-
1
-
-
33644804271
-
The therapeutic potential of drugs that target cannabinoid receptors or modulate the tissue levels or actions of endocannabinoids
-
Pertwee, R. G. The therapeutic potential of drugs that target cannabinoid receptors or modulate the tissue levels or actions of endocannabinoids AAPS J. 2005, 7, E625-E654
-
(2005)
AAPS J.
, vol.7
, pp. 625-E654
-
-
Pertwee, R.G.1
-
2
-
-
4644331847
-
Cannabinoid physiology and pharmacology: 30 years of progress
-
Howlett, A. C.; Breivogel, C. S.; Childers, S. R.; Deadwyler, S. A.; Hampson, R. E.; Porrino, L. J. Cannabinoid physiology and pharmacology: 30 years of progress Neuropharmacology 2004, 47 (Suppl. 1) 345-358
-
(2004)
Neuropharmacology
, vol.47
, pp. 345-358
-
-
Howlett, A.C.1
Breivogel, C.S.2
Childers, S.R.3
Deadwyler, S.A.4
Hampson, R.E.5
Porrino, L.J.6
-
3
-
-
30444457225
-
Cannabinoid pharmacology: The first 66 years
-
Pertwee, R. G. Cannabinoid pharmacology: the first 66 years Br. J. Pharmacol. 2006, 147 (Suppl. 1) S163-S171
-
(2006)
Br. J. Pharmacol.
, vol.147
, pp. 163-S171
-
-
Pertwee, R.G.1
-
4
-
-
33244484802
-
Structural-activity relationship study on C-4 carbon atom of the CB1 antagonist SR141716: Synthesis and pharmacological evaluation of 1,2,4-triazole-3-carboxamides
-
Jagerovic, N.; Hernandez-Folgado, L.; Alkorta, I.; Goya, P.; Martin, M. I.; Dannert, M. T.; Alsasua, A.; Frigola, J.; Cuberes, M. R.; Dordal, A.; Holenz, J. Structural-activity relationship study on C-4 carbon atom of the CB1 antagonist SR141716: synthesis and pharmacological evaluation of 1,2,4-triazole-3-carboxamides Eur. J. Med. Chem. 2006, 41, 114-120
-
(2006)
Eur. J. Med. Chem.
, vol.41
, pp. 114-120
-
-
Jagerovic, N.1
Hernandez-Folgado, L.2
Alkorta, I.3
Goya, P.4
Martin, M.I.5
Dannert, M.T.6
Alsasua, A.7
Frigola, J.8
Cuberes, M.R.9
Dordal, A.10
Holenz, J.11
-
5
-
-
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
-
6
-
-
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
-
7
-
-
43249100162
-
Targeting the endocannabinoid system: To enhance or reduce?
-
Di Marzo, V. Targeting the endocannabinoid system: to enhance or reduce? Nat. Rev. Drug Discovery 2008, 7, 438-455
-
(2008)
Nat. Rev. Drug Discovery
, vol.7
, pp. 438-455
-
-
Di Marzo, V.1
-
8
-
-
84901279661
-
2012 Division of Medicinal Chemistry Award Address. Trekking the cannabinoid road: A personal perspective
-
Makriyannis, A. 2012 Division of Medicinal Chemistry Award Address. Trekking the cannabinoid road: a personal perspective J. Med. Chem. 2014, 57, 3891-3911
-
(2014)
J. Med. Chem.
, vol.57
, pp. 3891-3911
-
-
Makriyannis, A.1
-
9
-
-
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
-
10
-
-
40349113029
-
CB1 cannabinoid antagonists: Structure-activity relationships and potential therapeutic applications
-
Jagerovic, N.; Fernandez-Fernandez, C.; Goya, P. CB1 cannabinoid antagonists: structure-activity relationships and potential therapeutic applications Curr. Top. Med. Chem. 2008, 8, 205-230
-
(2008)
Curr. Top. Med. Chem.
, vol.8
, pp. 205-230
-
-
Jagerovic, N.1
Fernandez-Fernandez, C.2
Goya, P.3
-
11
-
-
61649089261
-
Central side-effects of therapies based on CB1 cannabinoid receptor agonists and antagonists: Focus on anxiety and depression
-
Moreira, F. A.; Grieb, M.; Lutz, B. Central side-effects of therapies based on CB1 cannabinoid receptor agonists and antagonists: focus on anxiety and depression Best Pract. Res., Clin. Endocrinol. Metab. 2009, 23, 133-144
-
(2009)
Best Pract. Res., Clin. Endocrinol. Metab.
, vol.23
, pp. 133-144
-
-
Moreira, F.A.1
Grieb, M.2
Lutz, B.3
-
12
-
-
84868128338
-
Targeting the endocannabinoid system with cannabinoid receptor agonists: Pharmacological strategies and therapeutic possibilities
-
Pertwee, R. G. Targeting the endocannabinoid system with cannabinoid receptor agonists: pharmacological strategies and therapeutic possibilities Philos. Trans. R. Soc. London, Ser. B 2012, 367, 3353-3363
-
(2012)
Philos. Trans. R. Soc. London, Ser. B
, vol.367
, pp. 3353-3363
-
-
Pertwee, R.G.1
-
13
-
-
84857375139
-
Allosteric modulation of seven transmembrane spanning receptors: Theory, practice, and opportunities for central nervous system drug discovery
-
Melancon, B. J.; Hopkins, C. R.; Wood, M. R.; Emmitte, K. A.; Niswender, C. M.; Christopoulos, A.; Conn, P. J.; Lindsley, C. W. Allosteric modulation of seven transmembrane spanning receptors: theory, practice, and opportunities for central nervous system drug discovery J. Med. Chem. 2012, 55, 1445-1464
-
(2012)
J. Med. Chem.
, vol.55
, pp. 1445-1464
-
-
Melancon, B.J.1
Hopkins, C.R.2
Wood, M.R.3
Emmitte, K.A.4
Niswender, C.M.5
Christopoulos, A.6
Conn, P.J.7
Lindsley, C.W.8
-
14
-
-
77952354490
-
Seven transmembrane receptors as shapeshifting proteins: The impact of allosteric modulation and functional selectivity on new drug discovery
-
Kenakin, T.; Miller, L. J. Seven transmembrane receptors as shapeshifting proteins: the impact of allosteric modulation and functional selectivity on new drug discovery Pharmacol. Rev. 2010, 62, 265-304
-
(2010)
Pharmacol. Rev.
, vol.62
, pp. 265-304
-
-
Kenakin, T.1
Miller, L.J.2
-
15
-
-
0036258990
-
G protein-coupled receptor allosterism and complexing
-
Christopoulos, A.; Kenakin, T. G protein-coupled receptor allosterism and complexing Pharmacol. Rev. 2002, 54, 323-374
-
(2002)
Pharmacol. Rev.
, vol.54
, pp. 323-374
-
-
Christopoulos, A.1
Kenakin, T.2
-
16
-
-
58149193205
-
Allosteric modulators of GPCRs: A novel approach for the treatment of CNS disorders
-
Conn, P. J.; Christopoulos, A.; Lindsley, C. W. Allosteric modulators of GPCRs: a novel approach for the treatment of CNS disorders Nat. Rev. Drug Discovery 2009, 8, 41-54
-
(2009)
Nat. Rev. Drug Discovery
, vol.8
, pp. 41-54
-
-
Conn, P.J.1
Christopoulos, A.2
Lindsley, C.W.3
-
17
-
-
84896891638
-
Allosteric modulation of a cannabinoid G protein-coupled receptor: Binding site elucidation and relationship to G protein signaling
-
Shore, D. M.; Baillie, G. L.; Hurst, D. H.; Navas, F., III; Seltzman, H. H.; Marcu, J. P.; Abood, M. E.; Ross, R. A.; Reggio, P. H. Allosteric modulation of a cannabinoid G protein-coupled receptor: binding site elucidation and relationship to G protein signaling J. Biol. Chem. 2014, 289, 5828-5845
-
(2014)
J. Biol. Chem.
, vol.289
, pp. 5828-5845
-
-
Shore, D.M.1
Baillie, G.L.2
Hurst, D.H.3
-
18
-
-
0036490942
-
Allosteric binding sites on cell-surface receptors: Novel targets for drug discovery
-
Christopoulos, A. Allosteric binding sites on cell-surface receptors: novel targets for drug discovery Nat. Rev. Drug Discovery 2002, 1, 198-210
-
(2002)
Nat. Rev. Drug Discovery
, vol.1
, pp. 198-210
-
-
Christopoulos, A.1
-
19
-
-
53449093828
-
G-protein-coupled receptors: From classical modes of modulation to allosteric mechanisms
-
Bridges, T. M.; Lindsley, C. W. G-protein-coupled receptors: from classical modes of modulation to allosteric mechanisms ACS Chem. Biol. 2008, 3, 530-541
-
(2008)
ACS Chem. Biol.
, vol.3
, pp. 530-541
-
-
Bridges, T.M.1
Lindsley, C.W.2
-
20
-
-
67650648706
-
Positive allosteric modulation of the human cannabinoid (CB) receptor by RTI-371, a selective inhibitor of the dopamine transporter
-
Navarro, H. A.; Howard, J. L.; Pollard, G. T.; Carroll, F. I. Positive allosteric modulation of the human cannabinoid (CB) receptor by RTI-371, a selective inhibitor of the dopamine transporter Br. J. Pharmacol. 2009, 156, 1178-1184
-
(2009)
Br. J. Pharmacol.
, vol.156
, pp. 1178-1184
-
-
Navarro, H.A.1
Howard, J.L.2
Pollard, G.T.3
Carroll, F.I.4
-
21
-
-
84871380135
-
Anti-inflammatory lipoxin A4 is an endogenous allosteric enhancer of CB1 cannabinoid receptor
-
Pamplona, F. A.; Ferreira, J.; Menezes de Lima, O., Jr.; Duarte, F. S.; Bento, A. F.; Forner, S.; Villarinho, J. G.; Bellocchio, L.; Wotjak, C. T.; Lerner, R.; Monory, K.; Lutz, B.; Canetti, C.; Matias, I.; Calixto, J. B.; Marsicano, G.; Guimaraes, M. Z.; Takahashi, R. N. Anti-inflammatory lipoxin A4 is an endogenous allosteric enhancer of CB1 cannabinoid receptor Proc. Natl. Acad. Sci. U.S.A. 2012, 109, 21134-21139
-
(2012)
Proc. Natl. Acad. Sci. U.S.A.
, vol.109
, pp. 21134-21139
-
-
Pamplona, F.A.1
Ferreira, J.2
Menezes De Lima, O.3
Duarte, F.S.4
Bento, A.F.5
Forner, S.6
Villarinho, J.G.7
Bellocchio, L.8
Wotjak, C.T.9
Lerner, R.10
Monory, K.11
Lutz, B.12
Canetti, C.13
Matias, I.14
Calixto, J.B.15
Marsicano, G.16
Guimaraes, M.Z.17
Takahashi, R.N.18
-
22
-
-
84868237301
-
Identification and quantification of a new family of peptide endocannabinoids (Pepcans) showing negative allosteric modulation at CB1 receptors
-
Bauer, M.; Chicca, A.; Tamborrini, M.; Eisen, D.; Lerner, R.; Lutz, B.; Poetz, O.; Pluschke, G.; Gertsch, J. Identification and quantification of a new family of peptide endocannabinoids (Pepcans) showing negative allosteric modulation at CB1 receptors J. Biol. Chem. 2012, 287, 36944-36967
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 36944-36967
-
-
Bauer, M.1
Chicca, A.2
Tamborrini, M.3
Eisen, D.4
Lerner, R.5
Lutz, B.6
Poetz, O.7
Pluschke, G.8
Gertsch, J.9
-
23
-
-
24044539957
-
Allosteric modulation of the cannabinoid CB1 receptor
-
Price, M. R.; Baillie, G. L.; Thomas, A.; Stevenson, L. A.; Easson, M.; Goodwin, R.; McLean, A.; McIntosh, L.; Goodwin, G.; Walker, G.; Westwood, P.; Marrs, J.; Thomson, F.; Cowley, P.; Christopoulos, A.; Pertwee, R. G.; Ross, R. A. Allosteric modulation of the cannabinoid CB1 receptor Mol. Pharmacol. 2005, 68, 1484-1495
-
(2005)
Mol. Pharmacol.
, vol.68
, pp. 1484-1495
-
-
Price, M.R.1
Baillie, G.L.2
Thomas, A.3
Stevenson, L.A.4
Easson, M.5
Goodwin, R.6
McLean, A.7
McIntosh, L.8
Goodwin, G.9
Walker, G.10
Westwood, P.11
Marrs, J.12
Thomson, F.13
Cowley, P.14
Christopoulos, A.15
Pertwee, R.G.16
Ross, R.A.17
-
24
-
-
35648985647
-
PSNCBAM-1, a novel allosteric antagonist at cannabinoid CB1 receptors with hypophagic effects in rats
-
Horswill, J. G.; Bali, U.; Shaaban, S.; Keily, J. F.; Jeevaratnam, P.; Babbs, A. J.; Reynet, C.; Wong Kai In, P. PSNCBAM-1, a novel allosteric antagonist at cannabinoid CB1 receptors with hypophagic effects in rats Br. J. Pharmacol. 2007, 152, 805-814
-
(2007)
Br. J. Pharmacol.
, vol.152
, pp. 805-814
-
-
Horswill, J.G.1
Bali, U.2
Shaaban, S.3
Keily, J.F.4
Jeevaratnam, P.5
Babbs, A.J.6
Reynet, C.7
Wong Kai In, P.8
-
25
-
-
35648962852
-
Allosterism and cannabinoid CB(1) receptors: The shape of things to come
-
Ross, R. A. Allosterism and cannabinoid CB(1) receptors: the shape of things to come Trends Pharmacol. Sci. 2007, 28, 567-572
-
(2007)
Trends Pharmacol. Sci.
, vol.28
, pp. 567-572
-
-
Ross, R.A.1
-
26
-
-
35648987701
-
Tuning the endocannabinoid system: Allosteric modulators of the CB1 receptor
-
Ross, R. A. Tuning the endocannabinoid system: allosteric modulators of the CB1 receptor Br. J. Pharmacol. 2007, 152, 565-566
-
(2007)
Br. J. Pharmacol.
, vol.152
, pp. 565-566
-
-
Ross, R.A.1
-
27
-
-
84859479825
-
Allosteric modulator ORG27569 induces CB1 cannabinoid receptor high affinity agonist binding state, receptor internalization, and Gi protein-independent ERK1/2 kinase activation
-
Ahn, K. H.; Mahmoud, M. M.; Kendall, D. A. Allosteric modulator ORG27569 induces CB1 cannabinoid receptor high affinity agonist binding state, receptor internalization, and Gi protein-independent ERK1/2 kinase activation J. Biol. Chem. 2012, 287, 12070-12082
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 12070-12082
-
-
Ahn, K.H.1
Mahmoud, M.M.2
Kendall, D.A.3
-
28
-
-
84874117655
-
Profiling two indole-2-carboxamides for allosteric modulation of the CB1 receptor
-
Ahn, K. H.; Mahmoud, M. M.; Samala, S.; Lu, D.; Kendall, D. A. Profiling two indole-2-carboxamides for allosteric modulation of the CB1 receptor J. Neurochem. 2013, 124, 584-589
-
(2013)
J. Neurochem.
, vol.124
, pp. 584-589
-
-
Ahn, K.H.1
Mahmoud, M.M.2
Samala, S.3
Lu, D.4
Kendall, D.A.5
-
29
-
-
79953007668
-
Effects of the allosteric antagonist 1-(4-chlorophenyl)-3-[3-(6-pyrrolidin-1-ylpyridin-2-yl)phenyl]urea (PSNCBAM-1) on CB1 receptor modulation in the cerebellum
-
Wang, X.; Horswill, J. G.; Whalley, B. J.; Stephens, G. J. Effects of the allosteric antagonist 1-(4-chlorophenyl)-3-[3-(6-pyrrolidin-1-ylpyridin-2-yl)phenyl]urea (PSNCBAM-1) on CB1 receptor modulation in the cerebellum Mol. Pharmacol. 2011, 79, 758-767
-
(2011)
Mol. Pharmacol.
, vol.79
, pp. 758-767
-
-
Wang, X.1
Horswill, J.G.2
Whalley, B.J.3
Stephens, G.J.4
-
30
-
-
84872716271
-
CB(1) receptor allosteric modulators display both agonist and signaling pathway specificity
-
Baillie, G. L.; Horswill, J. G.; Anavi-Goffer, S.; Reggio, P. H.; Bolognini, D.; Abood, M. E.; McAllister, S.; Strange, P. G.; Stephens, G. J.; Pertwee, R. G.; Ross, R. A. CB(1) receptor allosteric modulators display both agonist and signaling pathway specificity Mol. Pharmacol. 2013, 83, 322-338
-
(2013)
Mol. Pharmacol.
, vol.83
, pp. 322-338
-
-
Baillie, G.L.1
Horswill, J.G.2
Anavi-Goffer, S.3
Reggio, P.H.4
Bolognini, D.5
Abood, M.E.6
McAllister, S.7
Strange, P.G.8
Stephens, G.J.9
Pertwee, R.G.10
Ross, R.A.11
-
31
-
-
84866952392
-
A key agonist-induced conformational change in the cannabinoid receptor CB1 is blocked by the allosteric ligand Org 27569
-
Fay, J. F.; Farrens, D. L. A key agonist-induced conformational change in the cannabinoid receptor CB1 is blocked by the allosteric ligand Org 27569 J. Biol. Chem. 2012, 287, 33873-33882
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 33873-33882
-
-
Fay, J.F.1
Farrens, D.L.2
-
32
-
-
84862272370
-
Indole-2-carboxamides as allosteric modulators of the cannabinoid CB(1) receptor
-
Piscitelli, F.; Ligresti, A.; La Regina, G.; Coluccia, A.; Morera, L.; Allara, M.; Novellino, E.; Di Marzo, V.; Silvestri, R. Indole-2-carboxamides as allosteric modulators of the cannabinoid CB(1) receptor J. Med. Chem. 2012, 55, 5627-5631
-
(2012)
J. Med. Chem.
, vol.55
, pp. 5627-5631
-
-
Piscitelli, F.1
Ligresti, A.2
La Regina, G.3
Coluccia, A.4
Morera, L.5
Allara, M.6
Novellino, E.7
Di Marzo, V.8
Silvestri, R.9
-
33
-
-
84886571455
-
Structure-activity relationship study of indole-2-carboxamides identifies a potent allosteric modulator for the cannabinoid receptor 1 (CB1)
-
Mahmoud, M. M.; Ali, H. I.; Ahn, K. H.; Damaraju, A.; Samala, S.; Pulipati, V. K.; Kolluru, S.; Kendall, D. A.; Lu, D. Structure-activity relationship study of indole-2-carboxamides identifies a potent allosteric modulator for the cannabinoid receptor 1 (CB1) J. Med. Chem. 2013, 56, 7965-7975
-
(2013)
J. Med. Chem.
, vol.56
, pp. 7965-7975
-
-
Mahmoud, M.M.1
Ali, H.I.2
Ahn, K.H.3
Damaraju, A.4
Samala, S.5
Pulipati, V.K.6
Kolluru, S.7
Kendall, D.A.8
Lu, D.9
-
34
-
-
84898460777
-
Optimization of chemical functionalities of indole-2-carboxamides to improve allosteric parameters for the cannabinoid receptor 1 (CB1)
-
Khurana, L.; Ali, H. I.; Olszewska, T.; Ahn, K. H.; Damaraju, A.; Kendall, D. A.; Lu, D. Optimization of chemical functionalities of indole-2-carboxamides to improve allosteric parameters for the cannabinoid receptor 1 (CB1) J. Med. Chem. 2014, 57, 3040-3052
-
(2014)
J. Med. Chem.
, vol.57
, pp. 3040-3052
-
-
Khurana, L.1
Ali, H.I.2
Olszewska, T.3
Ahn, K.H.4
Damaraju, A.5
Kendall, D.A.6
Lu, D.7
-
35
-
-
57549086217
-
Indole synthesis via rhodium catalyzed oxidative coupling of acetanilides and internal alkynes
-
Stuart, D. R.; Bertrand-Laperle, M.; Burgess, K. M.; Fagnou, K. Indole synthesis via rhodium catalyzed oxidative coupling of acetanilides and internal alkynes J. Am. Chem. Soc. 2008, 130, 16474-16475
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 16474-16475
-
-
Stuart, D.R.1
Bertrand-Laperle, M.2
Burgess, K.M.3
Fagnou, K.4
-
36
-
-
84884214425
-
Substituted tetrahydroisoquinolines as selective antagonists for the orexin 1 receptor
-
Perrey, D. A.; German, N. A.; Gilmour, B. P.; Li, J. X.; Harris, D. L.; Thomas, B. F.; Zhang, Y. Substituted tetrahydroisoquinolines as selective antagonists for the orexin 1 receptor J. Med. Chem. 2013, 56, 6901-6916
-
(2013)
J. Med. Chem.
, vol.56
, pp. 6901-6916
-
-
Perrey, D.A.1
German, N.A.2
Gilmour, B.P.3
Li, J.X.4
Harris, D.L.5
Thomas, B.F.6
Zhang, Y.7
-
37
-
-
0033603507
-
Studies on the mechanism of action of 2-formyl-4-pyrrolidinopyridine: Isolation and characterization of a reactive intermediate
-
Sammakia, T.; Hurley, T. B. Studies on the mechanism of action of 2-formyl-4-pyrrolidinopyridine: isolation and characterization of a reactive intermediate J. Org. Chem. 1999, 64, 4652-4664
-
(1999)
J. Org. Chem.
, vol.64
, pp. 4652-4664
-
-
Sammakia, T.1
Hurley, T.B.2
-
38
-
-
64049108084
-
Synthesis and structure-activity relationships of amide derivatives of (4,4-difluoro-1,2,3,4-tetrahydro-5 H -1-benzazepin-5-ylidene)acetic acid as selective arginine vasopressin V2 receptor agonists
-
Tsukamoto, I.; Koshio, H.; Kuramochi, T.; Saitoh, C.; Yanai-Inamura, H.; Kitada-Nozawa, C.; Yamamoto, E.; Yatsu, T.; Shimada, Y.; Sakamoto, S.; Tsukamoto, S. Synthesis and structure-activity relationships of amide derivatives of (4,4-difluoro-1,2,3,4-tetrahydro-5 H -1-benzazepin-5-ylidene)acetic acid as selective arginine vasopressin V2 receptor agonists Bioorg. Med. Chem. 2009, 17, 3130-3141
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 3130-3141
-
-
Tsukamoto, I.1
Koshio, H.2
Kuramochi, T.3
Saitoh, C.4
Yanai-Inamura, H.5
Kitada-Nozawa, C.6
Yamamoto, E.7
Yatsu, T.8
Shimada, Y.9
Sakamoto, S.10
Tsukamoto, S.11
-
39
-
-
1842452582
-
A modular synthesis of the lamellarins: Total synthesis of lamellarin G trimethyl ether
-
Handy, S. T.; Zhang, Y.; Bregman, H. A modular synthesis of the lamellarins: total synthesis of lamellarin G trimethyl ether J. Org. Chem. 2004, 69, 2362-2366
-
(2004)
J. Org. Chem.
, vol.69
, pp. 2362-2366
-
-
Handy, S.T.1
Zhang, Y.2
Bregman, H.3
-
40
-
-
27344434132
-
Approaches to the synthesis of the lamellarins and related natural products. A review
-
Handy, S. T.; Zhang, Y. N. Approaches to the synthesis of the lamellarins and related natural products. A review Org. Prep. Proced. Int. 2005, 37, 411-445
-
(2005)
Org. Prep. Proced. Int.
, vol.37
, pp. 411-445
-
-
Handy, S.T.1
Zhang, Y.N.2
-
41
-
-
77957908601
-
Synthesis and biological evaluation of bivalent ligands for the cannabinoid 1 receptor
-
Zhang, Y.; Gilliam, A.; Maitra, R.; Damaj, M. I.; Tajuba, J. M.; Seltzman, H. H.; Thomas, B. F. Synthesis and biological evaluation of bivalent ligands for the cannabinoid 1 receptor J. Med. Chem. 2010, 53, 7048-7060
-
(2010)
J. Med. Chem.
, vol.53
, pp. 7048-7060
-
-
Zhang, Y.1
Gilliam, A.2
Maitra, R.3
Damaj, M.I.4
Tajuba, J.M.5
Seltzman, H.H.6
Thomas, B.F.7
-
42
-
-
84870037980
-
Diphenyl purine derivatives as peripherally selective cannabinoid receptor 1 antagonists
-
Fulp, A.; Bortoff, K.; Zhang, Y.; Seltzman, H.; Mathews, J.; Snyder, R.; Fennell, T.; Maitra, R. Diphenyl purine derivatives as peripherally selective cannabinoid receptor 1 antagonists J. Med. Chem. 2012, 55, 10022-10032
-
(2012)
J. Med. Chem.
, vol.55
, pp. 10022-10032
-
-
Fulp, A.1
Bortoff, K.2
Zhang, Y.3
Seltzman, H.4
Mathews, J.5
Snyder, R.6
Fennell, T.7
Maitra, R.8
-
43
-
-
84863358433
-
Design and synthesis of cannabinoid receptor 1 antagonists for peripheral selectivity
-
Fulp, A.; Bortoff, K.; Seltzman, H.; Zhang, Y.; Mathews, J.; Snyder, R.; Fennell, T.; Maitra, R. Design and synthesis of cannabinoid receptor 1 antagonists for peripheral selectivity J. Med. Chem. 2012, 55, 2820-2834
-
(2012)
J. Med. Chem.
, vol.55
, pp. 2820-2834
-
-
Fulp, A.1
Bortoff, K.2
Seltzman, H.3
Zhang, Y.4
Mathews, J.5
Snyder, R.6
Fennell, T.7
Maitra, R.8
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