-
1
-
-
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(5090), 1946-1949.
-
(1992)
Science
, vol.258
, Issue.5090
, 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
-
2
-
-
0027185227
-
Anandamide, an endogenous cannabimimetic eicosanoid, binds to the cloned human cannabinoid receptor and stimulates receptor-mediated signal transduction
-
Felder, C.C.; Briley, E.M.; Axelrod, J.; Simpson, J.T.; Mackie, K.; Devane, W.A. Anandamide, an endogenous cannabimimetic eicosanoid, binds to the cloned human cannabinoid receptor and stimulates receptor-mediated signal transduction. Proc. Natl. Acad. Sci. USA, 1993, 90(16), 7656-7660.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, Issue.16
, pp. 7656-7660
-
-
Felder, C.C.1
Briley, E.M.2
Axelrod, J.3
Simpson, J.T.4
Mackie, K.5
Devane, W.A.6
-
3
-
-
44849141696
-
Enzymatic pathways that regulate endocannabinoid signaling in the nervous system
-
Ahn, K.; McKinney, M.K.; Cravatt, B.F. Enzymatic pathways that regulate endocannabinoid signaling in the nervous system. Chem. Rev., 2008, 108(5), 1687-1707.
-
(2008)
Chem. Rev
, vol.108
, Issue.5
, pp. 1687-1707
-
-
Ahn, K.1
McKinney, M.K.2
Cravatt, B.F.3
-
4
-
-
0037207094
-
Cell signaling by endocannabinoids and their congeners: Questions of selectivity and other challenges
-
Schmid, H.H.; Schmid, P.C.; Berdyshev, E.V. Cell signaling by endocannabinoids and their congeners: questions of selectivity and other challenges. Chem. Phys. Lipids, 2002, 121(1-2), 111-134.
-
(2002)
Chem. Phys. Lipids
, vol.121
, Issue.1-2
, pp. 111-134
-
-
Schmid, H.H.1
Schmid, P.C.2
Berdyshev, E.V.3
-
5
-
-
1242294480
-
Molecular characterization of a phospholipase D generating anandamide and its congeners
-
Okamoto, Y.; Morishita, J.; Tsuboi, K.; Tonai, T.; Ueda, N. Molecular characterization of a phospholipase D generating anandamide and its congeners. J. Biol. Chem., 2004, 279(7), 5298-5305.
-
(2004)
J. Biol. Chem
, vol.279
, Issue.7
, pp. 5298-5305
-
-
Okamoto, Y.1
Morishita, J.2
Tsuboi, K.3
Tonai, T.4
Ueda, N.5
-
6
-
-
0028589390
-
Formation and inactivation of endogenous cannabinoid anandamide in central neurons
-
Di Marzo, V.; Fontana, A.; Cadas, H.; Schinelli, S.; Cimino, G.; Schwartz, J.C.; Piomelli, D. Formation and inactivation of endogenous cannabinoid anandamide in central neurons. Nature, 1994, 372(6507), 686-691.
-
(1994)
Nature
, vol.372
, Issue.6507
, 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
-
7
-
-
0031033841
-
Occurrence and biosynthesis of endogenous cannabinoid precursor, N-arachidonoyl phosphatidylethanolamine, in rat brain
-
Cadas, H.; di Tomaso, E.; Piomelli, D. Occurrence and biosynthesis of endogenous cannabinoid precursor, N-arachidonoyl phosphatidylethanolamine, in rat brain. J. Neurosci., 1997, 17(4), 1226- 1242.
-
(1997)
J. Neurosci
, vol.17
, Issue.4
, pp. 1226-1242
-
-
Cadas, H.1
di Tomaso, E.2
Piomelli, D.3
-
8
-
-
0035053627
-
Retrograde inhibition of presynaptic calcium influx by endogenous cannabinoids at excitatory synapses onto Purkinje cells
-
Kreitzer, A.C.; Regehr, W.G. Retrograde inhibition of presynaptic calcium influx by endogenous cannabinoids at excitatory synapses onto Purkinje cells. Neuron, 2001, 29(3), 717-727.
-
(2001)
Neuron
, vol.29
, Issue.3
, pp. 717-727
-
-
Kreitzer, A.C.1
Regehr, W.G.2
-
9
-
-
0035967145
-
Endogenous cannabinoids mediate retrograde signalling at hippocampal synapses
-
Wilson, R.I.; Nicoll, R.A. Endogenous cannabinoids mediate retrograde signalling at hippocampal synapses. Nature, 2001, 410(6828), 588-592.
-
(2001)
Nature
, vol.410
, Issue.6828
, pp. 588-592
-
-
Wilson, R.I.1
Nicoll, R.A.2
-
10
-
-
0035050883
-
Endogenous cannabinoids mediate retrograde signals from depolarized postsynaptic neurons to presynaptic terminals
-
Ohno-Shosaku, T.; Maejima, T.; Kano, M. Endogenous cannabinoids mediate retrograde signals from depolarized postsynaptic neurons to presynaptic terminals. Neuron, 2001, 29(3), 729-738.
-
(2001)
Neuron
, vol.29
, Issue.3
, pp. 729-738
-
-
Ohno-Shosaku, T.1
Maejima, T.2
Kano, M.3
-
11
-
-
0033574179
-
Brain regional distribution of endocannabinoids: Implications for their biosynthesis and biological function
-
Bisogno, T.; Berrendero, F.; Ambrosino, G.; Cebeira, M.; Ramos, J.A.; Fernandez-Ruiz, J.J.; Di Marzo, V. Brain regional distribution of endocannabinoids: implications for their biosynthesis and biological function. Biochem. Biophys. Res. Commun., 1999, 256(2), 377-380.
-
(1999)
Biochem. Biophys. Res Commun
, vol.256
, Issue.2
, pp. 377-380
-
-
Bisogno, T.1
Berrendero, F.2
Ambrosino, G.3
Cebeira, M.4
Ramos, J.A.5
Fernandez-Ruiz, J.J.6
di Marzo, V.7
-
12
-
-
0033048369
-
GC/MS analysis of anandamide and quantification of Narachidonoylphosphatidylethanolamides in various brain regions, spinal cord, testis, and spleen of the rat
-
Yang, H.Y.; Karoum, F.; Felder, C.; Badger, H.; Wang, T.C.; Markey, S.P. GC/MS analysis of anandamide and quantification of Narachidonoylphosphatidylethanolamides in various brain regions, spinal cord, testis, and spleen of the rat. J. Neurochem., 1999, 72(5), 1959-1968.
-
(1999)
J. Neurochem
, vol.72
, Issue.5
, pp. 1959-1968
-
-
Yang, H.Y.1
Karoum, F.2
Felder, C.3
Badger, H.4
Wang, T.C.5
Markey, S.P.6
-
13
-
-
0025325535
-
Structure of a cannabinoid receptor and functional expression of the cloned cDNA
-
Matsuda, L.A.; Lolait, S.J.; Brownstein, M.J.; Young, A.C.; Bonner, T.I. Structure of a cannabinoid receptor and functional expression of the cloned cDNA. Nature, 1990, 346(6284), 561-564.
-
(1990)
Nature
, vol.346
, Issue.6284
, pp. 561-564
-
-
Matsuda, L.A.1
Lolait, S.J.2
Brownstein, M.J.3
Young, A.C.4
Bonner, T.I.5
-
14
-
-
0027515373
-
Molecular characterization of a peripheral receptor for cannabinoids
-
Munro, S.; Thomas, K.L.; Abu-Shaar, M. Molecular characterization of a peripheral receptor for cannabinoids. Nature, 1993, 365(6441), 61-65.
-
(1993)
Nature
, vol.365
, Issue.6441
, pp. 61-65
-
-
Munro, S.1
Thomas, K.L.2
Abu-Shaar, M.3
-
15
-
-
0025954862
-
Characterization and localization of cannabinoid receptors in rat brain: A quantitative in vitro autoradiographic study
-
Herkenham, M.; Lynn, A.B.; Johnson, M.R.; Melvin, L.S.; de Costa, B.R.; Rice, K.C. Characterization and localization of cannabinoid receptors in rat brain: a quantitative in vitro autoradiographic study. J. Neurosci., 1991, 11(2), 563-583.
-
(1991)
J. Neurosci
, vol.11
, Issue.2
, pp. 563-583
-
-
Herkenham, M.1
Lynn, A.B.2
Johnson, M.R.3
Melvin, L.S.4
de Costa, B.R.5
Rice, K.C.6
-
16
-
-
0025236913
-
Cannabinoid receptor localization in brain
-
Herkenham, M.; Lynn, A.B.; Little, M.D.; Johnson, M.R.; Melvin, L.S.; de Costa, B.R.; Rice, K.C. Cannabinoid receptor localization in brain. Proc. Natl. Acad. Sci. USA, 1990, 87(5), 1932-1936.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, Issue.5
, pp. 1932-1936
-
-
Herkenham, M.1
Lynn, A.B.2
Little, M.D.3
Johnson, M.R.4
Melvin, L.S.5
de Costa, B.R.6
Rice, K.C.7
-
17
-
-
0031047273
-
Cannabinoid receptors in the human brain: A detailed anatomical and quantitative autoradiographic study in the fetal, neonatal and adult human brain
-
Glass, M.; Dragunow, M.; Faull, R.L. Cannabinoid receptors in the human brain: a detailed anatomical and quantitative autoradiographic study in the fetal, neonatal and adult human brain. Neuroscience, 1997, 77(2), 299-318.
-
(1997)
Neuroscience
, vol.77
, Issue.2
, pp. 299-318
-
-
Glass, M.1
Dragunow, M.2
Faull, R.L.3
-
18
-
-
0028325790
-
Localization of cannabinoid receptors and nonsaturable high-density cannabinoid binding sites in peripheral tissues of the rat: Implications for receptor-mediated immune modulation by cannabinoids
-
Lynn, A.B.; Herkenham, M. Localization of cannabinoid receptors and nonsaturable high-density cannabinoid binding sites in peripheral tissues of the rat: implications for receptor-mediated immune modulation by cannabinoids. J. Pharmacol. Exp. Ther., 1994, 268(3), 1612-1623.
-
(1994)
J. Pharmacol. Exp. Ther
, vol.268
, Issue.3
, pp. 1612-1623
-
-
Lynn, A.B.1
Herkenham, M.2
-
19
-
-
32844465920
-
Cannabinoid CB2 receptors: Immunohistochemical localization in rat brain
-
Gong, J.P.; Onaivi, E.S.; Ishiguro, H.; Liu, Q.R.; Tagliaferro, P.A.; Brusco, A.; Uhl, G.R. Cannabinoid CB2 receptors: immunohistochemical localization in rat brain. Brain Res., 2006, 1071(1), 10-23.
-
(2006)
Brain Res
, vol.1071
, Issue.1
, pp. 10-23
-
-
Gong, J.P.1
Onaivi, E.S.2
Ishiguro, H.3
Liu, Q.R.4
Tagliaferro, P.A.5
Brusco, A.6
Uhl, G.R.7
-
20
-
-
26844504226
-
Identification and functional characterization of brainstem cannabinoid CB2 receptors
-
Van Sickle, M.D.; Duncan, M.; Kingsley, P.J.; Mouihate, A.; Urbani, P.; Mackie, K.; Stella, N.; Makriyannis, A.; Piomelli, D.; Davison, J.S.; Marnett, L.J.; Di Marzo, V.; Pittman, Q.J.; Patel, K.D.; Sharkey, K.A. Identification and functional characterization of brainstem cannabinoid CB2 receptors. Science, 2005, 310(5746), 329-332.
-
(2005)
Science
, vol.310
, Issue.5746
, pp. 329-332
-
-
van Sickle, M.D.1
Duncan, M.2
Kingsley, P.J.3
Mouihate, A.4
Urbani, P.5
Mackie, K.6
Stella, N.7
Makriyannis, A.8
Piomelli, D.9
Davison, J.S.10
Marnett, L.J.11
di Marzo, V.12
Pittman, Q.J.13
Patel, K.D.14
Sharkey, K.A.15
-
21
-
-
0030611978
-
Pharmacology of cannabinoid CB1 and CB2 receptors
-
Pertwee, R.G. Pharmacology of cannabinoid CB1 and CB2 receptors. Pharmacol. Ther., 1997, 74(2), 129-180.
-
(1997)
Pharmacol. Ther
, vol.74
, Issue.2
, pp. 129-180
-
-
Pertwee, R.G.1
-
22
-
-
0033614984
-
Vanilloid receptors on sensory nerves mediate the vasodilator action of anandamide
-
Zygmunt, P.M.; Petersson, J.; Andersson, D.A.; Chuang, H.; Sorgard, M.; Di Marzo, V.; Julius, D.; Hogestatt, E.D. Vanilloid receptors on sensory nerves mediate the vasodilator action of anandamide. Nature, 1999, 400(6743), 452-457.
-
(1999)
Nature
, vol.400
, Issue.6743
, pp. 452-457
-
-
Zygmunt, P.M.1
Petersson, J.2
Andersson, D.A.3
Chuang, H.4
Sorgard, M.5
di Marzo, V.6
Julius, D.7
Hogestatt, E.D.8
-
23
-
-
35649015179
-
The orphan receptor GPR55 is a novel cannabinoid receptor
-
Ryberg, E.; Larsson, N.; Sjogren, S.; Hjorth, S.; Hermansson, N.O.; Leonova, J.; Elebring, T.; Nilsson, K.; Drmota, T.; Greasley, P.J. The orphan receptor GPR55 is a novel cannabinoid receptor. Br. J. Pharmacol., 2007, 152(7), 1092-1101.
-
(2007)
Br. J. Pharmacol
, vol.152
, Issue.7
, pp. 1092-1101
-
-
Ryberg, E.1
Larsson, N.2
Sjogren, S.3
Hjorth, S.4
Hermansson, N.O.5
Leonova, J.6
Elebring, T.7
Nilsson, K.8
Drmota, T.9
Greasley, P.J.10
-
24
-
-
0033984992
-
The endogenous lipid anandamide is a full agonist at the human vanilloid receptor (hVR1)
-
Smart, D.; Gunthorpe, M.J.; Jerman, J.C.; Nasir, S.; Gray, J.; Muir, A.I.; Chambers, J.K.; Randall, A.D.; Davis, J.B. The endogenous lipid anandamide is a full agonist at the human vanilloid receptor (hVR1). Br. J. Pharmacol., 2000, 129(2), 227-230.
-
(2000)
Br. J. Pharmacol
, vol.129
, Issue.2
, pp. 227-230
-
-
Smart, D.1
Gunthorpe, M.J.2
Jerman, J.C.3
Nasir, S.4
Gray, J.5
Muir, A.I.6
Chambers, J.K.7
Randall, A.D.8
Davis, J.B.9
-
25
-
-
70349687538
-
Pharmacology and treatment of neuropathic pains
-
Jensen, T.S.; Madsen, C.S.; Finnerup, N.B. Pharmacology and treatment of neuropathic pains. Curr. Opin. Neurol., 2009, 22(5), 467-474.
-
(2009)
Opin. Neurol
, vol.22
, Issue.5
, pp. 467-474
-
-
Jensen, T.S.1
Madsen, C.S.2
Finnerup, N.B.3
-
26
-
-
23044447712
-
Delta9-tetrahydrocannbinol accounts for the antinociceptive, hypothermic, and cataleptic effects of marijuana in mice
-
Varvel, S.A.; Bridgen, D.T.; Tao, Q.; Thomas, B.F.; Martin, B.R.; Lichtman, A.H. Delta9-tetrahydrocannbinol accounts for the antinociceptive, hypothermic, and cataleptic effects of marijuana in mice. J. Pharmacol. Exp. Ther., 2005, 314(1), 329-337.
-
(2005)
J. Pharmacol. Exp. Ther
, vol.314
, Issue.1
, pp. 329-337
-
-
Varvel, S.A.1
Bridgen, D.T.2
Tao, Q.3
Thomas, B.F.4
Martin, B.R.5
Lichtman, A.H.6
-
27
-
-
0034951162
-
The synthetic cannabinoid WIN55,212-2 attenuates hyperalgesia and allodynia in a rat model of neuropathic pain
-
Bridges, D.; Ahmad, K.; Rice, A.S. The synthetic cannabinoid WIN55,212-2 attenuates hyperalgesia and allodynia in a rat model of neuropathic pain. Br. J. Pharmacol., 2001, 133(4), 586-594.
-
(2001)
Br. J. Pharmacol
, vol.133
, Issue.4
, pp. 586-594
-
-
Bridges, D.1
Ahmad, K.2
Rice, A.S.3
-
28
-
-
0030044427
-
Suppression of noxious stimulus- evoked expression of Fos protein-like immunoreactivity in rat spinal cord by a selective cannabinoid agonist
-
Tsou, K.; Lowitz, K.A.; Hohmann, A.G.; Martin, W.J.; Hathaway, C.B.; Bereiter, D.A.; Walker, J.M. Suppression of noxious stimulus- evoked expression of Fos protein-like immunoreactivity in rat spinal cord by a selective cannabinoid agonist. Neuroscience, 1996, 70(3), 791-798.
-
(1996)
Neuroscience
, vol.70
, Issue.3
, pp. 791-798
-
-
Tsou, K.1
Lowitz, K.A.2
Hohmann, A.G.3
Martin, W.J.4
Hathaway, C.B.5
Bereiter, D.A.6
Walker, J.M.7
-
29
-
-
0015804583
-
Antipyretic, analgesic and anti-inflammatory effects of delta 9-tetrahydrocannabinol in the rat
-
Kosersky, D.S.; Dewey, W.L.; Harris, L.S. Antipyretic, analgesic and anti-inflammatory effects of delta 9-tetrahydrocannabinol in the rat. Eur. J. Pharmacol., 1973, 24(1), 1-7.
-
(1973)
Eur. J. Pharmacol
, vol.24
, Issue.1
, pp. 1-7
-
-
Kosersky, D.S.1
Dewey, W.L.2
Harris, L.S.3
-
30
-
-
34347339442
-
NOP receptor antagonist, JTC-801, blocks cannabinoid-evoked hypothermia in rats
-
Rawls, S.M.; Schroeder, J.A.; Ding, Z.; Rodriguez, T.; Zaveri, N. NOP receptor antagonist, JTC-801, blocks cannabinoid-evoked hypothermia in rats. Neuropeptides, 2007, 41(4), 239-247.
-
(2007)
Neuropeptides
, vol.41
, Issue.4
, pp. 239-247
-
-
Rawls, S.M.1
Schroeder, J.A.2
Ding, Z.3
Rodriguez, T.4
Zaveri, N.5
-
31
-
-
0028291118
-
The pharmacological activity of anandamide, a putative endogenous cannabinoid, in mice
-
Smith, P.B.; Compton, D.R.; Welch, S.P.; Razdan, R.K.; Mechoulam, R.; Martin, B.R. The pharmacological activity of anandamide, a putative endogenous cannabinoid, in mice. J. Pharmacol. Exp. Ther., 1994, 270(1), 219-227.
-
(1994)
J. Pharmacol. Exp. Ther
, vol.270
, Issue.1
, pp. 219-227
-
-
Smith, P.B.1
Compton, D.R.2
Welch, S.P.3
Razdan, R.K.4
Mechoulam, R.5
Martin, B.R.6
-
32
-
-
0032160418
-
Differential blockade of the antinociceptive effects of centrally administered cannabinoids by SR141716A
-
Welch, S.P.; Huffman, J.W.; Lowe, J. Differential blockade of the antinociceptive effects of centrally administered cannabinoids by SR141716A. J. Pharmacol. Exp. Ther., 1998, 286(3), 1301-1308.
-
(1998)
J. Pharmacol. Exp. Ther
, vol.286
, Issue.3
, pp. 1301-1308
-
-
Welch, S.P.1
Huffman, J.W.2
Lowe, J.3
-
33
-
-
33646748276
-
Antihyperalgesic effects of local injections of anandamide, ibuprofen, rofecoxib and their combinations in a model of neuropathic pain
-
Guindon, J.; Beaulieu, P. Antihyperalgesic effects of local injections of anandamide, ibuprofen, rofecoxib and their combinations in a model of neuropathic pain. Neuropharmacology, 2006, 50(7), 814-823.
-
(2006)
Neuropharmacology
, vol.50
, Issue.7
, pp. 814-823
-
-
Guindon, J.1
Beaulieu, P.2
-
34
-
-
32244432341
-
Actions of the FAAH Inhibitor URB597 In Neuropathic and Inflammatory Chronic Pain Models
-
Jayamanne, A.; Greenwood, R.; Mitchell, V.A.; Aslan, S.; Piomelli, D.; Vaughan, C.W. Actions of the FAAH inhibitor URB597 in neuropathic and inflammatory chronic pain models. Br. J. Pharmacol., 2006, 147(3), 281-288.
-
(2006)
Br. J. Pharmacol
, vol.147
, Issue.3
, pp. 281-288
-
-
Jayamanne, A.1
Greenwood, R.2
Mitchell, V.A.3
Aslan, S.4
Piomelli, D.5
Vaughan, C.W.6
-
35
-
-
33845799619
-
Analgesic effects of fatty acid amide hydrolase inhibition in a rat model of neuropathic pain
-
Jhaveri, M.D.; Richardson, D.; Kendall, D.A.; Barrett, D.A.; Chapman, V. Analgesic effects of fatty acid amide hydrolase inhibition in a rat model of neuropathic pain. J. Neurosci., 2006, 26(51), 13318-13327.
-
(2006)
J. Neurosci
, vol.26
, Issue.51
, pp. 13318-13327
-
-
Jhaveri, M.D.1
Richardson, D.2
Kendall, D.A.3
Barrett, D.A.4
Chapman, V.5
-
36
-
-
33646772896
-
Modulation of neuropathic and inflammatory pain by the endocannabinoid transport inhibitor AM404 [N-(4- hydroxyphenyl)-eicosa-5,8,11,14-tetraenamide
-
La Rana, G.; Russo, R.; Campolongo, P.; Bortolato, M.; Mangieri, R.A.; Cuomo, V.; Iacono, A.; Raso, G.M.; Meli, R.; Piomelli, D.; Calignano, A. Modulation of neuropathic and inflammatory pain by the endocannabinoid transport inhibitor AM404 [N-(4- hydroxyphenyl)-eicosa-5,8,11,14-tetraenamide]. J. Pharmacol. Exp. Ther., 2006, 317(3), 1365-1371.
-
(2006)
J. Pharmacol. Exp. Ther
, vol.317
, Issue.3
, pp. 1365-1371
-
-
la Rana, G.1
Russo, R.2
Campolongo, P.3
Bortolato, M.4
Mangieri, R.A.5
Cuomo, V.6
Iacono, A.7
Raso, G.M.8
Meli, R.9
Piomelli, D.10
Calignano, A.11
-
37
-
-
0035979244
-
Supersensitivity to anandamide and enhanced endogenous cannabinoid signaling in mice lacking fatty acid amide hydrolase
-
Cravatt, B.F.; Demarest, K.; Patricelli, M.P.; Bracey, M.H.; Giang, D.K.; Martin, B.R.; Lichtman, A.H. Supersensitivity to anandamide and enhanced endogenous cannabinoid signaling in mice lacking fatty acid amide hydrolase. Proc. Natl. Acad. Sci. USA, 2001, 98(16), 9371-9376.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, Issue.16
, pp. 9371-9376
-
-
Cravatt, B.F.1
Demarest, K.2
Patricelli, M.P.3
Bracey, M.H.4
Giang, D.K.5
Martin, B.R.6
Lichtman, A.H.7
-
38
-
-
34347342722
-
Cannabinoids mediate analgesia largely via peripheral type 1 cannabinoid receptors in nociceptors
-
Agarwal, N.; Pacher, P.; Tegeder, I.; Amaya, F.; Constantin, C.E.; Brenner, G.J.; Rubino, T.; Michalski, C.W.; Marsicano, G.; Monory, K.; Mackie, K.; Marian, C.; Batkai, S.; Parolaro, D.; Fischer, M.J.; Reeh, P.; Kunos, G.; Kress, M.; Lutz, B.; Woolf, C.J.; Kuner, R. Cannabinoids mediate analgesia largely via peripheral type 1 cannabinoid receptors in nociceptors. Nat. Neurosci., 2007, 10(7), 870-879.
-
(2007)
Nat. Neurosci
, vol.10
, Issue.7
, pp. 870-879
-
-
Agarwal, N.1
Pacher, P.2
Tegeder, I.3
Amaya, F.4
Constantin, C.E.5
Brenner, G.J.6
Rubino, T.7
Michalski, C.W.8
Marsicano, G.9
Monory, K.10
Mackie, K.11
Marian, C.12
Batkai, S.13
Parolaro, D.14
Fischer, M.J.15
Reeh, P.16
Kunos, G.17
Kress, M.18
Lutz, B.19
Woolf, C.J.20
Kuner, R.21
more..
-
39
-
-
0032940633
-
Localization of central cannabinoid CB1 receptor messenger RNA in neuronal subpopulations of rat dorsal root ganglia: A double-label in situ hybridization study
-
Hohmann, A.G.; Herkenham, M. Localization of central cannabinoid CB1 receptor messenger RNA in neuronal subpopulations of rat dorsal root ganglia: a double-label in situ hybridization study. Neuroscience, 1999, 90(3), 923-931.
-
(1999)
Neuroscience
, vol.90
, Issue.3
, pp. 923-931
-
-
Hohmann, A.G.1
Herkenham, M.2
-
40
-
-
64849099556
-
Localization of the endocannabinoid-degrading enzyme fatty acid amide hydrolase in rat dorsal root ganglion cells and its regulation after peripheral nerve injury
-
Lever, I.J.; Robinson, M.; Cibelli, M.; Paule, C.; Santha, P.; Yee, L.; Hunt, S.P.; Cravatt, B.F.; Elphick, M.R.; Nagy, I.; Rice, A.S. Localization of the endocannabinoid-degrading enzyme fatty acid amide hydrolase in rat dorsal root ganglion cells and its regulation after peripheral nerve injury. J. Neurosci., 2009, 29(12), 3766- 3780.
-
(2009)
J. Neurosci
, vol.29
, Issue.12
, pp. 3766-3780
-
-
Lever, I.J.1
Robinson, M.2
Cibelli, M.3
Paule, C.4
Santha, P.5
Yee, L.6
Hunt, S.P.7
Cravatt, B.F.8
Elphick, M.R.9
Nagy, I.10
Rice, A.S.11
-
41
-
-
33751244807
-
Sitespecific increases in peripheral cannabinoid receptors and their endogenous ligands in a model of neuropathic pain
-
Mitrirattanakul, S.; Ramakul, N.; Guerrero, A.V.; Matsuka, Y.; Ono, T.; Iwase, H.; Mackie, K.; Faull, K.F.; Spigelman, I. Sitespecific increases in peripheral cannabinoid receptors and their endogenous ligands in a model of neuropathic pain. Pain, 2006, 126(1-3), 102-114.
-
(2006)
Pain
, vol.126
, Issue.1-3
, pp. 102-114
-
-
Mitrirattanakul, S.1
Ramakul, N.2
Guerrero, A.V.3
Matsuka, Y.4
Ono, T.5
Iwase, H.6
Mackie, K.7
Faull, K.F.8
Spigelman, I.9
-
42
-
-
0029070520
-
Inhibition of noxious stimulus-evoked activity of spinal cord dorsal horn neurons by the cannabinoid WIN 55,212-2
-
Hohmann, A.G.; Martin, W.J.; Tsou, K.; Walker, J.M. Inhibition of noxious stimulus-evoked activity of spinal cord dorsal horn neurons by the cannabinoid WIN 55,212-2. Life Sci., 1995, 56(23-24), 2111-2118.
-
(1995)
Life Sci
, vol.56
, Issue.23-24
, pp. 2111-2118
-
-
Hohmann, A.G.1
Martin, W.J.2
Tsou, K.3
Walker, J.M.4
-
43
-
-
0032778413
-
Cannabinoid WIN 55,212-2 inhibits the activity-dependent facilitation of spinal nociceptive responses
-
Strangman, N.M.; Walker, J.M. Cannabinoid WIN 55,212-2 inhibits the activity-dependent facilitation of spinal nociceptive responses. J. Neurophysiol., 1999, 82(1), 472-477.
-
(1999)
J. Neurophysiol
, vol.82
, Issue.1
, pp. 472-477
-
-
Strangman, N.M.1
Walker, J.M.2
-
44
-
-
0033064793
-
Cannabinoid suppression of noxious heat-evoked activity in wide dynamic range neurons in the lumbar dorsal horn of the rat
-
Hohmann, A.G.; Tsou, K.; Walker, J.M. Cannabinoid suppression of noxious heat-evoked activity in wide dynamic range neurons in the lumbar dorsal horn of the rat. J. Neurophysiol., 1999, 81(2), 575-583.
-
(1999)
J. Neurophysiol
, vol.81
, Issue.2
, pp. 575-583
-
-
Hohmann, A.G.1
Tsou, K.2
Walker, J.M.3
-
45
-
-
0029036140
-
An examination of the central sites of action of cannabinoidinduced antinociception in the rat
-
Martin, W.J.; Patrick, S.L.; Coffin, P.O.; Tsou, K.; Walker, J.M. An examination of the central sites of action of cannabinoidinduced antinociception in the rat. Life Sci., 1995, 56(23-24), 2103-2109.
-
(1995)
Life Sci
, vol.56
, Issue.23-24
, pp. 2103-2109
-
-
Martin, W.J.1
Patrick, S.L.2
Coffin, P.O.3
Tsou, K.4
Walker, J.M.5
-
46
-
-
0032489002
-
Cannabinoid receptormediated inhibition of the rat tail-flick reflex after microinjection into the rostral ventromedial medulla
-
Martin, W.J.; Tsou, K.; Walker, J.M. Cannabinoid receptormediated inhibition of the rat tail-flick reflex after microinjection into the rostral ventromedial medulla. Neurosci. Lett., 1998, 242(1), 33-36.
-
(1998)
Neurosci. Lett
, vol.242
, Issue.1
, pp. 33-36
-
-
Martin, W.J.1
Tsou, K.2
Walker, J.M.3
-
47
-
-
0043073239
-
Effects of direct periaqueductal grey administration of a cannabinoid receptor agonist on nociceptive and aversive responses in rats
-
Finn, D.P.; Jhaveri, M.D.; Beckett, S.R.; Roe, C.H.; Kendall, D.A.; Marsden, C.A.; Chapman, V. Effects of direct periaqueductal grey administration of a cannabinoid receptor agonist on nociceptive and aversive responses in rats. Neuropharmacology, 2003, 45(5), 594-604.
-
(2003)
Neuropharmacology
, vol.45
, Issue.5
, pp. 594-604
-
-
Finn, D.P.1
Jhaveri, M.D.2
Beckett, S.R.3
Roe, C.H.4
Kendall, D.A.5
Marsden, C.A.6
Chapman, V.7
-
48
-
-
0032716177
-
Pain modulation by release of the endogenous cannabinoid anandamide
-
Walker, J.M.; Huang, S.M.; Strangman, N.M.; Tsou, K.; Sanudo- Pena, M.C. Pain modulation by release of the endogenous cannabinoid anandamide. Proc. Natl. Acad. Sci. USA, 1999, 96(21), 12198-12203.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, Issue.21
, pp. 12198-12203
-
-
Walker, J.M.1
Huang, S.M.2
Strangman, N.M.3
Tsou, K.4
Sanudo-Pena, M.C.5
-
49
-
-
33846389346
-
Changes in spinal and supraspinal endocannabinoid levels in neuropathic rats
-
Petrosino, S.; Palazzo, E.; de Novellis, V.; Bisogno, T.; Rossi, F.; Maione, S.; Di Marzo, V. Changes in spinal and supraspinal endocannabinoid levels in neuropathic rats. Neuropharmacology, 2007, 52(2), 415-422.
-
(2007)
Neuropharmacology
, vol.52
, Issue.2
, pp. 415-422
-
-
Petrosino, S.1
Palazzo, E.2
de Novellis, V.3
Bisogno, T.4
Rossi, F.5
Maione, S.6
di Marzo, V.7
-
50
-
-
0034936663
-
Mechanisms of inflammatory pain
-
Kidd, B.L.; Urban, L.A. Mechanisms of inflammatory pain. Br. J. Anaesth., 2001, 87(1), 3-11.
-
(2001)
Br. J. Anaesth
, vol.87
, Issue.1
, pp. 3-11
-
-
Kidd, B.L.1
Urban, L.A.2
-
51
-
-
0032056333
-
Characterization of delta9-tetrahydrocannabinol and anandamide antinociception in nonarthritic and arthritic rats
-
Smith, F.L.; Fujimori, K.; Lowe, J.; Welch, S.P. Characterization of delta9-tetrahydrocannabinol and anandamide antinociception in nonarthritic and arthritic rats. Pharmacol. Biochem. Behav., 1998, 60(1), 183-191.
-
(1998)
Pharmacol. Biochem. Behav
, vol.60
, Issue.1
, pp. 183-191
-
-
Smith, F.L.1
Fujimori, K.2
Lowe, J.3
Welch, S.P.4
-
52
-
-
64749114255
-
Discovery and characterization of a highly selective FAAH inhibitor that reduces inflammatory pain
-
Ahn, K.; Johnson, D.S.; Mileni, M.; Beidler, D.; Long, J.Z.; McKinney, M.K.; Weerapana, E.; Sadagopan, N.; Liimatta, M.; Smith, S.E.; Lazerwith, S.; Stiff, C.; Kamtekar, S.; Bhattacharya, K.; Zhang, Y.; Swaney, S.; Van Becelaere, K.; Stevens, R.C.; Cravatt, B.F. Discovery and characterization of a highly selective FAAH inhibitor that reduces inflammatory pain. Chem. Biol., 2009, 16(4), 411-420.
-
(2009)
Chem. Biol
, vol.16
, Issue.4
, 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
-
53
-
-
0031776783
-
The antihyperalgesic actions of the cannabinoid anandamide and the putative CB2 receptor agonist palmitoylethanolamide in visceral and somatic inflammatory pain
-
Jaggar, S.I.; Hasnie, F.S.; Sellaturay, S.; Rice, A.S. The antihyperalgesic actions of the cannabinoid anandamide and the putative CB2 receptor agonist palmitoylethanolamide in visceral and somatic inflammatory pain. Pain, 1998, 76(1-2), 189-199.
-
(1998)
Pain
, vol.76
, Issue.1-2
, pp. 189-199
-
-
Jaggar, S.I.1
Hasnie, F.S.2
Sellaturay, S.3
Rice, A.S.4
-
54
-
-
0031779305
-
Cannabinoids reduce hyperalgesia and inflammation via interaction with peripheral CB1 receptors
-
Richardson, J.D.; Kilo, S.; Hargreaves, K.M. Cannabinoids reduce hyperalgesia and inflammation via interaction with peripheral CB1 receptors. Pain, 1998, 75(1), 111-119.
-
(1998)
Pain
, vol.75
, Issue.1
, pp. 111-119
-
-
Richardson, J.D.1
Kilo, S.2
Hargreaves, K.M.3
-
55
-
-
0035089509
-
Administration of endocannabinoids prevents a referred hyperalgesia associated with inflammation of the urinary bladder
-
discussion 506A
-
Farquhar-Smith, W.P.; Rice, A.S. Administration of endocannabinoids prevents a referred hyperalgesia associated with inflammation of the urinary bladder. Anesthesiology, 2001, 94(3), 507-513 discussion 506A.
-
(2001)
Anesthesiology
, vol.94
, Issue.3
, pp. 507-513
-
-
Farquhar-Smith, W.P.1
Rice, A.S.2
-
56
-
-
0029012014
-
Identification of an endogenous 2-monoglyceride, present in canine gut, that binds to cannabinoid receptors
-
Mechoulam, R.; Ben-Shabat, S.; Hanus, L.; Ligumsky, M.; Kaminski, N.E.; Schatz, A.R.; Gopher, A.; Almog, S.; Martin, B.R.; Compton, D.R.; Pertwee, R.G.; Griffin, G.; Bayewitch, M.; Barg, J.; Vogel, Z. Identification of an endogenous 2-monoglyceride, present in canine gut, that binds to cannabinoid receptors. Biochem. Pharmacol., 1995, 50(1), 83-90.
-
(1995)
Biochem. Pharmacol
, vol.50
, Issue.1
, pp. 83-90
-
-
Mechoulam, R.1
Ben-Shabat, S.2
Hanus, L.3
Ligumsky, M.4
Kaminski, N.E.5
Schatz, A.R.6
Gopher, A.7
Almog, S.8
Martin, B.R.9
Compton, D.R.10
Pertwee, R.G.11
Griffin, G.12
Bayewitch, M.13
Barg, J.14
Vogel, Z.15
-
57
-
-
0028970517
-
2-Arachidonoylglycerol: A possible endogenous cannabinoid receptor ligand in brain. B
-
Sugiura, T.; Kondo, S.; Sukagawa, A.; Nakane, S.; Shinoda, A.; Itoh, K.; Yamashita, A.; Waku, K. 2-Arachidonoylglycerol: a possible endogenous cannabinoid receptor ligand in brain. Biochem. Biophys. Res. Commun., 1995, 215(1), 89-97.
-
(1995)
Iochem. Biophys. Res. Commun
, vol.215
, Issue.1
, pp. 89-97
-
-
Sugiura, T.1
Kondo, S.2
Sukagawa, A.3
Nakane, S.4
Shinoda, A.5
Itoh, K.6
Yamashita, A.7
Waku, K.8
-
58
-
-
0031044290
-
Biosynthesis, release and degradation of the novel endogenous cannabimimetic metabolite 2-arachidonoylglycerol in mouse neuroblastoma cells
-
Bisogno, T.; Sepe, N.; Melck, D.; Maurelli, S.; De Petrocellis, L.; Di Marzo, V. Biosynthesis, release and degradation of the novel endogenous cannabimimetic metabolite 2-arachidonoylglycerol in mouse neuroblastoma cells. Biochem. J., 1997, 322(2), 671-677.
-
(1997)
Biochem. J
, vol.322
, Issue.2
, pp. 671-677
-
-
Bisogno, T.1
Sepe, N.2
Melck, D.3
Maurelli, S.4
de Petrocellis, L.5
di Marzo, V.6
-
59
-
-
0030870722
-
A second endogenous cannabinoid that modulates long-term potentiation
-
Stella, N.; Schweitzer, P.; Piomelli, D. A second endogenous cannabinoid that modulates long-term potentiation. Nature, 1997, 388(6644), 773-778.
-
(1997)
Nature
, vol.388
, Issue.6644
, pp. 773-778
-
-
Stella, N.1
Schweitzer, P.2
Piomelli, D.3
-
60
-
-
0242268553
-
The molecular logic of endocannabinoid signalling
-
Piomelli, D. The molecular logic of endocannabinoid signalling. Nat. Rev. Neurosci., 2003, 4(11), 873-884.
-
(2003)
Nat. Rev. Neurosci
, vol.4
, Issue.11
, pp. 873-884
-
-
Piomelli, D.1
-
61
-
-
0035910626
-
Rapid generation of 2- arachidonoylglycerol, an endogenous cannabinoid receptor ligand, in rat brain after decapitation
-
Sugiura, T.; Yoshinaga, N.; Waku, K. Rapid generation of 2- arachidonoylglycerol, an endogenous cannabinoid receptor ligand, in rat brain after decapitation. Neurosci. Lett., 2001, 297(3), 175-178.
-
(2001)
Neurosci. Lett
, vol.297
, Issue.3
, pp. 175-178
-
-
Sugiura, T.1
Yoshinaga, N.2
Waku, K.3
-
62
-
-
0032777296
-
Liquid chromatographic- mass spectrometric measurement of the endogenous cannabinoid 2-arachidonylglycerol in the spinal cord and peripheral nervous system
-
Huang, S.M.; Strangman, N.M.; Walker, J.M. Liquid chromatographic- mass spectrometric measurement of the endogenous cannabinoid 2-arachidonylglycerol in the spinal cord and peripheral nervous system. Zhongguo Yao Li Xue Bao, 1999, 20(12), 1098-1102.
-
(1999)
Zhongguo Yao Li Xue Bao
, vol.20
, Issue.12
, pp. 1098-1102
-
-
Huang, S.M.1
Strangman, N.M.2
Walker, J.M.3
-
63
-
-
0032511165
-
2+-dependent and -independent mechanisms
-
2+-dependent and -independent mechanisms. FEBS Lett., 1998, 429(2), 152-156.
-
(1998)
FEBS Lett
, vol.429
, Issue.2
, pp. 152-156
-
-
Kondo, S.1
Kondo, H.2
Nakane, S.3
Kodaka, T.4
Tokumura, A.5
Waku, K.6
Sugiura, T.7
-
64
-
-
33744974528
-
Molecular composition of the endocannabinoid system at glutamatergic synapses
-
Katona, I.; Urban, G.M.; Wallace, M.; Ledent, C.; Jung, K.M.; Piomelli, D.; Mackie, K.; Freund, T.F. Molecular composition of the endocannabinoid system at glutamatergic synapses. J. Neurosci., 2006, 26(21), 5628-5637.
-
(2006)
J. Neurosci
, vol.26
, Issue.21
, pp. 5628-5637
-
-
Katona, I.1
Urban, G.M.2
Wallace, M.3
Ledent, C.4
Jung, K.M.5
Piomelli, D.6
Mackie, K.7
Freund, T.F.8
-
65
-
-
33646932964
-
Localization of diacylglycerol lipasealpha around postsynaptic spine suggests close proximity between production site of an endocannabinoid, 2-arachidonoyl-glycerol, and presynaptic cannabinoid CB1 receptor
-
Yoshida, T.; Fukaya, M.; Uchigashima, M.; Miura, E.; Kamiya, H.; Kano, M.; Watanabe, M. Localization of diacylglycerol lipasealpha around postsynaptic spine suggests close proximity between production site of an endocannabinoid, 2-arachidonoyl-glycerol, and presynaptic cannabinoid CB1 receptor. J. Neurosci., 2006, 26(18), 4740-4751.
-
(2006)
J. Neurosci
, vol.26
, Issue.18
, pp. 4740-4751
-
-
Yoshida, T.1
Fukaya, M.2
Uchigashima, M.3
Miura, E.4
Kamiya, H.5
Kano, M.6
Watanabe, M.7
-
66
-
-
37349043211
-
Identification of the sites of 2- arachidonoylglycerol synthesis and action imply retrograde endocannabinoid signaling at both GABAergic and glutamatergic synapses in the ventral tegmental area
-
Matyas, F.; Urban, G.M.; Watanabe, M.; Mackie, K.; Zimmer, A.; Freund, T.F.; Katona, I. Identification of the sites of 2- arachidonoylglycerol synthesis and action imply retrograde endocannabinoid signaling at both GABAergic and glutamatergic synapses in the ventral tegmental area. Neuropharmacology, 2008, 54(1), 95-107.
-
(2008)
Neuropharmacology
, vol.54
, Issue.1
, pp. 95-107
-
-
Matyas, F.1
Urban, G.M.2
Watanabe, M.3
Mackie, K.4
Zimmer, A.5
Freund, T.F.6
Katona, I.7
-
67
-
-
0043267987
-
Anandamide and arachidonic acid use epoxyeicosatrienoic acids to activate TRPV4 channels
-
Watanabe, H.; Vriens, J.; Prenen, J.; Droogmans, G.; Voets, T.; Nilius, B. Anandamide and arachidonic acid use epoxyeicosatrienoic acids to activate TRPV4 channels. Nature, 2003, 424(6947), 434-438.
-
(2003)
Nature
, vol.424
, Issue.6947
, pp. 434-438
-
-
Watanabe, H.1
Vriens, J.2
Prenen, J.3
Droogmans, G.4
Voets, T.5
Nilius, B.6
-
68
-
-
21344444379
-
An endocannabinoid mechanism for stress-induced analgesia
-
Hohmann, A.G.; Suplita, R.L.; Bolton, N.M.; Neely, M.H.; Fegley, D.; Mangieri, R.; Krey, J.F.; Walker, J.M.; Holmes, P.V.; Crystal, J.D.; Duranti, A.; Tontini, A.; Mor, M.; Tarzia, G.; Piomelli, D. An endocannabinoid mechanism for stress-induced analgesia. Nature, 2005, 435(7045), 1108-1112.
-
(2005)
Nature
, vol.435
, Issue.7045
, pp. 1108-1112
-
-
Hohmann, A.G.1
Suplita, R.L.2
Bolton, N.M.3
Neely, M.H.4
Fegley, D.5
Mangieri, R.6
Krey, J.F.7
Walker, J.M.8
Holmes, P.V.9
Crystal, J.D.10
Duranti, A.11
Tontini, A.12
Mor, M.13
Tarzia, G.14
Piomelli, D.15
-
69
-
-
70349110145
-
Blockade of endocannabinoid- degrading enzymes attenuates neuropathic pain
-
Kinsey, S.G.; Long, J.Z.; O'Neal, S.T.; Abdullah, R.A.; Poklis, J.L.; Boger, D.L.; Cravatt, B.F.; Lichtman, A.H. Blockade of endocannabinoid- degrading enzymes attenuates neuropathic pain. J. Pharmacol. Exp. Ther., 2009, 330(3), 902-910.
-
(2009)
J. Pharmacol. Exp. Ther
, vol.330
, Issue.3
, 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
-
70
-
-
57349137829
-
Modulation of the anti-nociceptive effects of 2-arachidonoyl glycerol by peripherally administered FAAH and MGL inhibitors in a neuropathic pain model
-
Desroches, J.; Guindon, J.; Lambert, C.; Beaulieu, P. Modulation of the anti-nociceptive effects of 2-arachidonoyl glycerol by peripherally administered FAAH and MGL inhibitors in a neuropathic pain model. Br. J. Pharmacol., 2008, 155(6), 913-924.
-
(2008)
Br. J. Pharmacol
, vol.155
, Issue.6
, pp. 913-924
-
-
Desroches, J.1
Guindon, J.2
Lambert, C.3
Beaulieu, P.4
-
71
-
-
35648973242
-
The inhibition of monoacylglycerol lipase by URB602 showed an antiinflammatory and anti-nociceptive effect in a murine model of acute inflammation
-
Comelli, F.; Giagnoni, G.; Bettoni, I.; Colleoni, M.; Costa, B. The inhibition of monoacylglycerol lipase by URB602 showed an antiinflammatory and anti-nociceptive effect in a murine model of acute inflammation. Br. J. Pharmacol., 2007, 152(5), 787-794.
-
(2007)
Br. J. Pharmacol
, vol.152
, Issue.5
, pp. 787-794
-
-
Comelli, F.1
Giagnoni, G.2
Bettoni, I.3
Colleoni, M.4
Costa, B.5
-
72
-
-
0035957425
-
2-arachidonyl glyceryl ether, an endogenous agonist of the cannabinoid CB1 receptor
-
Hanus, L.; Abu-Lafi, S.; Fride, E.; Breuer, A.; Vogel, Z.; Shalev, D.E.; Kustanovich, I.; Mechoulam, R. 2-arachidonyl glyceryl ether, an endogenous agonist of the cannabinoid CB1 receptor. Proc. Natl. Acad. Sci. USA, 2001, 98(7), 3662-3665.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, Issue.7
, pp. 3662-3665
-
-
Hanus, L.1
Abu-Lafi, S.2
Fride, E.3
Breuer, A.4
Vogel, Z.5
Shalev, D.E.6
Kustanovich, I.7
Mechoulam, R.8
-
73
-
-
33845656509
-
Quantitative profiling of endocannabinoids and related compounds in rat brain using liquid chromatography-tandem electrospray ionization mass spectrometry
-
Richardson, D.; Ortori, C.A.; Chapman, V.; Kendall, D.A.; Barrett, D.A. Quantitative profiling of endocannabinoids and related compounds in rat brain using liquid chromatography-tandem electrospray ionization mass spectrometry. Anal. Biochem., 2007, 360(2), 216-226.
-
(2007)
Anal. Biochem
, vol.360
, Issue.2
, pp. 216-226
-
-
Richardson, D.1
Ortori, C.A.2
Chapman, V.3
Kendall, D.A.4
Barrett, D.A.5
-
74
-
-
0034332637
-
N-acyl-dopamines: Novel synthetic CB(1) cannabinoid-receptor ligands and inhibitors of anandamide inactivation with cannabimimetic activity in vitro and in vivo
-
Bisogno, T.; Melck, D.; Bobrov, M.; Gretskaya, N.M.; Bezuglov, V.V.; De Petrocellis, L.; Di Marzo, V. N-acyl-dopamines: novel synthetic CB(1) cannabinoid-receptor ligands and inhibitors of anandamide inactivation with cannabimimetic activity in vitro and in vivo. Biochem. J., 2000, 351(3), 817-824.
-
(2000)
Biochem. J
, vol.351
, Issue.3
, pp. 817-824
-
-
Bisogno, T.1
Melck, D.2
Bobrov, M.3
Gretskaya, N.M.4
Bezuglov, V.V.5
de Petrocellis, L.6
di Marzo, V.7
-
75
-
-
0037062411
-
An endogenous capsaicin-like substance with high potency at recombinant and native vanilloid VR1 receptors
-
Huang, S.M.; Bisogno, T.; Trevisani, M.; Al-Hayani, A.; De Petrocellis, L.; Fezza, F.; Tognetto, M.; Petros, T.J.; Krey, J.F.; Chu, C.J.; Miller, J.D.; Davies, S.N.; Geppetti, P.; Walker, J.M.; Di Marzo, V. An endogenous capsaicin-like substance with high potency at recombinant and native vanilloid VR1 receptors. Proc. Natl. Acad. Sci. USA, 2002, 99(12), 8400-8405.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, Issue.12
, pp. 8400-8405
-
-
Huang, S.M.1
Bisogno, T.2
Trevisani, M.3
Al-Hayani, A.4
de Petrocellis, L.5
Fezza, F.6
Tognetto, M.7
Petros, T.J.8
Krey, J.F.9
Chu, C.J.10
Miller, J.D.11
Davies, S.N.12
Geppetti, P.13
Walker, J.M.14
di Marzo, V.15
-
76
-
-
0001162640
-
The identification of N-2(hydroxyethyl)-palmitamide as a naturally occurring anti-inflammatory agent
-
Kuehl, F.A.; Jacob, T.A.; Ganley, O.H.; Ormond, R.E.; Meisinger, M.A.P. The identification of N-2(hydroxyethyl)-palmitamide as a naturally occurring anti-inflammatory agent. J. Am. Chem. Soc., 1957, 79, 5577-5578.
-
(1957)
J. Am. Chem. Soc
, vol.79
, pp. 5577-5578
-
-
Kuehl, F.A.1
Jacob, T.A.2
Ganley, O.H.3
Ormond, R.E.4
Meisinger, M.A.P.5
-
77
-
-
0037207087
-
Endocannabinoids and related fatty acid derivatives in pain modulation
-
Walker, J.M.; Krey, J.F.; Chu, C.J.; Huang, S.M. Endocannabinoids and related fatty acid derivatives in pain modulation. Chem. Phys. Lipids, 2002, 121(1-2), 159-172.
-
(2002)
Chem. Phys. Lipids
, vol.121
, Issue.1 c2
, pp. 159-172
-
-
Walker, J.M.1
Krey, J.F.2
Chu, C.J.3
Huang, S.M.4
-
78
-
-
78651171367
-
Fatty Acid Amides of Ethanolamine in Mammalian Tissues
-
Bachur, N.R.; Masek, K.; Melmon, K.L.; Udenfriend, S. Fatty Acid Amides of Ethanolamine in Mammalian Tissues. J. Biol. Chem., 1965, 240(3), 1019-1024.
-
(1965)
J. Biol. Chem
, vol.240
, Issue.3
, pp. 1019-1024
-
-
Bachur, N.R.1
Masek, K.2
Melmon, K.L.3
Udenfriend, S.4
-
79
-
-
27944505915
-
PPARs in diseases: Control mechanisms of inflammation
-
Kostadinova, R.; Wahli, W.; Michalik, L. PPARs in diseases: control mechanisms of inflammation. Curr. Med. Chem., 2005, 12(25), 2995-3009.
-
(2005)
Curr. Med. Chem
, vol.12
, Issue.25
, pp. 2995-3009
-
-
Kostadinova, R.1
Wahli, W.2
Michalik, L.3
-
80
-
-
11244328917
-
The nuclear receptor peroxisome proliferator- activated receptor-alpha mediates the anti-inflammatory actions of palmitoylethanolamide
-
Lo Verme, J.; Fu, J.; Astarita, G.; La Rana, G.; Russo, R.; Calignano, A.; Piomelli, D. The nuclear receptor peroxisome proliferator- activated receptor-alpha mediates the anti-inflammatory actions of palmitoylethanolamide. Mol. Pharmacol., 2005, 67(1), 15-19.
-
(2005)
Mol. Pharmacol.
, vol.67
, Issue.1
, pp. 15-19
-
-
lo Verme, J.1
Fu, J.2
Astarita, G.3
la Rana, G.4
Russo, R.5
Calignano, A.6
Piomelli, D.7
-
81
-
-
33751166817
-
Rapid broad-spectrum analgesia through activation of peroxisome proliferator-activated receptor-alpha
-
LoVerme, J.; Russo, R.; La Rana, G.; Fu, J.; Farthing, J.; Mattace- Raso, G.; Meli, R.; Hohmann, A.; Calignano, A.; Piomelli, D. Rapid broad-spectrum analgesia through activation of peroxisome proliferator-activated receptor-alpha. J. Pharmacol. Exp. Ther., 2006, 319(3), 1051-1061.
-
(2006)
J. Pharmacol. Exp. Ther
, vol.319
, Issue.3
, pp. 1051-1061
-
-
Loverme, J.1
Russo, R.2
la Rana, G.3
Fu, J.4
Farthing, J.5
Mattace-Raso, G.6
Meli, R.7
Hohmann, A.8
Calignano, A.9
Piomelli, D.10
-
82
-
-
14844282831
-
The expanding field of cannabimimetic and related lipid mediators
-
Bradshaw, H.B.; Walker, J.M. The expanding field of cannabimimetic and related lipid mediators. Br. J. Pharmacol., 2005, 144(4), 459-465.
-
(2005)
Br. J. Pharmacol
, vol.144
, Issue.4
, pp. 459-465
-
-
Bradshaw, H.B.1
Walker, J.M.2
-
83
-
-
0032537734
-
Control of pain initiation by endogenous cannabinoids
-
Calignano, A.; La Rana, G.; Giuffrida, A.; Piomelli, D. Control of pain initiation by endogenous cannabinoids. Nature, 1998, 394(6690), 277-281.
-
(1998)
Nature
, vol.394
, Issue.6690
, pp. 277-281
-
-
Calignano, A.1
la Rana, G.2
Giuffrida, A.3
Piomelli, D.4
-
84
-
-
0035843772
-
Antinociceptive activity of the endogenous fatty acid amide, palmitylethanolamide
-
Calignano, A.; La Rana, G.; Piomelli, D. Antinociceptive activity of the endogenous fatty acid amide, palmitylethanolamide. Eur. J. Pharmacol., 2001, 419(2-3), 191-198.
-
(2001)
Eur. J. Pharmacol
, vol.419
, Issue.2-3
, pp. 191-198
-
-
Calignano, A.1
la Rana, G.2
Piomelli, D.3
-
85
-
-
23044438547
-
The search for the palmitoylethanolamide receptor
-
LoVerme, J.; La Rana, G.; Russo, R.; Calignano, A.; Piomelli, D. The search for the palmitoylethanolamide receptor. Life Sci., 2005, 77(14), 1685-1698.
-
(2005)
Life Sci
, vol.77
, Issue.14
, pp. 1685-1698
-
-
Loverme, J.1
la Rana, G.2
Russo, R.3
Calignano, A.4
Piomelli, D.5
-
86
-
-
53349089891
-
The endogenous fatty acid amide, palmitoylethanolamide, has antiallodynic and anti-hyperalgesic effects in a murine model of neuropathic pain: Involvement of CB(1), TRPV1 and PPARgamma receptors and neurotrophic factors
-
Costa, B.; Comelli, F.; Bettoni, I.; Colleoni, M.; Giagnoni, G. The endogenous fatty acid amide, palmitoylethanolamide, has antiallodynic and anti-hyperalgesic effects in a murine model of neuropathic pain: involvement of CB(1), TRPV1 and PPARgamma receptors and neurotrophic factors. Pain, 2008, 139(3), 541-550.
-
(2008)
Pain
, vol.139
, Issue.3
, pp. 541-550
-
-
Costa, B.1
Comelli, F.2
Bettoni, I.3
Colleoni, M.4
Giagnoni, G.5
-
87
-
-
0041321275
-
Oleylethanolamide regulates feeding and body weight through activation of the nuclear receptor PPAR-alpha
-
Fu, J.; Gaetani, S.; Oveisi, F.; Lo Verme, J.; Serrano, A.; Rodriguez De Fonseca, F.; Rosengarth, A.; Luecke, H.; Di Giacomo, B.; Tarzia, G.; Piomelli, D. Oleylethanolamide regulates feeding and body weight through activation of the nuclear receptor PPAR-alpha. Nature, 2003, 425(6953), 90-93.
-
(2003)
Nature
, vol.425
, Issue.6953
, pp. 90-93
-
-
Fu, J.1
Gaetani, S.2
Oveisi, F.3
lo Verme, J.4
Serrano, A.5
de Rodriguez, F.F.6
Rosengarth, A.7
Luecke, H.8
di Giacomo, B.9
Tarzia, G.10
Piomelli, D.11
-
88
-
-
0035829625
-
An anorexic lipid mediator regulated by feeding
-
Rodriguez de Fonseca, F.; Navarro, M.; Gomez, R.; Escuredo, L.; Nava, F.; Fu, J.; Murillo-Rodriguez, E.; Giuffrida, A.; LoVerme, J.; Gaetani, S.; Kathuria, S.; Gall, C.; Piomelli, D. An anorexic lipid mediator regulated by feeding. Nature, 2001, 414(6860), 209-212.
-
(2001)
Nature
, vol.414
, Issue.6860
, pp. 209-212
-
-
de Rodriguez, F.F.1
Navarro, M.2
Gomez, R.3
Escuredo, L.4
Nava, F.5
Fu, J.6
Murillo-Rodriguez, E.7
Giuffrida, A.8
Loverme, J.9
Gaetani, S.10
Kathuria, S.11
Gall, C.12
Piomelli, D.13
-
89
-
-
33644627958
-
Deorphanization of a G protein-coupled receptor for oleoylethanolamide and its use in the discovery of small-molecule hypophagic agents
-
Overton, H.A.; Babbs, A.J.; Doel, S.M.; Fyfe, M.C.; Gardner, L.S.; Griffin, G.; Jackson, H.C.; Procter, M.J.; Rasamison, C.M.; Tang- Christensen, M.; Widdowson, P.S.; Williams, G.M.; Reynet, C. Deorphanization of a G protein-coupled receptor for oleoylethanolamide and its use in the discovery of small-molecule hypophagic agents. Cell Metab., 2006, 3(3), 167-175.
-
(2006)
Cell Metab
, vol.3
, Issue.3
, pp. 167-175
-
-
Overton, H.A.1
Babbs, A.J.2
Doel, S.M.3
Fyfe, M.C.4
Gardner, L.S.5
Griffin, G.6
Jackson, H.C.7
Procter, M.J.8
Rasamison, C.M.9
Tang- Christensen, M.10
Widdowson, P.S.11
Williams, G.M.12
Reynet, C.13
-
90
-
-
17844392649
-
Oleoylethanolamide excites vagal sensory neurones, induces visceral pain and reduces shortterm food intake in mice via capsaicin receptor TRPV1
-
Wang, X.; Miyares, R.L.; Ahern, G.P. Oleoylethanolamide excites vagal sensory neurones, induces visceral pain and reduces shortterm food intake in mice via capsaicin receptor TRPV1. J. Physiol., 2005, 564(Pt 2), 541-547.
-
(2005)
J. Physiol
, vol.564
, Issue.Pt 2
, pp. 541-547
-
-
Wang, X.1
Miyares, R.L.2
Ahern, G.P.3
-
91
-
-
36249015507
-
Analgesic properties of oleoylethanolamide (OEA) in visceral and inflammatory pain
-
Suardiaz, M.; Estivill-Torrus, G.; Goicoechea, C.; Bilbao, A.; Rodriguez de Fonseca, F. Analgesic properties of oleoylethanolamide (OEA) in visceral and inflammatory pain. Pain, 2007, 133(1-3), 99-110.
-
(2007)
Pain
, vol.133
, Issue.1-3
, pp. 99-110
-
-
Suardiaz, M.1
Estivill-Torrus, G.2
Goicoechea, C.3
Bilbao, A.4
de Rodriguez, F.F.5
-
92
-
-
0031051583
-
Structural requirements for binding of anandamide-type compounds to the brain cannabinoid receptor
-
Sheskin, T.; Hanus, L.; Slager, J.; Vogel, Z.; Mechoulam, R. Structural requirements for binding of anandamide-type compounds to the brain cannabinoid receptor. J. Med. Chem., 1997, 40(5), 659-667.
-
(1997)
J. Med. Chem
, vol.40
, Issue.5
, pp. 659-667
-
-
Sheskin, T.1
Hanus, L.2
Slager, J.3
Vogel, Z.4
Mechoulam, R.5
-
93
-
-
0035900694
-
Identification of a new class of molecules, the arachidonyl amino acids, and characterization of one member that inhibits pain
-
Huang, S.M.; Bisogno, T.; Petros, T.J.; Chang, S.Y.; Zavitsanos, P.A.; Zipkin, R.E.; Sivakumar, R.; Coop, A.; Maeda, D.Y.; De Petrocellis, L.; Burstein, S.; Di Marzo, V.; Walker, J.M. Identification of a new class of molecules, the arachidonyl amino acids, and characterization of one member that inhibits pain. J. Biol. Chem., 2001, 276(46), 42639-42644.
-
(2001)
J. Biol. Chem
, vol.276
, Issue.46
, pp. 42639-42644
-
-
Huang, S.M.1
Bisogno, T.2
Petros, T.J.3
Chang, S.Y.4
Zavitsanos, P.A.5
Zipkin, R.E.6
Sivakumar, R.7
Coop, A.8
Maeda, D.Y.9
de Petrocellis, L.10
Burstein, S.11
di Marzo, V.12
Walker, J.M.13
-
94
-
-
33746382543
-
Identification of N-arachidonylglycine as the endogenous ligand for orphan G-protein-coupled receptor GPR18
-
Kohno, M.; Hasegawa, H.; Inoue, A.; Muraoka, M.; Miyazaki, T.; Oka, K.; Yasukawa, M. Identification of N-arachidonylglycine as the endogenous ligand for orphan G-protein-coupled receptor GPR18. Biochem. Biophys. Res. Commun., 2006, 347(3), 827-832.
-
(2006)
Biochem. Biophys. Res. Commun
, vol.347
, Issue.3
, pp. 827-832
-
-
Kohno, M.1
Hasegawa, H.2
Inoue, A.3
Muraoka, M.4
Miyazaki, T.5
Oka, K.6
Yasukawa, M.7
-
95
-
-
51049093412
-
Identification of Farnesyl Pyrophosphate and N-arachidonylglycine As Endogenous Ligands For GPR92
-
Oh, D.Y.; Yoon, J.M.; Moon, M.J.; Hwang, J.I.; Choe, H.; Lee, J.Y.; Kim, J.I.; Kim, S.; Rhim, H.; O'Dell, D.K.; Walker, J.M.; Na, H.S.; Lee, M.G.; Kwon, H.B.; Kim, K.; Seong, J.Y. Identification of farnesyl pyrophosphate and N-arachidonylglycine as endogenous ligands for GPR92. J. Biol. Chem., 2008, 283(30), 21054-21064.
-
(2008)
J. Biol. Chem
, vol.283
, Issue.30
, pp. 21054-21064
-
-
Oh, D.Y.1
Yoon, J.M.2
Moon, M.J.3
Hwang, J.I.4
Choe, H.5
Lee, J.Y.6
Kim, J.I.7
Kim, S.8
Rhim, H.9
O'Dell, D.K.10
Walker, J.M.11
Na, H.S.12
Lee, M.G.13
Kwon, H.B.14
Kim, K.15
Seong, J.Y.16
-
96
-
-
37449026229
-
Actions of Narachidonyl- glycine in a rat neuropathic pain model
-
Vuong, L.A.; Mitchell, V.A.; Vaughan, C.W. Actions of Narachidonyl- glycine in a rat neuropathic pain model. Neuropharmacology, 2008, 54(1), 189-193.
-
(2008)
Neuropharmacology
, vol.54
, Issue.1
, pp. 189-193
-
-
Vuong, L.A.1
Mitchell, V.A.2
Vaughan, C.W.3
-
97
-
-
35648937451
-
Actions of Narachidonyl- glycine in a rat inflammatory pain model
-
Succar, R.; Mitchell, V.A.; Vaughan, C.W. Actions of Narachidonyl- glycine in a rat inflammatory pain model. Mol. Pain, 2007, 3, 24.
-
(2007)
Mol. Pain
, vol.3
, pp. 24
-
-
Succar, R.1
Mitchell, V.A.2
Vaughan, C.W.3
-
98
-
-
0036774131
-
Regulation of anandamide tissue levels by Narachidonylglycine
-
Burstein, S.H.; Huang, S.M.; Petros, T.J.; Rossetti, R.G.; Walker, J.M.; Zurier, R.B. Regulation of anandamide tissue levels by Narachidonylglycine. Biochem. Pharmacol., 2002, 64(7), 1147-1150.
-
(2002)
Biochem. Pharmacol
, vol.64
, Issue.7
, pp. 1147-1150
-
-
Burstein, S.H.1
Huang, S.M.2
Petros, T.J.3
Rossetti, R.G.4
Walker, J.M.5
Zurier, R.B.6
-
99
-
-
0346725821
-
A structure-activity relationship studyon N-arachidonoyl-amino acids as possible endogenous inhibitors of fatty acid amide hydrolase
-
Grazia Cascio, M.; Minassi, A.; Ligresti, A.; Appendino, G.; Burstein, S.; Di Marzo, V. A structure-activity relationship studyon N-arachidonoyl-amino acids as possible endogenous inhibitors of fatty acid amide hydrolase. Biochem. Biophys. Res. Commun., 2004, 314(1), 192-196.
-
(2004)
Biochem. Biophys. Res. Commun
, vol.314
, Issue.1
, pp. 192-196
-
-
Grazia, C.M.1
Minassi, A.2
Ligresti, A.3
Appendino, G.4
Burstein, S.5
di Marzo, V.A.6
-
100
-
-
70350335061
-
T-type calcium channel inhibition underlies the analgesic effects of the endogenous lipoamino acids
-
Barbara, G.; Alloui, A.; Nargeot, J.; Lory, P.; Eschalier, A.; Bourinet, E.; Chemin, J. T-type calcium channel inhibition underlies the analgesic effects of the endogenous lipoamino acids. J. Neurosci., 2009, 29(42), 13106-13114.
-
(2009)
J. Neurosci
, vol.29
, Issue.42
, pp. 13106-13114
-
-
Barbara, G.1
Alloui, A.2
Nargeot, J.3
Lory, P.4
Eschalier, A.5
Bourinet, E.6
Chemin, J.7
-
101
-
-
75949116246
-
The endocannabinoid 2- arachidonoylglycerol produced by diacylglycerol lipase alpha mediates retrograde suppression of synaptic transmission
-
Tanimura, A.; Yamazaki, M.; Hashimotodani, Y.; Uchigashima, M.; Kawata, S.; Abe, M.; Kita, Y.; Hashimoto, K.; Shimizu, T.; Watanabe, M.; Sakimura, K.; Kano, M. The endocannabinoid 2- arachidonoylglycerol produced by diacylglycerol lipase alpha mediates retrograde suppression of synaptic transmission. Neuron, 2010, 65(3), 320-327.
-
(2010)
Neuron
, vol.65
, Issue.3
, pp. 320-327
-
-
Tanimura, A.1
Yamazaki, M.2
Hashimotodani, Y.3
Uchigashima, M.4
Kawata, S.5
Abe, M.6
Kita, Y.7
Hashimoto, K.8
Shimizu, T.9
Watanabe, M.10
Sakimura, K.11
Kano, M.12
-
102
-
-
0029904838
-
Molecular characterization of an enzyme that degrades neuromodulatory fatty-acid amides
-
Cravatt, B.F.; Giang, D.K.; Mayfield, S.P.; Boger, D.L.; Lerner, R.A.; Gilula, N.B. Molecular characterization of an enzyme that degrades neuromodulatory fatty-acid amides. Nature, 1996, 384(6604), 83-87.
-
(1996)
Nature
, vol.384
, Issue.6604
, pp. 83-87
-
-
Cravatt, B.F.1
Giang, D.K.2
Mayfield, S.P.3
Boger, D.L.4
Lerner, R.A.5
Gilula, N.B.6
-
103
-
-
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(5599), 1793-1796.
-
(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
-
104
-
-
74849116058
-
X-ray crystallographic analysis of alpha- ketoheterocycle inhibitors bound to a humanized variant of fatty acid amide hydrolase
-
Mileni, M.; Garfunkle, J.; Ezzili, C.; Kimball, F.S.; Cravatt, B.F.; Stevens, R.C.; Boger, D.L. X-ray crystallographic analysis of alpha- ketoheterocycle inhibitors bound to a humanized variant of fatty acid amide hydrolase. J. Med. Chem., 2010, 53(1), 230-240.
-
(2010)
J. Med. Chem
, vol.53
, Issue.1
, pp. 230-240
-
-
Mileni, M.1
Garfunkle, J.2
Ezzili, C.3
Kimball, F.S.4
Cravatt, B.F.5
Stevens, R.C.6
Boger, D.L.7
-
105
-
-
51349143217
-
Structure-guided inhibitor design for human FAAH by interspecies active site conversion
-
Mileni, M.; Johnson, D.S.; Wang, Z.; Everdeen, D.S.; Liimatta, M.; Pabst, B.; Bhattacharya, K.; Nugent, R.A.; Kamtekar, S.; Cravatt, B.F.; Ahn, K.; Stevens, R.C. Structure-guided inhibitor design for human FAAH by interspecies active site conversion. Proc. Natl. Acad. Sci. USA, 2008, 105(35), 12820-12824.
-
(2008)
Proc. Natl. Acad. Sci. USA
, vol.105
, Issue.35
, 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
-
106
-
-
0033520099
-
Chemical and mutagenic investigations of fatty acid amide hydrolase: Evidence for a family of serine hydrolases with distinct catalytic properties
-
Patricelli, M.P.; Lovato, M.A.; Cravatt, B.F. Chemical and mutagenic investigations of fatty acid amide hydrolase: evidence for a family of serine hydrolases with distinct catalytic properties. Biochemistry, 1999, 38(31), 9804-9812.
-
(1999)
Biochemistry
, vol.38
, Issue.31
, pp. 9804-9812
-
-
Patricelli, M.P.1
Lovato, M.A.2
Cravatt, B.F.3
-
107
-
-
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(23), 7327-7343.
-
(2008)
J. Med. Chem
, vol.51
, Issue.23
, pp. 7327-7343
-
-
Seierstad, M.1
Breitenbucher, J.G.2
-
108
-
-
0030903752
-
Molecular characterization of human and mouse fatty acid amide hydrolases
-
Giang, D.K.; Cravatt, B.F. Molecular characterization of human and mouse fatty acid amide hydrolases. Proc. Natl. Acad. Sci. USA, 1997, 94(6), 2238-2242.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, Issue.6
, pp. 2238-2242
-
-
Giang, D.K.1
Cravatt, B.F.2
-
109
-
-
0038738350
-
Comparative analysis of fatty acid amide hydrolase and cb(1) cannabinoid receptor expression in the mouse brain: Evidence of a widespread role for fatty acid amide hydrolase in regulation of endocannabinoid signaling
-
Egertova, M.; Cravatt, B.F.; Elphick, M.R. Comparative analysis of fatty acid amide hydrolase and cb(1) cannabinoid receptor expression in the mouse brain: evidence of a widespread role for fatty acid amide hydrolase in regulation of endocannabinoid signaling. Neuroscience, 2003, 119(2), 481-496.
-
(2003)
Neuroscience
, vol.119
, Issue.2
, pp. 481-496
-
-
Egertova, M.1
Cravatt, B.F.2
Elphick, M.R.3
-
110
-
-
0032494704
-
A new perspective on cannabinoid signalling: Complementary localization of fatty acid amide hydrolase and the CB1 receptor in rat brain
-
Egertova, M.; Giang, D.K.; Cravatt, B.F.; Elphick, M.R. A new perspective on cannabinoid signalling: complementary localization of fatty acid amide hydrolase and the CB1 receptor in rat brain. Proc. Biol. Sci., 1998, 265(1410), 2081-2085.
-
(1998)
Proc. Biol. Sci
, vol.265
, Issue.1410
, pp. 2081-2085
-
-
Egertova, M.1
Giang, D.K.2
Cravatt, B.F.3
Elphick, M.R.4
-
111
-
-
3242751838
-
Segregation of two endocannabinoidhydrolyzing enzymes into pre- and postsynaptic compartments in the rat hippocampus, cerebellum and amygdala
-
Gulyas, A.I.; Cravatt, B.F.; Bracey, M.H.; Dinh, T.P.; Piomelli, D.; Boscia, F.; Freund, T.F. Segregation of two endocannabinoidhydrolyzing enzymes into pre- and postsynaptic compartments in the rat hippocampus, cerebellum and amygdala. Eur. J. Neurosci., 2004, 20(2), 441-458.
-
(2004)
Eur. J. Neurosci
, vol.20
, Issue.2
, pp. 441-458
-
-
Gulyas, A.I.1
Cravatt, B.F.2
Bracey, M.H.3
Dinh, T.P.4
Piomelli, D.5
Boscia, F.6
Freund, T.F.7
-
112
-
-
0030823213
-
The biodisposition and metabolism of anandamide in mice
-
Willoughby, K.A.; Moore, S.F.; Martin, B.R.; Ellis, E.F. The biodisposition and metabolism of anandamide in mice. J. Pharmacol. Exp. Ther., 1997, 282(1), 243-247.
-
(1997)
J. Pharmacol. Exp. Ther
, vol.282
, Issue.1
, pp. 243-247
-
-
Willoughby, K.A.1
Moore, S.F.2
Martin, B.R.3
Ellis, E.F.4
-
113
-
-
2442510225
-
Mice lacking fatty acid amide hydrolase exhibit a cannabinoid receptormediated phenotypic hypoalgesia
-
Lichtman, A.H.; Shelton, C.C.; Advani, T.; Cravatt, B.F. Mice lacking fatty acid amide hydrolase exhibit a cannabinoid receptormediated phenotypic hypoalgesia. Pain, 2004, 109(3), 319-327.
-
(2004)
Pain
, vol.109
, Issue.3
, pp. 319-327
-
-
Lichtman, A.H.1
Shelton, C.C.2
Advani, T.3
Cravatt, B.F.4
-
114
-
-
3242710172
-
Functional disassociation of the central and peripheral fatty acid amide signaling systems
-
Cravatt, B.F.; Saghatelian, A.; Hawkins, E.G.; Clement, A.B.; Bracey, M.H.; Lichtman, A.H. Functional disassociation of the central and peripheral fatty acid amide signaling systems. Proc. Natl. Acad. Sci. USA, 2004, 101(29), 10821-10826.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, Issue.29
, pp. 10821-10826
-
-
Cravatt, B.F.1
Saghatelian, A.2
Hawkins, E.G.3
Clement, A.B.4
Bracey, M.H.5
Lichtman, A.H.6
-
115
-
-
33845981826
-
A second fatty acid amide hydrolase with variable distribution among placental mammals
-
Wei, B.Q.; Mikkelsen, T.S.; McKinney, M.K.; Lander, E.S.; Cravatt, B.F. A second fatty acid amide hydrolase with variable distribution among placental mammals. J. Biol. Chem., 2006, 281(48), 36569-36578.
-
(2006)
J. Biol. Chem
, vol.281
, Issue.48
, pp. 36569-36578
-
-
Wei, B.Q.1
Mikkelsen, T.S.2
McKinney, M.K.3
Lander, E.S.4
Cravatt, B.F.A.5
-
116
-
-
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
-
Karbarz, M.J.; Luo, L.; Chang, L.; Tham, C.S.; Palmer, J.A.; Wilson, S.J.; Wennerholm, M.L.; Brown, S.M.; Scott, B.P.; Apodaca, R.L.; Keith, J.M.; Wu, J.; Breitenbucher, J.G.; Chaplan, S.R.; Webb, M. 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., 2009, 108(1), 316-329.
-
(2009)
Anesth. Analg
, vol.108
, Issue.1
, 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
-
117
-
-
0032055496
-
The novel endogenous cannabinoid 2-arachidonoylglycerol is inactivated by neuronal- and basophil-like cells: Connections with anandamide
-
Di Marzo, V.; Bisogno, T.; Sugiura, T.; Melck, D.; De Petrocellis, L. The novel endogenous cannabinoid 2-arachidonoylglycerol is inactivated by neuronal- and basophil-like cells: connections with anandamide. Biochem. J., 1998, 331(1), 15-19.
-
(1998)
Biochem. J
, vol.331
, Issue.1
, pp. 15-19
-
-
di Marzo, V.1
Bisogno, T.2
Sugiura, T.3
Melck, D.4
de Petrocellis, L.5
-
118
-
-
0032559369
-
Anandamide amidohydrolase reacting with 2-arachidonoylglycerol, another cannabinoid receptor ligand
-
Goparaju, S.K.; Ueda, N.; Yamaguchi, H.; Yamamoto, S. Anandamide amidohydrolase reacting with 2-arachidonoylglycerol, another cannabinoid receptor ligand. FEBS Lett., 1998, 422(1), 69-73.
-
(1998)
FEBS Lett
, vol.422
, Issue.1
, pp. 69-73
-
-
Goparaju, S.K.1
Ueda, N.2
Yamaguchi, H.3
Yamamoto, S.4
-
119
-
-
45849112147
-
Fatty acid amide hydrolase inhibition enhances the anti-allodynic actions of endocannabinoids in a model of acute pain adapted for the mouse
-
Palmer, J.A.; Higuera, E.S.; Chang, L.; Chaplan, S.R. Fatty acid amide hydrolase inhibition enhances the anti-allodynic actions of endocannabinoids in a model of acute pain adapted for the mouse. Neuroscience, 2008, 154(4), 1554-1561.
-
(2008)
Neuroscience
, vol.154
, Issue.4
, pp. 1554-1561
-
-
Palmer, J.A.1
Higuera, E.S.2
Chang, L.3
Chaplan, S.R.4
-
120
-
-
0036678094
-
Brain monoglyceride lipase participating in endocannabinoid inactivation
-
Dinh, T.P.; Carpenter, D.; Leslie, F.M.; Freund, T.F.; Katona, I.; Sensi, S.L.; Kathuria, S.; Piomelli, D. Brain monoglyceride lipase participating in endocannabinoid inactivation. Proc. Natl. Acad. Sci. USA, 2002, 99(16), 10819-10824.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, Issue.16
, pp. 10819-10824
-
-
Dinh, T.P.1
Carpenter, D.2
Leslie, F.M.3
Freund, T.F.4
Katona, I.5
Sensi, S.L.6
Kathuria, S.7
Piomelli, D.8
-
121
-
-
6944247598
-
RNA interference suggests a primary role for monoacylglycerol lipase in the degradation of the endocannabinoid 2-arachidonoylglycerol
-
Dinh, T.P.; Kathuria, S.; Piomelli, D. RNA interference suggests a primary role for monoacylglycerol lipase in the degradation of the endocannabinoid 2-arachidonoylglycerol. Mol. Pharmacol., 2004, 66(5), 1260-1264.
-
(2004)
Mol. Pharmacol
, vol.66
, Issue.5
, pp. 1260-1264
-
-
Dinh, T.P.1
Kathuria, S.2
Piomelli, D.3
-
122
-
-
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(1), 76-81.
-
(2003)
Nat. Med
, vol.9
, Issue.1
, 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
-
123
-
-
57749087828
-
Selective blockade of 2- arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects
-
Long, J.Z.; Li, W.; Booker, L.; Burston, J.J.; Kinsey, S.G.; Schlosburg, J.E.; Pavon, F.J.; Serrano, A.M.; Selley, D.E.; Parsons, L.H.; Lichtman, A.H.; Cravatt, B.F. Selective blockade of 2- arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects. Nat. Chem. Biol., 2009, 5(1), 37-44.
-
(2009)
Nat. Chem. Biol
, vol.5
, Issue.1
, 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
Pavon, F.J.7
Serrano, A.M.8
Selley, D.E.9
Parsons, L.H.10
Lichtman, A.H.11
Cravatt, B.F.12
-
124
-
-
37149013708
-
A comprehensive profile of brain enzymes that hydrolyze the endocannabinoid 2- arachidonoylglycerol
-
Blankman, J.L.; Simon, G.M.; Cravatt, B.F. A comprehensive profile of brain enzymes that hydrolyze the endocannabinoid 2- arachidonoylglycerol. Chem. Biol., 2007, 14(12), 1347-1356.
-
(2007)
Chem. Biol
, vol.14
, Issue.12
, pp. 1347-1356
-
-
Blankman, J.L.1
Simon, G.M.2
Cravatt, B.F.A.3
-
125
-
-
15744378565
-
Molecular characterization of N-acylethanolamine-hydrolyzing acid amidase, a novel member of the choloylglycine hydrolase family with structural and functional similarity to acid ceramidase
-
Tsuboi, K.; Sun, Y.X.; Okamoto, Y.; Araki, N.; Tonai, T.; Ueda, N. Molecular characterization of N-acylethanolamine-hydrolyzing acid amidase, a novel member of the choloylglycine hydrolase family with structural and functional similarity to acid ceramidase. J. Biol. Chem., 2005, 280(12), 11082-11092.
-
(2005)
J. Biol. Chem
, vol.280
, Issue.12
, pp. 11082-11092
-
-
Tsuboi, K.1
Sun, Y.X.2
Okamoto, Y.3
Araki, N.4
Tonai, T.5
Ueda, N.6
-
126
-
-
0035929564
-
Purification and characterization of an acid amidase selective for Npalmitoylethanolamine, a putative endogenous anti-inflammatory substance
-
Ueda, N.; Yamanaka, K.; Yamamoto, S. Purification and characterization of an acid amidase selective for Npalmitoylethanolamine, a putative endogenous anti-inflammatory substance. J. Biol. Chem., 2001, 276(38), 35552-35557.
-
(2001)
J. Biol. Chem
, vol.276
, Issue.38
, pp. 35552-35557
-
-
Ueda, N.1
Yamanaka, K.2
Yamamoto, S.3
-
127
-
-
73949084238
-
Selective N-acylethanolamine-hydrolyzing acid amidase inhibition reveals a key role for endogenous palmitoylethanolamide in inflammation
-
Solorzano, C.; Zhu, C.; Battista, N.; Astarita, G.; Lodola, A.; Rivara, S.; Mor, M.; Russo, R.; Maccarrone, M.; Antonietti, F.; Duranti, A.; Tontini, A.; Cuzzocrea, S.; Tarzia, G.; Piomelli, D. Selective N-acylethanolamine-hydrolyzing acid amidase inhibition reveals a key role for endogenous palmitoylethanolamide in inflammation. Proc. Natl. Acad. Sci. USA, 2009, 106(49), 20966-20971.
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, Issue.49
, pp. 20966-20971
-
-
Solorzano, C.1
Zhu, C.2
Battista, N.3
Astarita, G.4
Lodola, A.5
Rivara, S.6
Mor, M.7
Russo, R.8
Maccarrone, M.9
Antonietti, F.10
Duranti, A.11
Tontini, A.12
Cuzzocrea, S.13
Tarzia, G.14
Piomelli, D.15
-
128
-
-
33947330328
-
Identification of a novel endocannabinoid-hydrolyzing enzyme expressed by microglial cells
-
Muccioli, G.G.; Xu, C.; Odah, E.; Cudaback, E.; Cisneros, J.A.; Lambert, D.M.; Lopez Rodriguez, M.L.; Bajjalieh, S.; Stella, N. Identification of a novel endocannabinoid-hydrolyzing enzyme expressed by microglial cells. J. Neurosci., 2007, 27(11), 2883-2889.
-
(2007)
J. Neurosci
, vol.27
, Issue.11
, pp. 2883-2889
-
-
Muccioli, G.G.1
Xu, C.2
Odah, E.3
Cudaback, E.4
Cisneros, J.A.5
Lambert, D.M.6
Lopez Rodriguez, M.L.7
Bajjalieh, S.8
Stella, N.9
-
129
-
-
34547789923
-
A functional proteomic strategy to discover inhibitors for uncharacterized hydrolases
-
Li, W.; Blankman, J.L.; Cravatt, B.F. A functional proteomic strategy to discover inhibitors for uncharacterized hydrolases. J. Am. Chem. Soc., 2007, 129(31), 9594-9595.
-
(2007)
J. Am. Chem. Soc
, vol.129
, Issue.31
, pp. 9594-9595
-
-
Li, W.1
Blankman, J.L.2
Cravatt, B.F.3
-
130
-
-
67650732783
-
Fatty acid amide hydrolase as a potential therapeutic target for the treatment of pain and CNS disorders
-
Ahn, K.; Johnson, D.S.; Cravatt, B.F. Fatty acid amide hydrolase as a potential therapeutic target for the treatment of pain and CNS disorders. Expert Opin. Drug Discov., 2009, 4(7), 763-784.
-
(2009)
Expert Opin. Drug Discov
, vol.4
, Issue.7
, pp. 763-784
-
-
Ahn, K.1
Johnson, D.S.2
Cravatt, B.F.3
-
131
-
-
74549185125
-
FAAH and MAGL inhibitors: Therapeutic opportunities from regulating endocannabinoid levels
-
Petrosino, S.; Di Marzo, V. FAAH and MAGL inhibitors: therapeutic opportunities from regulating endocannabinoid levels. Curr. Opin. Investig. Drugs, 2010, 11(1), 51-62.
-
(2010)
Curr. Opin. Investig. Drugs
, vol.11
, Issue.1
, pp. 51-62
-
-
Petrosino, S.1
di Marzo, V.2
-
132
-
-
33947319316
-
Analgesic actions of N-arachidonoyl-serotonin, a fatty acid amide hydrolase inhibitor with antagonistic activity at vanilloid TRPV1 receptors
-
Maione, S.; De Petrocellis, L.; de Novellis, V.; Moriello, A.S.; Petrosino, S.; Palazzo, E.; Rossi, F.S.; Woodward, D.F.; Di Marzo, V. Analgesic actions of N-arachidonoyl-serotonin, a fatty acid amide hydrolase inhibitor with antagonistic activity at vanilloid TRPV1 receptors. Br. J. Pharmacol., 2007, 150(6), 766-781.
-
(2007)
Br. J. Pharmacol
, vol.150
, Issue.6
, pp. 766-781
-
-
Maione, S.1
de Petrocellis, L.2
de Novellis, V.3
Moriello, A.S.4
Petrosino, S.5
Palazzo, E.6
Rossi, F.S.7
Woodward, D.F.8
di Marzo, V.9
-
133
-
-
54049133600
-
The analgesic effect of N-arachidonoyl-serotonin, a FAAH inhibitor and TRPV1 receptor antagonist, associated with changes in rostral ventromedial medulla and locus coeruleus cell activity in rats
-
de Novellis, V.; Palazzo, E.; Rossi, F.; De Petrocellis, L.; Petrosino, S.; Guida, F.; Luongo, L.; Migliozzi, A.; Cristino, L.; Marabese, I.; Starowicz, K.; Di Marzo, V.; Maione, S. The analgesic effect of N-arachidonoyl-serotonin, a FAAH inhibitor and TRPV1 receptor antagonist, associated with changes in rostral ventromedial medulla and locus coeruleus cell activity in rats. Neuropharmacology, 2008, 55(7), 1105-1113.
-
(2008)
Neuropharmacology
, vol.55
, Issue.7
, pp. 1105-1113
-
-
de Novellis, V.1
Palazzo, E.2
Rossi, F.3
de Petrocellis, L.4
Petrosino, S.5
Guida, F.6
Luongo, L.7
Migliozzi, A.8
Cristino, L.9
Marabese, I.10
Starowicz, K.11
di Marzo, V.12
Maione, S.13
-
134
-
-
77952885551
-
The dual fatty acid amide hydrolase/TRPV1 blocker, Narachidonoyl- serotonin, relieves carrageenan-induced inflammation and hyperalgesia in mice
-
Costa, B.; Bettoni, I.; Petrosino, S.; Comelli, F.; Giagnoni, G.; Di Marzo, V. The dual fatty acid amide hydrolase/TRPV1 blocker, Narachidonoyl- serotonin, relieves carrageenan-induced inflammation and hyperalgesia in mice. Pharmacol. Res., 2010, 61(6), 537-546.
-
(2010)
Pharmacol. Res
, vol.61
, Issue.6
, pp. 537-546
-
-
Costa, B.1
Bettoni, I.2
Petrosino, S.3
Comelli, F.4
Giagnoni, G.5
di Marzo, V.6
-
135
-
-
33749341230
-
AM404, an inhibitor of anandamide uptake, prevents pain behaviour and modulates cytokine and apoptotic pathways in a rat model of neuropathic pain
-
Costa, B.; Siniscalco, D.; Trovato, A.E.; Comelli, F.; Sotgiu, M.L.; Colleoni, M.; Maione, S.; Rossi, F.; Giagnoni, G. AM404, an inhibitor of anandamide uptake, prevents pain behaviour and modulates cytokine and apoptotic pathways in a rat model of neuropathic pain. Br. J. Pharmacol., 2006, 148(7), 1022-1032.
-
(2006)
Br. J. Pharmacol
, vol.148
, Issue.7
, pp. 1022-1032
-
-
Costa, B.1
Siniscalco, D.2
Trovato, A.E.3
Comelli, F.4
Sotgiu, M.L.5
Colleoni, M.6
Maione, S.7
Rossi, F.8
Giagnoni, G.9
-
136
-
-
34548693209
-
Actions of the endocannabinoid transport inhibitor AM404 in neuropathic and inflammatory pain models
-
Mitchell, V.A.; Greenwood, R.; Jayamanne, A.; Vaughan, C.W. Actions of the endocannabinoid transport inhibitor AM404 in neuropathic and inflammatory pain models. Clin. Exp. Pharmacol. Physiol., 2007, 34(11), 1186-1190.
-
(2007)
Clin. Exp. Pharmacol. Physiol
, vol.34
, Issue.11
, pp. 1186-1190
-
-
Mitchell, V.A.1
Greenwood, R.2
Jayamanne, A.3
Vaughan, C.W.4
-
137
-
-
67849128393
-
The endocannabinoid transport inhibitor AM404 modulates nociception in cholestasis
-
Hasanein, P. The endocannabinoid transport inhibitor AM404 modulates nociception in cholestasis. Neurosci. Lett., 2009, 462(3), 230-234.
-
(2009)
Neurosci. Lett
, vol.462
, Issue.3
, pp. 230-234
-
-
Hasanein, P.1
-
138
-
-
34547566970
-
The effect of the palmitoylethanolamide analogue, palmitoylallylamide (L-29) on pain behaviour in rodent models of neuropathy
-
Wallace, V.C.; Segerdahl, A.R.; Lambert, D.M.; Vandevoorde, S.; Blackbeard, J.; Pheby, T.; Hasnie, F.; Rice, A.S. The effect of the palmitoylethanolamide analogue, palmitoylallylamide (L-29) on pain behaviour in rodent models of neuropathy. Br. J. Pharmacol., 2007, 151(7), 1117-1128.
-
(2007)
Br. J. Pharmacol
, vol.151
, Issue.7
, pp. 1117-1128
-
-
Wallace, V.C.1
Segerdahl, A.R.2
Lambert, D.M.3
Vandevoorde, S.4
Blackbeard, J.5
Pheby, T.6
Hasnie, F.7
Rice, A.S.8
-
139
-
-
0034693147
-
Neurobehavioral activity in mice of N-vanillyl-arachidonyl-amide
-
Di Marzo, V.; Breivogel, C.; Bisogno, T.; Melck, D.; Patrick, G.; Tao, Q.; Szallasi, A.; Razdan, R.K.; Martin, B.R. Neurobehavioral activity in mice of N-vanillyl-arachidonyl-amide. Eur. J. Pharmacol., 2000, 406(3), 363-374.
-
(2000)
Eur. J. Pharmacol
, vol.406
, Issue.3
, pp. 363-374
-
-
di Marzo, V.1
Breivogel, C.2
Bisogno, T.3
Melck, D.4
Patrick, G.5
Tao, Q.6
Szallasi, A.7
Razdan, R.K.8
Martin, B.R.9
-
140
-
-
2942657757
-
A structure/activity relationship study on arvanil, an endocannabinoid and vanilloid hybrid
-
Di Marzo, V.; Griffin, G.; De Petrocellis, L.; Brandi, I.; Bisogno, T.; Williams, W.; Grier, M.C.; Kulasegram, S.; Mahadevan, A.; Razdan, R.K.; Martin, B.R. A structure/activity relationship study on arvanil, an endocannabinoid and vanilloid hybrid. J. Pharmacol. Exp. Ther., 2002, 300(3), 984-991.
-
(2002)
J. Pharmacol. Exp. Ther
, vol.300
, Issue.3
, pp. 984-991
-
-
di Marzo, V.1
Griffin, G.2
de Petrocellis, L.3
Brandi, I.4
Bisogno, T.5
Williams, W.6
Grier, M.C.7
Kulasegram, S.8
Mahadevan, A.9
Razdan, R.K.10
Martin, B.R.11
-
141
-
-
0037192605
-
Arvanil-induced inhibition of spasticity and persistent pain: Evidence for therapeutic sites of action different from the vanilloid VR1 receptor and cannabinoid CB(1)/CB(2) receptors
-
Brooks, J.W.; Pryce, G.; Bisogno, T.; Jaggar, S.I.; Hankey, D.J.; Brown, P.; Bridges, D.; Ledent, C.; Bifulco, M.; Rice, A.S.; Di Marzo, V.; Baker, D. Arvanil-induced inhibition of spasticity and persistent pain: evidence for therapeutic sites of action different from the vanilloid VR1 receptor and cannabinoid CB(1)/CB(2) receptors. Eur. J. Pharmacol., 2002, 439(1-3), 83-92.
-
(2002)
Eur. J. Pharmacol
, vol.439
, Issue.1-3
, pp. 83-92
-
-
Brooks, J.W.1
Pryce, G.2
Bisogno, T.3
Jaggar, S.I.4
Hankey, D.J.5
Brown, P.6
Bridges, D.7
Ledent, C.8
Bifulco, M.9
Rice, A.S.10
di Marzo, V.11
Baker, D.12
-
142
-
-
33748457916
-
Non-cannabinoid CB1, non-cannabinoid CB2 antinociceptive effects of several novel compounds in the PPQ stretch test in mice
-
Haller, V.L.; Cichewicz, D.L.; Welch, S.P. Non-cannabinoid CB1, non-cannabinoid CB2 antinociceptive effects of several novel compounds in the PPQ stretch test in mice. Eur. J. Pharmacol., 2006, 546(1-3), 60-68.
-
(2006)
Eur. J. Pharmacol
, vol.546
, Issue.1-3
, pp. 60-68
-
-
Haller, V.L.1
Cichewicz, D.L.2
Welch, S.P.3
-
143
-
-
20144377098
-
Discovery of a Potent, Selective, and Efficacious Class of Reversible Alphaketoheterocycle 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 alphaketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics. J. Med. Chem., 2005, 48(6), 1849-1856.
-
(2005)
J. Med. Chem
, vol.48
, Issue.6
, 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
-
144
-
-
4644354869
-
Reversible inhibitors of fatty acid amide hydrolase that promote analgesia: Evidence for an unprecedented combination of potency and selectivity
-
Lichtman, A.H.; Leung, D.; Shelton, C.C.; Saghatelian, A.; Hardouin, C.; Boger, D.L.; Cravatt, B.F. Reversible inhibitors of fatty acid amide hydrolase that promote analgesia: evidence for an unprecedented combination of potency and selectivity. J. Pharmacol. Exp. Ther., 2004, 311(2), 441-448.
-
(2004)
J. Pharmacol. Exp. Ther
, 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
-
145
-
-
33646431125
-
Inhibition of fatty acid amide hydrolase produces analgesia by multiple mechanisms
-
Chang, L.; Luo, L.; Palmer, J.A.; Sutton, S.; Wilson, S.J.; Barbier, A.J.; Breitenbucher, J.G.; Chaplan, S.R.; Webb, M. Inhibition of fatty acid amide hydrolase produces analgesia by multiple mechanisms. Br. J. Pharmacol., 2006, 148(1), 102-113.
-
(2006)
Br. J. Pharmacol
, vol.148
, Issue.1
, pp. 102-113
-
-
Chang, L.1
Luo, L.2
Palmer, J.A.3
Sutton, S.4
Wilson, S.J.5
Barbier, A.J.6
Breitenbucher, J.G.7
Chaplan, S.R.8
Webb, M.9
-
146
-
-
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(1), 48-56.
-
(2009)
J. Pharmacol. Exp. Ther
, vol.329
, Issue.1
, pp. 48-56
-
-
Naidu, P.S.1
Booker, L.2
Cravatt, B.F.3
Lichtman, A.H.4
-
147
-
-
0038361307
-
Discovering potent and selective reversible inhibitors of enzymes in complex proteomes
-
Leung, D.; Hardouin, C.; Boger, D.L.; Cravatt, B.F. Discovering potent and selective reversible inhibitors of enzymes in complex proteomes. Nat. Biotechnol., 2003, 21(6), 687-691.
-
(2003)
Nat. Biotechnol
, vol.21
, Issue.6
, pp. 687-691
-
-
Leung, D.1
Hardouin, C.2
Boger, D.L.3
Cravatt, B.F.4
-
148
-
-
33847283286
-
Fatty acid amide hydrolase inhibitors display broad selectivity and inhibit multiple carboxylesterases as offtargets
-
Zhang, D.; Saraf, A.; Kolasa, T.; Bhatia, P.; Zheng, G.Z.; Patel, M.; Lannoye, G.S.; Richardson, P.; Stewart, A.; Rogers, J.C.; Brioni, J.D.; Surowy, C.S. Fatty acid amide hydrolase inhibitors display broad selectivity and inhibit multiple carboxylesterases as offtargets. Neuropharmacology, 2007, 52(4), 1095-1105.
-
(2007)
Neuropharmacology
, vol.52
, Issue.4
, pp. 1095-1105
-
-
Zhang, D.1
Saraf, A.2
Kolasa, T.3
Bhatia, P.4
Zheng, G.Z.5
Patel, M.6
Lannoye, G.S.7
Richardson, P.8
Stewart, A.9
Rogers, J.C.10
Brioni, J.D.11
Surowy, C.S.12
-
149
-
-
36048978697
-
Novel mechanistic class of fatty acid amide hydrolase inhibitors with remarkable selectivity
-
Ahn, K.; Johnson, D.S.; Fitzgerald, L.R.; Liimatta, M.; Arendse, A.; Stevenson, T.; Lund, E.T.; Nugent, R.A.; Nomanbhoy, T.K.; Alexander, J.P.; Cravatt, B.F. Novel mechanistic class of fatty acid amide hydrolase inhibitors with remarkable selectivity. Biochemistry, 2007, 46(45), 13019-13030.
-
(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
-
150
-
-
34250750792
-
The fatty acid amide hydrolase inhibitor URB597 (cyclohexylcarbamic acid 3'-carbamoylbiphenyl-3-yl ester) reduces neuropathic pain after oral administration in mice
-
Russo, R.; Loverme, J.; La Rana, G.; Compton, T.R.; Parrott, J.; Duranti, A.; Tontini, A.; Mor, M.; Tarzia, G.; Calignano, A.; Piomelli, D. 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., 2007, 322(1), 236-242.
-
(2007)
J. Pharmacol. Exp. Ther
, 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
-
151
-
-
48149107173
-
Targeting endocannabinoid degradation protects against experimental colitis in mice: Involvement of CB1 and CB2 receptors
-
Storr, M.A.; Keenan, C.M.; Emmerdinger, D.; Zhang, H.; Yuce, B.; Sibaev, A.; Massa, F.; Buckley, N.E.; Lutz, B.; Goke, B.; Brand, S.; Patel, K.D.; Sharkey, K.A. Targeting endocannabinoid degradation protects against experimental colitis in mice: involvement of CB1 and CB2 receptors. J. Mol. Med., 2008, 86(8), 925-936.
-
(2008)
J. Mol. Med
, vol.86
, Issue.8
, pp. 925-936
-
-
Storr, M.A.1
Keenan, C.M.2
Emmerdinger, D.3
Zhang, H.4
Yuce, B.5
Sibaev, A.6
Massa, F.7
Buckley, N.E.8
Lutz, B.9
Goke, B.10
Brand, S.11
Patel, K.D.12
Sharkey, K.A.13
-
152
-
-
48749116524
-
Effects of URB597 as an inhibitor of fatty acid amide hydrolase on modulation of nociception in a rat model of cholestasis
-
Hasanein, P.; Shahidi, S.; Komaki, A.; Mirazi, N. Effects of URB597 as an inhibitor of fatty acid amide hydrolase on modulation of nociception in a rat model of cholestasis. Eur. J. Pharmacol., 2008, 591(1-3), 132-135.
-
(2008)
Eur. J. Pharmacol
, vol.591
, Issue.1-3
, pp. 132-135
-
-
Hasanein, P.1
Shahidi, S.2
Komaki, A.3
Mirazi, N.4
-
153
-
-
57349146897
-
Inhibition of fatty acid amide hydrolase produces PPAR-alpha-mediated analgesia in a rat model of inflammatory pain
-
Sagar, D.R.; Kendall, D.A.; Chapman, V. Inhibition of fatty acid amide hydrolase produces PPAR-alpha-mediated analgesia in a rat model of inflammatory pain. Br. J. Pharmacol., 2008, 155(8), 1297-1306.
-
(2008)
Br. J. Pharmacol
, vol.155
, Issue.8
, pp. 1297-1306
-
-
Sagar, D.R.1
Kendall, D.A.2
Chapman, V.3
-
154
-
-
45849106100
-
Inhibition of fatty acid amide hydrolase and cyclooxygenase-2 increases levels of endocannabinoid related molecules and produces analgesia via peroxisome proliferator- activated receptor-alpha in a model of inflammatory pain
-
Jhaveri, M.D.; Richardson, D.; Robinson, I.; Garle, M.J.; Patel, A.; Sun, Y.; Sagar, D.R.; Bennett, A.J.; Alexander, S.P.; Kendall, D.A.; Barrett, D.A.; Chapman, V. Inhibition of fatty acid amide hydrolase and cyclooxygenase-2 increases levels of endocannabinoid related molecules and produces analgesia via peroxisome proliferator- activated receptor-alpha in a model of inflammatory pain. Neuropharmacology, 2008, 55(1), 85-93.
-
(2008)
Neuropharmacology
, vol.55
, Issue.1
, pp. 85-93
-
-
Jhaveri, M.D.1
Richardson, D.2
Robinson, I.3
Garle, M.J.4
Patel, A.5
Sun, Y.6
Sagar, D.R.7
Bennett, A.J.8
Alexander, S.P.9
Kendall, D.A.10
Barrett, D.A.11
Chapman, V.12
-
155
-
-
56149118394
-
A decrease in anandamide signaling contributes to the maintenance of cutaneous mechanical hyperalgesia in a model of bone cancer pain
-
Khasabova, I.A.; Khasabov, S.G.; Harding-Rose, C.; Coicou, L.G.; Seybold, B.A.; Lindberg, A.E.; Steevens, C.D.; Simone, D.A.; Seybold, V.S. A decrease in anandamide signaling contributes to the maintenance of cutaneous mechanical hyperalgesia in a model of bone cancer pain. J. Neurosci., 2008, 28(44), 11141-11152.
-
(2008)
J. Neurosci
, vol.28
, Issue.44
, pp. 11141-11152
-
-
Khasabova, I.A.1
Khasabov, S.G.2
Harding-Rose, C.3
Coicou, L.G.4
Seybold, B.A.5
Lindberg, A.E.6
Steevens, C.D.7
Simone, D.A.8
Seybold, V.S.9
-
156
-
-
34249687699
-
Novel inhibitors of fatty acid amide hydrolase
-
Sit, S.Y.; Conway, C.; Bertekap, R.; Xie, K.; Bourin, C.; Burris, K.; Deng, H. Novel inhibitors of fatty acid amide hydrolase. Bioorg. Med. Chem. Lett., 2007, 17(12), 3287-3291.
-
(2007)
Bioorg. Med. Chem. Lett
, 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
-
157
-
-
65349167368
-
Benzothiophene piperazine and piperidine urea inhibitors of fatty acid amide hydrolase (FAAH
-
Johnson, D.S.; Ahn, K.; Kesten, S.; Lazerwith, S.E.; Song, Y.; Morris, M.; Fay, L.; Gregory, T.; Stiff, C.; Dunbar, J.B., Jr.; Liimatta, M.; Beidler, D.; Smith, S.; Nomanbhoy, T.K.; Cravatt, B.F. Benzothiophene piperazine and piperidine urea inhibitors of fatty acid amide hydrolase (FAAH). Bioorg. Med. Chem. Lett., 2009, 19(10), 2865-2869.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.10
, pp. 2865-2869
-
-
Johnson, D.S.1
Ahn, K.2
Kesten, S.3
Lazerwith, S.E.4
Song, Y.5
Morris, M.6
Fay, L.7
Gregory, T.8
Stiff, C.9
Dunbar Jr., J.B.10
Liimatta, M.11
Beidler, D.12
Smith, S.13
Nomanbhoy, T.K.14
Cravatt, B.F.15
-
158
-
-
49849094981
-
Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase
-
Keith, J.M.; Apodaca, R.; Xiao, W.; Seierstad, M.; Pattabiraman, K.; Wu, J.; Webb, M.; Karbarz, M.J.; Brown, S.; Wilson, S.; Scott, B.; Tham, C.S.; Luo, L.; Palmer, J.; Wennerholm, M.; Chaplan, S.; Breitenbucher, J.G. Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase. Bioorg. Med. Chem. Lett., 2008, 18(17), 4838-4843.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, Issue.17
, pp. 4838-4843
-
-
Keith, J.M.1
Apodaca, R.2
Xiao, W.3
Seierstad, M.4
Pattabiraman, K.5
Wu, J.6
Webb, M.7
Karbarz, M.J.8
Brown, S.9
Wilson, S.10
Scott, B.11
Tham, C.S.12
Luo, L.13
Palmer, J.14
Wennerholm, M.15
Chaplan, S.16
Breitenbucher, J.G.17
-
159
-
-
27744466783
-
Mechanism of carbamate inactivation of FAAH: Implications for the design of covalent inhibitors and in vivo functional probes for enzymes
-
Alexander, J.P.; Cravatt, B.F. Mechanism of carbamate inactivation of FAAH: implications for the design of covalent inhibitors and in vivo functional probes for enzymes. Chem. Biol., 2005, 12(11), 1179-1187.
-
(2005)
Chem. Biol
, vol.12
, Issue.11
, pp. 1179-1187
-
-
Alexander, J.P.1
Cravatt, B.F.2
-
160
-
-
67650003004
-
Fatty acid amide hydrolase inhibitors. Surprising selectivity of chiral azetidine ureas
-
Hart, T.; Macias, A.T.; Benwell, K.; Brooks, T.; D'Alessandro, J.; Dokurno, P.; Francis, G.; Gibbons, B.; Haymes, T.; Kennett, G.; Lightowler, S.; Mansell, H.; Matassova, N.; Misra, A.; Padfield, A.; Parsons, R.; Pratt, R.; Robertson, A.; Walls, S.; Wong, M.; Roughley, S. Fatty acid amide hydrolase inhibitors. Surprising selectivity of chiral azetidine ureas. Bioorg. Med. Chem. Lett., 2009, 19(15), 4241-4244.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.15
, pp. 4241-4244
-
-
Hart, T.1
Macias, A.T.2
Benwell, K.3
Brooks, T.4
D'Alessandro, J.5
Dokurno, P.6
Francis, G.7
Gibbons, B.8
Haymes, T.9
Kennett, G.10
Lightowler, S.11
Mansell, H.12
Matassova, N.13
Misra, A.14
Padfield, A.15
Parsons, R.16
Pratt, R.17
Robertson, A.18
Walls, S.19
Wong, M.20
Roughley, S.21
more..
-
161
-
-
70349199021
-
Structure based design of novel irreversible FAAH inhibitors
-
Wang, J.L.; Bowen, S.J.; Schweitzer, B.A.; Madsen, H.M.; McDonald, J.; Pelc, M.J.; Tenbrink, R.E.; Beidler, D.; Thorarensen, A. Structure based design of novel irreversible FAAH inhibitors. Bioorg. Med. Chem. Lett., 2009, 19(20), 5970-5974.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.20
, pp. 5970-5974
-
-
Wang, J.L.1
Bowen, S.J.2
Schweitzer, B.A.3
Madsen, H.M.4
McDonald, J.5
Pelc, M.J.6
Tenbrink, R.E.7
Beidler, D.8
Thorarensen, A.9
-
162
-
-
24944508307
-
Characterization of the sulfhydryl-sensitive site in the enzyme responsible for hydrolysis of 2-arachidonoylglycerol in rat cerebellar membranes
-
Saario, S.M.; Salo, O.M.; Nevalainen, T.; Poso, A.; Laitinen, J.T.; Jarvinen, T.; Niemi, R. Characterization of the sulfhydryl-sensitive site in the enzyme responsible for hydrolysis of 2-arachidonoylglycerol in rat cerebellar membranes. Chem. Biol., 2005, 12(6), 649-656.
-
(2005)
Chem. Biol
, vol.12
, Issue.6
, pp. 649-656
-
-
Saario, S.M.1
Salo, O.M.2
Nevalainen, T.3
Poso, A.4
Laitinen, J.T.5
Jarvinen, T.6
Niemi, R.7
-
163
-
-
54349098736
-
N-arachidonyl maleimide potentiates the pharmacological and biochemical effects of the endocannabinoid 2-arachidonylglycerol through inhibition of monoacylglycerol lipase
-
Burston, J.J.; Sim-Selley, L.J.; Harloe, J.P.; Mahadevan, A.; Razdan, R.K.; Selley, D.E.; Wiley, J.L. N-arachidonyl maleimide potentiates the pharmacological and biochemical effects of the endocannabinoid 2-arachidonylglycerol through inhibition of monoacylglycerol lipase. J. Pharmacol. Exp. Ther., 2008, 327(2), 546-553.
-
(2008)
J. Pharmacol. Exp. Ther
, vol.327
, Issue.2
, pp. 546-553
-
-
Burston, J.J.1
Sim-Selley, L.J.2
Harloe, J.P.3
Mahadevan, A.4
Razdan, R.K.5
Selley, D.E.6
Wiley, J.L.7
-
164
-
-
25844440525
-
Selective inhibition of 2-AG hydrolysis enhances endocannabinoid signaling in hippocampus
-
Makara, J.K.; Mor, M.; Fegley, D.; Szabo, S.I.; Kathuria, S.; Astarita, G.; Duranti, A.; Tontini, A.; Tarzia, G.; Rivara, S.; Freund, T.F.; Piomelli, D. Selective inhibition of 2-AG hydrolysis enhances endocannabinoid signaling in hippocampus. Nat. Neurosci., 2005, 8(9), 1139-1141.
-
(2005)
Nat. Neurosci
, vol.8
, Issue.9
, pp. 1139-1141
-
-
Makara, J.K.1
Mor, M.2
Fegley, D.3
Szabo, S.I.4
Kathuria, S.5
Astarita, G.6
Duranti, A.7
Tontini, A.8
Tarzia, G.9
Rivara, S.10
Freund, T.F.11
Piomelli, D.12
-
165
-
-
31844433721
-
Endocannabinoids at the spinal level regulate, but do not mediate, nonopioid stress-induced analgesia
-
Suplita, R.L., 2nd; Gutierrez, T.; Fegley, D.; Piomelli, D.; Hohmann, A.G. Endocannabinoids at the spinal level regulate, but do not mediate, nonopioid stress-induced analgesia. Neuropharmacology, 2006, 50(3), 372-379.
-
(2006)
Neuropharmacology
, vol.50
, Issue.3
, pp. 372-379
-
-
Suplita 2nd., R.L.1
Gutierrez, T.2
Fegley, D.3
Piomelli, D.4
Hohmann, A.G.5
-
166
-
-
33947302244
-
The antinociceptive effects of intraplantar injections of 2-arachidonoyl glycerol are mediatedby cannabinoid CB2 receptors
-
Guindon, J.; Desroches, J.; Beaulieu, P. The antinociceptive effects of intraplantar injections of 2-arachidonoyl glycerol are mediatedby cannabinoid CB2 receptors. Br. J. Pharmacol., 2007, 150(6), 693-701.
-
(2007)
Br. J. Pharmacol
, vol.150
, Issue.6
, pp. 693-701
-
-
Guindon, J.1
Desroches, J.2
Beaulieu, P.3
-
167
-
-
33846551684
-
Lack of selectivity of URB602 for 2- oleoylglycerol compared to anandamide hydrolysis in vitro
-
Vandevoorde, S.; Jonsson, K.O.; Labar, G.; Persson, E.; Lambert, D.M.; Fowler, C.J. Lack of selectivity of URB602 for 2- oleoylglycerol compared to anandamide hydrolysis in vitro. Br. J. Pharmacol., 2007, 150(2), 186-191.
-
(2007)
Br. J. Pharmacol
, vol.150
, Issue.2
, pp. 186-191
-
-
Vandevoorde, S.1
Jonsson, K.O.2
Labar, G.3
Persson, E.4
Lambert, D.M.5
Fowler, C.J.6
-
168
-
-
33747333630
-
URB754 has no effect on the hydrolysis or signaling capacity of 2-AG in the rat brain
-
Saario, S.M.; Palomaki, V.; Lehtonen, M.; Nevalainen, T.; Jarvinen, T.; Laitinen, J.T. URB754 has no effect on the hydrolysis or signaling capacity of 2-AG in the rat brain. Chem. Biol., 2006, 13(8), 811-814.
-
(2006)
Chem. Biol
, vol.13
, Issue.8
, pp. 811-814
-
-
Saario, S.M.1
Palomaki, V.2
Lehtonen, M.3
Nevalainen, T.4
Jarvinen, T.5
Laitinen, J.T.6
-
169
-
-
68249133858
-
Inhibitors of endocannabinoidmetabolizing enzymes reduce precipitated withdrawal responses in THC-dependent mice
-
Schlosburg, J.E.; Carlson, B.L.; Ramesh, D.; Abdullah, R.A.; Long, J.Z.; Cravatt, B.F.; Lichtman, A.H. Inhibitors of endocannabinoidmetabolizing enzymes reduce precipitated withdrawal responses in THC-dependent mice. AAPS J., 2009, 11(2), 342-352.
-
(2009)
AAPS J
, vol.11
, Issue.2
, pp. 342-352
-
-
Schlosburg, J.E.1
Carlson, B.L.2
Ramesh, D.3
Abdullah, R.A.4
Long, J.Z.5
Cravatt, B.F.6
Lichtman, A.H.7
-
170
-
-
73949109254
-
Dual blockade of FAAH and MAGL identifies behavioral processes regulated by endocannabinoid crosstalk in vivo
-
Long, J.Z.; Nomura, D.K.; Vann, R.E.; Walentiny, D.M.; Booker, L.; Jin, X.; Burston, J.J.; Sim-Selley, L.J.; Lichtman, A.H.; Wiley, J.L.; Cravatt, B.F. Dual blockade of FAAH and MAGL identifies behavioral processes regulated by endocannabinoid crosstalk in vivo. Proc. Natl. Acad. Sci. USA, 2009, 106(48), 20270-20275.
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, Issue.48
, 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
Burston, J.J.7
Sim-Selley, L.J.8
Lichtman, A.H.9
Wiley, J.L.10
Cravatt, B.F.11
-
171
-
-
77649198453
-
Characterization of tunable piperidine and piperazine carbamates as inhibitors of endocannabinoid hydrolases
-
Long, J.Z.; Jin, X.; Adibekian, A.; Li, W.; Cravatt, B.F. Characterization of tunable piperidine and piperazine carbamates as inhibitors of endocannabinoid hydrolases. J. Med. Chem., 2010, 53(4), 1830-1842.
-
(2010)
J. Med. Chem
, vol.53
, Issue.4
, pp. 1830-1842
-
-
Long, J.Z.1
Jin, X.2
Adibekian, A.3
Li, W.4
Cravatt, B.F.5
-
172
-
-
0035037811
-
Cannabinoid CB(1) receptor agonists produce cerebellar dysfunction in mice
-
Patel, S.; Hillard, C.J. Cannabinoid CB(1) receptor agonists produce cerebellar dysfunction in mice. J. Pharmacol. Exp. Ther., 2001, 297(2), 629-637.
-
(2001)
J. Pharmacol. Exp. Ther
, vol.297
, Issue.2
, pp. 629-637
-
-
Patel, S.1
Hillard, C.J.2
-
173
-
-
57649192489
-
Development of a potent inhibitor of 2-arachidonoylglycerol hydrolysis with antinociceptive activity in vivo
-
Bisogno, T.; Ortar, G.; Petrosino, S.; Morera, E.; Palazzo, E.; Nalli, M.; Maione, S.; Di Marzo, V. Development of a potent inhibitor of 2-arachidonoylglycerol hydrolysis with antinociceptive activity in vivo. Biochim. Biophys. Acta, 2009, 1791(1), 53-60.
-
(2009)
Biochim. Biophys. Acta
, vol.1791
, Issue.1
, pp. 53-60
-
-
Bisogno, T.1
Ortar, G.2
Petrosino, S.3
Morera, E.4
Palazzo, E.5
Nalli, M.6
Maione, S.7
di Marzo, V.8
-
174
-
-
71149108705
-
Discovery of potent and reversible monoacylglycerol lipase inhibitors
-
King, A.R.; Dotsey, E.Y.; Lodola, A.; Jung, K.M.; Ghomian, A.; Qiu, Y.; Fu, J.; Mor, M.; Piomelli, D. Discovery of potent and reversible monoacylglycerol lipase inhibitors. Chem. Biol., 2009, 16(10), 1045-1052.
-
(2009)
Chem. Biol
, vol.16
, Issue.10
, pp. 1045-1052
-
-
King, A.R.1
Dotsey, E.Y.2
Lodola, A.3
Jung, K.M.4
Ghomian, A.5
Qiu, Y.6
Fu, J.7
Mor, M.8
Piomelli, D.9
-
175
-
-
70350339817
-
A critical cysteine residue in monoacylglycerol lipase is targeted by a new class of isothiazolinone-based enzyme inhibitors
-
King, A.R.; Lodola, A.; Carmi, C.; Fu, J.; Mor, M.; Piomelli, D. A critical cysteine residue in monoacylglycerol lipase is targeted by a new class of isothiazolinone-based enzyme inhibitors. Br. J. Pharmacol., 2009, 157(6), 974-983.
-
(2009)
Br. J. Pharmacol
, vol.157
, Issue.6
, pp. 974-983
-
-
King, A.R.1
Lodola, A.2
Carmi, C.3
Fu, J.4
Mor, M.5
Piomelli, D.6
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