-
1
-
-
0019775230
-
Spinal opiate analgesia: Characteristics and principles of action
-
Yaksh, T. L. Spinal opiate analgesia: characteristics and principles of action. Pain 1981, 11, 293-346.
-
(1981)
Pain
, vol.11
, pp. 293-346
-
-
Yaksh, T.L.1
-
2
-
-
0034214841
-
NK1 (substance P) receptor antagonists - why are they not analgesic in humans?
-
Hill, R. NK1 (substance P) receptor antagonists - why are they not analgesic in humans? Trends Pharmacol. Sci. 2000, 21, 244-246.
-
(2000)
Trends Pharmacol. Sci
, vol.21
, pp. 244-246
-
-
Hill, R.1
-
3
-
-
14644439235
-
Improving opioid effectiveness: From ideas to evidence
-
Kalso, E. Improving opioid effectiveness: from ideas to evidence. Eur. J. Pain 2005, 9, 131-135.
-
(2005)
Eur. J. Pain
, vol.9
, pp. 131-135
-
-
Kalso, E.1
-
4
-
-
0037109674
-
Spinal neurons that possess the substance P receptor are required for the development of central sensitization
-
Khasabov, S. G.; Rogers, S. D.; Ghilardi, J. R.; Peters, C. M.; Mantyh, P. W.; Simone, D. A. Spinal neurons that possess the substance P receptor are required for the development of central sensitization. J. Neurosci. 2002, 22, 9086-9098.
-
(2002)
J. Neurosci
, vol.22
, pp. 9086-9098
-
-
Khasabov, S.G.1
Rogers, S.D.2
Ghilardi, J.R.3
Peters, C.M.4
Mantyh, P.W.5
Simone, D.A.6
-
5
-
-
0028928491
-
Rapid endocytosis of a G protein coupled receptor: Substance P evoked internalization of its receptor in the rat striatum in vivo
-
Mantyh, P. W.; Allen, C. J.; Ghilardi, J. R.; Rogers, S. D.; Mantyh, C. R.; Liu, H.; Basbaum, A. I.; Vigna, S. R.; Maggio, J. E. Rapid endocytosis of a G protein coupled receptor: substance P evoked internalization of its receptor in the rat striatum in vivo. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 2622-2626.
-
(1995)
Proc. Natl. Acad. Sci. U.S.A
, vol.92
, pp. 2622-2626
-
-
Mantyh, P.W.1
Allen, C.J.2
Ghilardi, J.R.3
Rogers, S.D.4
Mantyh, C.R.5
Liu, H.6
Basbaum, A.I.7
Vigna, S.R.8
Maggio, J.E.9
-
6
-
-
0021277125
-
Hyperalgesia produced by intrathecal substance P and related peptides: Desensitization and cross desensitization
-
Moochhala, S. M.; Sawynok, J. Hyperalgesia produced by intrathecal substance P and related peptides: desensitization and cross desensitization. Br. J. Pharmacol. 1984, 82, 381-388.
-
(1984)
Br. J. Pharmacol
, vol.82
, pp. 381-388
-
-
Moochhala, S.M.1
Sawynok, J.2
-
7
-
-
13044305848
-
Transmission of chronic nociception by spinal neurons expressing the substance P receptor
-
Nichols, M. L.; Allen, B. J.; Rogers, S. D.; Ghilardi, J. R.; Honore, P.; Luger, N. M.; Finke, M. P.; Li, J.; Lappi, D. A.; Simone, D. A.; Mantyh, P. W. Transmission of chronic nociception by spinal neurons expressing the substance P receptor. Science 1999, 286, 1558-1561.
-
(1999)
Science
, vol.286
, pp. 1558-1561
-
-
Nichols, M.L.1
Allen, B.J.2
Rogers, S.D.3
Ghilardi, J.R.4
Honore, P.5
Luger, N.M.6
Finke, M.P.7
Li, J.8
Lappi, D.A.9
Simone, D.A.10
Mantyh, P.W.11
-
8
-
-
21844474563
-
Role of NK-1 neurotransmission in opioid-induced hyperalgesia
-
King, T.; Gardell, L. R.; Wang, R.; Vardanyan, A.; Ossipov, M. H.; Malan, T. P., Jr.; Vanderah, T. W.; Hunt, S. P.; Hruby, V. J.; Lai, J.; Porreca, F. Role of NK-1 neurotransmission in opioid-induced hyperalgesia. Pain 2005, 116 (3), 276-288.
-
(2005)
Pain
, vol.116
, Issue.3
, pp. 276-288
-
-
King, T.1
Gardell, L.R.2
Wang, R.3
Vardanyan, A.4
Ossipov, M.H.5
Malan Jr., T.P.6
Vanderah, T.W.7
Hunt, S.P.8
Hruby, V.J.9
Lai, J.10
Porreca, F.11
-
9
-
-
26244461682
-
Is paradoxical pain induced by sustained opioid exposure an underlying mechanism of opioid antinociceptive tolerance?
-
King, T.; Ossipov, M. H.; Vanderah, T. W.; Porreca, F.; Lai, J. Is paradoxical pain induced by sustained opioid exposure an underlying mechanism of opioid antinociceptive tolerance? Neurosignals 2005, 14 (4), 194-205.
-
(2005)
Neurosignals
, vol.14
, Issue.4
, pp. 194-205
-
-
King, T.1
Ossipov, M.H.2
Vanderah, T.W.3
Porreca, F.4
Lai, J.5
-
10
-
-
0034675028
-
Morphine treatment induced calcitonin gene-related peptide and substance P increases in cultured dorsal root ganglion neurons
-
Ma, W.; Zheng, W. H.; Kar, S.; Quirion, R. Morphine treatment induced calcitonin gene-related peptide and substance P increases in cultured dorsal root ganglion neurons. Neuroscience 2000, 99 (3), 529-539.
-
(2000)
Neuroscience
, vol.99
, Issue.3
, pp. 529-539
-
-
Ma, W.1
Zheng, W.H.2
Kar, S.3
Quirion, R.4
-
11
-
-
0141705322
-
Inhibition of neurokinin-1-substance P receptor and prostanoid activity prevents and reverses the development of morphine tolerance in vivo and the morphine-induced increase in CGRP expression in cultured dorsal root ganglion neurons
-
Powell, K. J.; Quirion, R.; Jhamandas, K. Inhibition of neurokinin-1-substance P receptor and prostanoid activity prevents and reverses the development of morphine tolerance in vivo and the morphine-induced increase in CGRP expression in cultured dorsal root ganglion neurons. Eur. J. Neurosci. 2003, 18 (6), 1572-1583.
-
(2003)
Eur. J. Neurosci
, vol.18
, Issue.6
, pp. 1572-1583
-
-
Powell, K.J.1
Quirion, R.2
Jhamandas, K.3
-
12
-
-
0028255873
-
Spinal co-administration of peptide substance P antagonist increases antinociceptive effect of the opioid peptide biphalin
-
Misterek, K.; Maszczynska, I.; Dorociak, A.; Gumulka, S. W.; Carr, D. B.; Szyfelbein, S. K.; Lipkowski, A. W. Spinal co-administration of peptide substance P antagonist increases antinociceptive effect of the opioid peptide biphalin. Life Sci. 1994, 54 (14), 939-944.
-
(1994)
Life Sci
, vol.54
, Issue.14
, pp. 939-944
-
-
Misterek, K.1
Maszczynska, I.2
Dorociak, A.3
Gumulka, S.W.4
Carr, D.B.5
Szyfelbein, S.K.6
Lipkowski, A.W.7
-
13
-
-
23944462196
-
Resting and evoked spinal substance P release during chronic intrathecal morphine infusion: Parallels with tolerance and dependence
-
Gu, G.; Kondo, I.; Hua, X. Y.; Yaksh, T. L. Resting and evoked spinal substance P release during chronic intrathecal morphine infusion: parallels with tolerance and dependence. J. Pharmacol. Exp. Ther. 2005, 314 (3), 1362-1369.
-
(2005)
J. Pharmacol. Exp. Ther
, vol.314
, Issue.3
, pp. 1362-1369
-
-
Gu, G.1
Kondo, I.2
Hua, X.Y.3
Yaksh, T.L.4
-
14
-
-
0016717712
-
Immunohistochemical studies on the localization and distribution of substance P in cat primary sensory neurons
-
Hokfelt, T.; Kellereth, J. O.; Nilsson, G. Immunohistochemical studies on the localization and distribution of substance P in cat primary sensory neurons. Brain Res. 1975, 100, 235-252.
-
(1975)
Brain Res
, vol.100
, pp. 235-252
-
-
Hokfelt, T.1
Kellereth, J.O.2
Nilsson, G.3
-
15
-
-
12944335078
-
Substance P and Somatostatin levels in rhumatioid arthesis, molecular physiology
-
New York Academy of Science: New York
-
Marchand, J. E.; Kream, R. M. Substance P and Somatostatin levels in rhumatioid arthesis, molecular physiology. In Substance P and Related Peptides: Cellular and Molecular Physiology; New York Academy of Science: New York, 1990; pp 437-438.
-
(1990)
Substance P and Related Peptides: Cellular and Molecular Physiology
, pp. 437-438
-
-
Marchand, J.E.1
Kream, R.M.2
-
16
-
-
17044429802
-
Inhibition by spinal mu- and delta-opioid agonists of afferent-evoked substance P release
-
Kondo, I.; Marvizon, J. C.; Song, B.; Salgado, F.; Codeluppi, S.; Hua, X. Y.; Yaksh, T. L. Inhibition by spinal mu- and delta-opioid agonists of afferent-evoked substance P release. J. Neurosci. 2005, 25 (14), 3651-3660.
-
(2005)
J. Neurosci
, vol.25
, Issue.14
, pp. 3651-3660
-
-
Kondo, I.1
Marvizon, J.C.2
Song, B.3
Salgado, F.4
Codeluppi, S.5
Hua, X.Y.6
Yaksh, T.L.7
-
17
-
-
0025813255
-
Opioid receptor binding properties of analgesic analogues of cholecystokinin octapeptide
-
Slaninova, J.; Knapp, R. J.; Wu, J.; Fang, S. N.; Kramer, T.; Hruby, V. J.; Yamamura, H. I. Opioid receptor binding properties of analgesic analogues of cholecystokinin octapeptide. Eur. J. Pharmacol. 1991, 200, 195-198.
-
(1991)
Eur. J. Pharmacol
, vol.200
, pp. 195-198
-
-
Slaninova, J.1
Knapp, R.J.2
Wu, J.3
Fang, S.N.4
Kramer, T.5
Hruby, V.J.6
Yamamura, H.I.7
-
18
-
-
33644863475
-
Design and synthesis of novel hydrazide-linked bifunctional peptides as delta/mu opioid receptor agonists and CCK-1/CCK-2 receptor antagonists
-
2006
-
Lee, Y. S.; Agnes, R. S.; Badghisi, H.; Davis, P.; Ma, S. W.; Lai, J.; Porreca, F.; Hruby, V. J. Design and synthesis of novel hydrazide-linked bifunctional peptides as delta/mu opioid receptor agonists and CCK-1/CCK-2 receptor antagonists. J. Med. Chem. 2006, 49 (5),-1773-1780.
-
(1773)
J. Med. Chem
, vol.49
, Issue.5
-
-
Lee, Y.S.1
Agnes, R.S.2
Badghisi, H.3
Davis, P.4
Ma, S.W.5
Lai, J.6
Porreca, F.7
Hruby, V.J.8
-
19
-
-
0037498433
-
Design of novel peptide ligands which have opioid agonist activity and CCK antagonist activity for the treatment of pain
-
Hruby, V. J.; Agnes, R. S.; Davis, P.; Ma, S. W.; Lee, Y. S.; Vanderah, T. W.; Lai, J.; Porreca, F. Design of novel peptide ligands which have opioid agonist activity and CCK antagonist activity for the treatment of pain. Life Sci. 2003, 73 (6), 699-704.
-
(2003)
Life Sci
, vol.73
, Issue.6
, pp. 699-704
-
-
Hruby, V.J.1
Agnes, R.S.2
Davis, P.3
Ma, S.W.4
Lee, Y.S.5
Vanderah, T.W.6
Lai, J.7
Porreca, F.8
-
20
-
-
33646722004
-
Structure-activity relationships of bifunctional peptides based on overlapping pharmacophores at opioid and cholecystokinin receptors
-
Agnes, R. S.; Lee, Y. S.; Davis, P.; Ma, S. W.; Badghisi, H.; Porreca, F.; Lai, J.; Hruby, V. J. Structure-activity relationships of bifunctional peptides based on overlapping pharmacophores at opioid and cholecystokinin receptors. J. Med. Chem. 2006, 49 (10), 2868-2875.
-
(2006)
J. Med. Chem
, vol.49
, Issue.10
, pp. 2868-2875
-
-
Agnes, R.S.1
Lee, Y.S.2
Davis, P.3
Ma, S.W.4
Badghisi, H.5
Porreca, F.6
Lai, J.7
Hruby, V.J.8
-
21
-
-
1642398888
-
Spinal antinociceptive effects of AA501, a novel chimeric peptide with opioid receptor agonist and tachykinin receptor antagonist moieties
-
Bonney, I. M.; Foran, S. E.; Marchand, J. E.; Lipkowski, A. W.; Carr, D. B. Spinal antinociceptive effects of AA501, a novel chimeric peptide with opioid receptor agonist and tachykinin receptor antagonist moieties. Eur. J. Pharmacol. 2004, 488 (1-3), 91-99.
-
(2004)
Eur. J. Pharmacol
, vol.488
, Issue.1-3
, pp. 91-99
-
-
Bonney, I.M.1
Foran, S.E.2
Marchand, J.E.3
Lipkowski, A.W.4
Carr, D.B.5
-
22
-
-
0032942522
-
Opioid activity of sendide, a tachykinin NK1 receptor antagonist
-
Sakurada, T.; Yuhki, M.; Inoue, M.; Sakurada, C.; Tan-No, K.; Ohba, M.; Kisara, K.; Sakurada, S. Opioid activity of sendide, a tachykinin NK1 receptor antagonist. Eur. J. Pharmacol. 1999, 369 (3), 261-266.
-
(1999)
Eur. J. Pharmacol
, vol.369
, Issue.3
, pp. 261-266
-
-
Sakurada, T.1
Yuhki, M.2
Inoue, M.3
Sakurada, C.4
Tan-No, K.5
Ohba, M.6
Kisara, K.7
Sakurada, S.8
-
23
-
-
23844480802
-
Endomorphins interact with tachykinin receptors
-
Kosson, P.; Bonney, I.; Carr, D. B.; Lipkowski, A. W. Endomorphins interact with tachykinin receptors. Peptides 2005, 26 (9), 1667-1669.
-
(2005)
Peptides
, vol.26
, Issue.9
, pp. 1667-1669
-
-
Kosson, P.1
Bonney, I.2
Carr, D.B.3
Lipkowski, A.W.4
-
24
-
-
2142658722
-
New Torends in the Development of Opioid Peptide Analogues as Advanced Remedies for pain Relief
-
Gentilucci, L. New Torends in the Development of Opioid Peptide Analogues as Advanced Remedies for pain Relief. Curr. Topics Med. Chem. 2004, 4, 19-38.
-
(2004)
Curr. Topics Med. Chem
, vol.4
, pp. 19-38
-
-
Gentilucci, L.1
-
25
-
-
0025960130
-
Development of delta opioid peptides as nonaddicting analgesics
-
Rapaka, R. S.; Porreca, F. Development of delta opioid peptides as nonaddicting analgesics. Pharm. Res. 1991, 8 (1), 1-8.
-
(1991)
Pharm. Res
, vol.8
, Issue.1
, pp. 1-8
-
-
Rapaka, R.S.1
Porreca, F.2
-
26
-
-
0030983867
-
Non-peptide δ opioid agonists and antagonists
-
Dondio, G.; Ronzoni, S.; Petrillo, P. Non-peptide δ opioid agonists and antagonists. Expert Opin. Ther. Pat. 1997, 7, 1075-1098.
-
(1997)
Expert Opin. Ther. Pat
, vol.7
, pp. 1075-1098
-
-
Dondio, G.1
Ronzoni, S.2
Petrillo, P.3
-
27
-
-
0028937898
-
SNC 80, a selective, nonpeptidic and systemically active opioid delta agonist
-
Bilsky, E. J.; Calderon, S. N.; Wang, T.; Bernstein, R. N.; Davis, P.; Hruby, V. J.; McNutt, R. W.; Rothman, R. B.; Rice, K. C.; Porreca, F. SNC 80, a selective, nonpeptidic and systemically active opioid delta agonist. J. Pharmacol. Exp. Ther. 1995, 273, 359-366.
-
(1995)
J. Pharmacol. Exp. Ther
, vol.273
, pp. 359-366
-
-
Bilsky, E.J.1
Calderon, S.N.2
Wang, T.3
Bernstein, R.N.4
Davis, P.5
Hruby, V.J.6
McNutt, R.W.7
Rothman, R.B.8
Rice, K.C.9
Porreca, F.10
-
28
-
-
0032866115
-
The delta-opioid receptor: Molecular pharmacology, signal transduction, and the determination of drug efficacy
-
Quock, R. M.; Burkey, T. H.; Varga, E.; Hosohata, Y.; Hosohata, K.; Cowell, S. M.; Slate, C. A.; Ehlert, F. J.; Roeske, W. R.; Yamamura, H. I. The delta-opioid receptor: molecular pharmacology, signal transduction, and the determination of drug efficacy. Pharmacol. Rev. 1999, 51 (3), 503-532.
-
(1999)
Pharmacol. Rev
, vol.51
, Issue.3
, pp. 503-532
-
-
Quock, R.M.1
Burkey, T.H.2
Varga, E.3
Hosohata, Y.4
Hosohata, K.5
Cowell, S.M.6
Slate, C.A.7
Ehlert, F.J.8
Roeske, W.R.9
Yamamura, H.I.10
-
29
-
-
0022929968
-
Design Principles: Enkephalins With Predictable Mu/Delta Receptor Specificity
-
Shimohigashi, Y. Design Principles: Enkephalins With Predictable Mu/Delta Receptor Specificity. NIDA Res. Monogr. 1986, 69, 65-100.
-
(1986)
NIDA Res. Monogr
, vol.69
, pp. 65-100
-
-
Shimohigashi, Y.1
-
30
-
-
0027379024
-
Antinociceptive Profile of Biphalin, a Dimeric Enkephalin Analog
-
Horan, P. J.; Mattia, A.; Bilsky, E. J.; Weber, S.; Davis, T. P.; Yamamura, H. J.; Malatynska, E.; Appleyard, S. M.; Slaninova, J.; Misicka, A.; Lipowski, A. W.; Hruby, V. J.; Porreca, F. Antinociceptive Profile of Biphalin, a Dimeric Enkephalin Analog. J. Pharmacol. Exp. Ther. 1993, 265, 1446-1454.
-
(1993)
J. Pharmacol. Exp. Ther
, vol.265
, pp. 1446-1454
-
-
Horan, P.J.1
Mattia, A.2
Bilsky, E.J.3
Weber, S.4
Davis, T.P.5
Yamamura, H.J.6
Malatynska, E.7
Appleyard, S.M.8
Slaninova, J.9
Misicka, A.10
Lipowski, A.W.11
Hruby, V.J.12
Porreca, F.13
-
31
-
-
0027214178
-
N-Acyl-L-tryptophan benzyl esters: Potent substance P receptor antagonists
-
Macleod, A. M.; Merchant, K. J.; Cascieri, M. A.; Sadowski, S.; Ber, E.; Swain, C. J.; Baker, R. N-Acyl-L-tryptophan benzyl esters: potent substance P receptor antagonists. J. Med Chem. 1993, 14, 2044-2045.
-
(1993)
J. Med Chem
, vol.14
, pp. 2044-2045
-
-
Macleod, A.M.1
Merchant, K.J.2
Cascieri, M.A.3
Sadowski, S.4
Ber, E.5
Swain, C.J.6
Baker, R.7
-
32
-
-
0028318167
-
Characterization of the interaction of N-acyl-L-tryptophan benzyl ester neurokinin antagonists with the human neurokinin-1 receptor
-
Cascieri, M. A.; Macleod, A. M.; Underwood, D.; Shiao, L. L.; Ber, E.; Sadowski, S.; Yu, H.; Merchant, K. J.; Swain, C. J.; Strader, C. D.; Fong, T. M. Characterization of the interaction of N-acyl-L-tryptophan benzyl ester neurokinin antagonists with the human neurokinin-1 receptor. J. Biol. Chem. 1994, 269 (9), 6587-6591.
-
(1994)
J. Biol. Chem
, vol.269
, Issue.9
, pp. 6587-6591
-
-
Cascieri, M.A.1
Macleod, A.M.2
Underwood, D.3
Shiao, L.L.4
Ber, E.5
Sadowski, S.6
Yu, H.7
Merchant, K.J.8
Swain, C.J.9
Strader, C.D.10
Fong, T.M.11
-
33
-
-
0034931327
-
2 deduced from two-dimensional 1H-NMR and conformational energy calculations is related to its affinity for NK1-receptor
-
2 deduced from two-dimensional 1H-NMR and conformational energy calculations is related to its affinity for NK1-receptor. J. Pept. Sci. 2001, 7 (6), 323-330.
-
(2001)
J. Pept. Sci
, vol.7
, Issue.6
, pp. 323-330
-
-
Millet, R.1
Goossens, L.2
Goossens, J.F.3
Chavatte, P.4
Bertrand-Caumont, K.5
Houssin, R.6
Henichart, J.P.7
-
34
-
-
0033053308
-
2 as NK1/NK2 ligands
-
2 as NK1/NK2 ligands. Lett. Pep. Sci. 1999, 6, 255-262.
-
(1999)
Lett. Pep. Sci
, vol.6
, pp. 255-262
-
-
Millet, R.1
Goossens, L.2
Bertrand-Caumont, K.3
Chavatte, P.4
Houssin, R.5
Henichart, J.P.6
-
35
-
-
0028233389
-
Glycopeptide enkephalin analogues produce analgesia in mice: Evidence for penetration of the blood-brain barrier
-
Polt, R.; Porreca, F.; Szabo, L. Z.; Bilsky, E. J.; Davis, P.; Abbruscato, T. J.; Davis, T. P.; Horvath, R.; Yamamura, H. I.; Hruby, V. J. Glycopeptide enkephalin analogues produce analgesia in mice: evidence for penetration of the blood-brain barrier. Proc. Natl. Acad. Sci. U.S.A. 1994, 91 (15), 7114-7118.
-
(1994)
Proc. Natl. Acad. Sci. U.S.A
, vol.91
, Issue.15
, pp. 7114-7118
-
-
Polt, R.1
Porreca, F.2
Szabo, L.Z.3
Bilsky, E.J.4
Davis, P.5
Abbruscato, T.J.6
Davis, T.P.7
Horvath, R.8
Yamamura, H.I.9
Hruby, V.J.10
-
36
-
-
0026701796
-
Topographical requirements for delta opioid ligands: Common structural features of dermenkephalin and deltorphin
-
Misicka, A.; Lipkowski, A. W.; Horvath, R.; Davis, P.; Kramer, T. H.; Yamamura, H. I.; Hruby, V. J. Topographical requirements for delta opioid ligands: common structural features of dermenkephalin and deltorphin. Life Sci. 1992, 51 (13), 1025-1032.
-
(1992)
Life Sci
, vol.51
, Issue.13
, pp. 1025-1032
-
-
Misicka, A.1
Lipkowski, A.W.2
Horvath, R.3
Davis, P.4
Kramer, T.H.5
Yamamura, H.I.6
Hruby, V.J.7
-
37
-
-
0017735536
-
Endogenous opioid peptides: Multiple agonists and receptors
-
Lord, J. A. H; Waterfield, A. A.; Hughes, J.; Kosterlitz, H. W. Endogenous opioid peptides: multiple agonists and receptors. Nature 1977, 207, 495-499.
-
(1977)
Nature
, vol.207
, pp. 495-499
-
-
Lord, J.A.H.1
Waterfield, A.A.2
Hughes, J.3
Kosterlitz, H.W.4
-
38
-
-
0020682345
-
Methionine oxidation enhances opioid activity of an enkephalin analog
-
Kiritsy-Roy, J. A.; Chan, S. K.; Iwamoto, E. T. Methionine oxidation enhances opioid activity of an enkephalin analog. Life Sci. 1983, 32 (8), 889-893.
-
(1983)
Life Sci
, vol.32
, Issue.8
, pp. 889-893
-
-
Kiritsy-Roy, J.A.1
Chan, S.K.2
Iwamoto, E.T.3
-
39
-
-
0025343103
-
Effects of metkephamid (LY127623), a selective delta opioid receptor agonist, on gastric function
-
Glavin, G. B.; Pinsky, C.; Hall, A. M. Effects of metkephamid (LY127623), a selective delta opioid receptor agonist, on gastric function. Life Sci. 1990, 46 (15), 1075-1079.
-
(1990)
Life Sci
, vol.46
, Issue.15
, pp. 1075-1079
-
-
Glavin, G.B.1
Pinsky, C.2
Hall, A.M.3
-
40
-
-
0020464432
-
Metkephamid (Tyr-D-ala-Gly-Phe-N(Me)Met-NH2), a potent opioid peptide: Receptor binding and analgesic properties
-
Burkhardt, C.; Frederickson, R. C.; Pasternak, G. W. Metkephamid (Tyr-D-ala-Gly-Phe-N(Me)Met-NH2), a potent opioid peptide: receptor binding and analgesic properties. Peptides 1982, 3 (5), 869-871.
-
(1982)
Peptides
, vol.3
, Issue.5
, pp. 869-871
-
-
Burkhardt, C.1
Frederickson, R.C.2
Pasternak, G.W.3
-
41
-
-
0019381209
-
-
Frederickson, R. C.; Smithwick, E. L.; Shuman, R.; Bemis, K. G. Metkephamid, a systemically active analog of methionine enkephalin with potent opioid alpha-receptor activity. Science 1981, 211, 603-605.
-
Frederickson, R. C.; Smithwick, E. L.; Shuman, R.; Bemis, K. G. Metkephamid, a systemically active analog of methionine enkephalin with potent opioid alpha-receptor activity. Science 1981, 211, 603-605.
-
-
-
-
42
-
-
0344448273
-
Coherence transfer by isotropic mixing: Application to proton correlation spectroscopy
-
Braunschweiler, L.; Ernst, R. R. Coherence transfer by isotropic mixing: Application to proton correlation spectroscopy. J. Magn. Reson. 1983, 53, 521-528.
-
(1983)
J. Magn. Reson
, vol.53
, pp. 521-528
-
-
Braunschweiler, L.1
Ernst, R.R.2
-
43
-
-
33845378943
-
Assignment of complex 1H-NMR spectra via two-dimensional homonuclear Hartmann-Hahn spectroscopy
-
Davis, D. G.; Bax, A. Assignment of complex 1H-NMR spectra via two-dimensional homonuclear Hartmann-Hahn spectroscopy. J. Am Chem. Soc. 1985, 107, 2820-2821.
-
(1985)
J. Am Chem. Soc
, vol.107
, pp. 2820-2821
-
-
Davis, D.G.1
Bax, A.2
-
44
-
-
45949124222
-
Generation of pure phase NMR subspectra for measurement of homonuclear coupling constants
-
Subramanian, S.; Bax, A. Generation of pure phase NMR subspectra for measurement of homonuclear coupling constants. J. Magn. Reson. 1987, 71, 325-330.
-
(1987)
J. Magn. Reson
, vol.71
, pp. 325-330
-
-
Subramanian, S.1
Bax, A.2
-
45
-
-
45949117739
-
Improved techniques for homonuclear rotating-frame and isotropic mixing experiments
-
Rance, M. Improved techniques for homonuclear rotating-frame and isotropic mixing experiments. J. Magn. Reson. 1987, 74, 557-564.
-
(1987)
J. Magn. Reson
, vol.74
, pp. 557-564
-
-
Rance, M.1
-
46
-
-
5144233105
-
MLEV-17-based two-dimensional homonuclear magnetization transfer spectroscopy
-
Bax, A.; Davis, D. G. MLEV-17-based two-dimensional homonuclear magnetization transfer spectroscopy. J. Magn. Reson. 1985, 65, 355-360.
-
(1985)
J. Magn. Reson
, vol.65
, pp. 355-360
-
-
Bax, A.1
Davis, D.G.2
-
47
-
-
0021114895
-
Application of phase sensitive two-dimensional correlated spectroscopy (COSY) for measurements of 1H-1H spin-spin coupling constants in proteins
-
Marion, D.; Wuthrich, K. Application of phase sensitive two-dimensional correlated spectroscopy (COSY) for measurements of 1H-1H spin-spin coupling constants in proteins. Biochem. Biophys. Res. Commun. 1983, 113, 967-974.
-
(1983)
Biochem. Biophys. Res. Commun
, vol.113
, pp. 967-974
-
-
Marion, D.1
Wuthrich, K.2
-
48
-
-
0030069077
-
The peptide binding site of the substance P (NK-1) receptor localized by a photoreactive analogue of substance P: Presence of a disulfide bond
-
Boyd, N. D.; Kage, R.; Dumas, J. J.; Krause, J. E.; Leeman, S. E. The peptide binding site of the substance P (NK-1) receptor localized by a photoreactive analogue of substance P: presence of a disulfide bond, Proc. Natl. Acad. Sci. U.S.A. 1996, 93, 433-437.
-
(1996)
Proc. Natl. Acad. Sci. U.S.A
, vol.93
, pp. 433-437
-
-
Boyd, N.D.1
Kage, R.2
Dumas, J.J.3
Krause, J.E.4
Leeman, S.E.5
-
49
-
-
0027250490
-
Measurement of guanine nucleotide-binding protein activation by A1 adenosine receptor agonists in bovine brain membranes: Stimulation of guanosine-5′-O-(3-[35S]mio) triphosphate binding
-
Lorenzen, A.; Fuss, M.; Vogt, H.; Schwabe, U. Measurement of guanine nucleotide-binding protein activation by A1 adenosine receptor agonists in bovine brain membranes: stimulation of guanosine-5′-O-(3-[35S]mio) triphosphate binding. Mol. Pharmacol. 1993, 44 (1),115-123.
-
(1993)
Mol. Pharmacol
, vol.44
, Issue.1
, pp. 115-123
-
-
Lorenzen, A.1
Fuss, M.2
Vogt, H.3
Schwabe, U.4
-
50
-
-
0020608003
-
Affinity of normorphine for its pharmacologic receptor in the naive and morphine-tolerant guinea-pig isolated ileum
-
Porreca, F.; Burks, T. F. Affinity of normorphine for its pharmacologic receptor in the naive and morphine-tolerant guinea-pig isolated ileum. J. Pharmacol. Exp. Ther. 1983, 225 (3), 688-693.
-
(1983)
J. Pharmacol. Exp. Ther
, vol.225
, Issue.3
, pp. 688-693
-
-
Porreca, F.1
Burks, T.F.2
-
51
-
-
0025344555
-
Opioid agonist affinity in the guinea-pig ileum and mouse vas deferens
-
Porreca, F.; LoPresti, D; Ward, S. J. Opioid agonist affinity in the guinea-pig ileum and mouse vas deferens. Eur. J. Pharmacol. 1990, 179 (1-2), 129-139.
-
(1990)
Eur. J. Pharmacol
, vol.179
, Issue.1-2
, pp. 129-139
-
-
Porreca, F.1
LoPresti, D.2
Ward, S.J.3
-
52
-
-
0033588946
-
Biological activity of fragments and analogues of the potent dimeric opioid peptide, biphalin
-
Lipkowski, A. W.; Misicka, A.; Davis, P.; Stropova, D.; Janders, J.; Lachwa, M.; Porreca, F.; Yamamura, H. I.; Hruby, V. J. Biological activity of fragments and analogues of the potent dimeric opioid peptide, biphalin. Bioorg. Med. Chem. Lett. 1999, 9 (18), 2763-6.
-
(1999)
Bioorg. Med. Chem. Lett
, vol.9
, Issue.18
, pp. 2763-2766
-
-
Lipkowski, A.W.1
Misicka, A.2
Davis, P.3
Stropova, D.4
Janders, J.5
Lachwa, M.6
Porreca, F.7
Yamamura, H.I.8
Hruby, V.J.9
-
53
-
-
0022051507
-
Characterization of [3H][2-D-{penicillamine,5-D-p}enicillamine]-enkephalin Binding to delta Opiate Receptors in the Rat Brain and Neuroblastoma-Glioma Hybrid Cell Line (NG 108-15)
-
Akiyama, K.; Gee, K. W.; Mosberg, H. I.; Hruby, V. J.; Yamamura, H. I. Characterization of [3H][2-D-{penicillamine,5-D-p}enicillamine]-enkephalin Binding to delta Opiate Receptors in the Rat Brain and Neuroblastoma-Glioma Hybrid Cell Line (NG 108-15), Proc. Natl. Acad. Sci. U.S.A. 1985, 82, 2543-2547.
-
(1985)
Proc. Natl. Acad. Sci. U.S.A
, vol.82
, pp. 2543-2547
-
-
Akiyama, K.1
Gee, K.W.2
Mosberg, H.I.3
Hruby, V.J.4
Yamamura, H.I.5
-
54
-
-
0000440578
-
-
Mosberg, H. I.; Hurst, M. R.; Hruby, V. J.; Gee, H. K.; Yamamura, H. I.; Galligan, J. J. Burks, T. F. Bis-Penicillamine Enkephalins Possess Highly Improved Specificity toward delta Receptors Proc. Natl. Acad. Sci. U.S.A. 1983, 80, 5871-5874.
-
Mosberg, H. I.; Hurst, M. R.; Hruby, V. J.; Gee, H. K.; Yamamura, H. I.; Galligan, J. J. Burks, T. F. Bis-Penicillamine Enkephalins Possess Highly Improved Specificity toward delta Receptors Proc. Natl. Acad. Sci. U.S.A. 1983, 80, 5871-5874.
-
-
-
-
55
-
-
0021023120
-
Cyclic penicillamine containing enkephalin analogs display profound delta receptor selectivities
-
Mosberg, H. I.; Hurst, R.; Hruby, V. J.; Gee, K.; Akiyama, K.; Yamamura, H. I.; Galligan, J. J.; Burks, T. F. Cyclic penicillamine containing enkephalin analogs display profound delta receptor selectivities. Life Sci. 1983, 33 (Suppl 1), 447-50.
-
(1983)
Life Sci
, vol.33
, Issue.SUPPL. 1
, pp. 447-450
-
-
Mosberg, H.I.1
Hurst, R.2
Hruby, V.J.3
Gee, K.4
Akiyama, K.5
Yamamura, H.I.6
Galligan, J.J.7
Burks, T.F.8
-
56
-
-
34250826440
-
Structure-Activity Relationships and Biological Evaluation of Novel Bifunctional C-terminal Modified Peptides for delta/ mu Opioid Receptor Agonists and Neurokinin-1 Receptor Antagonists. American Chemical Society
-
Yamamoto, T.; Nair, P.; Davis, P.; Ma, S-W.; Moye, S.; Largent, T.; Vanderah, T. W.; Lai, J.; Porreca, F.; Yamamura, H. I.; Hruby, V. J. Design, Structure-Activity Relationships and Biological Evaluation of Novel Bifunctional C-terminal Modified Peptides for delta/ mu Opioid Receptor Agonists and Neurokinin-1 Receptor Antagonists. American Chemical Society, 232nd National Meeting, San Francisco, CA, Sep. 10-14, 2006; p MEDI-7.
-
232nd National Meeting, San Francisco, CA, Sep. 10-14, 2006; p MEDI-7
-
-
Yamamoto, T.1
Nair, P.2
Davis, P.3
Ma, S.-W.4
Moye, S.5
Largent, T.6
Vanderah, T.W.7
Lai, J.8
Porreca, F.9
Yamamura, H.I.10
Hruby, V.11
Design, J.12
|