-
1
-
-
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., and Gilula, N. B. (1996) Molecular characterization of an enzyme that degrades neuromodulatory fatty-acid amides, Nature 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., and Cravatt, B. F. (1997) Molecular characterization of human and mouse fatty acid amide hydrolases, Proc. Natl. Acad. Sci. U.S.A. 94, 2238-2242.
-
(1997)
Proc. Natl. Acad. Sci. U.S.A
, vol.94
, pp. 2238-2242
-
-
Giang, D.K.1
Cravatt, B.F.2
-
3
-
-
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., and Mechoulam, R. (1992) Isolation and structure of a brain constituent that binds to the cannabinoid receptor, Science 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
-
4
-
-
0036216311
-
The palmitoylethanolamide family: A new class of anti-inflammatory agents?
-
Lambert, D. M., Vandevoorde, S., Jonsson, K. O., and Fowler, C. J. (2002) The palmitoylethanolamide family: a new class of anti-inflammatory agents?, Curr. Med. Chem. 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
-
5
-
-
0029004101
-
Chemical characterization of a family of brain lipids that induce sleep
-
Cravatt, B. F., Prospero-Garcia, O., Siuzdak, G., Gilula, N. B., Henriksen, S. J., Boger, D. L., and Lerner, R. A. (1995) Chemical characterization of a family of brain lipids that induce sleep, Science 268, 1506-1509.
-
(1995)
Science
, vol.268
, pp. 1506-1509
-
-
Cravatt, B.F.1
Prospero-Garcia, O.2
Siuzdak, G.3
Gilula, N.B.4
Henriksen, S.J.5
Boger, D.L.6
Lerner, R.A.7
-
6
-
-
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., and Piomelli, D. (2001) An anorexic lipid mediator regulated by feeding, Nature 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-Rodriguez, E.7
Giuffrida, A.8
LoVerme, J.9
Gaetani, S.10
Kathuria, S.11
Gall, C.12
Piomelli, D.13
-
7
-
-
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., and Lichtman, A. H. (2001) Supersensitivity to anandamide and enhanced endogenous cannabinoid signaling in mice lacking fatty acid amide hydrolase, Proc. Natl. Acad. Sci. U.S.A. 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
-
8
-
-
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., and Piomelli, D. (2003) Modulation of anxiety through blockade of anandamide hydrolysis, Nat. Med. 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
-
9
-
-
2442510225
-
Mice lacking fatty acid amide hydrolase exhibit a cannabinoid receptor-mediated phenotypic hypoalgesia
-
Lichtman, A. H., Shelton, C. C., Advani, T., and Cravatt, B. F. (2004) Mice lacking fatty acid amide hydrolase exhibit a cannabinoid receptor-mediated phenotypic hypoalgesia, Pain 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
-
10
-
-
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., and Piomelli, D. (2005) An endocannabinoid mechanism for stress-induced analgesia, Nature 435, 1108-1112.
-
(2005)
Nature
, vol.435
, 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
-
11
-
-
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., and Webb, M. (2006) Inhibition of fatty acid amide hydrolase produces analgesia by multiple mechanisms, Br. J. Pharmacol. 148, 102-113.
-
(2006)
Br. J. Pharmacol
, vol.148
, 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
-
12
-
-
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., and Vaughan, C. W. (2006) Actions of the FAAH inhibitor URB597 in neuropathic and inflammatory chronic pain models, Br. J. Pharmacol. 147, 281-288.
-
(2006)
Br. J. Pharmacol
, vol.147
, pp. 281-288
-
-
Jayamanne, A.1
Greenwood, R.2
Mitchell, V.A.3
Aslan, S.4
Piomelli, D.5
Vaughan, C.W.6
-
13
-
-
34250750792
-
The fatty-acid amide hydrolase inhibitor URB597 (cyclohexyl carbamic acid 3′-carbamoyl-biphenyl-3-yl ester) reduces neuropathic pain after oral administration in mice
-
Russo, R., LoVerme, J., La Rana, G., Compton, T., Parrot, J., Duranti, A., Tontini, A., Mor, M., Tarzia, G., Calignano, A., and Piomelli, D. (2007) The fatty-acid amide hydrolase inhibitor URB597 (cyclohexyl carbamic acid 3′-carbamoyl-biphenyl-3-yl ester) reduces neuropathic pain after oral administration in mice, J. Pharmacol. Exp. Ther. 322, 236-242.
-
(2007)
J. Pharmacol. Exp. Ther
, vol.322
, pp. 236-242
-
-
Russo, R.1
LoVerme, J.2
La Rana, G.3
Compton, T.4
Parrot, J.5
Duranti, A.6
Tontini, A.7
Mor, M.8
Tarzia, G.9
Calignano, A.10
Piomelli, D.11
-
14
-
-
29444460231
-
Antidepressant-like activity and modulation of brain monoaminergic transmission by blockade of anandamide hydrolysis
-
Gobbi, G., Bambico, F. R., Mangieri, R., Bortolato, M., Campolongo, P., Solinas, M., Cassano, T., Morgese, M. G., Debonnel, G., Duranti, A., Tontini, A., Tarzia, G., Mor, M., Trezza, V., Goldberg, S. R., Cuomo, V., and Piomelli, D. (2005) Antidepressant-like activity and modulation of brain monoaminergic transmission by blockade of anandamide hydrolysis, Proc. Natl. Acad. Sei. U.S.A. 102, 18620-18625.
-
(2005)
Proc. Natl. Acad. Sei. U.S.A
, vol.102
, pp. 18620-18625
-
-
Gobbi, G.1
Bambico, F.R.2
Mangieri, R.3
Bortolato, M.4
Campolongo, P.5
Solinas, M.6
Cassano, T.7
Morgese, M.G.8
Debonnel, G.9
Duranti, A.10
Tontini, A.11
Tarzia, G.12
Mor, M.13
Trezza, V.14
Goldberg, S.R.15
Cuomo, V.16
Piomelli, D.17
-
15
-
-
34247605930
-
Evaluation of fatty acid amide hydrolase inhibition in murine models of emotionality
-
Naiu, P. S., Varvel, S. A., Ahn, K., Cravatt, B. F., Martin, B. R., and Lichtman, A. H. (2006) Evaluation of fatty acid amide hydrolase inhibition in murine models of emotionality, Psychopharmacology 192, 61-70.
-
(2006)
Psychopharmacology
, vol.192
, pp. 61-70
-
-
Naiu, P.S.1
Varvel, S.A.2
Ahn, K.3
Cravatt, B.F.4
Martin, B.R.5
Lichtman, A.H.6
-
16
-
-
4143074761
-
Characterization of the sleep-wake patterns in mice lacking fatty acid amide hydrolase
-
Huitron-Resendiz, S., Sanchez-Alavez, M., Wills, D. N., Cravatt, B. F., and Henriksen, S. J. (2004) Characterization of the sleep-wake patterns in mice lacking fatty acid amide hydrolase, Sleep 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
-
-
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., and Lichtman, A. H. (2004) Functional disassociation of the central and peripheral fatty acid amide signaling systems, Proc. Natl. Acad. Sci. U.S.A. 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
-
18
-
-
27144431754
-
Inhibitors of fatty acid amide hydrolase reduce carrageenan-induced hind paw inflammation in pentobarbital-treated mice: Comparison with indomethacin and possible involvement of cannabinoid receptors
-
Holt, S., Comelli, F., Costa, B., and Fowler, C. J. (2005) Inhibitors of fatty acid amide hydrolase reduce carrageenan-induced hind paw inflammation in pentobarbital-treated mice: comparison with indomethacin and possible involvement of cannabinoid receptors, Br. J. Pharmacol. 146, 467-476.
-
(2005)
Br. J. Pharmacol
, vol.146
, pp. 467-476
-
-
Holt, S.1
Comelli, F.2
Costa, B.3
Fowler, C.J.4
-
19
-
-
0030571562
-
Study of the amidase signature group
-
Chebrou, H., Bigey, F., Arnaud, A., and Galzy, P. (1996) Study of the amidase signature group, Biochim. Biophys. Acta 1298, 285-293.
-
(1996)
Biochim. Biophys. Acta
, vol.1298
, pp. 285-293
-
-
Chebrou, H.1
Bigey, F.2
Arnaud, A.3
Galzy, P.4
-
20
-
-
22244484464
-
Structure and function of fatty acid amide hydrolase
-
McKinney, M. K., and Cravatt, B. F. (2005) Structure and function of fatty acid amide hydrolase, Annu. Rev. Biochem. 74, 411-432.
-
(2005)
Annu. Rev. Biochem
, vol.74
, pp. 411-432
-
-
McKinney, M.K.1
Cravatt, B.F.2
-
21
-
-
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., and Cravatt, B. F. (1999) Chemical and mutagenic investigations of fatty acid amide hydrolase: evidence for a family of serine hydrolases with distinct catalytic properties, Biochemistry 38, 9804-9812.
-
(1999)
Biochemistry
, vol.38
, pp. 9804-9812
-
-
Patricelli, M.P.1
Lovato, M.A.2
Cravatt, B.F.3
-
22
-
-
0030037917
-
Inhibition of oleamide hydrolase catalyzed hydrolysis of the endogenous sleep-inducing lipid cis-9-octadecenamide
-
Patterson, J. E., Ollman, I. R., Cravatt, B. F., Boger, D. L., Wong, C. H., and Lerner, R. A. (1996) Inhibition of oleamide hydrolase catalyzed hydrolysis of the endogenous sleep-inducing lipid cis-9-octadecenamide, J. Am. Chem. Soc. 118, 5938-5945.
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 5938-5945
-
-
Patterson, J.E.1
Ollman, I.R.2
Cravatt, B.F.3
Boger, D.L.4
Wong, C.H.5
Lerner, R.A.6
-
23
-
-
33847783305
-
Potent and selective alpha-ketoheterocycle-based inhibitors of the anandamide and oleamide catabolizing enzyme, fatty acid amide hydrolase
-
Romero, A., Du, W., Hwang, I., Rayl, T. J., F. Kimball, S., Leung, D., Hoover, H. S., Apodaca, R. L., Breitenbucher, J. G., Cravatt, B. F., and Boger, D. L. (2007) Potent and selective alpha-ketoheterocycle-based inhibitors of the anandamide and oleamide catabolizing enzyme, fatty acid amide hydrolase, J. Med. Chem. 50, 1058-1068.
-
(2007)
J. Med. Chem
, vol.50
, pp. 1058-1068
-
-
Romero, A.1
Du, W.2
Hwang, I.3
Rayl, T.J.F.4
Kimball, 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
-
24
-
-
20144377098
-
Discovery of a potent, selective, and efficacious class of reversible α-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics
-
Boger, D. L., Miyauchi, H., Du, W., Hardouin, C., Fecik, R. A., Cheng, H., Hwang, I., Hedrick, M. P., Leung, D., Acevedo, O., Guimaraes, C. R. W., Jorgensen, W. L., and Cravatt, B. F. (2005) Discovery of a potent, selective, and efficacious class of reversible α-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics, J. Med. Chem. 48, 1849-1856.
-
(2005)
J. Med. Chem
, vol.48
, pp. 1849-1856
-
-
Boger, D.L.1
Miyauchi, H.2
Du, W.3
Hardouin, C.4
Fecik, R.A.5
Cheng, H.6
Hwang, I.7
Hedrick, M.P.8
Leung, D.9
Acevedo, O.10
Guimaraes, C.R.W.11
Jorgensen, W.L.12
Cravatt, B.F.13
-
25
-
-
0038361307
-
Discovering potent and selective reversible inhibitors of enzymes in complex proteomes
-
Leung, D., Hardouin, C., Boger, D. L., and Cravatt, B. F. (2003) Discovering potent and selective reversible inhibitors of enzymes in complex proteomes, Nat. Biotechnol. 21, 687-691.
-
(2003)
Nat. Biotechnol
, vol.21
, pp. 687-691
-
-
Leung, D.1
Hardouin, C.2
Boger, D.L.3
Cravatt, B.F.4
-
26
-
-
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., and Cravatt, B. F. (2004) Reversible inhibitors of fatty acid amide hydrolase that promote analgesia: evidence for an unprecedented combination of potency and selectivity, J. Pharmacol. Exp. Ther. 311, 441-448.
-
(2004)
J. Pharmacol. Exp. Ther
, vol.311
, 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
-
27
-
-
27744466783
-
Mechanism of carbamate inactivation of FAAH: Implications for the design of covalent inhibitors and in vivo functional probes for enzymes
-
Alexander, J. P., and Cravatt, B. F. (2005) Mechanism of carbamate inactivation of FAAH: Implications for the design of covalent inhibitors and in vivo functional probes for enzymes, Chem. Biol. 12, 1179-87.
-
(2005)
Chem. Biol
, vol.12
, pp. 1179-1187
-
-
Alexander, J.P.1
Cravatt, B.F.2
-
28
-
-
33847283286
-
Fatty acid amide hydrolase inhibitors display broad selectivity and inhibit multiple carboxylesterases as off-targets
-
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., and Surowy, C. S. (2007) Fatty acid amide hydrolase inhibitors display broad selectivity and inhibit multiple carboxylesterases as off-targets, Neuropharmacology 52, 1095-1105.
-
(2007)
Neuropharmacology
, vol.52
, 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
-
29
-
-
0035469599
-
Direct visualization of serine hydrolase activities in complex proteome using fluorescent active site-directed probes
-
Patricelli, M. P., Giang, D. K., Stamp, L. M., and Burbaum, J. J. (2001) Direct visualization of serine hydrolase activities in complex proteome using fluorescent active site-directed probes, Proteomics 1, 1067-1071.
-
(2001)
Proteomics
, vol.1
, pp. 1067-1071
-
-
Patricelli, M.P.1
Giang, D.K.2
Stamp, L.M.3
Burbaum, J.J.4
-
30
-
-
36049022331
-
-
Apodaca, R., Breitenbucher, J. G., Pattabiraman, K., Seierstad, M., and Xiao, W. (2006) Piperazinyl and piperidinyl ureas as modulators of fatty acid amide hydrolase, WO 2006/074025.
-
Apodaca, R., Breitenbucher, J. G., Pattabiraman, K., Seierstad, M., and Xiao, W. (2006) Piperazinyl and piperidinyl ureas as modulators of fatty acid amide hydrolase, WO 2006/074025.
-
-
-
-
31
-
-
0032573124
-
Comparative characterization of a wild type and transmembrane domain-deleted fatty acid amide hydrolase: Identification of the transmembrane domain as a site for oligomerization
-
Patricelli, M. P., Lashuel, H. A., Giang, D. K., Kelly, J. W., and Cravatt, B. F. (1998) Comparative characterization of a wild type and transmembrane domain-deleted fatty acid amide hydrolase: identification of the transmembrane domain as a site for oligomerization, Biochemistry 37, 15177-87.
-
(1998)
Biochemistry
, vol.37
, pp. 15177-15187
-
-
Patricelli, M.P.1
Lashuel, H.A.2
Giang, D.K.3
Kelly, J.W.4
Cravatt, B.F.5
-
32
-
-
36049032279
-
-
Ahn, K. (2006) Fatty acid amide hydrolase assay, WO 2006/085196.
-
Ahn, K. (2006) Fatty acid amide hydrolase assay, WO 2006/085196.
-
-
-
-
33
-
-
15744389868
-
A spectrophotometric assay for fatty acid amide hydrolase suitable for high-throughput screening
-
De Bank, P. A., Kendall, D. A., and Alexander, S. P. (2005) A spectrophotometric assay for fatty acid amide hydrolase suitable for high-throughput screening, Biochem. Pharmacol. 69, 1187-93.
-
(2005)
Biochem. Pharmacol
, vol.69
, pp. 1187-1193
-
-
De Bank, P.A.1
Kendall, D.A.2
Alexander, S.P.3
-
34
-
-
0029927505
-
Mass spectrometric sequencing of proteins from silver-stained Polyacrylamide gels
-
Shevchenko, A., Wilm, M., Vorm, O., and Mann, M. (1996) Mass spectrometric sequencing of proteins from silver-stained Polyacrylamide gels, Anal. Chem. 68, 850-8.
-
(1996)
Anal. Chem
, vol.68
, pp. 850-858
-
-
Shevchenko, A.1
Wilm, M.2
Vorm, O.3
Mann, M.4
-
35
-
-
0033434080
-
Probability-based protein identification by searching sequence databases using mass spectrometry data
-
Perkins, D. N., Pappin, D. J. C., Creasy, D. M., and Cottrell, J. S.(1999) Probability-based protein identification by searching sequence databases using mass spectrometry data, Electrophoresis 20, 3551-67.
-
(1999)
Electrophoresis
, vol.20
, pp. 3551-3567
-
-
Perkins, D.N.1
Pappin, D.J.C.2
Creasy, D.M.3
Cottrell, J.S.4
-
36
-
-
3242716915
-
Inhibitor focusing: Direct selection of drug targets from proteomes using activity-based probes
-
Nomanbhoy, T. K., Rosenblum, J., Aban, A., and Burbaum, J. J. (2003) Inhibitor focusing: direct selection of drug targets from proteomes using activity-based probes, Assay Drug Dev. Technol. 1, 137-146.
-
(2003)
Assay Drug Dev. Technol
, vol.1
, pp. 137-146
-
-
Nomanbhoy, T.K.1
Rosenblum, J.2
Aban, A.3
Burbaum, J.J.4
-
37
-
-
0036678119
-
Enzyme activity profiles of the secreted and membrane proteome that depict cancer cell invasiveness
-
Jessani, N., Liu, Y., Humphrey, M., and Cravatt, B. F. (2002) Enzyme activity profiles of the secreted and membrane proteome that depict cancer cell invasiveness, Proc. Natl. Acad. Sci. U.S.A. 99, 10335-10340.
-
(2002)
Proc. Natl. Acad. Sci. U.S.A
, vol.99
, pp. 10335-10340
-
-
Jessani, N.1
Liu, Y.2
Humphrey, M.3
Cravatt, B.F.4
-
38
-
-
17044407508
-
High-resolution functional proteomics by active-site peptide profiling
-
Okerberg, E. S., Wu, J., Zhang, B., Samii, B., Blackford, K., Winn, D. T., Shreder, K. R., Burbaum, J. J., and Patricelli, M. P. (2005) High-resolution functional proteomics by active-site peptide profiling, Proc. Natl. Acad. ScL U.S.A. 102, 4996-5001.
-
(2005)
Proc. Natl. Acad. ScL U.S.A
, vol.102
, pp. 4996-5001
-
-
Okerberg, E.S.1
Wu, J.2
Zhang, B.3
Samii, B.4
Blackford, K.5
Winn, D.T.6
Shreder, K.R.7
Burbaum, J.J.8
Patricelli, M.P.9
-
39
-
-
33846248354
-
Functional interrogation of the kinome using nucleotide acyl phosphates
-
Patricelli, M. P., Szardenings, A. K., Liyanage, M., Nomanbhoy, T. K., Wu, M., Weissig, H., Aban, A., Chun, D., Tanner, S., and Kozarich, J. W. (2007) Functional interrogation of the kinome using nucleotide acyl phosphates, Biochemistry 46, 350-358.
-
(2007)
Biochemistry
, vol.46
, pp. 350-358
-
-
Patricelli, M.P.1
Szardenings, A.K.2
Liyanage, M.3
Nomanbhoy, T.K.4
Wu, M.5
Weissig, H.6
Aban, A.7
Chun, D.8
Tanner, S.9
Kozarich, J.W.10
-
40
-
-
0029644596
-
Method to correlate tandem mass spectra of modified peptides to amino acid sequences in the protein database
-
Yates, J. R., III, Eng, J. K., McCormack, A. L., and Schieltz, D. (1995) Method to correlate tandem mass spectra of modified peptides to amino acid sequences in the protein database, Anal. Chem. 67, 1426-1436.
-
(1995)
Anal. Chem
, vol.67
, pp. 1426-1436
-
-
Yates III, J.R.1
Eng, J.K.2
McCormack, A.L.3
Schieltz, D.4
-
41
-
-
0033593013
-
Activity-based protein profiling: The serine hydrolases
-
Liu, Y., Patricelli, M. P., and Cravatt, B. F. (1999) Activity-based protein profiling: the serine hydrolases, Proc. Natl. Acad. Sci. U.S.A. 96, 14694-14699.
-
(1999)
Proc. Natl. Acad. Sci. U.S.A
, vol.96
, pp. 14694-14699
-
-
Liu, Y.1
Patricelli, M.P.2
Cravatt, B.F.3
-
42
-
-
2242490907
-
Structural adaptation in a membrane enzyme that terminates endocannabinoid signaling
-
Bracey, M. A., Hanson, M. A., Masuda, K. R., Stevens, R. C., and Cravatt, B. F. (2002) Structural adaptation in a membrane enzyme that terminates endocannabinoid signaling, Science 298, 1793-1796.
-
(2002)
Science
, vol.298
, pp. 1793-1796
-
-
Bracey, M.A.1
Hanson, M.A.2
Masuda, K.R.3
Stevens, R.C.4
Cravatt, B.F.5
-
43
-
-
0004216822
-
-
2nd ed, pp, Wiley-VCH Press, New York
-
Copeland, R. A. (2000) Enzymes: A practical introduction to structure, mechanism, and data analysis, 2nd ed., pp 318-349, Wiley-VCH Press, New York.
-
(2000)
Enzymes: A practical introduction to structure, mechanism, and data analysis
, pp. 318-349
-
-
Copeland, R.A.1
-
44
-
-
17244362388
-
Mechanistic basis of enzyme-targeted drugs
-
Robertson, J. G. (2005) Mechanistic basis of enzyme-targeted drugs, Biochemistry 44, 5561-5571.
-
(2005)
Biochemistry
, vol.44
, pp. 5561-5571
-
-
Robertson, J.G.1
-
45
-
-
33746605204
-
The putative endocannabinoid transport blocker LY2183240 is a potent inhibitor of FAAH and several other brain serine hydrolases
-
Alexander, J. P., and Cravatt, B. F. (2006) The putative endocannabinoid transport blocker LY2183240 is a potent inhibitor of FAAH and several other brain serine hydrolases, J. Am. Chem. Soc. 128, 9699-9704.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 9699-9704
-
-
Alexander, J.P.1
Cravatt, B.F.2
-
46
-
-
0036051482
-
Chemical approaches for functionally probing the proteome
-
Greenbaum, D., Baruch, A., Hayrapetian, L., Darula, Z., Burlin-game, A., Medzihradszky, K. F., and Bogyo, M. (2002) Chemical approaches for functionally probing the proteome, Mol. Cell. Proteomics 1, 60-68.
-
(2002)
Mol. Cell. Proteomics
, vol.1
, pp. 60-68
-
-
Greenbaum, D.1
Baruch, A.2
Hayrapetian, L.3
Darula, Z.4
Burlin-game, A.5
Medzihradszky, K.F.6
Bogyo, M.7
-
47
-
-
36049004794
-
-
Matsumoto, T., Kori, M., Miyazaki, J., and Kiyota, Y. (2006) Preparation of piperidinecarboxamides and piperazinecarboxamides as fatty acid amide hydrolase (FAAH) inhibitors, WO 2006/054652.
-
Matsumoto, T., Kori, M., Miyazaki, J., and Kiyota, Y. (2006) Preparation of piperidinecarboxamides and piperazinecarboxamides as fatty acid amide hydrolase (FAAH) inhibitors, WO 2006/054652.
-
-
-
-
48
-
-
0033607236
-
Fatty acid amide hydrolase competitively degrades bioactive amides and esters through a nonconventional catalytic mechanism
-
Patricelli, M. P., and Cravatt, B. F. (1999) Fatty acid amide hydrolase competitively degrades bioactive amides and esters through a nonconventional catalytic mechanism, Biochemistry 38, 14125-14130.
-
(1999)
Biochemistry
, vol.38
, pp. 14125-14130
-
-
Patricelli, M.P.1
Cravatt, B.F.2
-
49
-
-
0141733197
-
Evidence for the distinct roles in catalysis for residues of the serine-serine-lysine catalytic triad of fatty acid amide hydrolase
-
McKinney, M. K., and Cravatt, B. F. (2003) Evidence for the distinct roles in catalysis for residues of the serine-serine-lysine catalytic triad of fatty acid amide hydrolase, J. Biol. Chem. 278, 37393-37399.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 37393-37399
-
-
McKinney, M.K.1
Cravatt, B.F.2
-
50
-
-
0031081549
-
Catalysis of the CC-1065 and duocarmycin DNA alkylation reaction: DNA binding induced conformational change in the agent results in activation
-
Boger, D. L., and Garbaccio, R. M. (1997) Catalysis of the CC-1065 and duocarmycin DNA alkylation reaction: DNA binding induced conformational change in the agent results in activation, Bioorg. Med. Chem. 5, 263-276.
-
(1997)
Bioorg. Med. Chem
, vol.5
, pp. 263-276
-
-
Boger, D.L.1
Garbaccio, R.M.2
|