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Volumn 13, Issue 12, 2003, Pages 1825-1837

TRPV1 (vanilloid receptor, capsaicin receptor) agonists and antagonists

Author keywords

Analgesics; Capsaicin; Chronic pain; Transient receptor potential (TRP) channels; TRPV1; Vanilloid receptors

Indexed keywords

5 IODORESINFERATOXIN; ANANDAMIDE; ARVANIL; CANNABIDIOL; CAPSAICIN; CAPSAICIN DERIVATIVE; CAPSAVANIL; CAPSAZEPINE; CATION CHANNEL; DOXEPIN; EUGENOL; EVODIAMINE; GLYCERYL TRINITRATE; INDOMETACIN; ISOVELLERAL; KAVA; LIDOCAINE; MORPHINE; N (4 HYDROXYPHENYL)ARACHIDONAMIDE; OLVANIL; PARACETAMOL; PROPANOCAINE; PROPOFOL; RESINIFERATOXIN; RETVANIL; RINVANIL; SB 366791; SDZ 249665; SESQUITERPENE LACTONE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG; VANILLOID RECEPTOR;

EID: 0346752069     PISSN: 13543776     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543776.13.12.1825     Document Type: Review
Times cited : (36)

References (55)
  • 1
    • 0037040395 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 39
  • 40
    • 0024382437 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.