, 341 (5), 288-293.
-
(2008)
Arch. Pharm. Chem. Life Sci.
, vol.341
, Issue.5
, pp. 288-293
-
-
Sun, X.-Y.1
Wei, C.-X.2
Chai, K.-Y.3
Piao, H.-R.4
Quan, Z.-S.5
-
86
-
-
1642409766
-
Tetrazolo[ 1,5-A]quinoline as a potential promising new scaffold for the synthesis of novel anti-inflammatory and antibacterial agents
-
Bekhit, A. A.; El-Sayed, O. A.; Aboulmagd, E.; Park, J. Y. Tetrazolo[ 1,5-a]quinoline as a potential promising new scaffold for the synthesis of novel anti-inflammatory and antibacterial agents. Eur. J. Med. Chem., 2004, 39(3), 249-255.
-
(2004)
Eur. J. Med. Chem.
, vol.39
, Issue.3
, pp. 249-255
-
-
Bekhit, A.A.1
El-Sayed, O.A.2
Aboulmagd, E.3
Park, J.Y.4
-
87
-
-
34447306306
-
Anti-inflammatory thiazine alkaloids isolated from the New Zealand Ascidian Aplidium sp. : IIInhibitors of the neutrophil respiratory burst in a model of gouty arthritis
-
Pearce, A. N.; Chia, E. W.; Berridge, M. V.; Clark, G. R.; Harper, J. L.; Larsen, L.; Maas, E. W.; Page, M. J.; Perry, N. B.; Webb, V. L.; Copp, B. R. Anti-inflammatory thiazine alkaloids isolated from the New Zealand Ascidian Aplidium sp.: Inhibitors of the neutrophil respiratory burst in a model of gouty arthritis. J. Nat. Prod., 2007, 70(6), 936-940.
-
(2007)
J. Nat. Prod.
, vol.70
, Issue.6
, pp. 936-940
-
-
Pearce, A.N.1
Chia, E.W.2
Berridge, M.V.3
Clark, G.R.4
Harper, J.L.5
Larsen, L.6
Maas, E.W.7
Page, M.J.8
Perry, N.B.9
Webb, V.L.10
Copp, B.R.11
-
88
-
-
53949104202
-
Synthesis and anti-inflammatory structure-activity relationships of thiazine-quinoline-quinones: Inhibitors of the neutrophil respiratory burst in a model of acute gouty arthritis
-
Chia, E. W.; Pearce, A. N.; Berridge, M. V.; Larsen, L.; Perry, N. B.; Sansom, C. E. Godfrey, C. A.; Hanton, L. R.; (Leon) Lu, G.-L.; Walton, M.; Denny, W. A.; Webb, V. L.; Copp, B. R.; Harper, J. L. Synthesis and anti-inflammatory structure-activity relationships of thiazine-quinoline- quinones: Inhibitors of the neutrophil respiratory burst in a model of acute gouty arthritis. Bioorg. Med. Chem., 2008, 16(21), 9432-9442.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, Issue.21
, pp. 9432-9442
-
-
Chia, E.W.1
Pearce, A.N.2
Berridge, M.V.3
Larsen, L.4
Perry, N.B.5
Sansom, C.E.6
Godfrey, C.A.7
Hanton, L.R.8
Lu, G.-L.9
Walton, M.10
Denny, W.A.11
Webb, V.L.12
Copp, B.R.13
Harper, J.L.14
-
89
-
-
40949138241
-
Synthesis, analgesic, anti-inflammatory, and antimicrobial activity of some novel pyrimido[4,5-b]quinolin-4-ones
-
El-Gazzar, A.-R. B. A.; El-Enanyb, M. M.; Mahmouda, M. N. Synthesis, analgesic, anti-inflammatory, and antimicrobial activity of some novel pyrimido[4,5-b]quinolin-4-ones. Bioorg. Med. Chem., 2008, 16(6), 3261-3273.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, Issue.6
, pp. 3261-3273
-
-
El-Gazzar, A.-R.B.A.1
El-Enanyb, M.M.2
Mahmouda, M.N.3
-
90
-
-
61449168879
-
New acyclic nucleosides analogues as potential analgesic, antiinflammatory, anti-oxidant and anti-microbial derived from pyrimido[4,5-b]quinolines Eur
-
El-Gazzar, A. B. A.; Hafez, H. N.; Nawwar, G. A. M. New acyclic nucleosides analogues as potential analgesic, antiinflammatory, anti-oxidant and anti-microbial derived from pyrimido[4,5-b]quinolines Eur. J. Med. Chem., 2009, 44(4), 1427-1436.
-
(2009)
J. Med. Chem.
, vol.44
, Issue.4
, pp. 1427-1436
-
-
El-Gazzar, A.B.A.1
Hafez, H.N.2
Nawwar, G.A.M.3
-
92
-
-
0036082487
-
Pharmacology of N-(3,5-Dichloro-1-oxido-4-pyridinyl)-8-methoxy-2- (trifluoromethyl)-5-quinoline carboxamide (SCH351591), a novel, orally active phosphodiesterase 4 inhibitor
-
Billah, M. M.; Cooper, N.; Minnicozzi, M.; Warneck, J.; Wang, P.; Hey, J. A.; Kreutner, W.; Rizzo, C.A.; Smith, S. R.; Young, S.; Chapman, R. W.; Dyke, H.; Shih, N.-Y.; Piwinski, J. J.; Cuss, F. M.; Montana, J.; Ganguly, A. K.; Egan, R. W. Pharmacology of N-(3,5-Dichloro-1-oxido-4-pyridinyl)-8-methoxy-2- (trifluoromethyl)-5-quinoline carboxamide (SCH351591), a novel, orally active phosphodiesterase 4 inhibitor. J. Pharmacol. Exp. Ther. 2002, 302 (1), 127-137.
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.302
, Issue.1
, pp. 127-137
-
-
Billah, M.M.1
Cooper, N.2
Minnicozzi, M.3
Warneck, J.4
Wang, P.5
Hey, J.A.6
Kreutner, W.7
Rizzo, C.A.8
Smith, S.R.9
Young, S.10
Chapman, R.W.11
Dyke, H.12
Shih, N.-Y.13
Piwinski, J.J.14
Cuss, F.M.15
Montana, J.16
Ganguly, A.K.17
Egan, R.W.18
-
93
-
-
2542487257
-
The toxicity of SCH351591, a novel phosphodiesterase-4
-
Losco, P. E.; Evans, E. W.; Barat, S. A.; Blackshear, P. E.; Reyderman, L.; Fine, J. S.; Bober, L. A.; Anthes, J. C.; Mirro, E. J.; Cuss, F. M. The toxicity of SCH351591, a novel phosphodiesterase-4. Tox. Pathol., 2004, 32, 295-308.
-
(2004)
Tox. Pathol.
, vol.32
, pp. 295-308
-
-
Losco, P.E.1
Evans, E.W.2
Barat, S.A.3
Blackshear, P.E.4
Reyderman, L.5
Fine, J.S.6
Bober, L.A.7
Anthes, J.C.8
Mirro, E.J.9
Cuss, F.M.10
-
94
-
-
84887877781
-
-
Available from: http://www.gsk-clinicalstudyregister.com/quicksearch- list.jsp?item=GSK256066&type=Compound&letterrange=G-K&studyType= All&phase=All&population=All&marketing=All.
-
-
-
-
95
-
-
84860662131
-
Anti-inflammatory iridoids of botanical origin
-
Viljoen, A.; Mncwangi, N.; Vermaak, I. Anti-Inflammatory Iridoids of Botanical Origin. Curr. Med. Chem., 2012, 19(14), 2104-2127.
-
(2012)
Curr. Med. Chem.
, vol.19
, Issue.14
, pp. 2104-2127
-
-
Viljoen, A.1
Mncwangi, N.2
Vermaak, I.3
-
96
-
-
84861881610
-
Discovery of selective small molecular TACE inhibitors for the treatment of rheumatoid arthritis
-
Li, N.G.; Shi, Z.H.; Tang, Y.P.; Wei-Li.; Lian-Yin.; Duan, J.A. Discovery of Selective Small Molecular TACE Inhibitors for the Treatment of Rheumatoid Arthritis. Curr. Med. Chem., 2012, 19(18), 2924-2956.
-
(2012)
Curr. Med. Chem.
, vol.19
, Issue.18
, pp. 2924-2956
-
-
Li, N.G.1
Shi, Z.H.2
Tang, Y.P.3
|