-
1
-
-
36048978697
-
Novel mechanistic class of fatty acid amide hydrolase inhibitors with remarkable selectivity
-
DOI 10.1021/bi701378g
-
K. Ahn, D.S. Johnson, L.R. Fitzgerald, M. Liimatta, A. Arendse, T. Stevenson, E.T. Lund, R.A. Nugent, T.K. Nomanbhoy, J.P. Alexander, and B.F. Cravatt Novel mechanistic class of fatty acid amide hydrolase inhibitors with remarkable selectivity Biochemistry 46 2007 13019 13030 (Pubitemid 350086220)
-
(2007)
Biochemistry
, vol.46
, Issue.45
, pp. 13019-13030
-
-
Ahn, K.1
Johnson, D.S.2
Fitzgerald, L.R.3
Liimatta, M.4
Arendse, A.5
Stevenson, T.6
Lund, E.T.7
Nugent, R.A.8
Nomanbhoy, T.K.9
Alexander, J.P.10
Cravatt, B.F.11
-
2
-
-
67650732783
-
Fatty acid amide hydrolase as a potential therapeutic target for the treatment of pain and CNS disorders
-
K. Ahn, D.S. Johnson, and B.F. Cravatt Fatty acid amide hydrolase as a potential therapeutic target for the treatment of pain and CNS disorders Expert Opin. Drug Discov. 4 2009 763 784
-
(2009)
Expert Opin. Drug Discov.
, vol.4
, pp. 763-784
-
-
Ahn, K.1
Johnson, D.S.2
Cravatt, B.F.3
-
3
-
-
64749114255
-
Discovery and characterization of a highly selective FAAH inhibitor that reduces inflammatory pain
-
K. Ahn, D.S. Johnson, M. Mileni, D. Beidler, J.Z. Long, M.K. McKinney, E. Weerapana, N. Sadagopan, M. Liimatta, S.E. Smith, S. Lazerwith, C. Stiff, S. Kamtekar, K. Bhattacharya, Y. Zhang, S. Swaney, K. Van Becelaere, R.C. Stevens, and B.F. Cravatt Discovery and characterization of a highly selective FAAH inhibitor that reduces inflammatory pain Chem. Biol. 16 2009 411 420
-
(2009)
Chem. Biol.
, vol.16
, pp. 411-420
-
-
Ahn, K.1
Johnson, D.S.2
Mileni, M.3
Beidler, D.4
Long, J.Z.5
McKinney, M.K.6
Weerapana, E.7
Sadagopan, N.8
Liimatta, M.9
Smith, S.E.10
Lazerwith, S.11
Stiff, C.12
Kamtekar, S.13
Bhattacharya, K.14
Zhang, Y.15
Swaney, S.16
Van Becelaere, K.17
Stevens, R.C.18
Cravatt, B.F.19
-
4
-
-
27744466783
-
Mechanism of carbamate inactivation of FAAH: Implications for the design of covalent inhibitors and in vivo functional probes for enzymes
-
DOI 10.1016/j.chembiol.2005.08.011, PII S107455210500267X
-
J.P. Alexander, and B.F. Cravatt Mechanism of carbamate inactivation of FAAH: implications for the design of covalent inhibitors and in vivo functional probes for enzymes Chem. Biol. 12 2005 1179 1187 (Pubitemid 41628253)
-
(2005)
Chemistry and Biology
, vol.12
, Issue.11
, pp. 1179-1187
-
-
Alexander, J.P.1
Cravatt, B.F.2
-
5
-
-
9244223576
-
Efficacy of two cannabis based medicinal extracts for relief of central neuropathic pain from brachial plexus avulsion: Results of a randomised controlled trial
-
DOI 10.1016/j.pain.2004.09.013, PII S0304395904004415
-
J.S. Berman, C. Symonds, and R. Birch Efficacy of two cannabis based medicinal extracts for relief of central neuropathic pain from brachial plexus avulsion: results of a randomised controlled trial Pain 112 2004 299 306 (Pubitemid 39550730)
-
(2004)
Pain
, vol.112
, Issue.3
, pp. 299-306
-
-
Berman, J.S.1
Symonds, C.2
Birch, R.3
-
6
-
-
2242490907
-
Structural adaptations in a membrane enzyme that terminates endocannabinoid signaling
-
DOI 10.1126/science.1076535
-
M.H. Bracey, M.A. Hanson, K.R. Masuda, R.C. Stevens, and B.F. Cravatt Structural adaptations in a membrane enzyme that terminates endocannabinoid signaling Science 298 2002 1793 1796 (Pubitemid 35404124)
-
(2002)
Science
, vol.298
, Issue.5599
, pp. 1793-1796
-
-
Bracey, M.H.1
Hanson, M.A.2
Masuda, K.R.3
Stevens, R.C.4
Cravatt, B.F.5
-
7
-
-
0034951162
-
The synthetic cannabinoid WIN55,212-2 attenuates hyperalgesia and allodynia in a rat model of neuropathic pain
-
D. Bridges, K. Ahmad, and A.S. Rice The synthetic cannabinoid WIN55,212-2 attenuates hyperalgesia and allodynia in a rat model of neuropathic pain Br. J. Pharmacol. 133 2001 586 594 (Pubitemid 32591925)
-
(2001)
British Journal of Pharmacology
, vol.133
, Issue.4
, pp. 586-594
-
-
Bridges, D.1
Ahmad, K.2
Rice, A.S.C.3
-
8
-
-
0028589390
-
Formation and inactivation of endogenous cannabinoid anandamide in central neurons
-
V. Di Marzo, A. Fontana, H. Cadas, S. Schinelli, G. Cimino, J.C. Schwartz, and D. Piomelli Formation and inactivation of endogenous cannabinoid anandamide in central neurons Nature 372 1994 686 691
-
(1994)
Nature
, vol.372
, pp. 686-691
-
-
Di Marzo, V.1
Fontana, A.2
Cadas, H.3
Schinelli, S.4
Cimino, G.5
Schwartz, J.C.6
Piomelli, D.7
-
9
-
-
45849097898
-
Biosynthesis, degradation and pharmacological importance of the fatty acid amides
-
E.K. Farrell, and D.J. Merkler Biosynthesis, degradation and pharmacological importance of the fatty acid amides Drug Discov. Today 13 2008 558 568
-
(2008)
Drug Discov. Today
, vol.13
, pp. 558-568
-
-
Farrell, E.K.1
Merkler, D.J.2
-
10
-
-
15744385109
-
Characterization of the fatty acid amide hydrolase inhibitor cyclohexyl carbamic acid 3′-carbamoyl-biphenyl-3-yl ester (URB597): Effects on anandamide and oleoylethanolamide deactivation
-
DOI 10.1124/jpet.104.078980
-
D. Fegley, S. Gaetani, A. Duranti, A. Tontini, M. Mor, G. Tarzia, and D. Piomelli Characterization of the fatty acid amide hydrolase inhibitor cyclohexyl carbamic acid 3′-carbamoyl-biphenyl-3-yl ester (URB597): effects on anandamide and oleoylethanolamide deactivation J. Pharmacol. Exp. Ther. 313 2005 352 358 (Pubitemid 40411361)
-
(2005)
Journal of Pharmacology and Experimental Therapeutics
, vol.313
, Issue.1
, pp. 352-358
-
-
Fegley, D.1
Gaetani, S.2
Duranti, A.3
Tontini, A.4
Mor, M.5
Tarzia, G.6
Piomelli, D.7
-
11
-
-
70949088924
-
Beta-Lactams derived from a carbapenem chiron are selective inhibitors of human fatty acid amide hydrolase versus human monoacylglycerol lipase
-
M. Feledziak, C. Michaux, A. Urbach, G. Labar, G.G. Muccioli, D.M. Lambert, and J. Marchand-Brynaert beta-Lactams derived from a carbapenem chiron are selective inhibitors of human fatty acid amide hydrolase versus human monoacylglycerol lipase J. Med. Chem. 52 2009 7054 7068
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7054-7068
-
-
Feledziak, M.1
Michaux, C.2
Urbach, A.3
Labar, G.4
Muccioli, G.G.5
Lambert, D.M.6
Marchand-Brynaert, J.7
-
12
-
-
77955429194
-
A new group of oxime carbamates as reversible inhibitors of fatty acid amide hydrolase
-
S. Gattinoni, C.D. Simone, S. Dallavalle, F. Fezza, R. Nannei, N. Battista, P. Minetti, G. Quattrociocchi, A. Caprioli, F. Borsini, W. Cabri, S. Penco, L. Merlini, and M. Maccarrone A new group of oxime carbamates as reversible inhibitors of fatty acid amide hydrolase Bioorg. Med. Chem. Lett. 20 2010 4406 4411
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 4406-4411
-
-
Gattinoni, S.1
Simone, C.D.2
Dallavalle, S.3
Fezza, F.4
Nannei, R.5
Battista, N.6
Minetti, P.7
Quattrociocchi, G.8
Caprioli, A.9
Borsini, F.10
Cabri, W.11
Penco, S.12
Merlini, L.13
MacCarrone, M.14
-
15
-
-
33847670594
-
A high throughput fluorescent assay for measuring the activity of fatty acid amide hydrolase
-
DOI 10.1016/j.jneumeth.2006.10.006, PII S016502700600505X
-
K.L. Kage, P.L. Richardson, L. Traphagen, J. Severin, A. Pereda-Lopez, T. Lubben, R. Davis-Taber, M.H. Vos, D. Bartley, K. Walter, J. Harlan, L. Solomon, U. Warrior, T.F. Holzman, C. Faltynek, C.S. Surowy, and V.E. Scott A high throughput fluorescent assay for measuring the activity of fatty acid amide hydrolase J. Neurosci. Meth. 161 2007 47 54 (Pubitemid 46357569)
-
(2007)
Journal of Neuroscience Methods
, vol.161
, Issue.1
, pp. 47-54
-
-
Kage, K.L.1
Richardson, P.L.2
Traphagen, L.3
Severin, J.4
Pereda-Lopez, A.5
Lubben, T.6
Davis-Taber, R.7
Vos, M.H.8
Bartley, D.9
Walter, K.10
Harlan, J.11
Solomon, L.12
Warrior, U.13
Holzman, T.F.14
Faltynek, C.15
Surowy, C.S.16
Scott, V.E.17
-
16
-
-
58749088402
-
Biochemical and biological properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a mechanism-based inhibitor of fatty acid amide hydrolase
-
M.J. Karbarz, L. Luo, L. Chang, C.S. Tham, J.A. Palmer, S.J. Wilson, M.L. Wennerholm, S.M. Brown, B.P. Scott, R.L. Apodaca, J.M. Keith, J. Wu, J.G. Breitenbucher, S.R. Chaplan, and M. Webb Biochemical and biological properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a mechanism-based inhibitor of fatty acid amide hydrolase Anesth. Analg. 108 2009 316 329
-
(2009)
Anesth. Analg.
, vol.108
, pp. 316-329
-
-
Karbarz, M.J.1
Luo, L.2
Chang, L.3
Tham, C.S.4
Palmer, J.A.5
Wilson, S.J.6
Wennerholm, M.L.7
Brown, S.M.8
Scott, B.P.9
Apodaca, R.L.10
Keith, J.M.11
Wu, J.12
Breitenbucher, J.G.13
Chaplan, S.R.14
Webb, M.15
-
17
-
-
0141593561
-
Analgesic Effect of the Synthetic Cannabinoid CT-3 on Chronic Neuropathic Pain: A Randomized Controlled Trial
-
DOI 10.1001/jama.290.13.1757
-
M. Karst, K. Salim, S. Burstein, I. Conrad, L. Hoy, and U. Schneider Analgesic effect of the synthetic cannabinoid CT-3 on chronic neuropathic pain: a randomized controlled trial JAMA 290 2003 1757 1762 (Pubitemid 37430626)
-
(2003)
Journal of the American Medical Association
, vol.290
, Issue.13
, pp. 1757-1762
-
-
Karst, M.1
Salim, K.2
Burstein, S.3
Conrad, I.4
Hoy, L.5
Schneider, U.6
-
18
-
-
70349110145
-
Blockade of endocannabinoid-degrading enzymes attenuates neuropathic pain
-
S.G. Kinsey, J.Z. Long, S.T. O'Neal, R.A. Abdullah, J.L. Poklis, D.L. Boger, B.F. Cravatt, and A.H. Lichtman Blockade of endocannabinoid-degrading enzymes attenuates neuropathic pain J. Pharmacol. Exp. Ther. 330 2009 902 910
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.330
, pp. 902-910
-
-
Kinsey, S.G.1
Long, J.Z.2
O'Neal, S.T.3
Abdullah, R.A.4
Poklis, J.L.5
Boger, D.L.6
Cravatt, B.F.7
Lichtman, A.H.8
-
19
-
-
2442657939
-
Mechanism of γ-secretase cleavage activation: Is γ-secretase regulated through autoinhibition involving the presenilin-1 exon 9 loop?
-
DOI 10.1021/bi036072v
-
K.S. Knappenberger, G. Tian, X. Ye, C. Sobotka-Briner, S.V. Ghanekar, B.D. Greenberg, and C.W. Scott Mechanism of gamma-secretase cleavage activation: is gamma-secretase regulated through autoinhibition involving the presenilin-1 exon 9 loop? Biochemistry 43 2004 6208 6218 (Pubitemid 38669489)
-
(2004)
Biochemistry
, vol.43
, Issue.20
, pp. 6208-6218
-
-
Knappenberger, K.S.1
Tian, G.2
Ye, X.3
Sobotka-Briner, C.4
Ghanekar, S.V.5
Greenberg, B.D.6
Scott, C.W.7
-
20
-
-
4644354869
-
Reversible inhibitors of fatty acid amide hydrolase that promote analgesia: Evidence for an unprecedented combination of potency and selectivity
-
DOI 10.1124/jpet.104.069401
-
A.H. Lichtman, D. Leung, C.C. Shelton, A. Saghatelian, C. Hardouin, D.L. Boger, and B.F. Cravatt Reversible inhibitors of fatty acid amide hydrolase that promote analgesia: evidence for an unprecedented combination of potency and selectivity J. Pharmacol. Exp. Ther. 311 2004 441 448 (Pubitemid 39391527)
-
(2004)
Journal of Pharmacology and Experimental Therapeutics
, vol.311
, Issue.2
, pp. 441-448
-
-
Lichtman, A.H.1
Leung, D.2
Shelton, C.C.3
Saghatelian, A.4
Hardouin, C.5
Boger, D.L.6
Cravatt, B.F.7
-
21
-
-
78049232267
-
Intracellular trafficking of anandamide: New concepts for signaling
-
M. Maccarrone, E. Dainese, and S. Oddi Intracellular trafficking of anandamide: new concepts for signaling Trends Biochem. Sci. 35 2010 601 608
-
(2010)
Trends Biochem. Sci.
, vol.35
, pp. 601-608
-
-
MacCarrone, M.1
Dainese, E.2
Oddi, S.3
-
22
-
-
6944246102
-
Mechanism of action of cannabinoids: How it may lead to treatment of cachexia, emesis, and pain
-
B.R. Martin, and J.L. Wiley Mechanism of action of cannabinoids: how it may lead to treatment of cachexia, emesis, and pain J. Support. Oncol. 2 2004 305 314 (Pubitemid 39409773)
-
(2004)
Journal of Supportive Oncology
, vol.2
, Issue.4
, pp. 305-314
-
-
Martin, B.R.1
Wiley, J.L.2
-
23
-
-
22244484464
-
Structure and function of fatty acid amide hydrolase
-
DOI 10.1146/annurev.biochem.74.082803.133450
-
M.K. McKinney, and B.F. Cravatt Structure and function of fatty acid amide hydrolase Annu. Rev. Biochem. 74 2005 411 432 (Pubitemid 40995513)
-
(2005)
Annual Review of Biochemistry
, vol.74
, pp. 411-432
-
-
McKinney, M.K.1
Cravatt, B.E.2
-
24
-
-
51349143217
-
Structure-guided inhibitor design for human FAAH by interspecies active site conversion
-
M. Mileni, D.S. Johnson, Z. Wang, D.S. Everdeen, M. Liimatta, B. Pabst, K. Bhattacharya, R.A. Nugent, S. Kamtekar, B.F. Cravatt, K. Ahn, and R.C. Stevens Structure-guided inhibitor design for human FAAH by interspecies active site conversion Proc. Natl. Acad. Sci. U. S. A. 105 2008 12820 12824
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 12820-12824
-
-
Mileni, M.1
Johnson, D.S.2
Wang, Z.3
Everdeen, D.S.4
Liimatta, M.5
Pabst, B.6
Bhattacharya, K.7
Nugent, R.A.8
Kamtekar, S.9
Cravatt, B.F.10
Ahn, K.11
Stevens, R.C.12
-
25
-
-
68049090031
-
Binding and inactivation mechanism of a humanized fatty acid amide hydrolase by alpha-ketoheterocycle inhibitors revealed from cocrystal structures
-
M. Mileni, J. Garfunkle, J.K. DeMartino, B.F. Cravatt, D.L. Boger, and R.C. Stevens Binding and inactivation mechanism of a humanized fatty acid amide hydrolase by alpha-ketoheterocycle inhibitors revealed from cocrystal structures J. Am. Chem. Soc. 131 2009 10497 10506
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 10497-10506
-
-
Mileni, M.1
Garfunkle, J.2
Demartino, J.K.3
Cravatt, B.F.4
Boger, D.L.5
Stevens, R.C.6
-
26
-
-
77954379126
-
Discovery and development of endocannabinoid-hydrolyzing enzyme inhibitors
-
A. Minkkila, S. Saario, and T. Nevalainen Discovery and development of endocannabinoid-hydrolyzing enzyme inhibitors Curr. Top. Med. Chem. 10 2010 828 858
-
(2010)
Curr. Top. Med. Chem.
, vol.10
, pp. 828-858
-
-
Minkkila, A.1
Saario, S.2
Nevalainen, T.3
-
27
-
-
0034942112
-
Cannabinoid-induced presynaptic inhibition of glutamatergic EPSCs in substantia gelatinosa neurons of the rat spinal cord
-
V. Morisset, and L. Urban Cannabinoid-induced presynaptic inhibition of glutamatergic EPSCs in substantia gelatinosa neurons of the rat spinal cord J. Neurophysiol. 86 2001 40 48 (Pubitemid 32623210)
-
(2001)
Journal of Neurophysiology
, vol.86
, Issue.1
, pp. 40-48
-
-
Morisset, V.1
Urban, L.2
-
28
-
-
77954819357
-
Endocannabinoid biosynthesis and inactivation, from simple to complex
-
G.G. Muccioli Endocannabinoid biosynthesis and inactivation, from simple to complex Drug Discov. Today 15 2010 474 483
-
(2010)
Drug Discov. Today
, vol.15
, pp. 474-483
-
-
Muccioli, G.G.1
-
29
-
-
1842451973
-
Nitric oxide inhibits NMDA currents in a subpopulation of substantia gelatinosa neurons of the adult rat spinal cord
-
DOI 10.1016/j.neulet.2004.01.057, PII S0304394004001260
-
R. Nicholson, D. Spanswick, and K. Lee Nitric oxide inhibits NMDA currents in a subpopulation of substantia gelatinosa neurons of the adult rat spinal cord Neurosci. Lett. 359 2004 180 184 (Pubitemid 38446667)
-
(2004)
Neuroscience Letters
, vol.359
, Issue.3
, pp. 180-184
-
-
Nicholson, R.1
Spanswick, D.2
Lee, K.3
-
31
-
-
65449146377
-
Emerging strategies for exploiting cannabinoid receptor agonists as medicines
-
R.G. Pertwee Emerging strategies for exploiting cannabinoid receptor agonists as medicines Br. J. Pharmacol. 156 2009 397 411
-
(2009)
Br. J. Pharmacol.
, vol.156
, pp. 397-411
-
-
Pertwee, R.G.1
-
32
-
-
34250750792
-
The fatty acid amide hydrolase inhibitor URB597 (cyclohexylcarbamic acid 3′-carbamoylbiphenyl-3-yl ester) reduces neuropathic pain after oral administration in mice
-
DOI 10.1124/jpet.107.119941
-
R. Russo, J. Loverme, G. La Rana, T.R. Compton, J. Parrott, A. Duranti, A. Tontini, M. Mor, G. Tarzia, A. Calignano, and D. Piomelli The fatty acid amide hydrolase inhibitor URB597 (cyclohexylcarbamic acid 3′- carbamoylbiphenyl-3-yl ester) reduces neuropathic pain after oral administration in mice J. Pharmacol. Exp. Ther. 322 2007 236 242 (Pubitemid 46956375)
-
(2007)
Journal of Pharmacology and Experimental Therapeutics
, vol.322
, Issue.1
, pp. 236-242
-
-
Russo, R.1
LoVerme, J.2
La Rana, G.3
Compton, T.R.4
Parrott, J.5
Duranti, A.6
Tontini, A.7
Mor, M.8
Tarzia, G.9
Calignano, A.10
Piomelli, D.11
-
33
-
-
57349170752
-
Discovery and development of fatty acid amide hydrolase (FAAH) inhibitors
-
M. Seierstad, and J.G. Breitenbucher Discovery and development of fatty acid amide hydrolase (FAAH) inhibitors J. Med. Chem. 51 2008 7327 7343
-
(2008)
J. Med. Chem.
, vol.51
, pp. 7327-7343
-
-
Seierstad, M.1
Breitenbucher, J.G.2
-
34
-
-
34249687699
-
Novel inhibitors of fatty acid amide hydrolase
-
DOI 10.1016/j.bmcl.2007.04.009, PII S0960894X07004295
-
S.Y. Sit, C. Conway, R. Bertekap, K. Xie, C. Bourin, K. Burris, and H. Deng Novel inhibitors of fatty acid amide hydrolase Bioorg. Med. Chem. Lett. 17 2007 3287 3291 (Pubitemid 46830893)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.12
, pp. 3287-3291
-
-
Sit, S.Y.1
Conway, C.2
Bertekap, R.3
Xie, K.4
Bourin, C.5
Burris, K.6
Deng, H.7
-
35
-
-
38349102259
-
Nabilone for the treatment of pain in fibromyalgia
-
R.Q. Skrabek, L. Galimova, K. Ethans, and D. Perry Nabilone for the treatment of pain in fibromyalgia J. Pain 9 2008 164 173
-
(2008)
J. Pain
, vol.9
, pp. 164-173
-
-
Skrabek, R.Q.1
Galimova, L.2
Ethans, K.3
Perry, D.4
-
36
-
-
0042206671
-
The mechanism of γ-secretase. Multiple inhibitor binding sites for transition state analogs and small molecule inhibitors
-
DOI 10.1074/jbc.M300905200
-
G. Tian, S.V. Ghanekar, D. Aharony, A.B. Shenvi, R.T. Jacobs, X. Liu, and B.D. Greenberg The mechanism of gamma-secretase: multiple inhibitor binding sites for transition state analogs and small molecule inhibitors J. Biol. Chem. 278 2003 28968 28975 (Pubitemid 36935808)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.31
, pp. 28968-28975
-
-
Tian, G.1
Ghanekar, S.V.2
Aharony, D.3
Shenvi, A.B.4
Jacobs, R.T.5
Liu, X.6
Greenberg, B.D.7
-
37
-
-
80052030628
-
-
submitted for publication
-
Tian, G., Paschetto, K.P., Gharahdaghi, F., Gordon, E., Wilkins, D.E., Luo, X., Scott, C., submitted for publication. Mechanism of Inhibition of Fatty Acid Amide Hydrolase by Sulfonamide Containing Benzothiazoles: Long Residence Time Derived from Increased Kinetic Barrier and Not Exclusively from Thermodynamic Potency.
-
Mechanism of Inhibition of Fatty Acid Amide Hydrolase by Sulfonamide Containing Benzothiazoles: Long Residence Time Derived from Increased Kinetic Barrier and Not Exclusively from Thermodynamic Potency
-
-
Tian, G.1
Paschetto, K.P.2
Gharahdaghi, F.3
Gordon, E.4
Wilkins, D.E.5
Luo, X.6
Scott, C.7
-
38
-
-
0036669790
-
Cannabinoid analgesia
-
DOI 10.1016/S0163-7258(02)00252-8, PII S0163725802002528
-
J.M. Walker, and S.M. Huang Cannabinoid analgesia Pharmacol. Ther. 95 2002 127 135 (Pubitemid 35232131)
-
(2002)
Pharmacology and Therapeutics
, vol.95
, Issue.2
, pp. 127-135
-
-
Walker J.Michael1
Huang, S.M.2
-
40
-
-
33744518269
-
A novel scintillation proximity assay for fatty acid amide hydrolase compatible with inhibitor screening
-
DOI 10.1016/j.ab.2006.04.005, PII S0003269706002703
-
Y. Wang, J. Xu, A. Uveges, M.K. Ramarao, K.E. Rogers, and P.G. Jones A novel scintillation proximity assay for fatty acid amide hydrolase compatible with inhibitor screening Anal. Biochem. 354 2006 35 42 (Pubitemid 43816392)
-
(2006)
Analytical Biochemistry
, vol.354
, Issue.1
, pp. 35-42
-
-
Wang, Y.1
Xu, J.2
Uveges, A.3
Ramarao, M.K.4
Rogers, K.E.5
Jones, P.G.6
-
41
-
-
59449100866
-
Synthesis and evaluation of benzothiazole-based analogues as novel, potent, and selective fatty acid amide hydrolase inhibitors
-
X. Wang, K. Sarris, K. Kage, D. Zhang, S.P. Brown, T. Kolasa, C. Surowy, O.F. El Kouhen, S.W. Muchmore, J.D. Brioni, and A.O. Stewart Synthesis and evaluation of benzothiazole-based analogues as novel, potent, and selective fatty acid amide hydrolase inhibitors J. Med. Chem. 52 2009 170 180
-
(2009)
J. Med. Chem.
, vol.52
, pp. 170-180
-
-
Wang, X.1
Sarris, K.2
Kage, K.3
Zhang, D.4
Brown, S.P.5
Kolasa, T.6
Surowy, C.7
El Kouhen, O.F.8
Muchmore, S.W.9
Brioni, J.D.10
Stewart, A.O.11
-
42
-
-
0038581558
-
A high-throughput-compatible assay for determining the activity of fatty acid amide hydrolase
-
DOI 10.1016/S0003-2697(03)00217-3
-
S. Wilson A high-throughput-compatible assay for determining the activity of fatty acid amide hydrolase Anal. Biochem. 318 2003 270 275 (Pubitemid 36694119)
-
(2003)
Analytical Biochemistry
, vol.318
, Issue.2
, pp. 270-275
-
-
Wilson, S.J.1
Lovenberg, T.W.2
Barbier, A.J.3
-
43
-
-
33750618230
-
Low dose treatment with the synthetic cannabinoid Nabilone significantly reduces spasticity-related pain: A double-blind placebo-controlled cross-over trial
-
DOI 10.1007/s00415-006-0218-8
-
J. Wissel, T. Haydn, J. Muller, C. Brenneis, T. Berger, W. Poewe, and L.D. Schelosky Low dose treatment with the synthetic cannabinoid Nabilone significantly reduces spasticity-related pain: a double-blind placebo-controlled cross-over trial J. Neurol. 253 2006 1337 1341 (Pubitemid 44691559)
-
(2006)
Journal of Neurology
, vol.253
, Issue.10
, pp. 1337-1341
-
-
Wissel, J.1
Haydn, T.2
Muller, J.3
Brenneis, C.4
Berger, T.5
Poewe, W.6
Schelosky, L.D.7
-
44
-
-
0024356486
-
Primary afferent-evoked synaptic responses and slow potential generation in rat substantia gelatinosa neurons in vitro
-
M. Yoshimura, and T.M. Jessell Primary afferent-evoked synaptic responses and slow potential generation in rat substantia gelatinosa neurons in vitro J. Neurophysiol. 62 1989 96 108 (Pubitemid 19180544)
-
(1989)
Journal of Neurophysiology
, vol.62
, Issue.1
, pp. 96-108
-
-
Yoshimura, M.1
Jessell, T.M.2
|