-
1
-
-
0029904838
-
Molecular characterization of an enzyme that degrades neuromodulator 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 neuromodulator fatty-acid amides. Nature 1996, 384, 83-87.
-
(1996)
Nature
, vol.384
, 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
-
2
-
-
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. U.S.A. 1997, 4, 2238-2242.
-
(1997)
Proc. Natl Acad. Sci. U.S.A.
, vol.4
, pp. 2238-2242
-
-
Giang, D.K.1
Cravatt, B.F.2
-
3
-
-
0035452256
-
Fatty acid amide hydrolase: Biochemistry, pharmacology, and therapeutic possibilities for an enzyme hydrolyzing anandamide, 2-arachidonoylglycerol, palmitoylethanolamide, and oleamide
-
Fowler, C. J.; Jonsson, K.-O.; Tiger, G. Fatty acid amide hydrolase: biochemistry, pharmacology, and therapeutic possibilities for an enzyme hydrolyzing anandamide, 2-arachidonoylglycerol, palmitoylethanolamide, and oleamide. Biochem. Pharmacol. 2001, 52, 517-526.
-
(2001)
Biochem. Pharmacol.
, vol.52
, pp. 517-526
-
-
Fowler, C.J.1
Jonsson, K.-O.2
Tiger, G.3
-
4
-
-
0035235117
-
Proteins regulating the biosynthesis and inactivation of neuromodulatory fatty acid amides
-
Patricelli, M. P.; Cravatt, B. F. Proteins regulating the biosynthesis and inactivation of neuromodulatory fatty acid amides. Vitam. Horm. 2001, 62, 663-674.
-
(2001)
Vitam. Horm.
, vol.62
, pp. 663-674
-
-
Patricelli, M.P.1
Cravatt, B.F.2
-
5
-
-
0027078685
-
Isolation and structure of a brain constituent that binds to the cannabinoid receptor
-
Devane, W. A.; Hanus, L.; Breuer, A.; Pertwee, R. G.; Stevenson, L. A.; Griffin, G.; Gibson, D.; Mandelbaum, A.; Etinger, A.; Mechoulam, R. Isolation and structure of a brain constituent that binds to the cannabinoid receptor. Science 1992, 258, 1946-1949.
-
(1992)
Science
, vol.258
, pp. 1946-1949
-
-
Devane, W.A.1
Hanus, L.2
Breuer, A.3
Pertwee, R.G.4
Stevenson, L.A.5
Griffin, G.6
Gibson, D.7
Mandelbaum, A.8
Etinger, A.9
Mechoulam, R.10
-
6
-
-
0035829625
-
An anorexic lipid mediator regulated by feeding
-
Rodriguez de Fonseca, F.; Navarro, M.; Gomez, R.; Escuredo, L.; Nava, F.; Fu, J.; Murillo-Rodríguez, E.; Giuffrida, A.; Lo Verme, J.; Gaetani, S.; Kathuria, S.; Gall, C.; Piomelli, D. An anorexic lipid mediator regulated by feeding. Nature 2001, 414, 209-212.
-
(2001)
Nature
, vol.414
, pp. 209-212
-
-
Rodriguez De Fonseca, F.1
Navarro, M.2
Gomez, R.3
Escuredo, L.4
Nava, F.5
Fu, J.6
Murillo-Rodríguez, E.7
Giuffrida, A.8
Lo Verme, J.9
Gaetani, S.10
Kathuria, S.11
Gall, C.12
Piomelli, D.13
-
7
-
-
0041321275
-
Oleylethanolamide regulates feeding and body weight through activation of the nuclear receptor PPAR-α
-
Fu, J.; Gaetani, S.; Oveisi, F.; LoVerme, 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-α. Nature 2003, 425, 90-93.
-
(2003)
Nature
, vol.425
, pp. 90-93
-
-
Fu, J.1
Gaetani, S.2
Oveisi, F.3
Loverme, J.4
Serrano, A.5
Rodriguez De Fonseca, F.6
Rosengarth, A.7
Luecke, H.8
Di Giacomo, B.9
Tarzia, G.10
Piomelli, D.11
-
8
-
-
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, 277-281.
-
(1998)
Nature
, vol.394
, pp. 277-281
-
-
Calignano, A.1
La Rana, G.2
Giuffrida, A.3
Piomelli, D.4
-
9
-
-
0036216311
-
The palmitoylethanolamide family: A new class of anti-inflammatory agents
-
Lambert, D. M.; Vandevoorde, S.; Jonsson, K.-O.; Fowler, C. J. The palmitoylethanolamide family: a new class of anti-inflammatory agents. Curr. Med. Chem. 2002, 9, 663-674.
-
(2002)
Curr. Med. Chem.
, vol.9
, pp. 663-674
-
-
Lambert, D.M.1
Vandevoorde, S.2
Jonsson, K.-O.3
Fowler, C.J.4
-
10
-
-
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. U.S.A. 2001, 98, 9371-9376.
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, 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
-
11
-
-
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, 319-327.
-
(2004)
Pain
, vol.109
, pp. 319-327
-
-
Lichtman, A.H.1
Shelton, C.C.2
Advani, T.3
Cravatt, B.F.4
-
12
-
-
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. U.S.A. 2004, 101, 10821-10826.
-
(2004)
Proc. Natl. Acad. Sci. U.S.A.
, vol.101
, 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
-
13
-
-
34250209535
-
Attenuation of allergic contact dermatitis through the endocannabinoid system
-
Karsak, M.; Gaffal, E.; Date, R.; Wang-Eckhardt, L.; Rehnelt, J.; Petrosino, S.; Starowicz, K.; Steuder, R.; Schlicker, E.; Cravatt, B. F.; Mechoulam, R.; Buettner, R.; Werner, S.; Di Marzo, V.; Tueting, T.; Zimmer, A. Attenuation of allergic contact dermatitis through the endocannabinoid system. Science 2007, 316, 1494-1497.
-
(2007)
Science
, vol.316
, pp. 1494-1497
-
-
Karsak, M.1
Gaffal, E.2
Date, R.3
Wang-Eckhardt, L.4
Rehnelt, J.5
Petrosino, S.6
Starowicz, K.7
Steuder, R.8
Schlicker, E.9
Cravatt, B.F.10
Mechoulam, R.11
Buettner, R.12
Werner, S.13
Di Marzo, V.14
Tueting, T.15
Zimmer, A.16
-
14
-
-
0029004101
-
Chemical characterization of a family of brain lipids that induce sleep
-
Cravatt, B. F.; Prospero-Garcia, O.; Suizdak, G.; Gilula, N. B.; Henriksen, S. J.; Boger, D. L.; Lerner, R. A. Chemical characterization of a family of brain lipids that induce sleep. Science 1995, 268, 1506-1509.
-
(1995)
Science
, vol.268
, pp. 1506-1509
-
-
Cravatt, B.F.1
Prospero-Garcia, O.2
Suizdak, G.3
Gilula, N.B.4
Henriksen, S.J.5
Boger, D.L.6
Lerner, R.A.7
-
15
-
-
0035211628
-
Effect of oleamide on sleep and its relationship to blood pressure, body temperature, and locomotor activity in rats
-
(a) Huitron-Resendiz, S.; Gombart, L.; Cravatt, B. F.; Henriksen, S. J. Effect of oleamide on sleep and its relationship to blood pressure, body temperature, and locomotor activity in rats. Exp. Neurol 2001, 172, 235-243.
-
(2001)
Exp. Neurol
, vol.172
, pp. 235-243
-
-
Huitron-Resendiz, S.1
Gombart, L.2
Cravatt, B.F.3
Henriksen, S.J.4
-
16
-
-
4143074761
-
Characterization of the sleep-wake patterns in mice lacking fatty acid amide hydrolase
-
(b) Huitron-Resendiz, S.; Sanchez-Alavez, M.; Wills, D. N.; Cravatt, B. F.; Henriksen, S. J. Characterization of the sleep-wake patterns in mice lacking fatty acid amide hydrolase. Sleep 2004, 27, 857-865.
-
(2004)
Sleep
, vol.27
, pp. 857-865
-
-
Huitron-Resendiz, S.1
Sanchez-Alavez, M.2
Wills, D.N.3
Cravatt, B.F.4
Henriksen, S.J.5
-
17
-
-
45749131042
-
The endocannabinoid system: From cell biology to therapy
-
Madras, B. K., Ed.; Cold Spring Harbor Laboratory Press: Woodbury, NY
-
Piomelli, D. The endocannabinoid system: from cell biology to therapy. In Cell Biology of Addiction; Madras, B. K., Ed.; Cold Spring Harbor Laboratory Press: Woodbury, NY, 2006; pp 223-237.
-
(2006)
Cell Biology of Addiction
, pp. 223-237
-
-
Piomelli, D.1
-
18
-
-
56249145659
-
The cannabinoid CB1 receptor and the endocannabinoid anandamide: Possible antidepressant targets
-
Bambico, F. R.; Gobbi, G. The cannabinoid CB1 receptor and the endocannabinoid anandamide: possible antidepressant targets. Expert. Opin. Ther. Targets 2008, 12, 1347-1366.
-
(2008)
Expert. Opin. Ther. Targets
, vol.12
, pp. 1347-1366
-
-
Bambico, F.R.1
Gobbi, G.2
-
19
-
-
67650635375
-
Endocannabinoids in the treatment of mood disorders: Evidence from animal models
-
Bambico, F. R.; Duranti, A.; Tontini, A.; Tarzia, G.; Gobbi, G. Endocannabinoids in the treatment of mood disorders: evidence from animal models. Curr. Pharm. Des. 2009, 15, 1623-1646.
-
(2009)
Curr. Pharm. Des.
, vol.15
, pp. 1623-1646
-
-
Bambico, F.R.1
Duranti, A.2
Tontini, A.3
Tarzia, G.4
Gobbi, G.5
-
20
-
-
0042572380
-
Fatty acid amide hydrolase: An emerging therapeutic target in the endocannabinoid system
-
Cravatt, B. J.; Lichtman, A. H. Fatty acid amide hydrolase: an emerging therapeutic target in the endocannabinoid system. Curr. Opin. Chem. Biol. 2003, 7, 469-475.
-
(2003)
Curr. Opin. Chem. Biol.
, vol.7
, pp. 469-475
-
-
Cravatt, B.J.1
Lichtman, A.H.2
-
21
-
-
23444432920
-
The endocannabinoid system: Drug targets, lead compounds, and potential therapeutic applications
-
Lambert, D. M.; Fowler, C. J. The endocannabinoid system: drug targets, lead compounds, and potential therapeutic applications. J. Med. Chem. 2005, 48, 5059-5087.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 5059-5087
-
-
Lambert, D.M.1
Fowler, C.J.2
-
22
-
-
57349170752
-
Discovery and development of fatty acid amide hydrolase (FAAH) inhibitors
-
Seierstad, M.; Breitenbucher, J. G. Discovery and development of fatty acid amide hydrolase (FAAH) inhibitors. J. Med. Chem. 2008, 51, 7327-7343.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 7327-7343
-
-
Seierstad, M.1
Breitenbucher, J.G.2
-
23
-
-
65549121665
-
Targeting fatty acid amide hydrolase (FAAH) to treat pain and inflammation
-
Schlosburg, J. E.; Kinsey, S. G.; Lichtman, A. H. Targeting fatty acid amide hydrolase (FAAH) to treat pain and inflammation. AAPS J. 2009, 11, 39-44.
-
(2009)
AAPS J.
, vol.11
, pp. 39-44
-
-
Schlosburg, J.E.1
Kinsey, S.G.2
Lichtman, A.H.3
-
24
-
-
57349170752
-
Discovery and development of fatty acid amide hydrolase (FAAH) inhibitors
-
Seierstad, M.; Breitenbucher, J. G. Discovery and development of fatty acid amide hydrolase (FAAH) inhibitors. J. Med. Chem. 2008, 51, 7327-7343.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 7327-7343
-
-
Seierstad, M.1
Breitenbucher, J.G.2
-
25
-
-
58149296562
-
Fatty acid amide hydrolase: A gate-keeper of the endocannabinoid system
-
Fezza, F.; De Simone, C.; Amadio, D.; Maccarrone, M. Fatty acid amide hydrolase: a gate-keeper of the endocannabinoid system. Subcell. Biochem. 2008, 49, 101-132.
-
(2008)
Subcell. Biochem.
, vol.49
, pp. 101-132
-
-
Fezza, F.1
De Simone, C.2
Amadio, D.3
Maccarrone, M.4
-
26
-
-
40349114245
-
Overview of the chemical families of fatty acid amide hydrolase and monoacylglycerol lipase inhibitors
-
Vandevoorde, S. Overview of the chemical families of fatty acid amide hydrolase and monoacylglycerol lipase inhibitors. Curr. Top. Med. Chem. 2008, 8, 247-267.
-
(2008)
Curr. Top. Med. Chem.
, vol.8
, pp. 247-267
-
-
Vandevoorde, S.1
-
27
-
-
20144377098
-
Discovery of a potent, selective, and efficacious class of reversible α-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics
-
Boger, D. L.; Miyauchi, H.; Du, W.; Hardouin, C.; Fecik, R. A.; Cheng, H.; Hwang, I.; Hedrick, M. P.; Acevedo, O.; Guimaraes, C. R. W.; Jorgensen, W. L.; Cravatt, B. F. Discovery of a potent, selective, and efficacious class of reversible α-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics. J. Med. Chem. 2005, 48, 1849-1856.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1849-1856
-
-
Boger, D.L.1
Miyauchi, H.2
Du, W.3
Hardouin, C.4
Fecik, R.A.5
Cheng, H.6
Hwang, I.7
Hedrick, M.P.8
Acevedo, O.9
Guimaraes, C.R.W.10
Jorgensen, W.L.11
Cravatt, B.F.12
-
28
-
-
33750487830
-
Delineation of a fundamental α-ketoheterocycle substituem effect for use in the design of enzyme inhibitors
-
Romero, F. A.; Hwang, I.; Boger, D. L. Delineation of a fundamental α-ketoheterocycle substituem effect for use in the design of enzyme inhibitors. J. Am. Chem. Soc. 2006, 128, 14004-14005.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 14004-14005
-
-
Romero, F.A.1
Hwang, I.2
Boger, D.L.3
-
29
-
-
33847783305
-
Potentand selective a-ketoheterocycle-based inhibitors of the anandamide and oleamide catabolizing enzyme, fatty acid amide hydrolase
-
Romero, F. A.; Du, W.; Hwang, I.; Rayl, T. J.; Kimball, F. S.; Leung, D.; Hoover, H. S.; Apodaca, R. L.; Breitenbucher, J. G.; Cravatt, B. F.; Boger, D. L. Potentand selective a-ketoheterocycle-based inhibitors of the anandamide and oleamide catabolizing enzyme, fatty acid amide hydrolase. J. Med. Chem. 2007, 50, 1058-1068.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 1058-1068
-
-
Romero, F.A.1
Du, W.2
Hwang, I.3
Rayl, T.J.4
Kimball, F.S.5
Leung, D.6
Hoover, H.S.7
Apodaca, R.L.8
Breitenbucher, J.G.9
Cravatt, B.F.10
Boger, D.L.11
-
30
-
-
34447538150
-
Structure-activity relationships of α-ketooxazole inhibitors of fatty acid amide hydrolase
-
Hardouin, C.; Kelso, M. J.; Romero, F. A.; Rayl, T. J.; Leung, D.; Hwang, I.; Cravatt, B. F.; Boger, D. L. Structure-activity relationships of α-ketooxazole inhibitors of fatty acid amide hydrolase. J. Med. Chem. 2007, 50, 3359-3368.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 3359-3368
-
-
Hardouin, C.1
Kelso, M.J.2
Romero, F.A.3
Rayl, T.J.4
Leung, D.5
Hwang, I.6
Cravatt, B.F.7
Boger, D.L.8
-
31
-
-
34548131105
-
Design, synthesis, and in vitro evaluation of carbamate derivatives of 2-benzoxazolyl- And 2-benzothiazolyl-(3-hydroxyphenyl)-methanones as novel fatty acid amide hydrolase inhibitors
-
Myllymäki, M. J.; Saario, S. M.; Kataja, A. O.; Castillo-Melendez, J. A.; Nevalainen, T.; Juvonen, R. O.; Jaervinen, T.; Koskinen, A. M. P. Design, synthesis, and in vitro evaluation of carbamate derivatives of 2-benzoxazolyl- and 2-benzothiazolyl-(3-hydroxyphenyl)-methanones as novel fatty acid amide hydrolase inhibitors. J. Med. Chem. 2007, 50, 4236-4242.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 4236-4242
-
-
Myllymäki, M.J.1
Saario, S.M.2
Kataja, A.O.3
Castillo-Melendez, J.A.4
Nevalainen, T.5
Juvonen, R.O.6
Jaervinen, T.7
Koskinen, A.M.P.8
-
32
-
-
49449114646
-
Optimization of the central heterocycle of α-ketoheterocycle inhibitors of fatty acid amide hydrolase
-
Garfunkle, J.; Ezzili, C.; Rayl, T. J.; Hochstatter, D. G.; Hwang, I.; Boger, D. L. Optimization of the central heterocycle of α-ketoheterocycle inhibitors of fatty acid amide hydrolase. J. Med. Chem. 2008, 51, 4392-4403.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4392-4403
-
-
Garfunkle, J.1
Ezzili, C.2
Rayl, T.J.3
Hochstatter, D.G.4
Hwang, I.5
Boger, D.L.6
-
33
-
-
55249090634
-
Exploration of a fundamental substituem effect of α-ketoheterocycle enzyme inhibitors: Potent and selective inhibitors of fatty acid amide hydrolase
-
DeMartino, J. K.; Garfunkle, J.; Hochstatter, D. G.; Cravatt, B. F.; Boger, D. L. Exploration of a fundamental substituem effect of α-ketoheterocycle enzyme inhibitors: potent and selective inhibitors of fatty acid amide hydrolase. Bioorg. Med. Chem. Lett. 2008, 18, 5842-5846.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 5842-5846
-
-
Demartino, J.K.1
Garfunkle, J.2
Hochstatter, D.G.3
Cravatt, B.F.4
Boger, D.L.5
-
34
-
-
38949167138
-
Inhibitors of proteases and amide hydrolases that employ an alpha-ketoheterocycle as a key enabling functionality
-
Maryanoff, B. E.; Costanzo, M. J. Inhibitors of proteases and amide hydrolases that employ an alpha-ketoheterocycle as a key enabling functionality. Bioorg. Med. Chem. 2008, 16, 1562-1595.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 1562-1595
-
-
Maryanoff, B.E.1
Costanzo, M.J.2
-
35
-
-
30444452978
-
Substituted 2-thioxoimidazolidin-4-ones and imidazolidine-2,4-diones as fatty acid amide hydrolase inhibitors templates
-
Muccioli, G. G.; Fazio, N.; Scriba, E. K. G.; Poppitz, W.; Cannata, F.; Poupaert, H. J.; Wouters, J.; Lambert, M. D. Substituted 2-thioxoimidazolidin-4- ones and imidazolidine-2,4-diones as fatty acid amide hydrolase inhibitors templates. J. Med. Chem. 2006, 49, 411-425.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 411-425
-
-
Muccioli, G.G.1
Fazio, N.2
Scriba, E.K.G.3
Poppitz, W.4
Cannata, F.5
Poupaert, H.J.6
Wouters, J.7
Lambert, M.D.8
-
36
-
-
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, 13019-13030.
-
(2007)
Biochemistry
, vol.46
, 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
-
37
-
-
0037234363
-
Modulation of anxiety through blockade of anandamide hydrolysis
-
Kathuria, S.; Gaetani, S.; Fegley, D.; Valino, F.; Duranti, A.; Tontini, A.; Mor, M.; Tarzia, G.; La Rana, G.; Calignano, A.; Giustino, A.; Tattoli, M.; Palmery, M.; Cuomo, V.; Piomelli, D. Modulation of anxiety through blockade of anandamide hydrolysis. Nat. Med. 2003, 9, 76-81.
-
(2003)
Nat. Med.
, vol.9
, pp. 76-81
-
-
Kathuria, S.1
Gaetani, S.2
Fegley, D.3
Valino, F.4
Duranti, A.5
Tontini, A.6
Mor, M.7
Tarzia, G.8
La Rana, G.9
Calignano, A.10
Giustino, A.11
Tattoli, M.12
Palmery, M.13
Cuomo, V.14
Piomelli, D.15
-
39
-
-
5744223570
-
Recent advances in the cannabinoids
-
Hertzog, D. L. Recent advances in the cannabinoids. Expert Opin. Ther. Pat. 2004, 14, 1435-1452.
-
(2004)
Expert Opin. Ther. Pat.
, vol.14
, pp. 1435-1452
-
-
Hertzog, D.L.1
-
40
-
-
12444260741
-
Design, synthesis, and structure-activity relationships of alkylcarbamic acid aryl esters, a new class of fatty acid amide hydrolase inhibitors
-
Tarzia, G.; Duranti, A.; Tontini, A.; Piersanti, G.; Mor, M.; Rivara, S.; Plazzi, P. V.; Park, C.; Kathuria, S.; Piomelli, D. Design, synthesis, and structure-activity relationships of alkylcarbamic acid aryl esters, a new class of fatty acid amide hydrolase inhibitors. J. Med. Chem. 2003, 46, 2352-2360.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2352-2360
-
-
Tarzia, G.1
Duranti, A.2
Tontini, A.3
Piersanti, G.4
Mor, M.5
Rivara, S.6
Plazzi, P.V.7
Park, C.8
Kathuria, S.9
Piomelli, D.10
-
41
-
-
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, 3287-3291.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, 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
-
42
-
-
45749124873
-
Synthesis and quantitative structure-activity relationship of fatty acid amide hydrolase inhibitors: Modulation at the n-portion of biphenyl-3-yl alkylcarbamates
-
Mor, M.; Lodola, A.; Rivara, A.; Vacondio, F.; Duranti, A.; Tontini, A.; Sanchini, S.; Piersanti, G.; Clapper, J. R.; King, A. R.; Giorgio Tarzia, G.; Piomelli, D. Synthesis and quantitative structure-activity relationship of fatty acid amide hydrolase inhibitors: modulation at the n-portion of biphenyl-3-yl alkylcarbamates. J. Med. Chem. 2008, 51, 3487-3498.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 3487-3498
-
-
Mor, M.1
Lodola, A.2
Rivara, A.3
Vacondio, F.4
Duranti, A.5
Tontini, A.6
Sanchini, S.7
Piersanti, G.8
Clapper, J.R.9
King, A.R.10
Giorgio Tarzia, G.11
Piomelli, D.12
-
43
-
-
67349206913
-
The synthesis and biological evaluation of para-substituted phenolic N-alkyl carbamates as endocannabinoid hydrolyzing enzyme inhibitors
-
Minkkilä, A.; Myllymäki, M. J.; Saario, S. M.; Castillo-Melendez, J. A.; Koskinen, A. M. P.; Fowler, C. J.; Leppanen, J.; Nevalainen, T. The synthesis and biological evaluation of para-substituted phenolic N-alkyl carbamates as endocannabinoid hydrolyzing enzyme inhibitors. Eur. J. Med. Chem. 2009, 44, 2994-3008.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 2994-3008
-
-
Minkkilä, A.1
Myllymäki, M.J.2
Saario, S.M.3
Castillo-Melendez, J.A.4
Koskinen, A.M.P.5
Fowler, C.J.6
Leppanen, J.7
Nevalainen, T.8
-
44
-
-
0034958490
-
Effects of pH on the inhibition of fatty acid amidohydrolase by ibuprofen
-
Holt, S.; Nilsson, J.; Omeir, R.; Tiger, G.; Fowler, C. J. Effects of pH on the inhibition of fatty acid amidohydrolase by ibuprofen. Br. J. Pharmacol. 2001, 133, 513-520.
-
(2001)
Br. J. Pharmacol.
, vol.133
, pp. 513-520
-
-
Holt, S.1
Nilsson, J.2
Omeir, R.3
Tiger, G.4
Fowler, C.J.5
-
45
-
-
0030730417
-
Ibuprofen inhibits rat brain deamidation of anandamide at pharmacologically relevant concentrations. Mode of inhibition and structure-activity relationship
-
Fowler, C. J.; Tiger, G.; Stenström, A. Ibuprofen inhibits rat brain deamidation of anandamide at pharmacologically relevant concentrations. Mode of inhibition and structure-activity relationship. J. Pharmacol. Exp. Ther. 1997, 283, 729-734.
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.283
, pp. 729-734
-
-
Fowler, C.J.1
Tiger, G.2
Stenström, A.3
-
46
-
-
34249091033
-
Inhibition of fatty acid amide hydrolase, a key endocannabinoid metabolizing enzyme, by analogues of ibuprofen and indomethacin
-
Holt, S.; Paylor, B.; Boldrup, L.; Alajakku, K.; Vandevoorde, S.; Sundström, A.; Cocco, M. T.; Onnis, V.; Fowler, C. J. Inhibition of fatty acid amide hydrolase, a key endocannabinoid metabolizing enzyme, by analogues of ibuprofen and indomethacin. Eur. J. Pharmacol. 2007, 565, 26-36.
-
(2007)
Eur. J. Pharmacol.
, vol.565
, pp. 26-36
-
-
Holt, S.1
Paylor, B.2
Boldrup, L.3
Alajakku, K.4
Vandevoorde, S.5
Sundström, A.6
Cocco, M.T.7
Onnis, V.8
Fowler, C.J.9
-
47
-
-
24744469860
-
Conversion of acetaminophen to the bioactive N-acylphenolamine AM404 via fatty acid amide hydrolase-dependent arachidonic acid conjugation in the nervous system
-
Högestätt, E. D.; Jonsson, B. A.; Ermund, A.; Andersson, D. A.; Bjork, H.; Alexander, J. P.; Cravatt, B. F.; Basbaum, A. I.; Zygmunt, P. M. Conversion of acetaminophen to the bioactive N-acylphenolamine AM404 via fatty acid amide hydrolase-dependent arachidonic acid conjugation in the nervous system. J. Biol. Chem. 2005, 280, 31405-31412.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 31405-31412
-
-
Högestätt, E.D.1
Jonsson, B.A.2
Ermund, A.3
Andersson, D.A.4
Bjork, H.5
Alexander, J.P.6
Cravatt, B.F.7
Basbaum, A.I.8
Zygmunt, P.M.9
-
48
-
-
0033545637
-
Substrate specificity and stereoselectivity of rat brain microsomal anandamide amidohydrolase
-
Lang, W.; Qin, C; Lin, S.; Khanolkar, A. D.; Goutopoulos, A.; Fan, P.; Abouzid, K.; Meng, Z.; Biegel, D.; Makriyannis, A. Substrate specificity and stereoselectivity of rat brain microsomal anandamide amidohydrolase. J. Med. Chem. 1999, 42, 896-902.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 896-902
-
-
Lang, W.1
Qin, C.2
Lin, S.3
Khanolkar, A.D.4
Goutopoulos, A.5
Fan, P.6
Abouzid, K.7
Meng, Z.8
Biegel, D.9
Makriyannis, A.10
-
49
-
-
0030865871
-
Functional role of high-affinity anandamide transport, as revealed by selective inhibition
-
Beltramo, M.; Stella, N.; Calignano, A.; Lin, S. Y.; Makriyannis, A.; Piomelli, D. Functional role of high-affinity anandamide transport, as revealed by selective inhibition. Science 1997, 277, 1094-1097.
-
(1997)
Science
, vol.277
, pp. 1094-1097
-
-
Beltramo, M.1
Stella, N.2
Calignano, A.3
Lin, S.Y.4
Makriyannis, A.5
Piomelli, D.6
-
50
-
-
0029960523
-
Head group analogs of arachidonylethanolamide, the endogenous cannabinoid ligand
-
Khanolkar, A. D.; Abadji, V.; Lin, S.; Hill, W. A.; Taha, G.; Abouzid, K.; Meng, Z.; Fan, P.; Makriyannis, A. Head group analogs of arachidonylethanolamide, the endogenous cannabinoid ligand. J. Med. Chem. 1996, 39, 4515-4519.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 4515-4519
-
-
Khanolkar, A.D.1
Abadji, V.2
Lin, S.3
Hill, W.A.4
Taha, G.5
Abouzid, K.6
Meng, Z.7
Fan, P.8
Makriyannis, A.9
-
51
-
-
0034640192
-
The anandamide transport inhibitor AM404 activates vanilloid receptors
-
Zygmunt, P. M.; Chuang, H.-h.; Movahed, P.; Julius, D.; Högestätt, E. D. The anandamide transport inhibitor AM404 activates vanilloid receptors. Eur. J. Pharmacol. 2000, 396, 39-42.
-
(2000)
Eur. J. Pharmacol.
, vol.396
, pp. 39-42
-
-
Zygmunt, P.M.1
Chuang, H.-H.2
Movahed, P.3
Julius, D.4
Högestätt, E.D.5
-
52
-
-
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, 1365-1371.
-
(2006)
J. Pharmacol. Exp. Ther.
, vol.317
, 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
-
54
-
-
34648844208
-
The local antinociceptive effects of paracetamol in neuropathic pain are mediated by cannabinoid receptors
-
Dani, M.; Guindon, J.; Lambert, C.; Beaulieu, P. The local antinociceptive effects of paracetamol in neuropathic pain are mediated by cannabinoid receptors. Eur. J. Pharmacol. 2007, 573, 214-215.
-
(2007)
Eur. J. Pharmacol.
, vol.573
, pp. 214-215
-
-
Dani, M.1
Guindon, J.2
Lambert, C.3
Beaulieu, P.4
-
55
-
-
51749108193
-
Endocannabinoid and serotonergic systems are needed for acetaminophen-induced analgesia
-
Mallet, C.; Daulhac, L.; Bonnefort, J.; Ledent, C.; Etienne, M.; Chapuy, E.; Libert, F.; Eschalier, A. Endocannabinoid and serotonergic systems are needed for acetaminophen-induced analgesia. Pain 2008, 139, 190-200.
-
(2008)
Pain
, vol.139
, pp. 190-200
-
-
Mallet, C.1
Daulhac, L.2
Bonnefort, J.3
Ledent, C.4
Etienne, M.5
Chapuy, E.6
Libert, F.7
Eschalier, A.8
-
56
-
-
58149102550
-
New analgesics synthetically derived from the paracetamol metabolite N(4-hydroxyphenyl)-(5Z,8Z,11Z,14Z)-icosatetra-5,8,11,14-enamide
-
Sinning, C.; Watzer, B.; Coste, O.; Nüsing, R. M.; Ott, I.; Ligresti, A.; Di Marzo, V.; Imming, P. New analgesics synthetically derived from the paracetamol metabolite N(4-hydroxyphenyl)-(5Z,8Z,11Z,14Z)-icosatetra-5,8, 11,14-enamide. J. Med. Chem. 2008, 51, 7800-7805.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 7800-7805
-
-
Sinning, C.1
Watzer, B.2
Coste, O.3
Nüsing, R.M.4
Ott, I.5
Ligresti, A.6
Di Marzo, V.7
Imming, P.8
-
57
-
-
57549112238
-
Dopamides, vanillylamides, ethanolamides, and arachidonic acid amides of anti-inflammatory and analgesic drug substances as TRPV1 ligands
-
Sinning, C.; Watzer, B.; De Petrocellis, L.; Di Marzo, V.; Imming, P. Dopamides, vanillylamides, ethanolamides, and arachidonic acid amides of anti-inflammatory and analgesic drug substances as TRPV1 ligands. ChemMedChem 2008, 3, 1956-1964.
-
(2008)
ChemMedChem
, vol.3
, pp. 1956-1964
-
-
Sinning, C.1
Watzer, B.2
De Petrocellis, L.3
Di Marzo, V.4
Imming, P.5
-
58
-
-
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, 766-781.
-
(2007)
Br. J. Pharmacol.
, vol.150
, 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
-
59
-
-
58149461157
-
Anxiolytic effects in mice of a dual blocker of fatty acid amide hydrolase and transient receptor potential vanilloid type-1 channels
-
Micale, V.; Cristino, L.; Tamburella, A.; Petrosino, S.; Leggio, G. M.; Drago, F.; Di Marzo, V. Anxiolytic effects in mice of a dual blocker of fatty acid amide hydrolase and transient receptor potential vanilloid type-1 channels. Neuropsychopharmacology 2009, 34, 593-606.
-
(2009)
Neuropsychopharmacology
, vol.34
, pp. 593-606
-
-
Micale, V.1
Cristino, L.2
Tamburella, A.3
Petrosino, S.4
Leggio, G.M.5
Drago, F.6
Di Marzo, V.7
-
60
-
-
29744441083
-
New potential anticancer agents based on the anthranilic acid scaffold. Synthesis and evaluation of biological activity
-
Congiu, C.; Coceo, M. T.; Lilliu, V.; Onnis, V. New potential anticancer agents based on the anthranilic acid scaffold. Synthesis and evaluation of biological activity. J. Med. Chem. 2005, 48, 8245-8252.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 8245-8252
-
-
Congiu, C.1
Coceo, M.T.2
Lilliu, V.3
Onnis, V.4
-
61
-
-
0242417539
-
Modifications of the ethanolamine head in N- Palmitoylethanolamine: Synthesis and evaluation of new agents interfering with the metabolism of anandamide
-
Vandevoorde, S.; Jonsson, K.-O.; Fowler, C. J.; Lambert, D. M. Modifications of the ethanolamine head in N- palmitoylethanolamine: synthesis and evaluation of new agents interfering with the metabolism of anandamide. J. Med. Chem. 2003, 46, 1440-1448.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 1440-1448
-
-
Vandevoorde, S.1
Jonsson, K.-O.2
Fowler, C.J.3
Lambert, D.M.4
-
62
-
-
0034986485
-
Role of fatty acid amide hydrolase in the transport of the endogenous canabinoid anandamide
-
Day, T. A.; Rakhshan, F.; Deutsch, D. G.; Barker, E. L. Role of fatty acid amide hydrolase in the transport of the endogenous canabinoid anandamide. Mol. Pharmacol. 2001, 59, 1369-1375.
-
(2001)
Mol. Pharmacol.
, vol.59
, pp. 1369-1375
-
-
Day, T.A.1
Rakhshan, F.2
Deutsch, D.G.3
Barker, E.L.4
-
63
-
-
33646928180
-
Anandamide uptake is consistent with rate-limited diffusion and is regulated by the degree of its hydrolysis by fatty acid amide hydrolase
-
Kaczocha, M.; Hermann, A.; Glaser, S. T.; Bojesen, I. N.; Deutsch, D. G. Anandamide uptake is consistent with rate-limited diffusion and is regulated by the degree of its hydrolysis by fatty acid amide hydrolase. J. Biol. Chem. 2006, 281, 9066-9075.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 9066-9075
-
-
Kaczocha, M.1
Hermann, A.2
Glaser, S.T.3
Bojesen, I.N.4
Deutsch, D.G.5
-
64
-
-
4744345923
-
A role for caveolae/lipid rafts in the uptake and recycling of the endogenous cannabinoid anandamide
-
McFarland, M. J.; Porter, A. C.; Rakhshan, F. R.; Rawat, D. S.; Gibbs, R. A.; Barker, E. L. A role for caveolae/lipid rafts in the uptake and recycling of the endogenous cannabinoid anandamide. J. Biol. Chem. 2004, 279, 41991-41997.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 41991-41997
-
-
McFarland, M.J.1
Porter, A.C.2
Rakhshan, F.R.3
Rawat, D.S.4
Gibbs, R.A.5
Barker, E.L.6
-
65
-
-
51349166122
-
Inhibition of fatty acid amide hydrolase by kaempferol and related naturally occurring flavonoids
-
Thors, L.; Belghiti, M.; Fowler, C. J. Inhibition of fatty acid amide hydrolase by kaempferol and related naturally occurring flavonoids. Br. J. Pharmacol. 2008, 155, 244-252.
-
(2008)
Br. J. Pharmacol.
, vol.155
, pp. 244-252
-
-
Thors, L.1
Belghiti, M.2
Fowler, C.J.3
-
66
-
-
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.; Pavón, 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, 31-44.
-
(2009)
Nat. Chem. Biol
, vol.5
, pp. 31-44
-
-
Long, J.Z.1
Li, W.2
Booker, L.3
Burston, J.J.4
Kinsey, S.G.5
Schlosburg, J.E.6
Pavón, F.J.7
Serrano, A.M.8
Selley, D.E.9
Parsons, L.H.10
Lichtman, A.H.11
Cravatt, B.F.12
-
67
-
-
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. U.S.A. 2002, 99, 10819-10824.
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, 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
-
68
-
-
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, 1347-1356.
-
(2007)
Chem. Biol
, vol.14
, pp. 1347-1356
-
-
Blankman, J.L.1
Simon, G.M.2
Cravatt, B.F.3
-
69
-
-
57649192489
-
Endocannabinoid research group. 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. Endocannabinoid Research Group. Development of a potent inhibitor of 2-arachidonoylglycerol hydrolysis with antinociceptive activity in vivo. Biochim. Biophys. Acta 2009, 1791, 53-60.
-
(2009)
Biochim. Biophys. Acta
, vol.1791
, 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
-
70
-
-
59449101653
-
CAY10499, a novel monoglyceride lipase inhibitor evidenced by an expeditious MGL assay
-
Muccioli, G. G.; Labar, G.; Lambert, D. M. CAY10499, a novel monoglyceride lipase inhibitor evidenced by an expeditious MGL assay. ChemBioChem 2008, 9, 2704-2710.
-
(2008)
ChemBioChem
, vol.9
, pp. 2704-2710
-
-
Muccioli, G.G.1
Labar, G.2
Lambert, D.M.3
-
71
-
-
10044228562
-
Inhibition of monoacylglycerol lipase and fatty acid amide hydrolase by analogues of 2-arachidonoylglycerol
-
Ghafouri, N.; Tiger, G.; Razdan, R. K.; Mahadevan, A.; Pertwee, R. G.; Martin, B. R.; Fowler, C. J. Inhibition of monoacylglycerol lipase and fatty acid amide hydrolase by analogues of 2-arachidonoylglycerol. Br. J. Pharmacol. 2004, 143, 774-784.
-
(2004)
Br. J. Pharmacol.
, vol.143
, pp. 774-784
-
-
Ghafouri, N.1
Tiger, G.2
Razdan, R.K.3
Mahadevan, A.4
Pertwee, R.G.5
Martin, B.R.6
Fowler, C.J.7
-
72
-
-
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.; Järvinen, 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, 649-656.
-
(2005)
Chem. Biol.
, vol.12
, pp. 649-656
-
-
Saario, S.M.1
Salo, O.M.2
Nevalainen, T.3
Poso, A.4
Laitinen, J.T.5
Järvinen, T.6
Niemi, R.7
-
73
-
-
77949395560
-
-
Hu, J.; Björklund, E.; Fowler, C. J. unpublished preliminary data
-
Hu, J.; Björklund, E.; Fowler, C. J. unpublished preliminary data.
-
-
-
-
74
-
-
0027480087
-
Differential inhibition of prostaglandin endoperoxide synthase (cyclooxygenase) isozymes by aspirin and other nonsteroidal anti-inflammatory drugs
-
Meade, E. A.; Smith, W. L.; DeWitt, D. L. Differential inhibition of prostaglandin endoperoxide synthase (cyclooxygenase) isozymes by aspirin and other nonsteroidal anti-inflammatory drugs. J. Biol. Chem. 1993, 268, 6610-6614.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 6610-6614
-
-
Meade, E.A.1
Smith, W.L.2
Dewitt, D.L.3
-
75
-
-
0035894284
-
2 synthases by ibuprofen, naproxen, and indomethacin
-
2 synthases by ibuprofen, naproxen, and indomethacin. Biochem. Pharmacol. 2001, 62, 1587-1595.
-
(2001)
Biochem. Pharmacol.
, vol.62
, pp. 1587-1595
-
-
Jaradat, M.S.1
Wongsud, B.2
Phornchirasilp, S.3
Rangwala, S.M.4
Shams, G.5
Sutton, M.6
Romstedt, K.J.7
Noonan, D.J.8
Feller, D.R.9
-
76
-
-
20044377747
-
Valdecoxib: Assessment of cyclooxygenase-2 potency and selectivity
-
Gierse, J. K.; Zhang, Y.; Hood, W. F.; Walker, M. C.; Trigg, J. S.; Maziasz, T. J.; Koboldt, C. M.; Muhammad, J. L.; Zweifel, B. S.; Masferrer, J. L.; Isakson, P. C.; Seibert, K. Valdecoxib: assessment of cyclooxygenase-2 potency and selectivity. J. Pharmacol. Exp. Ther. 2005, 312, 1206-1212.
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.312
, pp. 1206-1212
-
-
Gierse, J.K.1
Zhang, Y.2
Hood, W.F.3
Walker, M.C.4
Trigg, J.S.5
Maziasz, T.J.6
Koboldt, C.M.7
Muhammad, J.L.8
Zweifel, B.S.9
Masferrer, J.L.10
Isakson, P.C.11
Seibert, K.12
-
77
-
-
0033594911
-
Nonsteroid drug selectivities for cyclo-oxygenase-1 rather than cyclo-oxygenase-2 are associated with human gastrointestinal toxicity: A full in vitro analysis
-
Warner, T. D.; Giuliano, F.; Vojnovic, I.; Bukasa, A.; Mitchell, J. A.; Vane, J. R. Nonsteroid drug selectivities for cyclo-oxygenase-1 rather than cyclo-oxygenase-2 are associated with human gastrointestinal toxicity: a full in vitro analysis. Proc. Natl. Acad. Sci. U.S. A. 1999, 96, 7563-7568.
-
(1999)
Proc. Natl. Acad. Sci. U.S. A.
, vol.96
, pp. 7563-7568
-
-
Warner, T.D.1
Giuliano, F.2
Vojnovic, I.3
Bukasa, A.4
Mitchell, J.A.5
Vane, J.R.6
-
78
-
-
0024456528
-
Synthesis and biological properties of 3-methyl-10-propargyl-5,8- dideazafolic acid
-
Jones, T. R.; Betteridge, R. F.; Newell, D. R.; Jackman, A. L. Synthesis and biological properties of 3-methyl-10-propargyl-5,8-dideazafolic acid. J. Heterocycl Chem. 1989, 26, 1501-1508.
-
(1989)
J. Heterocycl Chem.
, vol.26
, pp. 1501-1508
-
-
Jones, T.R.1
Betteridge, R.F.2
Newell, D.R.3
Jackman, A.L.4
-
79
-
-
0029823888
-
Efficient Reagents for the Synthesis of 5-, 7-, and 5,7-Substituted Indoles Starting from Aromatic Amines: Scope and Limitations
-
Ezquerra, J.; Pedregal, C.; Lamas, C.; Barluenga, J.; Prez, M.; Garca-Martn, M. A.; Gonzlez, M. J. Efficient Reagents for the Synthesis of 5-, 7-, and 5,7-Substituted Indoles Starting from Aromatic Amines: Scope and Limitations. J. Org. Chem. 1996, 61, 5804-5812.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 5804-5812
-
-
Ezquerra, J.1
Pedregal, C.2
Lamas, C.3
Barluenga, J.4
Prez, M.5
Garca-Martn, M.A.6
Gonzlez, M.J.7
-
80
-
-
0020691086
-
Nonsteroidal antiinflammatory agents. 2. [(Heteroarylamino)-phenyl] alkanoic acids
-
Hino, K; Nakamura, H.; Nagai, Y.; Uno, H.; Nishimura, H. Nonsteroidal antiinflammatory agents. 2. [(Heteroarylamino)-phenyl]alkanoic acids. J. Med. Chem. 1983, 26, 222-226.
-
(1983)
J. Med. Chem.
, vol.26
, pp. 222-226
-
-
Hino, K.1
Nakamura, H.2
Nagai, Y.3
Uno, H.4
Nishimura, H.5
-
81
-
-
0010395773
-
-
Skinner, W. A.; Gram, H. F.; Mosher, C. W.; Baker, B. R. J. Am. Chem. Soc. 1959, 81, 4639-4643.
-
(1959)
J. Am. Chem. Soc.
, vol.81
, pp. 4639-4643
-
-
Skinner, W.A.1
Gram, H.F.2
Mosher, C.W.3
Baker, B.R.4
-
82
-
-
0025805362
-
Trihaloacetylated enol ethers - General synthetic procedure and heterocyclic ring closure reactions with hydroxylamine
-
Colla, A.; Martins, M. A. P.; Ciar, G.; Krimmer, S.; Fischer, P. Trihaloacetylated enol ethers - general synthetic procedure and heterocyclic ring closure reactions with hydroxylamine. Synthesis 1991, 483-486.
-
(1991)
Synthesis
, pp. 483-486
-
-
Colla, A.1
Martins, M.A.P.2
Ciar, G.3
Krimmer, S.4
Fischer, P.5
-
83
-
-
0018147775
-
Folate analogues altered in the C9-N10 bridge region: N'O-tosylisohomofolic acid and N'O-tosylisohomoaminopterin
-
Nair, M. G. Colleen O'Neal, P.; Baugh, C. M. Folate analogues altered in the C9-N10 bridge region: N'O-tosylisohomofolic acid and N'O- tosylisohomoaminopterin J. Med. Chem. 1978, 21, 673-677.
-
(1978)
J. Med. Chem.
, vol.21
, pp. 673-677
-
-
Nair, M.G.1
Colleen O'Neal, P.2
Baugh, C.M.3
-
84
-
-
3242664227
-
A simple stopped assay for fatty acid amide hydrolase avoiding the use of a chloroform extraction phase
-
Boldrup, L.; Wilson, S. J.; Barbier, A. J.; Fowler, C. J. A simple stopped assay for fatty acid amide hydrolase avoiding the use of a chloroform extraction phase. J. Biochem. Biophys. Methods 2004, 60, 171-177.
-
(2004)
J. Biochem. Biophys. Methods
, vol.60
, pp. 171-177
-
-
Boldrup, L.1
Wilson, S.J.2
Barbier, A.J.3
Fowler, C.J.4
-
85
-
-
33751044246
-
The potency of the fatty acid amide hydrolase inhibitor URB597 is dependent upon the assay pH
-
Paylor, B.; Holt, S.; Fowler, C. J. The potency of the fatty acid amide hydrolase inhibitor URB597 is dependent upon the assay pH. Pharmacol. Res. 2006, 54, 481-5.
-
(2006)
Pharmacol. Res.
, vol.54
, pp. 481-485
-
-
Paylor, B.1
Holt, S.2
Fowler, C.J.3
-
86
-
-
77949348000
-
-
Corrigendum published
-
Corrigendum published in Pharmacol. Res., 2007, 55, 80.
-
(2007)
Pharmacol. Res.
, vol.55
, pp. 80
-
-
-
87
-
-
0034054679
-
Carriermediated uptake of the endogenous cannabinoid anandamide in RBL-2H3 cells
-
Rakhshan, F.; Day, T. A.; Blakely, R. D.; Barker, E. L. Carriermediated uptake of the endogenous cannabinoid anandamide in RBL-2H3 cells, J. Pharmacol. Exp. Ther. 2000, 292, 960-967.
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.292
, pp. 960-967
-
-
Rakhshan, F.1
Day, T.A.2
Blakely, R.D.3
Barker, E.L.4
-
88
-
-
35648947398
-
Inhibition of the cellular uptake of anandamide by genistein and its analogue daidzein in cells with different levels of fatty acid amide hydrolase-driven uptake
-
Thors, L.; Eriksson, J.; Fowler, C.J. Inhibition of the cellular uptake of anandamide by genistein and its analogue daidzein in cells with different levels of fatty acid amide hydrolase-driven uptake. Br. J. Pharmacol. 2007, 152, 744-750.
-
(2007)
Br. J. Pharmacol.
, vol.152
, pp. 744-750
-
-
Thors, L.1
Eriksson, J.2
Fowler, C.J.3
-
89
-
-
2442713114
-
Reversible, temperature-dependent, and AM404-inhibitable adsorption of anandamide to cell culture wells as a confounding factor in release experiments
-
Karlsson, M.; Pahlsson, C.; Fowler, C. J. Reversible, temperature-dependent, and AM404-inhibitable adsorption of anandamide to cell culture wells as a confounding factor in release experiments. Eur. J. Pharm. Sci. 2004, 22, 181-189.
-
(2004)
Eur. J. Pharm. Sci.
, vol.22
, pp. 181-189
-
-
Karlsson, M.1
Pahlsson, C.2
Fowler, C.J.3
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