-
1
-
-
0036197504
-
Major depression and insomnia in chronic pain
-
Wilson, K. G.; Eriksson, M. Y.; DEon, J. L.; Mikail, S. F.; Emery, P. C. Major depression and insomnia in chronic pain Clin. J. Pain 2002, 18, 77-83
-
(2002)
Clin. J. Pain
, vol.18
, pp. 77-83
-
-
Wilson, K.G.1
Eriksson, M.Y.2
Deon, J.L.3
Mikail, S.F.4
Emery, P.C.5
-
2
-
-
0031742196
-
Self-reported sleep and mood disturbance in chronic pain patients
-
Morin, C. M.; Gibson, D.; Wade, J. Self-reported sleep and mood disturbance in chronic pain patients Clin. J. Pain 1998, 14, 311-314
-
(1998)
Clin. J. Pain
, vol.14
, pp. 311-314
-
-
Morin, C.M.1
Gibson, D.2
Wade, J.3
-
3
-
-
0034523887
-
Self-reported sleep quality and quality of life for individuals with chronic pain conditions
-
Menefee, L. A.; Frank, E. D.; Doghramji, K.; Picarello, K.; Park, J. J.; Jalali, S.; Perez-Schwartz, L. Self-reported sleep quality and quality of life for individuals with chronic pain conditions Clin. J. Pain 2000, 16, 290-297
-
(2000)
Clin. J. Pain
, vol.16
, pp. 290-297
-
-
Menefee, L.A.1
Frank, E.D.2
Doghramji, K.3
Picarello, K.4
Park, J.J.5
Jalali, S.6
Perez-Schwartz, L.7
-
4
-
-
6344282277
-
Understanding pain in depression
-
Stahl, S.; Briley, M. Understanding pain in depression Hum. Psychopharmacol. 2004, 19 (Suppl. 1) S9-S13
-
(2004)
Hum. Psychopharmacol.
, vol.19
, Issue.SUPPL. 1
-
-
Stahl, S.1
Briley, M.2
-
5
-
-
0034192592
-
A review of psychological risk factors in back and neck pain
-
Linton, S. J. A review of psychological risk factors in back and neck pain Spine (Philadelphia) 2000, 25, 1148-1156
-
(2000)
Spine (Philadelphia)
, vol.25
, pp. 1148-1156
-
-
Linton, S.J.1
-
6
-
-
0033161302
-
The association of chronic pain and suicide
-
Fishbain, D. A. The association of chronic pain and suicide Semin. Clin. Neuropsychiatry 1999, 4, 221-227
-
(1999)
Semin. Clin. Neuropsychiatry
, vol.4
, pp. 221-227
-
-
Fishbain, D.A.1
-
7
-
-
33645736058
-
Suicidality in chronic pain: A review of the prevalence, risk factors and psychological links
-
Tang, N. K.; Crane, C. Suicidality in chronic pain: a review of the prevalence, risk factors and psychological links Psychol. Med. 2006, 36, 575-586
-
(2006)
Psychol. Med.
, vol.36
, pp. 575-586
-
-
Tang, N.K.1
Crane, C.2
-
8
-
-
0035690330
-
Cyclooxygenase enzymes: Catalysis and inhibition
-
Kurumbail, R. G.; Kiefer, J. R.; Marnett, L. J. Cyclooxygenase enzymes: catalysis and inhibition Curr. Opin. Struct. Biol. 2001, 11, 752-760
-
(2001)
Curr. Opin. Struct. Biol.
, vol.11
, pp. 752-760
-
-
Kurumbail, R.G.1
Kiefer, J.R.2
Marnett, L.J.3
-
9
-
-
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, 1425-1441
-
(2007)
J. Med. Chem.
, vol.50
, pp. 1425-1441
-
-
Blobaum, A.L.1
Marnett, L.J.2
-
10
-
-
66349127141
-
Cyclooxygenases: Structural and functional insights
-
Rouzer, C. A.; Marnett, L. J. Cyclooxygenases: structural and functional insights J. Lipid Res. 2009, 50 (Suppl.) S29-S34
-
(2009)
J. Lipid Res.
, vol.50
, Issue.SUPPL.
-
-
Rouzer, C.A.1
Marnett, L.J.2
-
11
-
-
65249118795
-
The COXIB experience: A look in the rearview mirror
-
Marnett, L. J. The COXIB experience: a look in the rearview mirror Annu. Rev. Pharmacol. Toxicol. 2009, 49, 265-290
-
(2009)
Annu. Rev. Pharmacol. Toxicol.
, vol.49
, pp. 265-290
-
-
Marnett, L.J.1
-
12
-
-
32244441631
-
NSAID-associated adverse effects and acid control aids to prevent them: A review of current treatment options
-
Naesdal, J.; Brown, K. NSAID-associated adverse effects and acid control aids to prevent them: a review of current treatment options Drug Saf. 2006, 29, 119-132
-
(2006)
Drug Saf.
, vol.29
, pp. 119-132
-
-
Naesdal, J.1
Brown, K.2
-
13
-
-
6044267892
-
Failing the public health-rofecoxib, Merck, and the FDA
-
Topol, E. J. Failing the public health-rofecoxib, Merck, and the FDA N. Engl. J. Med. 2004, 351, 1707-1709
-
(2004)
N. Engl. J. Med.
, vol.351
, pp. 1707-1709
-
-
Topol, E.J.1
-
14
-
-
0033526928
-
The discovery of rofecoxib, [MK 966, Vioxx, 4-(4′- methylsulfonylphenyl)-3-phenyl-2(5H)-furanone], an orally active cyclooxygenase-2-inhibitor
-
Prasit, P.; Wang, Z.; Brideau, C.; Chan, C.-C.; Charleson, S.; Cromlish, W.; Ethier, D.; Evans, J. F.; Ford-Hutchinson, A. W.; Gauthier, J. Y.; Gordon, R.; Guay, J.; Gresser, M.; Kargman, S.; Kennedy, B.; Leblanc, Y.; Léger, S.; Mancini, J.; ONeill, G. P.; Ouellet, M.; Percival, M. D.; Perrier, H.; Riendeau, D.; Rodger, I.; Tagari, P.; Thérien, M.; Vickers, P.; Wong, E.; Xu, L.-J.; Young, R. N.; Zamboni, R.; Boyce, S.; Rupniak, N.; Forrest, M.; Visco, D.; Patrick, D. The discovery of rofecoxib, [MK 966, Vioxx, 4-(4′-methylsulfonylphenyl)-3-phenyl-2(5H)-furanone], an orally active cyclooxygenase-2-inhibitor Bioorg. Med. Chem. Lett. 1999, 9, 1773-1778
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 1773-1778
-
-
Prasit, P.1
Wang, Z.2
Brideau, C.3
Chan, C.-C.4
Charleson, S.5
Cromlish, W.6
Ethier, D.7
Evans, J.F.8
Ford-Hutchinson, A.W.9
Gauthier, J.Y.10
Gordon, R.11
Guay, J.12
Gresser, M.13
Kargman, S.14
Kennedy, B.15
Leblanc, Y.16
Léger, S.17
Mancini, J.18
Oneill, G.P.19
Ouellet, M.20
Percival, M.D.21
Perrier, H.22
Riendeau, D.23
Rodger, I.24
Tagari, P.25
Thérien, M.26
Vickers, P.27
Wong, E.28
Xu, L.-J.29
Young, R.N.30
Zamboni, R.31
Boyce, S.32
Rupniak, N.33
Forrest, M.34
Visco, D.35
Patrick, D.36
more..
-
15
-
-
21344432777
-
The endocannabinoid system: A drug discovery perspective
-
Piomelli, D. The endocannabinoid system: a drug discovery perspective Curr. Opin. Invest. Drugs (BioMed Cent.) 2005, 6, 672-679
-
(2005)
Curr. Opin. Invest. Drugs (BioMed Cent.)
, vol.6
, pp. 672-679
-
-
Piomelli, D.1
-
16
-
-
67650088165
-
The endocannabinoid system as a target for novel anxiolytic and antidepressant drugs
-
Gaetani, S.; Dipasquale, P.; Romano, A.; Righetti, L.; Cassano, T.; Piomelli, D.; Cuomo, V. The endocannabinoid system as a target for novel anxiolytic and antidepressant drugs Int. Rev. Neurobiol. 2009, 85, 57-72
-
(2009)
Int. Rev. Neurobiol.
, vol.85
, pp. 57-72
-
-
Gaetani, S.1
Dipasquale, P.2
Romano, A.3
Righetti, L.4
Cassano, T.5
Piomelli, D.6
Cuomo, V.7
-
17
-
-
29444460231
-
Antidepressant-like activity and modulation of brain monoaminergic transmission by blockade of anandamide hydrolysis
-
Gobbi, G.; Bambico, F. R.; Mangieri, R.; Bortolato, M.; Campolongo, P.; Solinas, M.; Cassano, T.; Morgese, M. G.; Debonnel, G.; Duranti, A.; Tontini, A.; Tarzia, G.; Mor, M.; Trezza, V.; Goldberg, S. R.; Cuomo, V.; Piomelli, D. Antidepressant-like activity and modulation of brain monoaminergic transmission by blockade of anandamide hydrolysis Proc. Natl. Acad. Sci. U.S.A. 2005, 102, 18620-18625
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 18620-18625
-
-
Gobbi, G.1
Bambico, F.R.2
Mangieri, R.3
Bortolato, M.4
Campolongo, P.5
Solinas, M.6
Cassano, T.7
Morgese, M.G.8
Debonnel, G.9
Duranti, A.10
Tontini, A.11
Tarzia, G.12
Mor, M.13
Trezza, V.14
Goldberg, S.R.15
Cuomo, V.16
Piomelli, D.17
-
18
-
-
77957263726
-
Anandamide suppresses pain initiation through a peripheral endocannabinoid mechanism
-
Clapper, J. R.; Moreno-Sanz, G.; Russo, R.; Guijarro, A.; Vacondio, F.; Duranti, A.; Tontini, A.; Sanchini, S.; Sciolino, N. R.; Spradley, J. M.; Hohmann, A. G.; Calignano, A.; Mor, M.; Tarzia, G.; Piomelli, D. Anandamide suppresses pain initiation through a peripheral endocannabinoid mechanism Nat. Neurosci. 2010, 13, 1265-1270
-
(2010)
Nat. Neurosci.
, vol.13
, pp. 1265-1270
-
-
Clapper, J.R.1
Moreno-Sanz, G.2
Russo, R.3
Guijarro, A.4
Vacondio, F.5
Duranti, A.6
Tontini, A.7
Sanchini, S.8
Sciolino, N.R.9
Spradley, J.M.10
Hohmann, A.G.11
Calignano, A.12
Mor, M.13
Tarzia, G.14
Piomelli, D.15
-
19
-
-
0037234363
-
Modulation of anxiety through blockade of anandamide hydrolysis
-
Kathuria, S.; Gaetani, S.; Fegley, D.; Valino, F.; Duranti, A.; Tontini, A.; Mor, M.; Tarzia, G.; La Rana, G.; Calignano, A.; Giustino, A.; Tattoli, M.; Palmery, M.; Cuomo, V.; Piomelli, D. Modulation of anxiety through blockade of anandamide hydrolysis Nat. Med. 2003, 9, 76-81
-
(2003)
Nat. Med.
, vol.9
, pp. 76-81
-
-
Kathuria, S.1
Gaetani, S.2
Fegley, D.3
Valino, F.4
Duranti, A.5
Tontini, A.6
Mor, M.7
Tarzia, G.8
La Rana, G.9
Calignano, A.10
Giustino, A.11
Tattoli, M.12
Palmery, M.13
Cuomo, V.14
Piomelli, D.15
-
20
-
-
0027078685
-
Isolation and structure of a brain constituent that binds to the cannabinoid receptor
-
Devane, W. A.; Hanus, L.; Breuer, A.; Pertwee, R. G.; Stevenson, L. A.; Griffin, G.; Gibson, D.; Mandelbaum, A.; Etinger, A.; Mechoulam, R. Isolation and structure of a brain constituent that binds to the cannabinoid receptor Science 1992, 258, 1946-1949
-
(1992)
Science
, vol.258
, pp. 1946-1949
-
-
Devane, W.A.1
Hanus, L.2
Breuer, A.3
Pertwee, R.G.4
Stevenson, L.A.5
Griffin, G.6
Gibson, D.7
Mandelbaum, A.8
Etinger, A.9
Mechoulam, R.10
-
21
-
-
0242268553
-
The molecular logic of endocannabinoid signalling
-
Piomelli, D. The molecular logic of endocannabinoid signalling Nat. Rev. Neurosci. 2003, 4, 873-884
-
(2003)
Nat. Rev. Neurosci.
, vol.4
, pp. 873-884
-
-
Piomelli, D.1
-
22
-
-
84155162653
-
A thickening network of lipids
-
Piomelli, D. A thickening network of lipids Pain 2012, 153, 3-4
-
(2012)
Pain
, vol.153
, pp. 3-4
-
-
Piomelli, D.1
-
23
-
-
84865277383
-
NSAIDs: ENdocannabinoid stimulating anti-inflammatory drugs?
-
Fowler, C. J. NSAIDs: eNdocannabinoid stimulating anti-inflammatory drugs? Trends Pharmacol. Sci. 2012, 33 (9) 468-473
-
(2012)
Trends Pharmacol. Sci.
, vol.33
, Issue.9
, pp. 468-473
-
-
Fowler, C.J.1
-
24
-
-
84874184618
-
Inhibitory properties of ibuprofen and its amide analogues towards the hydrolysis and cyclooxygenation of the endocannabinoid anandamide
-
in press.
-
Fowler, C. J.; Bjorklund, E.; Lichtman, A. H.; Naidu, P. S.; Congiu, C.; Onnis, V. Inhibitory properties of ibuprofen and its amide analogues towards the hydrolysis and cyclooxygenation of the endocannabinoid anandamide. J. Enzyme Inhib. Med. Chem. 2012, in press.
-
(2012)
J. Enzyme Inhib. Med. Chem.
-
-
Fowler, C.J.1
Bjorklund, E.2
Lichtman, A.H.3
Naidu, P.S.4
Congiu, C.5
Onnis, V.6
-
25
-
-
57349170752
-
Discovery and development of fatty acid amide hydrolase (FAAH) inhibitors
-
Seierstad, M.; Breitenbucher, J. G. Discovery and development of fatty acid amide hydrolase (FAAH) inhibitors J. Med. Chem. 2008, 51, 7327-7343
-
(2008)
J. Med. Chem.
, vol.51
, pp. 7327-7343
-
-
Seierstad, M.1
Breitenbucher, J.G.2
-
26
-
-
79960901769
-
The discovery and development of inhibitors of fatty acid amide hydrolase (FAAH)
-
Otrubova, K.; Ezzili, C.; Boger, D. L. The discovery and development of inhibitors of fatty acid amide hydrolase (FAAH) Bioorg. Med. Chem. Lett. 2011, 21, 4674-4685
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 4674-4685
-
-
Otrubova, K.1
Ezzili, C.2
Boger, D.L.3
-
27
-
-
80053926122
-
Covalent inhibitors of fatty acid amide hydrolase: A rationale for the activity of piperidine and piperazine aryl ureas
-
Palermo, G.; Branduardi, D.; Masetti, M.; Lodola, A.; Mor, M.; Piomelli, D.; Cavalli, A.; De Vivo, M. Covalent inhibitors of fatty acid amide hydrolase: a rationale for the activity of piperidine and piperazine aryl ureas J. Med. Chem. 2011, 54, 6612-6623
-
(2011)
J. Med. Chem.
, vol.54
, pp. 6612-6623
-
-
Palermo, G.1
Branduardi, D.2
Masetti, M.3
Lodola, A.4
Mor, M.5
Piomelli, D.6
Cavalli, A.7
De Vivo, M.8
-
28
-
-
20144377098
-
Discovery of a potent, selective, and efficacious class of reversible α-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics
-
Boger, D. L.; Miyauchi, H.; Du, W.; Hardouin, C.; Fecik, R. A.; Cheng, H.; Hwang, I.; Hedrick, M. P.; Leung, D.; Acevedo, O.; Guimaraes, C. R.; Jorgensen, W. L.; Cravatt, B. F. Discovery of a potent, selective, and efficacious class of reversible α-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics J. Med. Chem. 2005, 48, 1849-1856
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1849-1856
-
-
Boger, D.L.1
Miyauchi, H.2
Du, W.3
Hardouin, C.4
Fecik, R.A.5
Cheng, H.6
Hwang, I.7
Hedrick, M.P.8
Leung, D.9
Acevedo, O.10
Guimaraes, C.R.11
Jorgensen, W.L.12
Cravatt, B.F.13
-
29
-
-
69749121642
-
A second generation of carbamate-based fatty acid amide hydrolase inhibitors with improved activity in vivo
-
Clapper, J. R.; Vacondio, F.; King, A. R.; Duranti, A.; Tontini, A.; Silva, C.; Sanchini, S.; Tarzia, G.; Mor, M.; Piomelli, D. A second generation of carbamate-based fatty acid amide hydrolase inhibitors with improved activity in vivo ChemMedChem 2009, 4, 1505-1513
-
(2009)
ChemMedChem
, vol.4
, pp. 1505-1513
-
-
Clapper, J.R.1
Vacondio, F.2
King, A.R.3
Duranti, A.4
Tontini, A.5
Silva, C.6
Sanchini, S.7
Tarzia, G.8
Mor, M.9
Piomelli, D.10
-
30
-
-
69849098851
-
Structure-property relationships of a class of carbamate-based fatty acid amide hydrolase (FAAH) inhibitors: Chemical and biological stability
-
Vacondio, F.; Silva, C.; Lodola, A.; Fioni, A.; Rivara, S.; Duranti, A.; Tontini, A.; Sanchini, S.; Clapper, J. R.; Piomelli, D.; Mor, M.; Tarzia, G. Structure-property relationships of a class of carbamate-based fatty acid amide hydrolase (FAAH) inhibitors: chemical and biological stability ChemMedChem 2009, 4, 1495-1504
-
(2009)
ChemMedChem
, vol.4
, pp. 1495-1504
-
-
Vacondio, F.1
Silva, C.2
Lodola, A.3
Fioni, A.4
Rivara, S.5
Duranti, A.6
Tontini, A.7
Sanchini, S.8
Clapper, J.R.9
Piomelli, D.10
Mor, M.11
Tarzia, G.12
-
31
-
-
79951518976
-
Discovery of PF-04457845: A highly potent, orally bioavailable, and selective urea FAAH inhibitor
-
Johnson, D. S.; Stiff, C.; Lazerwith, S. E.; Kesten, S. R.; Fay, L. K.; Morris, M.; Beidler, D.; Liimatta, M. B.; Smith, S. E.; Dudley, D. T.; Sadagopan, N.; Bhattachar, S. N.; Kesten, S. J.; Nomanbhoy, T. K.; Cravatt, B. F.; Ahn, K. Discovery of PF-04457845: a highly potent, orally bioavailable, and selective urea FAAH inhibitor ACS Med. Chem. Lett. 2011, 2, 91-96
-
(2011)
ACS Med. Chem. Lett.
, vol.2
, pp. 91-96
-
-
Johnson, D.S.1
Stiff, C.2
Lazerwith, S.E.3
Kesten, S.R.4
Fay, L.K.5
Morris, M.6
Beidler, D.7
Liimatta, M.B.8
Smith, S.E.9
Dudley, D.T.10
Sadagopan, N.11
Bhattachar, S.N.12
Kesten, S.J.13
Nomanbhoy, T.K.14
Cravatt, B.F.15
Ahn, K.16
-
32
-
-
4744354729
-
Cyclohexylcarbamic acid 3′- or 4′-substituted biphenyl-3-yl esters as fatty acid amide hydrolase inhibitors: Synthesis, quantitative structure-activity relationships, and molecular modeling studies
-
Mor, M.; Rivara, S.; Lodola, A.; Plazzi, P. V.; Tarzia, G.; Duranti, A.; Tontini, A.; Piersanti, G.; Kathuria, S.; Piomelli, D. Cyclohexylcarbamic acid 3′- or 4′-substituted biphenyl-3-yl esters as fatty acid amide hydrolase inhibitors: synthesis, quantitative structure-activity relationships, and molecular modeling studies J. Med. Chem. 2004, 47, 4998-5008
-
(2004)
J. Med. Chem.
, vol.47
, pp. 4998-5008
-
-
Mor, M.1
Rivara, S.2
Lodola, A.3
Plazzi, P.V.4
Tarzia, G.5
Duranti, A.6
Tontini, A.7
Piersanti, G.8
Kathuria, S.9
Piomelli, D.10
-
33
-
-
63849146961
-
Synergy between enzyme inhibitors of fatty acid amide hydrolase and cyclooxygenase in visceral nociception
-
Naidu, P. S.; Booker, L.; Cravatt, B. F.; Lichtman, A. H. Synergy between enzyme inhibitors of fatty acid amide hydrolase and cyclooxygenase in visceral nociception J. Pharmacol. Exp. Ther. 2009, 329, 48-56
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.329
, pp. 48-56
-
-
Naidu, P.S.1
Booker, L.2
Cravatt, B.F.3
Lichtman, A.H.4
-
34
-
-
84859793552
-
Peripheral FAAH inhibition causes profound antinociception and protects against indomethacin-induced gastric lesions
-
Sasso, O.; Bertorelli, R.; Bandiera, T.; Scarpelli, R.; Colombano, G.; Armirotti, A.; Moreno-Sanz, G.; Reggiani, A.; Piomelli, D. Peripheral FAAH inhibition causes profound antinociception and protects against indomethacin-induced gastric lesions Pharmacol. Res. 2012, 65, 553-563
-
(2012)
Pharmacol. Res.
, vol.65
, pp. 553-563
-
-
Sasso, O.1
Bertorelli, R.2
Bandiera, T.3
Scarpelli, R.4
Colombano, G.5
Armirotti, A.6
Moreno-Sanz, G.7
Reggiani, A.8
Piomelli, D.9
-
35
-
-
39149091398
-
Multi-target-directed ligands to combat neurodegenerative diseases
-
Cavalli, A.; Bolognesi, M. L.; Minarini, A.; Rosini, M.; Tumiatti, V.; Recanatini, M.; Melchiorre, C. Multi-target-directed ligands to combat neurodegenerative diseases J. Med. Chem. 2008, 51, 347-372
-
(2008)
J. Med. Chem.
, vol.51
, pp. 347-372
-
-
Cavalli, A.1
Bolognesi, M.L.2
Minarini, A.3
Rosini, M.4
Tumiatti, V.5
Recanatini, M.6
Melchiorre, C.7
-
36
-
-
27144449695
-
Designed multiple ligands. An emerging drug discovery paradigm
-
Morphy, R.; Rankovic, Z. Designed multiple ligands. An emerging drug discovery paradigm J. Med. Chem. 2005, 48, 6523-6543
-
(2005)
J. Med. Chem.
, vol.48
, pp. 6523-6543
-
-
Morphy, R.1
Rankovic, Z.2
-
37
-
-
15044349115
-
The efficiency of multi-target drugs: The network approach might help drug design
-
Csermely, P.; Agoston, V.; Pongor, S. The efficiency of multi-target drugs: the network approach might help drug design Trends Pharmacol. Sci. 2005, 26, 178-182
-
(2005)
Trends Pharmacol. Sci.
, vol.26
, pp. 178-182
-
-
Csermely, P.1
Agoston, V.2
Pongor, S.3
-
38
-
-
33845762340
-
Multi-target therapeutics: When the whole is greater than the sum of the parts
-
Zimmermann, G. R.; Lehar, J.; Keith, C. T. Multi-target therapeutics: when the whole is greater than the sum of the parts Drug Discovery Today 2007, 12, 34-42
-
(2007)
Drug Discovery Today
, vol.12
, pp. 34-42
-
-
Zimmermann, G.R.1
Lehar, J.2
Keith, C.T.3
-
39
-
-
34249091033
-
Inhibition of fatty acid amide hydrolase, a key endocannabinoid metabolizing enzyme, by analogues of ibuprofen and indomethacin
-
Holt, S.; Paylor, B.; Boldrup, L.; Alajakku, K.; Vandevoorde, S.; Sundstrom, A.; Cocco, M. T.; Onnis, V.; Fowler, C. J. Inhibition of fatty acid amide hydrolase, a key endocannabinoid metabolizing enzyme, by analogues of ibuprofen and indomethacin Eur. J. Pharmacol. 2007, 565, 26-36
-
(2007)
Eur. J. Pharmacol.
, vol.565
, pp. 26-36
-
-
Holt, S.1
Paylor, B.2
Boldrup, L.3
Alajakku, K.4
Vandevoorde, S.5
Sundstrom, A.6
Cocco, M.T.7
Onnis, V.8
Fowler, C.J.9
-
40
-
-
78651287426
-
DrugBank 3.0: A comprehensive resource for 'omics' research on drugs
-
Knox, C.; Law, V.; Jewison, T.; Liu, P.; Ly, S.; Frolkis, A.; Pon, A.; Banco, K.; Mak, C.; Neveu, V.; Djoumbou, Y.; Eisner, R.; Guo, A. C.; Wishart, D. S. DrugBank 3.0: a comprehensive resource for 'omics' research on drugs Nucleic Acids Res. 2011, 39, D1035-D1041
-
(2011)
Nucleic Acids Res.
, vol.39
-
-
Knox, C.1
Law, V.2
Jewison, T.3
Liu, P.4
Ly, S.5
Frolkis, A.6
Pon, A.7
Banco, K.8
Mak, C.9
Neveu, V.10
Djoumbou, Y.11
Eisner, R.12
Guo, A.C.13
Wishart, D.S.14
-
41
-
-
33750991346
-
Benchmarking sets for molecular docking
-
Huang, N.; Shoichet, B. K.; Irwin, J. J. Benchmarking sets for molecular docking J. Med. Chem. 2006, 49, 6789-6801
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6789-6801
-
-
Huang, N.1
Shoichet, B.K.2
Irwin, J.J.3
-
43
-
-
33845931855
-
Scaffold of the cyclooxygenase-2 (COX-2) inhibitor carprofen provides Alzheimer γ-secretase modulators
-
Narlawar, R.; Perez Revuelta, B. I.; Haass, C.; Steiner, H.; Schmidt, B.; Baumann, K. Scaffold of the cyclooxygenase-2 (COX-2) inhibitor carprofen provides Alzheimer γ-secretase modulators J. Med. Chem. 2006, 49, 7588-7591
-
(2006)
J. Med. Chem.
, vol.49
, pp. 7588-7591
-
-
Narlawar, R.1
Perez Revuelta, B.I.2
Haass, C.3
Steiner, H.4
Schmidt, B.5
Baumann, K.6
-
44
-
-
77956274926
-
R-flurbiprofen reduces neuropathic pain in rodents by restoring endogenous cannabinoids
-
Bishay, P.; Schmidt, H.; Marian, C.; Haussler, A.; Wijnvoord, N.; Ziebell, S.; Metzner, J.; Koch, M.; Myrczek, T.; Bechmann, I.; Kuner, R.; Costigan, M.; Dehghani, F.; Geisslinger, G.; Tegeder, I. R-flurbiprofen reduces neuropathic pain in rodents by restoring endogenous cannabinoids PLoS One 2010, 5, e10628
-
(2010)
PLoS One
, vol.5
, pp. 10628
-
-
Bishay, P.1
Schmidt, H.2
Marian, C.3
Haussler, A.4
Wijnvoord, N.5
Ziebell, S.6
Metzner, J.7
Koch, M.8
Myrczek, T.9
Bechmann, I.10
Kuner, R.11
Costigan, M.12
Dehghani, F.13
Geisslinger, G.14
Tegeder, I.15
-
45
-
-
0033776148
-
Differences in the pharmacological properties of rat and chicken brain fatty acid amidohydrolase
-
Fowler, C. J.; Borjesson, M.; Tiger, G. Differences in the pharmacological properties of rat and chicken brain fatty acid amidohydrolase Br. J. Pharmacol. 2000, 131, 498-504
-
(2000)
Br. J. Pharmacol.
, vol.131
, pp. 498-504
-
-
Fowler, C.J.1
Borjesson, M.2
Tiger, G.3
-
46
-
-
78049405035
-
Molecular basis for cyclooxygenase inhibition by the non-steroidal anti-inflammatory drug naproxen
-
Duggan, K. C.; Walters, M. J.; Musee, J.; Harp, J. M.; Kiefer, J. R.; Oates, J. A.; Marnett, L. J. Molecular basis for cyclooxygenase inhibition by the non-steroidal anti-inflammatory drug naproxen J. Biol. Chem. 2010, 285, 34950-34959
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 34950-34959
-
-
Duggan, K.C.1
Walters, M.J.2
Musee, J.3
Harp, J.M.4
Kiefer, J.R.5
Oates, J.A.6
Marnett, L.J.7
-
47
-
-
0030730417
-
Ibuprofen inhibits rat brain deamidation of anandamide at pharmacologically relevant concentrations. Mode of inhibition and structure-activity relationship
-
Fowler, C. J.; Tiger, G.; Stenstrom, A. Ibuprofen inhibits rat brain deamidation of anandamide at pharmacologically relevant concentrations. Mode of inhibition and structure-activity relationship J. Pharmacol. Exp. Ther. 1997, 283, 729-734
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.283
, pp. 729-734
-
-
Fowler, C.J.1
Tiger, G.2
Stenstrom, A.3
-
48
-
-
0033557114
-
Inhibition of anandamide hydrolysis by the enantiomers of ibuprofen, ketorolac, and flurbiprofen
-
Fowler, C. J.; Janson, U.; Johnson, R. M.; Wahlstrom, G.; Stenstrom, A.; Norstrom, K.; Tiger, G. Inhibition of anandamide hydrolysis by the enantiomers of ibuprofen, ketorolac, and flurbiprofen Arch. Biochem. Biophys. 1999, 362, 191-196
-
(1999)
Arch. Biochem. Biophys.
, vol.362
, pp. 191-196
-
-
Fowler, C.J.1
Janson, U.2
Johnson, R.M.3
Wahlstrom, G.4
Stenstrom, A.5
Norstrom, K.6
Tiger, G.7
-
49
-
-
65449121973
-
The case for the development of novel analgesic agents targeting both fatty acid amide hydrolase and either cyclooxygenase or TRPV1
-
Fowler, C. J.; Naidu, P. S.; Lichtman, A.; Onnis, V. The case for the development of novel analgesic agents targeting both fatty acid amide hydrolase and either cyclooxygenase or TRPV1 Br. J. Pharmacol. 2009, 156, 412-419
-
(2009)
Br. J. Pharmacol.
, vol.156
, pp. 412-419
-
-
Fowler, C.J.1
Naidu, P.S.2
Lichtman, A.3
Onnis, V.4
-
50
-
-
0037320223
-
Acidic nonsteroidal anti-inflammatory drugs inhibit rat brain fatty acid amide hydrolase in a pH-dependent manner
-
Fowler, C. J.; Holt, S.; Tiger, G. Acidic nonsteroidal anti-inflammatory drugs inhibit rat brain fatty acid amide hydrolase in a pH-dependent manner J. Enzyme Inhib. Med. Chem. 2003, 18, 55-58
-
(2003)
J. Enzyme Inhib. Med. Chem.
, vol.18
, pp. 55-58
-
-
Fowler, C.J.1
Holt, S.2
Tiger, G.3
-
51
-
-
83855160816
-
Cannabinoids, endocannabinoids, and cancer
-
Hermanson, D. J.; Marnett, L. J. Cannabinoids, endocannabinoids, and cancer Cancer Metastasis Rev. 2011, 30, 599-612
-
(2011)
Cancer Metastasis Rev.
, vol.30
, pp. 599-612
-
-
Hermanson, D.J.1
Marnett, L.J.2
-
52
-
-
84862546573
-
Inflammation and cancer: Chemical approaches to mechanisms, imaging, and treatment
-
Marnett, L. J. Inflammation and cancer: chemical approaches to mechanisms, imaging, and treatment J. Org. Chem. 2012, 77, 5224-38
-
(2012)
J. Org. Chem.
, vol.77
, pp. 5224-5238
-
-
Marnett, L.J.1
-
53
-
-
59849106371
-
Protein promiscuity and its implications for biotechnology
-
Nobeli, I.; Favia, A. D.; Thornton, J. M. Protein promiscuity and its implications for biotechnology Nat. Biotechnol. 2009, 27, 157-167
-
(2009)
Nat. Biotechnol.
, vol.27
, pp. 157-167
-
-
Nobeli, I.1
Favia, A.D.2
Thornton, J.M.3
-
54
-
-
0141726877
-
A 'rule of three' for fragment-based lead discovery?
-
Congreve, M.; Carr, R.; Murray, C.; Jhoti, H. A 'rule of three' for fragment-based lead discovery? Drug Discovery Today 2003, 8, 876-877
-
(2003)
Drug Discovery Today
, vol.8
, pp. 876-877
-
-
Congreve, M.1
Carr, R.2
Murray, C.3
Jhoti, H.4
-
55
-
-
0021858796
-
Carprofen and the therapy of gastroduodenal ulcerations by ranitidine
-
Czarnobilski, Z.; Bem, S.; Czarnobilski, K.; Konturek, S. J. Carprofen and the therapy of gastroduodenal ulcerations by ranitidine Hepatogastroenterology 1985, 32, 20-23
-
(1985)
Hepatogastroenterology
, vol.32
, pp. 20-23
-
-
Czarnobilski, Z.1
Bem, S.2
Czarnobilski, K.3
Konturek, S.J.4
-
56
-
-
80054953106
-
(R)-Profens are substrate-selective inhibitors of endocannabinoid oxygenation by COX-2
-
Duggan, K. C.; Hermanson, D. J.; Musee, J.; Prusakiewicz, J. J.; Scheib, J. L.; Carter, B. D.; Banerjee, S.; Oates, J. A.; Marnett, L. J. (R)-Profens are substrate-selective inhibitors of endocannabinoid oxygenation by COX-2 Nat. Chem. Biol. 2011, 7, 803-809
-
(2011)
Nat. Chem. Biol.
, vol.7
, pp. 803-809
-
-
Duggan, K.C.1
Hermanson, D.J.2
Musee, J.3
Prusakiewicz, J.J.4
Scheib, J.L.5
Carter, B.D.6
Banerjee, S.7
Oates, J.A.8
Marnett, L.J.9
-
57
-
-
2242490907
-
Structural adaptations in a membrane enzyme that terminates endocannabinoid signaling
-
Bracey, M. H.; Hanson, M. A.; Masuda, K. R.; Stevens, R. C.; Cravatt, B. F. Structural adaptations in a membrane enzyme that terminates endocannabinoid signaling Science 2002, 298, 1793-1796
-
(2002)
Science
, vol.298
, pp. 1793-1796
-
-
Bracey, M.H.1
Hanson, M.A.2
Masuda, K.R.3
Stevens, R.C.4
Cravatt, B.F.5
-
58
-
-
0030461132
-
Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents
-
Kurumbail, R. G.; Stevens, A. M.; Gierse, J. K.; McDonald, J. J.; Stegeman, R. A.; Pak, J. Y.; Gildehaus, D.; Miyashiro, J. M.; Penning, T. D.; Seibert, K.; Isakson, P. C.; Stallings, W. C. Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents Nature 1996, 384, 644-648
-
(1996)
Nature
, vol.384
, pp. 644-648
-
-
Kurumbail, R.G.1
Stevens, A.M.2
Gierse, J.K.3
McDonald, J.J.4
Stegeman, R.A.5
Pak, J.Y.6
Gildehaus, D.7
Miyashiro, J.M.8
Penning, T.D.9
Seibert, K.10
Isakson, P.C.11
Stallings, W.C.12
-
59
-
-
70450106216
-
Improved prediction of protein side-chain conformations with SCWRL4
-
Krivov, G. G.; Shapovalov, M. V.; Dunbrack, R. L., Jr. Improved prediction of protein side-chain conformations with SCWRL4 Proteins 2009, 77, 778-795
-
(2009)
Proteins
, vol.77
, pp. 778-795
-
-
Krivov, G.G.1
Shapovalov, M.V.2
Dunbrack Jr., R.L.3
-
60
-
-
27344436659
-
Scalable molecular dynamics with NAMD
-
Phillips, J. C.; Braun, R.; Wang, W.; Gumbart, J.; Tajkhorshid, E.; Villa, E.; Chipot, C.; Skeel, R. D.; Kale, L.; Schulten, K. Scalable molecular dynamics with NAMD J. Comput. Chem. 2005, 26, 1781-1802
-
(2005)
J. Comput. Chem.
, vol.26
, pp. 1781-1802
-
-
Phillips, J.C.1
Braun, R.2
Wang, W.3
Gumbart, J.4
Tajkhorshid, E.5
Villa, E.6
Chipot, C.7
Skeel, R.D.8
Kale, L.9
Schulten, K.10
-
61
-
-
33748518255
-
Comparison of multiple Amber force fields and development of improved protein backbone parameters
-
Hornak, V.; Abel, R.; Okur, A.; Strockbine, B.; Roitberg, A.; Simmerling, C. Comparison of multiple Amber force fields and development of improved protein backbone parameters Proteins 2006, 65, 712-725
-
(2006)
Proteins
, vol.65
, pp. 712-725
-
-
Hornak, V.1
Abel, R.2
Okur, A.3
Strockbine, B.4
Roitberg, A.5
Simmerling, C.6
-
62
-
-
0033397980
-
Python: A programming language for software integration and development
-
Sanner, M. F. Python: a programming language for software integration and development J. Mol. Graphics Modell. 1999, 17, 57-61
-
(1999)
J. Mol. Graphics Modell.
, vol.17
, pp. 57-61
-
-
Sanner, M.F.1
-
63
-
-
76149120388
-
AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
-
Trott, O.; Olson, A. J. AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading J. Comput. Chem. 2010, 31, 455-61
-
(2010)
J. Comput. Chem.
, vol.31
, pp. 455-461
-
-
Trott, O.1
Olson, A.J.2
|