-
1
-
-
0037040395
-
The TRP channels, a remarkably functional family
-
MONTELL C, BIMBAUMER L, FLOCKERZI V: The TRP channels, a remarkably functional family. Cell (2002) 108:595-598.
-
(2002)
Cell
, vol.108
, pp. 595-598
-
-
Montell, C.1
Bimbaumer, L.2
Flockerzi, V.3
-
3
-
-
0030777012
-
The capsaicin receptor: A heat-activated ion channel in the pain pathway
-
CATERINA MJ, SCHUMACHER MA, TOMINAGA M et al.: The capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature (1997) 398:816-824.
-
(1997)
Nature
, vol.398
, pp. 816-824
-
-
Caterina, M.J.1
Schumacher, M.A.2
Tominaga, M.3
-
4
-
-
18244402941
-
A unified nomenclature for the superfamily of TRP cation channels
-
MONTELL C, BIRNBAUMER L, FLOCKERZI V et al.: A unified nomenclature for the superfamily of TRP cation channels. Mol. Cell (2002) 9:229-231.
-
(2002)
Mol. Cell
, vol.9
, pp. 229-231
-
-
Montell, C.1
Birnbaumer, L.2
Flockerzi, V.3
-
5
-
-
0037077041
-
A heat-sensitive TRP channel expressed in keratinocytes
-
PEIER AM, REEVE AJ, ANDERSSON DA et al.: A heat-sensitive TRP channel expressed in keratinocytes. Science (2002) 296:2046-2049.
-
(2002)
Science
, vol.296
, pp. 2046-2049
-
-
Peier, A.M.1
Reeve, A.J.2
Andersson, D.A.3
-
6
-
-
18444408683
-
TRPV3 is a temperature-sensitive vanilloid receptor-like protein
-
SMITH GD, GUNTHORPE MJ, KELSELL RE et al.: TRPV3 is a temperature-sensitive vanilloid receptor-like protein. Nature (2002) 418:186-190.
-
(2002)
Nature
, vol.418
, pp. 186-190
-
-
Smith, G.D.1
Gunthorpe, M.J.2
Kelsell, R.E.3
-
7
-
-
0037062915
-
TRPV3 is a calcium-permeable temperature-sensitive cation channel
-
XU H, RAMSEY IS, KOTECHA SA et al.: TRPV3 is a calcium-permeable temperature-sensitive cation channel. Nature (2002) 418:181-186.
-
(2002)
Nature
, vol.418
, pp. 181-186
-
-
Xu, H.1
Ramsey, I.S.2
Kotecha, S.A.3
-
8
-
-
0032721391
-
Novel natural vanilloid receptor agonists: New therapeutic targets for drug development
-
STERNER O, SZALLASI A: Novel natural vanilloid receptor agonists: new therapeutic targets for drug development. Trends Pharmacol. Sci.(1999) 20:431-439.
-
(1999)
Trends Pharmacol. Sci.
, vol.20
, pp. 431-439
-
-
Sterner, O.1
Szallasi, A.2
-
10
-
-
0036303675
-
Vanilloid (capsaicin) receptors in health and disease
-
SZALLASI A: Vanilloid (capsaicin) receptors in health and disease. Am. J. Clin. Pathol. (2002) 118:110-121.
-
(2002)
Am. J. Clin. Pathol.
, vol.118
, pp. 110-121
-
-
Szallasi, A.1
-
11
-
-
0032970173
-
Vanilloid (capsaicin) receptors and mechanisms
-
SZALLASI A, BLUMBERG PM: Vanilloid (capsaicin) receptors and mechanisms. Pharmacol. Rev. (1999) 51:159-211.
-
(1999)
Pharmacol. Rev.
, vol.51
, pp. 159-211
-
-
Szallasi, A.1
Blumberg, P.M.2
-
12
-
-
0037062411
-
An endogenous capsaicin-like substance with high potency at recombinant and native vanilloid VR1 receptors
-
HUANG SM, BISOGNO T, TREVISANI M et al.: An endogenous capsaicin-like substance with high potency at recombinant and native vanilloid VR1 receptors. Proc. Natl. Acad. Sci. USA (2002) 99:8400-8405.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 8400-8405
-
-
Huang, S.M.1
Bisogno, T.2
Trevisani, M.3
-
13
-
-
0038190980
-
N-Oleolydopamine, a novel endogenous capsaicin-like lipid that produces hyperalgesia
-
CHU CJ, HUANG SM, DE PETROCELLIS L et al.: N-Oleolydopamine, a novel endogenous capsaicin-like lipid that produces hyperalgesia. J. Biol. Chem. (2003) 278:13633-13639.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 13633-13639
-
-
Chu, C.J.1
Huang, S.M.2
De Petrocellis, L.3
-
14
-
-
0037799198
-
2 binding site as a determinant of capsaicin receptor sensitivity
-
2 binding site as a determinant of capsaicin receptor sensitivity. Science (2003) 300:1284-1288.
-
(2003)
Science
, vol.300
, pp. 1284-1288
-
-
Prescott, E.D.1
Julius, D.2
-
15
-
-
0034862596
-
Vanilloid receptor ligands. Hopes and realities for the future
-
SZALLASI A: Vanilloid receptor ligands. Hopes and realities for the future. Drugs Aging (2001) 18:561-573.
-
(2001)
Drugs Aging
, vol.18
, pp. 561-573
-
-
Szallasi, A.1
-
16
-
-
0037341020
-
Compounds acting at the endocannabinoid and/or endovanilloid systems reduce hyperkinesia in a rat model of Huntington's disease
-
LASTRES-BECKER I, DE MIGUEL R, DE PETROCELLIS L et al.: Compounds acting at the endocannabinoid and/or endovanilloid systems reduce hyperkinesia in a rat model of Huntington's disease. J. Neurochem. (2003) 84:1097-1109.
-
(2003)
J. Neurochem.
, vol.84
, pp. 1097-1109
-
-
Lastres-Becker, I.1
De Miguel, R.2
De Petrocellis, L.3
-
17
-
-
0038609734
-
Structural determinant of TRPV1 desensitization interacts with calmodulin
-
NUMAZAKI M, TOMINAGA T, KUMIKO T et al.: Structural determinant of TRPV1 desensitization interacts with calmodulin. Proc. Natl. Acad. Sci USA (2003) 100:8002-8006.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 8002-8006
-
-
Numazaki, M.1
Tominaga, T.2
Kumiko, T.3
-
18
-
-
0000713128
-
After a decade of intravescical vanilloid therapy: Still more questions than answers
-
SZALLASI A: After a decade of intravescical vanilloid therapy: still more questions than answers. Lancet Neurobiol. (2002) 1:167-172.
-
(2002)
Lancet Neurobiol.
, vol.1
, pp. 167-172
-
-
Szallasi, A.1
-
19
-
-
0030265431
-
The role of capsaicin-sensitive C-fiber afferent nerves in the cough reflex
-
KARLSSON JA: The role of capsaicin-sensitive C-fiber afferent nerves in the cough reflex. Pulm. Pharmacol. (1996) 9:315-321.
-
(1996)
Pulm. Pharmacol.
, vol.9
, pp. 315-321
-
-
Karlsson, J.A.1
-
20
-
-
0037348385
-
Metabolism of capsaicin by cytochrome P450 produces novel dehydrogenated metabolites and decreases cytotoxicity to lung and liver cells
-
REILLY CA, EHLHARDT WJ, JACKSON DA et al.: Metabolism of capsaicin by cytochrome P450 produces novel dehydrogenated metabolites and decreases cytotoxicity to lung and liver cells. Chem. Res. Toxicol. (2003) 16:336-349.
-
(2003)
Chem. Res. Toxicol.
, vol.16
, pp. 336-349
-
-
Reilly, C.A.1
Ehlhardt, W.J.2
Jackson, D.A.3
-
21
-
-
0043267987
-
Anandamide and arachidonic acid use epoxyeicosatrienoic acids to activate TRPV4 channels
-
WATANABE H, VRIENS J, PRENEN J et al.: Anandamide and arachidonic acid use epoxyeicosatrienoic acids to activate TRPV4 channels. Nature (2003) 424:438-441.
-
(2003)
Nature
, vol.424
, pp. 438-441
-
-
Watanabe, H.1
Vriens, J.2
Prenen, J.3
-
22
-
-
0037134482
-
Activation of TRPV4 channels (hVRL-2/mTRP12) by phorbol derivatives
-
WATANABE H, DAVIS JB, DARREN S et al.: Activation of TRPV4 channels (hVRL-2/mTRP12) by phorbol derivatives. J. Biol. Chem. (2002) 277:13569-13577.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 13569-13577
-
-
Watanabe, H.1
Davis, J.B.2
Darren, S.3
-
23
-
-
0035076126
-
Pharmacological differences between the human and the rat vanilloid receptor 1 (VR1)
-
MCINTYRE P, MCLATCHIE LM, CHAMBERS A et al.: Pharmacological differences between the human and the rat vanilloid receptor 1 (VR1). Br. J. Pharmacol. (2001) 132:1084-1094.
-
(2001)
Br. J. Pharmacol.
, vol.132
, pp. 1084-1094
-
-
Mcintyre, P.1
Mclatchie, L.M.2
Chambers, A.3
-
24
-
-
0036183319
-
Molecular basis for species-specific sensitivity to 'hot' chili pepper
-
JORDT SE, JULIUS D: Molecular basis for species-specific sensitivity to 'hot' chili pepper. Cell (2002) 108:421-430.
-
(2002)
Cell
, vol.108
, pp. 421-430
-
-
Jordt, S.E.1
Julius, D.2
-
25
-
-
0036711213
-
Cloning and functional characterization of the guinea-pig vanilloid receptor 1
-
SAVIDGE J, DAVIS C, SHAH K et al.: Cloning and functional characterization of the guinea-pig vanilloid receptor 1. Neuropharmacology (2002) 43:450-456.
-
(2002)
Neuropharmacology
, vol.43
, pp. 450-456
-
-
Savidge, J.1
Davis, C.2
Shah, K.3
-
26
-
-
0034815843
-
Capsaicin-like anti-obese activities of evodiamine from fruits Evodia rutaecarpa, a vanilloid receptor antagonist
-
KOBAYASHI Y, NAKANO Y, KIZAKI M et al.: Capsaicin-like anti-obese activities of evodiamine from fruits Evodia rutaecarpa, a vanilloid receptor antagonist. Planta Med. (2001) 67:628-633.
-
(2001)
Planta Med.
, vol.67
, pp. 628-633
-
-
Kobayashi, Y.1
Nakano, Y.2
Kizaki, M.3
-
27
-
-
0034751335
-
Molecular targets for cannabidiol and its synthetic analogues: Effects on vanilloid VR1 receptors and on cellular uptake and enzymatic hydrolysis of anandamide
-
BISOGNO T, HANUS L, DE PETROCELLIS L et al.: Molecular targets for cannabidiol and its synthetic analogues: effects on vanilloid VR1 receptors and on cellular uptake and enzymatic hydrolysis of anandamide. Br. J. Pharmacol (2001) 134:845-852.
-
(2001)
Br. J. Pharmacol.
, vol.134
, pp. 845-852
-
-
Bisogno, T.1
Hanus, L.2
De Petrocellis, L.3
-
28
-
-
0242367472
-
Activation of vanilloid receptor 1 (VR1) by eugenol
-
YANG BH, PIAO ZG, KIM YB et al.: Activation of vanilloid receptor 1 (VR1) by eugenol. J. Dent. Res. (2003) 82:781-785.
-
(2003)
J. Dent. Res.
, vol.82
, pp. 781-785
-
-
Yang, B.H.1
Piao, Z.G.2
Kim, Y.B.3
-
29
-
-
0036294731
-
Thapsigargicin binds to and inhibits the cloned vanilloid receptor-1
-
TOT A, KEDEI N, SZABO T et al.: Thapsigargicin binds to and inhibits the cloned vanilloid receptor-1. Biochem. Biophysi. Res. Commum. (2002) 293:777-782.
-
(2002)
Biochem. Biophysi. Res. Commum.
, vol.293
, pp. 777-782
-
-
Tot, A.1
Kedei, N.2
Szabo, T.3
-
30
-
-
0037410253
-
TRPV1 activation and induction of nociceptive response by a non-pungent capsaicin-like compound, capsiate
-
IIDA T, MORIYAMA T, KOBATA K et al.: TRPV1 activation and induction of nociceptive response by a non-pungent capsaicin-like compound, capsiate. Neuropharmacology (2003) 44:958-967.
-
(2003)
Neuropharmacology
, vol.44
, pp. 958-967
-
-
Iida, T.1
Moriyama, T.2
Kobata, K.3
-
31
-
-
0037222887
-
Non-pungent capsacinoids from sweet pepper. Synthesis and evaluation of the chemopreventive and anticancer potential
-
MACHO A, LUCENA C, SANCHO R et al.: Non-pungent capsacinoids from sweet pepper. Synthesis and evaluation of the chemopreventive and anticancer potential. Eur. J. Nutr. (2003) 42:2-9.
-
(2003)
Eur. J. Nutr.
, vol.42
, pp. 2-9
-
-
Macho, A.1
Lucena, C.2
Sancho, R.3
-
32
-
-
0035850979
-
Propofol activates vanilloid receptor channels expressed in human embryonic kidney-293 cells
-
TSUTUMI S, TOMIOKA A. SUDO M et al.: Propofol activates vanilloid receptor channels expressed in human embryonic kidney-293 cells. Nerosci. Lett. (2001) 312:45-49.
-
(2001)
Nerosci. Lett.
, vol.312
, pp. 45-49
-
-
Tsutumi, S.1
Tomioka, A.2
Sudo, M.3
-
33
-
-
0037103229
-
N-Acylvanillamides: Development of an expeditious synthesis and discovery of new acyl templates for powerful activation of the vanilloid receptor
-
APPENDINO G, MINASSI A, SCHIANO MORELLO A et al.: N-Acylvanillamides: development of an expeditious synthesis and discovery of new acyl templates for powerful activation of the vanilloid receptor. J. Med. Chem. (2002) 45:3739-3745.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3739-3745
-
-
Appendino, G.1
Minassi, A.2
Schiano Morello, A.3
-
34
-
-
0034672692
-
In vivo pharmacology of SDZ-249665, a novel, non-pungent capsaicin analogue
-
URBAN L, CAMPBELL EA, PANESAR M et al.: In vivo pharmacology of SDZ-249665, a novel, non-pungent capsaicin analogue. Pain (2000) 89:65-74.
-
(2000)
Pain
, vol.89
, pp. 65-74
-
-
Urban, L.1
Campbell, E.A.2
Panesar, M.3
-
35
-
-
0034640192
-
The anandamide transport inhibitor AM-404 activates vanilloid receptors
-
ZYGMUNT PM, CHUANG H, MOVAHED P et al.: The anandamide transport inhibitor AM-404 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.2
Movahed, P.3
-
36
-
-
0037111326
-
A role for endocannabinoids in indomethacin-induced spinal antinociception
-
GUHRING H, HAMZA M, SERGEJEVA M et al.: A role for endocannabinoids in indomethacin-induced spinal antinociception. Eur. J. Pharmacol. (2002) 454:153-163.
-
(2002)
Eur. J. Pharmacol.
, vol.454
, pp. 153-163
-
-
Guhring, H.1
Hamza, M.2
Sergejeva, M.3
-
37
-
-
0037308120
-
Endocannabinoids induce ileitis in rats via the capsaicin receptor (VR1)
-
MCVEY DC, SCHMID PC, SCHMID HHO et al.: Endocannabinoids induce ileitis in rats via the capsaicin receptor (VR1). J. Pharmacol. Exp. Ther. (2003) 304:713-722.
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.304
, pp. 713-722
-
-
Mcvey, D.C.1
Schmid, P.C.2
Schmid, H.H.O.3
-
38
-
-
0034505125
-
DA-5018 (Capsavanil, KR-25018)
-
PARK NS, SEONG CM, JUNG YS et al.: DA-5018 (Capsavanil, KR-25018). Drugs Fut. (2000) 25:1131-1137.
-
(2000)
Drugs Fut.
, vol.25
, pp. 1131-1137
-
-
Park, N.S.1
Seong, C.M.2
Jung, Y.S.3
-
40
-
-
0024382437
-
Resiniferatoxin, a phorbol-related diterpene, acts as an ultrapotent analogue of capsaicin, the irritant constituent in red pepper
-
SZALLASI A, BLUMBERG PM: Resiniferatoxin, a phorbol-related diterpene, acts as an ultrapotent analogue of capsaicin, the irritant constituent in red pepper. Neuroscience (1989) 30:515-520.
-
(1989)
Neuroscience
, vol.30
, pp. 515-520
-
-
Szallasi, A.1
Blumberg, P.M.2
-
41
-
-
0033581625
-
3-Acyloxy-2-phenalkylpropyl amides and esters of homovanillic acid as novel vanilloid receptor agonists
-
LEE J, PARK SU, KIM JY et al.: 3-Acyloxy-2-phenalkylpropyl amides and esters of homovanillic acid as novel vanilloid receptor agonists. Bioorg. Med. Chem. Lett. (1999) 9:2909-2914.
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 2909-2914
-
-
Lee, J.1
Park, S.U.2
Kim, J.Y.3
-
42
-
-
0036166972
-
Phenolic modification as an approach to improve the pharmacology of the 3-acyloxy-2-benzylpropyl homovanillic amides and thioureas, a promising class of vanilloid receptor agonists and analgesics
-
LEE J, LEE J, KANG MS et al.: Phenolic modification as an approach to improve the pharmacology of the 3-acyloxy-2-benzylpropyl homovanillic amides and thioureas, a promising class of vanilloid receptor agonists and analgesics. Bioorg. Med. Chem. (2002) 10:1171-1179.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 1171-1179
-
-
Lee, J.1
Lee, J.2
Kang, M.S.3
-
43
-
-
0035192117
-
N-(3-Acyloxy-2-benzylpropyl)-N′-(4-hydroxy-3-methoxybenzyl)thiourea derivatives as potent vanilloid receptor agonists and analgesics
-
LEE J, LEE J, KIM J et al.: N-(3-Acyloxy-2-benzylpropyl)-N′-(4-hydroxy-3-methoxybenzyl)thiourea derivatives as potent vanilloid receptor agonists and analgesics. Bioorg. Med. Chem. (2001) 9:19-22.
-
(2001)
Bioorg. Med. Chem.
, vol.9
, pp. 19-22
-
-
Lee, J.1
Lee, J.2
Kim, J.3
-
44
-
-
0028021842
-
The discovery of capsazepine, the first competitive antagonist of the sensory neuron excitants capsaicin and resiniferatoxin
-
WALPOLE CSI, BEVAN S, BOVERMANN G et al.: The discovery of capsazepine, the first competitive antagonist of the sensory neuron excitants capsaicin and resiniferatoxin. J. Med. Chem. (1994) 37:1942-1954.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1942-1954
-
-
Walpole, C.S.I.1
Bevan, S.2
Bovermann, G.3
-
45
-
-
0035173995
-
Iodo-resiniferatoxin, a new potent vanilloid receptor antagonist
-
WAHL P, FOGED C, TULLIN S et al.: Iodo-resiniferatoxin, a new potent vanilloid receptor antagonist. Mol. Pharmacol. (2001) 59:9-15.
-
(2001)
Mol. Pharmacol.
, vol.59
, pp. 9-15
-
-
Wahl, P.1
Foged, C.2
Tullin, S.3
-
46
-
-
0037156355
-
Synthesis and in vitro evaluation of a novel iodinated resiniferatoxin derivative that is an agonist at the human vanilloid VR1 receptor
-
MCDONNEL ME, ZHANG SP, DUBIN AE et al.: Synthesis and in vitro evaluation of a novel iodinated resiniferatoxin derivative that is an agonist at the human vanilloid VR1 receptor. Bioorg. Med. Chem. Lett. (2002) 12:1189-1192.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1189-1192
-
-
Mcdonnel, M.E.1
Zhang, S.P.2
Dubin, A.E.3
-
47
-
-
10744226892
-
Halogenation of a capsaicin analogue leads to novel vanilloid TRPV1 receptor antagonists
-
APPENDINO G, HARRISON S, DE PETROCELLIS L et al.: Halogenation of a capsaicin analogue leads to novel vanilloid TRPV1 receptor antagonists. Br. J. Pharmacol (2003) 139:1417-1424.
-
(2003)
Br. J. Pharmacol
, vol.139
, pp. 1417-1424
-
-
Appendino, G.1
Harrison, S.2
De Petrocellis, L.3
-
48
-
-
0036894895
-
Functional properties of the high-affinity TRPV1 (VR1) vanilloid receptor antagonist (4-hydroxy-5-iodo-3-methoxyphenylacetate ester) iodoresiniferatoxin
-
SEABROOK GR, SUTTON KG, JAROLIMEK W et al.: Functional properties of the high-affinity TRPV1 (VR1) vanilloid receptor antagonist (4-hydroxy-5-iodo-3-methoxyphenylacetate ester) iodoresiniferatoxin. J. Pharmacol. Exper. Therap. (2002) 303:1052-1060.
-
(2002)
J. Pharmacol. Exper. Therap.
, vol.303
, pp. 1052-1060
-
-
Seabrook, G.R.1
Sutton, K.G.2
Jarolimek, W.3
-
49
-
-
0038460841
-
N-(Methylsulfonylamino)benzyl thiourea analogues: Novel potent and high affinity antagonists of vanilloid receptors
-
LEE J, LEE J, KANG M et al.: N-(Methylsulfonylamino)benzyl thiourea analogues: novel potent and high affinity antagonists of vanilloid receptors. J. Med. Chem. (2003) 46:3116-3126.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 3116-3126
-
-
Lee, J.1
Lee, J.2
Kang, M.3
-
50
-
-
0346445338
-
Identification of SB-366791, a potent and selective antagonist of vanilloid receptor-1
-
RAMI HK, DAVIDS JB, GUNTHORPE MJ et al.: Identification of SB-366791, a potent and selective antagonist of vanilloid receptor-1. Drugs Fut. (2002) 27(Suppl.A):411.
-
(2002)
Drugs Fut.
, vol.27
, Issue.SUPPL. A
, pp. 411
-
-
Rami, H.K.1
Davids, J.B.2
Gunthorpe, M.J.3
-
51
-
-
12444319246
-
Chain-branched acyclic phenethylthiocarbamates as vanilloid receptor antagonists
-
YOON JW, CHOI HY, LEE HJ et al.: Chain-branched acyclic phenethylthiocarbamates as vanilloid receptor antagonists. Bioorg. Med. Chem. Lett. (2003) 13:1549-1552.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1549-1552
-
-
Yoon, J.W.1
Choi, H.Y.2
Lee, H.J.3
-
52
-
-
0007899884
-
Inhibition of capsaicin-induced single channel currents by cocaine
-
LEE SH, PREMKUMAR LS: Inhibition of capsaicin-induced single channel currents by cocaine. Soc. Neurosci. Abstr. (1999) 25:2255.
-
(1999)
Soc. Neurosci. Abstr.
, vol.25
, pp. 2255
-
-
Lee, S.H.1
Premkumar, L.S.2
-
53
-
-
0343729529
-
Ginsenosides inhibit capsaicin channels in rat dorsal root ganglion neurons
-
HAHN JH: Ginsenosides inhibit capsaicin channels in rat dorsal root ganglion neurons. Neurosci. Lett. (2000) 287:45-48.
-
(2000)
Neurosci. Lett.
, vol.287
, pp. 45-48
-
-
Hahn, J.H.1
-
54
-
-
0345814093
-
Vanilloid receptor antagonists: Structure-activity relationships via parallel and targeted synthesis
-
DAX S, DUBIN A, JETTER M et al.: Vanilloid receptor antagonists: structure-activity relationships via parallel and targeted synthesis. Drugs Fut. (2002) 27(Suppl.A):93.
-
(2002)
Drugs Fut.
, vol.27
, Issue.SUPPL. A
, pp. 93
-
-
Dax, S.1
Dubin, A.2
Jetter, M.3
-
55
-
-
0037215646
-
The VR1 antagonist capsazepine reverses mechanical hyperalgesia in models of inflammatory and neuropathic pain
-
WALKER KM, URBAN L, MEDHURST SJ et al.: The VR1 antagonist capsazepine reverses mechanical hyperalgesia in models of inflammatory and neuropathic pain. J. Pharmacol Exp. Ther. (2003) 304:56-62.
-
(2003)
J. Pharmacol Exp. Ther.
, vol.304
, pp. 56-62
-
-
Walker, K.M.1
Urban, L.2
Medhurst, S.J.3
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