-
1
-
-
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, and M.K. McKinney et al. 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
-
2
-
-
79959506821
-
Mechanistic and pharmacological characterization of PF-04457845: A highly potent and selective fatty acid amide hydrolase inhibitor that reduces inflammatory and noninflammatory pain
-
K. Ahn, S.E. Smith, M.B. Liimatta, D. Beidler, N. Sadagopan, and D.T. Dudley et al. Mechanistic and pharmacological characterization of PF-04457845: a highly potent and selective fatty acid amide hydrolase inhibitor that reduces inflammatory and noninflammatory pain J. Pharmacol. Exp. Ther. 338 2011 114 124
-
(2011)
J. Pharmacol. Exp. Ther.
, vol.338
, pp. 114-124
-
-
Ahn, K.1
Smith, S.E.2
Liimatta, M.B.3
Beidler, D.4
Sadagopan, N.5
Dudley, D.T.6
-
3
-
-
84859051245
-
The fatty acid amide hydrolase (FAAH) inhibitor PF-3845 acts in the nervous system to reverse LPS-induced tactile allodynia in mice
-
L. Booker, S.G. Kinsey, R.A. Abdullah, J.L. Blankman, J.Z. Long, and C. Ezzili et al. The fatty acid amide hydrolase (FAAH) inhibitor PF-3845 acts in the nervous system to reverse LPS-induced tactile allodynia in mice Br. J. Pharmacol. 165 2012 2485 2496
-
(2012)
Br. J. Pharmacol.
, vol.165
, pp. 2485-2496
-
-
Booker, L.1
Kinsey, S.G.2
Abdullah, R.A.3
Blankman, J.L.4
Long, J.Z.5
Ezzili, C.6
-
4
-
-
14844282831
-
The expanding field of cannabimimetic and related lipid mediators
-
H.B. Bradshaw, and J.M. Walker The expanding field of cannabimimetic and related lipid mediators Br. J. Pharmacol. 144 2005 459 465
-
(2005)
Br. J. Pharmacol.
, vol.144
, pp. 459-465
-
-
Bradshaw, H.B.1
Walker, J.M.2
-
5
-
-
0027933374
-
Quantitative assessment of tactile allodynia in the rat paw
-
S.R. Chaplan, F.W. Bach, J.W. Pogrel, J.M. Chung, and T.L. Yaksh Quantitative assessment of tactile allodynia in the rat paw J. Neurosci. Methods 53 1994 55 63
-
(1994)
J. Neurosci. Methods
, vol.53
, pp. 55-63
-
-
Chaplan, S.R.1
Bach, F.W.2
Pogrel, J.W.3
Chung, J.M.4
Yaksh, T.L.5
-
6
-
-
77957263726
-
Anandamide suppresses pain initiation through a peripheral endocannabinoid mechanism
-
J.R. Clapper, G. Moreno-Sanz, R. Russo, A. Guijarro, F. Vacondio, and A. Duranti et al. Anandamide suppresses pain initiation through a peripheral endocannabinoid mechanism Nat. Neurosci. 13 2010 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
-
7
-
-
0036221971
-
CB1 and CB2 cannabinoid receptors are implicated in inflammatory pain
-
N. Clayton, F.H. Marshall, C. Bountra, and C.T. O'Shaughnessy CB1 and CB2 cannabinoid receptors are implicated in inflammatory pain Pain 96 2002 253 260
-
(2002)
Pain
, vol.96
, pp. 253-260
-
-
Clayton, N.1
Marshall, F.H.2
Bountra, C.3
O'Shaughnessy, C.T.4
-
8
-
-
35648973242
-
The inhibition of monoacylglycerol lipase by URB602 showed an anti-inflammatory and anti-nociceptive effect in a murine model of acute inflammation
-
F. Comelli, G. Giagnoni, I. Bettoni, M. Colleoni, and B. Costa The inhibition of monoacylglycerol lipase by URB602 showed an anti-inflammatory and anti-nociceptive effect in a murine model of acute inflammation Br. J. Pharmacol. 152 2007 787 794
-
(2007)
Br. J. Pharmacol.
, vol.152
, pp. 787-794
-
-
Comelli, F.1
Giagnoni, G.2
Bettoni, I.3
Colleoni, M.4
Costa, B.5
-
9
-
-
2342498975
-
3-[2-cyano-3-(trifluoromethyl)phenoxy]phenyl-4,4,4-trifluoro-1- butanesulfonate (BAY 59-3074): A novel cannabinoid Cb1/Cb2 receptor partial agonist with antihyperalgesic and antiallodynic effects
-
J. De Vry, D. Denzer, E. Reissmueller, M. Eijckenboom, M. Heil, and H. Meier et al. 3-[2-cyano-3-(trifluoromethyl)phenoxy]phenyl-4,4,4-trifluoro-1- butanesulfonate (BAY 59-3074): a novel cannabinoid Cb1/Cb2 receptor partial agonist with antihyperalgesic and antiallodynic effects J. Pharmacol. Exp. Ther. 310 2004 620 632
-
(2004)
J. Pharmacol. Exp. Ther.
, vol.310
, pp. 620-632
-
-
De Vry, J.1
Denzer, D.2
Reissmueller, E.3
Eijckenboom, M.4
Heil, M.5
Meier, H.6
-
11
-
-
33645794041
-
The biosynthesis, fate and pharmacological properties of endocannabinoids
-
V. Di Marzo, L. De Petrocellis, and T. Bisogno The biosynthesis, fate and pharmacological properties of endocannabinoids Handb. Exp. Pharmacol. 2005 147 185
-
(2005)
Handb. Exp. Pharmacol.
, pp. 147-185
-
-
Di Marzo, V.1
De Petrocellis, L.2
Bisogno, T.3
-
12
-
-
28644451441
-
Activation of CB1 and CB2 receptors attenuates the induction and maintenance of inflammatory pain in the rat
-
S.J. Elmes, L.A. Winyard, S.J. Medhurst, N.M. Clayton, A.W. Wilson, and D.A. Kendall et al. Activation of CB1 and CB2 receptors attenuates the induction and maintenance of inflammatory pain in the rat Pain 118 2005 327 335
-
(2005)
Pain
, vol.118
, pp. 327-335
-
-
Elmes, S.J.1
Winyard, L.A.2
Medhurst, S.J.3
Clayton, N.M.4
Wilson, A.W.5
Kendall, D.A.6
-
13
-
-
84874649914
-
The monoacylglycerol lipase inhibitor JZL184 suppresses inflammatory pain in the mouse carrageenan model
-
S. Ghosh, L.E. Wise, Y. Chen, R. Gujjar, A. Mahadevan, and B.F. Cravatt et al. The monoacylglycerol lipase inhibitor JZL184 suppresses inflammatory pain in the mouse carrageenan model Life Sci. 92 2013 498 505
-
(2013)
Life Sci.
, vol.92
, pp. 498-505
-
-
Ghosh, S.1
Wise, L.E.2
Chen, Y.3
Gujjar, R.4
Mahadevan, A.5
Cravatt, B.F.6
-
14
-
-
69549116206
-
The therapeutic potential of the endocannabinoid system for the development of a novel class of antidepressants
-
M.N. Hill, C.J. Hillard, F.R. Bambico, S. Patel, B.B. Gorzalka, and G. Gobbi The therapeutic potential of the endocannabinoid system for the development of a novel class of antidepressants Trends Pharmacol. Sci. 30 2009 484 493
-
(2009)
Trends Pharmacol. Sci.
, vol.30
, pp. 484-493
-
-
Hill, M.N.1
Hillard, C.J.2
Bambico, F.R.3
Patel, S.4
Gorzalka, B.B.5
Gobbi, G.6
-
15
-
-
84864577250
-
An efficient randomised, placebo-controlled clinical trial with the irreversible fatty acid amide hydrolase-1 inhibitor PF-04457845, which modulates endocannabinoids but fails to induce effective analgesia in patients with pain due to osteoarthritis of the knee
-
J.P. Huggins, T.S. Smart, S. Langman, L. Taylor, and T. Young An efficient randomised, placebo-controlled clinical trial with the irreversible fatty acid amide hydrolase-1 inhibitor PF-04457845, which modulates endocannabinoids but fails to induce effective analgesia in patients with pain due to osteoarthritis of the knee Pain 153 2012 1837 1846
-
(2012)
Pain
, vol.153
, pp. 1837-1846
-
-
Huggins, J.P.1
Smart, T.S.2
Langman, S.3
Taylor, L.4
Young, T.5
-
16
-
-
32244432341
-
Actions of the FAAH inhibitor URB597 in neuropathic and inflammatory chronic pain models
-
A. Jayamanne, R. Greenwood, V.A. Mitchell, S. Aslan, D. Piomelli, and C.W. Vaughan Actions of the FAAH inhibitor URB597 in neuropathic and inflammatory chronic pain models Br. J. Pharmacol. 147 2006 281 288
-
(2006)
Br. J. Pharmacol.
, vol.147
, pp. 281-288
-
-
Jayamanne, A.1
Greenwood, R.2
Mitchell, V.A.3
Aslan, S.4
Piomelli, D.5
Vaughan, C.W.6
-
17
-
-
0038582327
-
A cannabinoid agonist differentially attenuates deep tissue hyperalgesia in animal models of cancer and inflammatory muscle pain
-
L.J. Kehl, D.T. Hamamoto, P.W. Wacnik, D.L. Croft, B.D. Norsted, and G.L. Wilcox et al. A cannabinoid agonist differentially attenuates deep tissue hyperalgesia in animal models of cancer and inflammatory muscle pain Pain 103 2003 175 186
-
(2003)
Pain
, vol.103
, pp. 175-186
-
-
Kehl, L.J.1
Hamamoto, D.T.2
Wacnik, P.W.3
Croft, D.L.4
Norsted, B.D.5
Wilcox, G.L.6
-
18
-
-
79960892570
-
Fatty acid amide hydrolase blockade attenuates the development of collagen-induced arthritis and related thermal hyperalgesia in mice
-
S.G. Kinsey, P.S. Naidu, B.F. Cravatt, D.T. Dudley, and A.H. Lichtman Fatty acid amide hydrolase blockade attenuates the development of collagen-induced arthritis and related thermal hyperalgesia in mice Pharmacol. Biochem. Behav. 99 2011 718 725
-
(2011)
Pharmacol. Biochem. Behav.
, vol.99
, pp. 718-725
-
-
Kinsey, S.G.1
Naidu, P.S.2
Cravatt, B.F.3
Dudley, D.T.4
Lichtman, A.H.5
-
19
-
-
78650619344
-
Inhibition of endocannabinoid catabolic enzymes elicits anxiolytic-like effects in the marble burying assay
-
S.G. Kinsey, S.T. O'Neal, J.Z. Long, B.F. Cravatt, and A.H. Lichtman Inhibition of endocannabinoid catabolic enzymes elicits anxiolytic-like effects in the marble burying assay Pharmacol. Biochem. Behav. 98 2011 21 27
-
(2011)
Pharmacol. Biochem. Behav.
, vol.98
, pp. 21-27
-
-
Kinsey, S.G.1
O'Neal, S.T.2
Long, J.Z.3
Cravatt, B.F.4
Lichtman, A.H.5
-
20
-
-
57749087828
-
Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects
-
J.Z. Long, W. Li, L. Booker, J.J. Burston, S.G. Kinsey, and J.E. Schlosburg et al. Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects Nat. Chem. Biol. 5 2009 37 44
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 37-44
-
-
Long, J.Z.1
Li, W.2
Booker, L.3
Burston, J.J.4
Kinsey, S.G.5
Schlosburg, J.E.6
-
21
-
-
73949109254
-
Dual blockade of FAAH and MAGL identifies behavioral processes regulated by endocannabinoid crosstalk in vivo
-
J.Z. Long, D.K. Nomura, R.E. Vann, D.M. Walentiny, L. Booker, and X. Jin et al. Dual blockade of FAAH and MAGL identifies behavioral processes regulated by endocannabinoid crosstalk in vivo Proc. Natl. Acad. Sci. U.S.A. 106 2009 20270 20275
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 20270-20275
-
-
Long, J.Z.1
Nomura, D.K.2
Vann, R.E.3
Walentiny, D.M.4
Booker, L.5
Jin, X.6
-
22
-
-
68749110973
-
Functional CB2 type cannabinoid receptors at CNS synapses
-
N.H. Morgan, I.M. Stanford, and G.L. Woodhall Functional CB2 type cannabinoid receptors at CNS synapses Neuropharmacology 57 2009 356 368
-
(2009)
Neuropharmacology
, vol.57
, pp. 356-368
-
-
Morgan, N.H.1
Stanford, I.M.2
Woodhall, G.L.3
-
23
-
-
77953775181
-
Regulation of inflammatory pain by inhibition of fatty acid amide hydrolase
-
P.S. Naidu, S.G. Kinsey, T.L. Guo, B.F. Cravatt, and A.H. Lichtman Regulation of inflammatory pain by inhibition of fatty acid amide hydrolase J. Pharmacol. Exp. Ther. 334 2010 182 190
-
(2010)
J. Pharmacol. Exp. Ther.
, vol.334
, pp. 182-190
-
-
Naidu, P.S.1
Kinsey, S.G.2
Guo, T.L.3
Cravatt, B.F.4
Lichtman, A.H.5
-
24
-
-
33748703859
-
The endocannabinoid system as an emerging target of pharmacotherapy
-
P. Pacher, S. Batkai, and G. Kunos The endocannabinoid system as an emerging target of pharmacotherapy Pharmacol. Rev. 58 2006 389 462
-
(2006)
Pharmacol. Rev.
, vol.58
, pp. 389-462
-
-
Pacher, P.1
Batkai, S.2
Kunos, G.3
-
25
-
-
74549185125
-
FAAH and MAGL inhibitors: Therapeutic opportunities from regulating endocannabinoid levels
-
S. Petrosino, and V. Di Marzo FAAH and MAGL inhibitors: therapeutic opportunities from regulating endocannabinoid levels Curr. Opin. Investig. Drugs 11 2010 51 62
-
(2010)
Curr. Opin. Investig. Drugs
, vol.11
, pp. 51-62
-
-
Petrosino, S.1
Di Marzo, V.2
-
26
-
-
0242268553
-
The molecular logic of endocannabinoid signalling
-
D. Piomelli The molecular logic of endocannabinoid signalling Nat. Rev. Neurosci. 4 2003 873 884
-
(2003)
Nat. Rev. Neurosci.
, vol.4
, pp. 873-884
-
-
Piomelli, D.1
-
27
-
-
84859324853
-
Inhibiting the breakdown of endogenous opioids and cannabinoids to alleviate pain
-
B.P. Roques, M.C. Fournie-Zaluski, and M. Wurm Inhibiting the breakdown of endogenous opioids and cannabinoids to alleviate pain Nat. Rev. Drug Discov. 11 2012 292 310
-
(2012)
Nat. Rev. Drug Discov.
, vol.11
, pp. 292-310
-
-
Roques, B.P.1
Fournie-Zaluski, M.C.2
Wurm, M.3
-
28
-
-
0032056333
-
Characterization of delta9-tetrahydrocannabinol and anandamide antinociception in nonarthritic and arthritic rats
-
F.L. Smith, K. Fujimori, J. Lowe, and S.P. Welch Characterization of delta9-tetrahydrocannabinol and anandamide antinociception in nonarthritic and arthritic rats Pharmacol. Biochem. Behav. 60 1998 183 191
-
(1998)
Pharmacol. Biochem. Behav.
, vol.60
, pp. 183-191
-
-
Smith, F.L.1
Fujimori, K.2
Lowe, J.3
Welch, S.P.4
-
29
-
-
34547566970
-
The effect of the palmitoylethanolamide analogue, palmitoylallylamide (L-29) on pain behaviour in rodent models of neuropathy
-
V.C. Wallace, A.R. Segerdahl, D.M. Lambert, S. Vandevoorde, J. Blackbeard, and T. Pheby et al. The effect of the palmitoylethanolamide analogue, palmitoylallylamide (L-29) on pain behaviour in rodent models of neuropathy Br. J. Pharmacol. 151 2007 1117 1128
-
(2007)
Br. J. Pharmacol.
, vol.151
, pp. 1117-1128
-
-
Wallace, V.C.1
Segerdahl, A.R.2
Lambert, D.M.3
Vandevoorde, S.4
Blackbeard, J.5
Pheby, T.6
-
30
-
-
84862101460
-
Dual fatty acid amide hydrolase and monoacylglycerol lipase blockade produces THC-like Morris water maze deficits in mice
-
L.E. Wise, K.A. Long, R.A. Abdullah, J.Z. Long, B.F. Cravatt, and A.H. Lichtman Dual fatty acid amide hydrolase and monoacylglycerol lipase blockade produces THC-like Morris water maze deficits in mice ACS Chem. Neurosci. 3 2012 369 378
-
(2012)
ACS Chem. Neurosci.
, vol.3
, pp. 369-378
-
-
Wise, L.E.1
Long, K.A.2
Abdullah, R.A.3
Long, J.Z.4
Cravatt, B.F.5
Lichtman, A.H.6
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