-
1
-
-
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, 61-65.
-
(1993)
Nature
, vol.365
, pp. 61-65
-
-
Munro, S.1
Thomas, K.L.2
Abu-Shaar, M.3
-
2
-
-
0029094470
-
-
Galiegue, S.; Mary, S.; Marchand, J.; Dussossoy, D.; Carriere, D.; Carayon, P.; Bouaboula, M.; Shire, D.; Le, Fur, G.; Casellas, P. Expression of central and peripheral cannabinoid receptors in human immune tissues and leukocyte subpopulations. Eur. J. Biochem. 1995, 232, 54-61.
-
Galiegue, S.; Mary, S.; Marchand, J.; Dussossoy, D.; Carriere, D.; Carayon, P.; Bouaboula, M.; Shire, D.; Le, Fur, G.; Casellas, P. Expression of central and peripheral cannabinoid receptors in human immune tissues and leukocyte subpopulations. Eur. J. Biochem. 1995, 232, 54-61.
-
-
-
-
3
-
-
0348010292
-
2 receptors and fatty acid amide hydrolase are selectively overexpressed in neuritic plaque-associated glia in Alzheimer's disease brains
-
2 receptors and fatty acid amide hydrolase are selectively overexpressed in neuritic plaque-associated glia in Alzheimer's disease brains. J. Neurosci. 2003, 23, 11136-11141.
-
(2003)
J. Neurosci
, vol.23
, pp. 11136-11141
-
-
Benito, C.1
Nunez, E.2
Tolon, R.M.3
Carrier, E.J.4
Rabano, A.5
Hillard, C.J.6
Romerio, J.7
-
4
-
-
26844504226
-
-
2 receptors. Science 2005, 310, 329-332.
-
2 receptors. Science 2005, 310, 329-332.
-
-
-
-
5
-
-
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, 561-564.
-
(1990)
Nature
, vol.346
, pp. 561-564
-
-
Matsuda, L.A.1
Lolait, S.J.2
Brownstein, M.J.3
Young, A.C.4
Bonner, T.I.5
-
6
-
-
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, 5069-5087.
-
(2005)
J. Med. Chem
, vol.48
, pp. 5069-5087
-
-
Lambert, D.M.1
Fowler, C.J.2
-
7
-
-
33144480327
-
Cannabinoid receptors as therapeutic targets
-
Mackie, K. Cannabinoid receptors as therapeutic targets. Annu. Rev. Pharmacol. Toxicol. 2006, 46, 101-122.
-
(2006)
Annu. Rev. Pharmacol. Toxicol
, vol.46
, pp. 101-122
-
-
Mackie, K.1
-
8
-
-
33748703859
-
The endocannabinoid system as an emerging target of pharmacotherapy
-
Pacher, P.; Batkai, S.; Kunos, G. The endocannabinoid system as an emerging target of pharmacotherapy. Pharmacol. Rev. 2006, 58, 389-462.
-
(2006)
Pharmacol. Rev
, vol.58
, pp. 389-462
-
-
Pacher, P.1
Batkai, S.2
Kunos, G.3
-
9
-
-
0034886018
-
2 cannabinoid receptor-mediated peripheral antinociception
-
2 cannabinoid receptor-mediated peripheral antinociception. Pain 2001, 93, 239-245.
-
(2001)
Pain
, vol.93
, pp. 239-245
-
-
Malan Jr., T.P.1
Ibrahim, M.M.2
Deng, H.3
Liu, Q.4
Mata, H.P.5
Vanderah, T.6
Porreca, F.7
Makriyannis, A.8
-
10
-
-
0041836218
-
2 cannabinoid receptors by AM1241 inhibits experimental neuropathic pain: Pain inhibition by receptors not present in the CNS
-
2 cannabinoid receptors by AM1241 inhibits experimental neuropathic pain: Pain inhibition by receptors not present in the CNS. Proc. Natl. Acad. Sci. U.S.A. 2003, 100, 10529-10533.
-
(2003)
Proc. Natl. Acad. Sci. U.S.A
, vol.100
, pp. 10529-10533
-
-
Ibrahim, M.M.1
Deng, H.2
Zvonok, A.3
Cockayne, D.A.4
Kwan, J.5
Mata, H.P.6
Vanderah, T.W.7
Lai, J.8
Porreca, F.9
Makriyannis, A.10
Malan Jr., T.P.11
-
12
-
-
0038521050
-
Selective activation of cannabinoid CB(2) receptors suppresses spinal fos protein expression and pain behavior in a rat model of inflammation
-
Nackley, A. G.; Makriyannis, A.; Hohmann, A. G. Selective activation of cannabinoid CB(2) receptors suppresses spinal fos protein expression and pain behavior in a rat model of inflammation. Neuroscience 2003, 119, 747-757.
-
(2003)
Neuroscience
, vol.119
, pp. 747-757
-
-
Nackley, A.G.1
Makriyannis, A.2
Hohmann, A.G.3
-
13
-
-
0141992217
-
2) receptor activation
-
2) receptor activation. Br. J. Pharmacol. 2003, 140, 261-268.
-
(2003)
Br. J. Pharmacol
, vol.140
, pp. 261-268
-
-
Patel, H.J.1
Birrell, M.A.2
Crispino, N.3
Hele, D.J.4
Venkatesan, P.5
Barnes, P.J.6
Yacoub, M.H.7
Belyisi, M.G.8
-
14
-
-
33745997333
-
2 receptor inverse agonist JTE-907 suppresses spontaneous itch-associated responses of NC mice, a model of atopic dermatitis
-
2 receptor inverse agonist JTE-907 suppresses spontaneous itch-associated responses of NC mice, a model of atopic dermatitis. Eur. J. Pharmacol. 2006, 542, 179-183.
-
(2006)
Eur. J. Pharmacol
, vol.542
, pp. 179-183
-
-
Maekawa, T.1
Nojima, H.2
Kuraishi, Y.3
Aisaka, K.4
-
15
-
-
0035422139
-
-
2 cannabinoid receptor. Cancer Res. 2001, 61, 5784-5789.
-
2 cannabinoid receptor". Cancer Res. 2001, 61, 5784-5789.
-
-
-
-
16
-
-
0037100312
-
2 cannabinoid receptors as a novel therapy to treat malignant lymphoblastic disease
-
2 cannabinoid receptors as a novel therapy to treat malignant lymphoblastic disease. Blood 2002, 100, 627-634.
-
(2002)
Blood
, vol.100
, pp. 627-634
-
-
McKallip, R.J.1
Lombard, C.2
Fisher, M.3
Martin, B.R.4
Ryu, S.5
Grants, S.6
Nagarkatti, P.S.7
Nagarkatti, M.8
-
18
-
-
21044458324
-
Current knowledge on the antagonists and inverse agonists of cannabinoid receptors
-
Muccioli, G. G.; Lambert, D. M. Current knowledge on the antagonists and inverse agonists of cannabinoid receptors. Curr. Med. Chem. 2005, 12, 1361-1394.
-
(2005)
Curr. Med. Chem
, vol.12
, pp. 1361-1394
-
-
Muccioli, G.G.1
Lambert, D.M.2
-
19
-
-
30444443786
-
2 cannabinoid receptors agonists: Synthesis, pharmacological properties, and molecular modeling
-
2 cannabinoid receptors agonists: Synthesis, pharmacological properties, and molecular modeling. J. Med. Chem. 2006, 49, 70-79.
-
(2006)
J. Med. Chem
, vol.49
, pp. 70-79
-
-
Stern, E.1
Muccioli, G.G.2
Millet, R.3
Goossens, J.-F.4
Farce, A.5
Chavatte, P.6
Poupaert, J.H.7
Lambert, D.M.8
Depreux, P.9
Hénichart, J.-P.10
-
20
-
-
0000139329
-
The synthesis of certain substituted quinolines and 5,6-benzoquinolines
-
Gould, R. G. and Jacobs, W. A. The synthesis of certain substituted quinolines and 5,6-benzoquinolines. J. Am. Chem. Soc. 1939, 61, 2890-2895.
-
(1939)
J. Am. Chem. Soc
, vol.61
, pp. 2890-2895
-
-
Gould, R.G.1
Jacobs, W.A.2
-
21
-
-
0017809797
-
Quinolone antimicrobial agents. 1. Versatile new synthesis of 1-alkyl-1,4-dihydro-4-oxo-3- quinoline carboxylic acids
-
Mitscher, L. A.; Gracey, H. E.; Clark, G. W.; Suzuki, T. Quinolone antimicrobial agents. 1. Versatile new synthesis of 1-alkyl-1,4-dihydro-4-oxo-3- quinoline carboxylic acids. J. Med. Chem., 1978, 21, 485-489.
-
(1978)
J. Med. Chem
, vol.21
, pp. 485-489
-
-
Mitscher, L.A.1
Gracey, H.E.2
Clark, G.W.3
Suzuki, T.4
-
22
-
-
0027339716
-
3 receptor antagonists. 2. 4-Hydroxy-3-quinolinecarboxylic acid derivatives
-
3 receptor antagonists. 2. 4-Hydroxy-3-quinolinecarboxylic acid derivatives. J. Med. Chem. 1993, 36, 617-626.
-
(1993)
J. Med. Chem
, vol.36
, pp. 617-626
-
-
Hayashi, H.1
Miwa, Y.2
Ichikawa, S.3
Yoda, N.4
Miki, I.5
Ishii, A.6
Kono, M.7
Yasuzawa, T.8
Suzuki, F.9
-
23
-
-
0035082307
-
-
Jung, J.-C.; Jung, Y.-J.; Park, O.-S. Synthesis of 4-hydroxyquinolin- 2(1H)-one analogues and 2-substituted quinolone derivatives. J. Heterocycl. Chem. 2001, 38, 61-67.
-
Jung, J.-C.; Jung, Y.-J.; Park, O.-S. Synthesis of 4-hydroxyquinolin- 2(1H)-one analogues and 2-substituted quinolone derivatives. J. Heterocycl. Chem. 2001, 38, 61-67.
-
-
-
-
24
-
-
0028137119
-
Synthetic studies of the pyrroloquinoline nucleus of the makaluvamine alkaloids. Synthesis of the topoisomerase II inhibitor makaluvamine D
-
White, J. D.; Yager, K. M.; Yakura, T. Synthetic studies of the pyrroloquinoline nucleus of the makaluvamine alkaloids. Synthesis of the topoisomerase II inhibitor makaluvamine D. J. Am. Chem. Soc. 1994, 116, 1831-1838.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 1831-1838
-
-
White, J.D.1
Yager, K.M.2
Yakura, T.3
-
25
-
-
33845557579
-
Palladium-catalyzed reaction of tributyltin hydride with acyl chlorides. A mild, selective, and general route to aldehydes
-
Four, P.; Guibe, F. Palladium-catalyzed reaction of tributyltin hydride with acyl chlorides. A mild, selective, and general route to aldehydes. J. Org. Chem. 1981, 46, 4439-4445.
-
(1981)
J. Org. Chem
, vol.46
, pp. 4439-4445
-
-
Four, P.1
Guibe, F.2
-
26
-
-
0037431376
-
Identification of N,N-disubstituted phenylalanines as a novel class of inhibitors of hepatitis C NS5B polymerase
-
Chan, L.; Reddy, T. J.; Proulx, M.; Das, S. K.; Pereira, O.; Wang, W.; Siddiqui, A.; Yannopoulos, C. G.; Poisson, C.; Turcotte, N.; Drouin, A.; Alaoui-Ismaili, M. H.; Bethell, R.; Hamel, M.; L'Heureux, L.; Bilimoria, D.; Nguyen-Ba, N. Identification of N,N-disubstituted phenylalanines as a novel class of inhibitors of hepatitis C NS5B polymerase. J. Med. Chem. 2003, 46, 1283-1285.
-
(2003)
J. Med. Chem
, vol.46
, pp. 1283-1285
-
-
Chan, L.1
Reddy, T.J.2
Proulx, M.3
Das, S.K.4
Pereira, O.5
Wang, W.6
Siddiqui, A.7
Yannopoulos, C.G.8
Poisson, C.9
Turcotte, N.10
Drouin, A.11
Alaoui-Ismaili, M.H.12
Bethell, R.13
Hamel, M.14
L'Heureux, L.15
Bilimoria, D.16
Nguyen-Ba, N.17
-
27
-
-
0034606467
-
Synthesis and biological evaluation of 2,5-dihydropyrazolo[4,3-c]quinolin-3-ones, a novel series of PDE 4 inhibitors with low emetic potential and antiasthmatic properties
-
Crespo, M, I.; Gràcia, J.; Puig, C.; Vega, A.; Bou, J.; Beleta, J.; Doménech, T.; Ryder, H.; Segarra, V.; Palacios, J. M. Synthesis and biological evaluation of 2,5-dihydropyrazolo[4,3-c]quinolin-3-ones, a novel series of PDE 4 inhibitors with low emetic potential and antiasthmatic properties. Bioorg. Med. Chem. Lett. 2000, 10, 2661-2664.
-
(2000)
Bioorg. Med. Chem. Lett
, vol.10
, pp. 2661-2664
-
-
Crespo, M.I.1
Gràcia, J.2
Puig, C.3
Vega, A.4
Bou, J.5
Beleta, J.6
Doménech, T.7
Ryder, H.8
Segarra, V.9
Palacios, J.M.10
-
28
-
-
0030505551
-
An NMR study of halogenated 1,4-dihydro-1-ethyl-4-oxoquinoline-3- carboxylates
-
Podányi, B.; Keresztúri, G.; Vasvári-Debreczy, L.; Hermecz, I. An NMR study of halogenated 1,4-dihydro-1-ethyl-4-oxoquinoline-3- carboxylates. Magn. Reson. Chem. 1998, 34, 972-978.
-
(1998)
Magn. Reson. Chem
, vol.34
, pp. 972-978
-
-
Podányi, B.1
Keresztúri, G.2
Vasvári-Debreczy, L.3
Hermecz, I.4
-
29
-
-
40849100075
-
2 receptor agonists by liquid chromatography on amylose stationary phases
-
in press, doi: 10.1016/j.jpba.2007.01.044
-
2 receptor agonists by liquid chromatography on amylose stationary phases. J. Pharm. Biomed. Anal. 2007, in press, doi: 10.1016/j.jpba.2007.01.044.
-
(2007)
J. Pharm. Biomed. Anal
-
-
Stern, E.1
Goossens, L.2
Vaccher, C.3
Bonte, J.-P.4
Depreux, P.5
Hénichart, J.-P.6
Goossens, J.-F.7
-
30
-
-
0004537706
-
Synthesis of antimalarials. VI. Synthesis of certain 1,5- and 1,8-naphthyridine derivatives
-
Adams, J. T.; Bradsher, C. K.; Breslow, D. S.; Amore, T.; Hauser, C. R. Synthesis of antimalarials. VI. Synthesis of certain 1,5- and 1,8-naphthyridine derivatives. J. Am. Chem. Soc. 1946, 68, 1317-1319.
-
(1946)
J. Am. Chem. Soc
, vol.68
, pp. 1317-1319
-
-
Adams, J.T.1
Bradsher, C.K.2
Breslow, D.S.3
Amore, T.4
Hauser, C.R.5
-
31
-
-
0038441368
-
-
Springfield, S. A.; Marcantonio, K.; Ceglia, S.; Albaneze-Walker, J.; Dormer, P. G.; Nelson, T. D.; Murry, J. A. A convenient one-pot synthesis of 1,8-naphthyridones. J. Org. Chem. 2003, 68, 4598-4599.
-
Springfield, S. A.; Marcantonio, K.; Ceglia, S.; Albaneze-Walker, J.; Dormer, P. G.; Nelson, T. D.; Murry, J. A. A convenient one-pot synthesis of 1,8-naphthyridones. J. Org. Chem. 2003, 68, 4598-4599.
-
-
-
-
32
-
-
4444366049
-
Solid phase synthesis of 6-acylamino-1-alkyl/aryl-4-oxo-1,4-dihydrocinnoline-3-carboxamides
-
Sereni, L.; Tató, M.; Sola, F.; Brill, W. K.-D. Solid phase synthesis of 6-acylamino-1-alkyl/aryl-4-oxo-1,4-dihydrocinnoline-3-carboxamides. Tetrahedron 2005, 60, 8561-8577.
-
(2005)
Tetrahedron
, vol.60
, pp. 8561-8577
-
-
Sereni, L.1
Tató, M.2
Sola, F.3
Brill, W.K.-D.4
-
33
-
-
0025868658
-
Oxybenzotriazole free peptide coupling reagents for N-methylated amino acids
-
Coste, J.; Frérot, E.; Jouin, P. Oxybenzotriazole free peptide coupling reagents for N-methylated amino acids. Tetrahedron Lett. 1991, 32, 1967-1970.
-
(1991)
Tetrahedron Lett
, vol.32
, pp. 1967-1970
-
-
Coste, J.1
Frérot, E.2
Jouin, P.3
-
34
-
-
8544221860
-
A versatile and efficient synthesis of 3-aroyl-1,4-dihydroquinolin-4-ones
-
Stern, E.; Millet, R.; Depreux, P.; Hénichart, J.-P. A versatile and efficient synthesis of 3-aroyl-1,4-dihydroquinolin-4-ones. Tetrahedron Lett. 2004, 45, 9257-9259.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 9257-9259
-
-
Stern, E.1
Millet, R.2
Depreux, P.3
Hénichart, J.-P.4
-
35
-
-
17144367660
-
1 cannabinoid receptor ligands: Synthesis and pharmacological evaluation
-
1 cannabinoid receptor ligands: Synthesis and pharmacological evaluation. J. Med. Chem. 2005, 48, 2509-2517.
-
(2005)
J. Med. Chem
, vol.48
, pp. 2509-2517
-
-
Muccioli, G.G.1
Martin, D.2
Scriba, G.K.E.3
Poppitz, W.4
Poupaert, J.H.5
Wouters, J.6
Lambert, D.M.7
-
36
-
-
28544451559
-
1 cannabinoid receptor inverse agonists
-
1 cannabinoid receptor inverse agonists. J. Med. Chem. 2005, 48, 7486-7490.
-
(2005)
J. Med. Chem
, vol.48
, pp. 7486-7490
-
-
Muccioli, G.G.1
Wouters, J.2
Scriba, G.K.E.3
Poppitz, W.4
Poupaert, J.H.5
Lambert, D.M.6
-
37
-
-
32344434497
-
-
1 cannabinoid receptor inverse agonists/ antagonists. J. Med. Chem. 2006, 49, 872-882.
-
1 cannabinoid receptor inverse agonists/ antagonists. J. Med. Chem. 2006, 49, 872-882.
-
-
-
-
38
-
-
33749236407
-
-
2 selective agonists. J. Med. Chem. 2006, 49, 5947-5957.
-
2 selective agonists. J. Med. Chem. 2006, 49, 5947-5957.
-
-
-
-
39
-
-
35848931598
-
-
Compound 30 in ref 19 corresponds to ALICB-179 (compound 3 in the present study).
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Compound 30 in ref 19 corresponds to ALICB-179 (compound 3 in the present study).
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