-
1
-
-
0030682389
-
Etorphines: μ-opioid receptor-selective antinociception and low physical dependence capacity
-
M.D. Aceto, L.S. Harris, and E.R. Bowman Etorphines: μ-opioid receptor-selective antinociception and low physical dependence capacity Eur. J. Pharmacol. 338 1997 215 223
-
(1997)
Eur. J. Pharmacol.
, vol.338
, pp. 215-223
-
-
Aceto, M.D.1
Harris, L.S.2
Bowman, E.R.3
-
2
-
-
4444381999
-
Long-term agonist effects of congeners of etorphine suggest interfacial location of mu opioid recognition site
-
J.A. Bell, and J.C. Schaeffer Long-term agonist effects of congeners of etorphine suggest interfacial location of mu opioid recognition site Abstr.-Soc. Neurosci. 23 479 1997 9
-
(1997)
Abstr.-Soc. Neurosci.
, vol.23
, Issue.479
, pp. 9
-
-
Bell, J.A.1
Schaeffer, J.C.2
-
3
-
-
0014213099
-
Novel analgesics and molecular rearrangements in the morphine-thebaine group: III. Alcohols of the 6,14-endo-ethenotetrahydrooripavine series and derived analogs of N-allylmorphine and -narcodeine
-
K.W. Bentley, and D.G. Hardy Novel analgesics and molecular rearrangements in the morphine-thebaine group: III. Alcohols of the 6,14-endo-ethenotetrahydrooripavine series and derived analogs of N-allylmorphine and -narcodeine J. Am. Chem. Soc. 89 1967 3281 3292
-
(1967)
J. Am. Chem. Soc.
, vol.89
, pp. 3281-3292
-
-
Bentley, K.W.1
Hardy, D.G.2
-
4
-
-
0028791123
-
Buprenorphine treatment of opioid dependence: A review
-
W.K. Bickel, and L. Amass Buprenorphine treatment of opioid dependence: a review Exp. Clin. Psychopharmacol. 3 1995 477 489
-
(1995)
Exp. Clin. Psychopharmacol.
, vol.3
, pp. 477-489
-
-
Bickel, W.K.1
Amass, L.2
-
5
-
-
0024552044
-
Chronic morphine increases μ-opiate receptor binding in rat brain: A quantitative autoradiographic study
-
L.S. Brady, M. Herkenham, J.B. Long, and R.B. Rothman Chronic morphine increases μ-opiate receptor binding in rat brain: a quantitative autoradiographic study Brain Res. 477 1989 382 386
-
(1989)
Brain Res.
, vol.477
, pp. 382-386
-
-
Brady, L.S.1
Herkenham, M.2
Long, J.B.3
Rothman, R.B.4
-
6
-
-
0027772479
-
A new consistent model explaining structure (conformation)-activity relationships of opiates with μ-selectivity
-
W. Brandt, A. Barth, and H.-D. Holtje A new consistent model explaining structure (conformation)-activity relationships of opiates with μ-selectivity Drug Des. Discov. 10 1993 257 283
-
(1993)
Drug Des. Discov.
, vol.10
, pp. 257-283
-
-
Brandt, W.1
Barth, A.2
Holtje, H.-D.3
-
7
-
-
0028284548
-
Differential effects of systemically administered nor-binaltorphimine (nor-BNI) on κ-opioid agonists in the mouse writhing assay
-
J.H. Broadbear, S.S. Negus, E.R. Butelman, B.R. deCosta, and J.H. Woods Differential effects of systemically administered nor-binaltorphimine (nor-BNI) on κ-opioid agonists in the mouse writhing assay Psychopharmacology 115 1994 311 319
-
(1994)
Psychopharmacology
, vol.115
, pp. 311-319
-
-
Broadbear, J.H.1
Negus, S.S.2
Butelman, E.R.3
Decosta, B.R.4
Woods, J.H.5
-
8
-
-
0033838122
-
Methocinnamox is a potent, long-lasting and selective antagonist of morphine-mediated antinociception in the mouse: Comparison with clocinnamox, β-funaltrexamine and β-chlornaltrexamine
-
J.H. Broadbear, T.L. Sumpter, T.F. Burke, S.M. Husbands, J.W. Lewis, J.H. Woods, and J.R. Traynor Methocinnamox is a potent, long-lasting and selective antagonist of morphine-mediated antinociception in the mouse: comparison with clocinnamox, β-funaltrexamine and β-chlornaltrexamine J. Pharmacol. Exp. Ther. 294 2000 933 940
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.294
, pp. 933-940
-
-
Broadbear, J.H.1
Sumpter, T.L.2
Burke, T.F.3
Husbands, S.M.4
Lewis, J.W.5
Woods, J.H.6
Traynor, J.R.7
-
9
-
-
0033847301
-
BU48: A novel buprenorphine analog that exhibits δ-opioid-mediated convulsions but not delta-mediated antinociception in mice
-
D.C. Broom, L. Gou, A. Coop, S.M. Husbands, J.H. Lewis, J.H. Woods, and J.R. Traynor BU48: a novel buprenorphine analog that exhibits δ-opioid-mediated convulsions but not delta-mediated antinociception in mice J. Pharmacol. Exp. Ther. 294 2000 1195 1200
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.294
, pp. 1195-1200
-
-
Broom, D.C.1
Gou, L.2
Coop, A.3
Husbands, S.M.4
Lewis, J.H.5
Woods, J.H.6
Traynor, J.R.7
-
10
-
-
0036827839
-
Comparison of receptor mechanisms and efficacy requirements for δ-agonist induced convulsive activity and antinociception in mice
-
D.C. Broom, J.F. Nitsche, J.E. Pintar, K.C. Rice, J.H. Woods, and J.R. Traynor Comparison of receptor mechanisms and efficacy requirements for δ-agonist induced convulsive activity and antinociception in mice J. Pharmacol. Exp. Ther. 303 2002 723 729
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.303
, pp. 723-729
-
-
Broom, D.C.1
Nitsche, J.F.2
Pintar, J.E.3
Rice, K.C.4
Woods, J.H.5
Traynor, J.R.6
-
11
-
-
0017714512
-
The animal pharmacology of buprenorphine: An oripavine analgesic agent
-
A. Cowan, J.C. Doxey, and E.J.R. Harry The animal pharmacology of buprenorphine: an oripavine analgesic agent Br. J. Pharmacol. 60 1977 547 554
-
(1977)
Br. J. Pharmacol.
, vol.60
, pp. 547-554
-
-
Cowan, A.1
Doxey, J.C.2
Harry, E.J.R.3
-
12
-
-
0017756322
-
Agonist and antagonist properties of buprenorphine, a new antinociceptive agent
-
A. Cowan, J.W. Lewis, and I.R. MacFarlane Agonist and antagonist properties of buprenorphine, a new antinociceptive agent Br. J. Pharmacol. 60 1977 537 545
-
(1977)
Br. J. Pharmacol.
, vol.60
, pp. 537-545
-
-
Cowan, A.1
Lewis, J.W.2
MacFarlane, I.R.3
-
13
-
-
0022479347
-
A tail withdrawal procedure for assessing analgesic activity in rhesus monkeys
-
L.A. Dykstra, and J.H. Woods A tail withdrawal procedure for assessing analgesic activity in rhesus monkeys J. Pharmacol. Methods 15 1986 263 269
-
(1986)
J. Pharmacol. Methods
, vol.15
, pp. 263-269
-
-
Dykstra, L.A.1
Woods, J.H.2
-
14
-
-
84935383230
-
Synthetic analgesics: II. Dithienylbutenyl- and dithienylbutylamines
-
N.B. Eddy, and D. Leimbach Synthetic analgesics: II. Dithienylbutenyl- and dithienylbutylamines J. Pharmacol. Exp. Ther. 107 1953 385
-
(1953)
J. Pharmacol. Exp. Ther.
, vol.107
, pp. 385
-
-
Eddy, N.B.1
Leimbach, D.2
-
15
-
-
0021217795
-
Discriminative stimulus effects of reversible and irreversible opiate antagonists: Morphine, oxymorphazone and buprenorphine
-
C. France, A.E. Jacobson, and J.H. Woods Discriminative stimulus effects of reversible and irreversible opiate antagonists: morphine, oxymorphazone and buprenorphine J. Pharmacol. Exp. Ther. 230 1984 652 657
-
(1984)
J. Pharmacol. Exp. Ther.
, vol.230
, pp. 652-657
-
-
France, C.1
Jacobson, A.E.2
Woods, J.H.3
-
16
-
-
0001878908
-
Clinical efficacy studies of buprenorphine for the treatment of opiate dependence
-
A. Cowan J.W. Lewis Wiley-Liss New York
-
P.J. Fudala, and R.E. Johnson Clinical efficacy studies of buprenorphine for the treatment of opiate dependence A. Cowan J.W. Lewis Buprenorphine: Combatting Drug Abuse with a Unique Opioid 1995 Wiley-Liss New York 213 219
-
(1995)
Buprenorphine: Combatting Drug Abuse with a Unique Opioid
, pp. 213-219
-
-
Fudala, P.J.1
Johnson, R.E.2
-
17
-
-
0002448256
-
The interaction of buprenorphine with the opiate receptor: Lipophilicity as a determining factor in drug-receptor kinetics
-
H.W. Kosterlitz Elsevier Amsterdam
-
J.M. Hambrook, and M.J. Rance The interaction of buprenorphine with the opiate receptor: lipophilicity as a determining factor in drug-receptor kinetics H.W. Kosterlitz Opiates and Endogenous Opioid Peptides 1976 Elsevier Amsterdam 295 301
-
(1976)
Opiates and Endogenous Opioid Peptides
, pp. 295-301
-
-
Hambrook, J.M.1
Rance, M.J.2
-
18
-
-
0034724851
-
Antinociceptive and other behavioral effects of the steroid SC17599 are mediated by the μ-opioid receptor
-
H. Houshyar, I.J. McFadyen, J.H. Woods, and J.R. Traynor Antinociceptive and other behavioral effects of the steroid SC17599 are mediated by the μ-opioid receptor Eur. J. Pharmacol. 395 2000 121 128
-
(2000)
Eur. J. Pharmacol.
, vol.395
, pp. 121-128
-
-
Houshyar, H.1
McFadyen, I.J.2
Woods, J.H.3
Traynor, J.R.4
-
19
-
-
0016632644
-
Effect of morphine on adrenergic transmission in the mouse vas deferens. Assessment of agonist and antagonist potencies of narcotic analgesics
-
J. Hughes, H.W. Kosterlitz, and F.M. Leslie Effect of morphine on adrenergic transmission in the mouse vas deferens. Assessment of agonist and antagonist potencies of narcotic analgesics Br. J. Pharmacol. 53 1975 371 381
-
(1975)
Br. J. Pharmacol.
, vol.53
, pp. 371-381
-
-
Hughes, J.1
Kosterlitz, H.W.2
Leslie, F.M.3
-
20
-
-
0028846956
-
Morphinan cyclic imines and pyrrolidines containing a constrained phenyl group: High affinity opioid agonists
-
S.M. Husbands, and J.W. Lewis Morphinan cyclic imines and pyrrolidines containing a constrained phenyl group: high affinity opioid agonists Bioorganic Med. Chem. Letters 5 1995 2969 2974
-
(1995)
Bioorganic Med. Chem. Letters
, vol.5
, pp. 2969-2974
-
-
Husbands, S.M.1
Lewis, J.W.2
-
21
-
-
84862410796
-
A bridged pyrrolomorphinan with potent, long-lasting κ-opioid agonism and delayed opioid antagonism
-
S.M. Husbands, C.L. Neilan, J. Broadbear, P. Grundt, S. Breeden, M.D. Aceto, J.H. Woods, J.W. Lewis, and J.R. Traynor A bridged pyrrolomorphinan with potent, long-lasting κ-opioid agonism and delayed opioid antagonism Eur. J. Pharmacol 2003 (submitted for publication)
-
(2003)
Eur. J. Pharmacol
-
-
Husbands, S.M.1
Neilan, C.L.2
Broadbear, J.3
Grundt, P.4
Breeden, S.5
Aceto, M.D.6
Woods, J.H.7
Lewis, J.W.8
Traynor, J.R.9
-
22
-
-
0027157469
-
The pharmacology of salmeterol
-
M. Johnson, P.R. Butchers, R.A. Coleman, A.T. Nials, P. Strong, M.J. Sumner, C.J. Vardey, and C.J. Whelan The pharmacology of salmeterol Life Sci. 52 1993 2131 2143
-
(1993)
Life Sci.
, vol.52
, pp. 2131-2143
-
-
Johnson, M.1
Butchers, P.R.2
Coleman, R.A.3
Nials, A.T.4
Strong, P.5
Sumner, M.J.6
Vardey, C.J.7
Whelan, C.J.8
-
23
-
-
0030572632
-
Agonist and antagonist properties of dihydroetorphine for mu-opioid receptors in mice
-
J. Kamei, T. Suzuki, and H. Nagase Agonist and antagonist properties of dihydroetorphine for mu-opioid receptors in mice Neurosci. Lett. 215 1996 87 90
-
(1996)
Neurosci. Lett.
, vol.215
, pp. 87-90
-
-
Kamei, J.1
Suzuki, T.2
Nagase, H.3
-
25
-
-
0032791257
-
Differential binding properties of oripavines at cloned mu- and delta-opioid receptors
-
K.O. Lee, H. Akil, J.H. Woods, and J.R. Traynor Differential binding properties of oripavines at cloned mu- and delta-opioid receptors Eur. J. Pharmacol. 378 1999 323 330
-
(1999)
Eur. J. Pharmacol.
, vol.378
, pp. 323-330
-
-
Lee, K.O.1
Akil, H.2
Woods, J.H.3
Traynor, J.R.4
-
27
-
-
0032893053
-
Nitrocinnamoyl and chlorocinnamoyl derivatives of dihydrocodeinone: In vivo and in vitro characterization of μ-selective agonist and antagonist activity
-
J.P. McLaughlin, K.P. Hill, Q. Jiang, A. Sebastian, S. Archer, and J.M. Bidlack Nitrocinnamoyl and chlorocinnamoyl derivatives of dihydrocodeinone: in vivo and in vitro characterization of μ-selective agonist and antagonist activity J. Pharmacol. Exp. Ther. 289 1999 304 311
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.289
, pp. 304-311
-
-
McLaughlin, J.P.1
Hill, K.P.2
Jiang, Q.3
Sebastian, A.4
Archer, S.5
Bidlack, J.M.6
-
28
-
-
0014446524
-
The inhibitory action of noradrenaline and adrenaline in acetylcholine output on guinea-pig longitudinal muscle strip
-
W.D.M. Paton, and E.S. Vizi The inhibitory action of noradrenaline and adrenaline in acetylcholine output on guinea-pig longitudinal muscle strip Br. J. Pharmacol. 35 1969 10 29
-
(1969)
Br. J. Pharmacol.
, vol.35
, pp. 10-29
-
-
Paton, W.D.M.1
Vizi, E.S.2
-
29
-
-
0013974234
-
Inhibition of writhing by narcotic antagonists
-
J. Pearl, and L.S. Harris Inhibition of writhing by narcotic antagonists J. Pharmacol. Exp. Ther. 154 1966 319 323
-
(1966)
J. Pharmacol. Exp. Ther.
, vol.154
, pp. 319-323
-
-
Pearl, J.1
Harris, L.S.2
-
30
-
-
0008249278
-
Molecular modeling of fumaramido and cinnamoylamido derivatives in epoxy-morphinans. Correlation with pharmacological profiles
-
N.G. Piggot, I. Derrick, H.A. Moynihan, S.M. Husbands, and J.W. Lewis Molecular modeling of fumaramido and cinnamoylamido derivatives in epoxy-morphinans. Correlation with pharmacological profiles Analgesia 1 1995 4 6
-
(1995)
Analgesia
, vol.1
, pp. 4-6
-
-
Piggot, N.G.1
Derrick, I.2
Moynihan, H.A.3
Husbands, S.M.4
Lewis, J.W.5
-
31
-
-
0020566912
-
Different receptor sites mediate opioid agonism and antagonism
-
P.S. Portoghese, and A.E. Takemori Different receptor sites mediate opioid agonism and antagonism J. Med. Chem. 26 1983 1341 1348
-
(1983)
J. Med. Chem.
, vol.26
, pp. 1341-1348
-
-
Portoghese, P.S.1
Takemori, A.E.2
-
32
-
-
0027367655
-
14β-p-Nitrocinnamoylamino-7,8-dihydromorphinones and their codeinone analogues: Synthesis and receptor activity
-
A. Sebastian, J.M. Bidlack, Q. Jiang, D. Deecher, M. Teitler, S.D. Glick, and S. Archer 14β-p-Nitrocinnamoylamino-7,8-dihydromorphinones and their codeinone analogues: synthesis and receptor activity J. Med. Chem. 36 1993 3154 3160
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3154-3160
-
-
Sebastian, A.1
Bidlack, J.M.2
Jiang, Q.3
Deecher, D.4
Teitler, M.5
Glick, S.D.6
Archer, S.7
-
34
-
-
0023093925
-
Decrease in delta and mu opioid receptor binding capacity in rat brain after chronic etorphine treatment
-
P. Tao, P. Law, and H.H. Loh Decrease in delta and mu opioid receptor binding capacity in rat brain after chronic etorphine treatment J. Pharmacol. Exp. Ther. 240 1987 809 816
-
(1987)
J. Pharmacol. Exp. Ther.
, vol.240
, pp. 809-816
-
-
Tao, P.1
Law, P.2
Loh, H.H.3
-
35
-
-
0023948749
-
Morphine-induced down regulation of μ-opioid receptors in neonatal rat brain
-
A. Tempel, J. Habas, W. Paredes, and G.A. Barr Morphine-induced down regulation of μ-opioid receptors in neonatal rat brain Dev. Brain Res. 41 1988 129 133
-
(1988)
Dev. Brain Res.
, vol.41
, pp. 129-133
-
-
Tempel, A.1
Habas, J.2
Paredes, W.3
Barr, G.A.4
-
36
-
-
0028986870
-
35]thio)triphosphate binding to membranes from human neuroblastoma SH-SY5Y cells
-
35]thio)triphosphate binding to membranes from human neuroblastoma SH-SY5Y cells Mol. Pharmacol. 47 1995 848 854
-
(1995)
Mol. Pharmacol.
, vol.47
, pp. 848-854
-
-
Traynor, J.R.1
Nahorski, S.R.2
-
37
-
-
0032747782
-
Ring-constrained orvinols as analogs of buprenorphine: Differences in opioid activity related to configuration of C20 hydroxyl group
-
J.R. Traynor, L. Guo, A. Coop, J.L. Lewis, and J.H. Woods Ring-constrained orvinols as analogs of buprenorphine: differences in opioid activity related to configuration of C20 hydroxyl group J. Pharmacol. Exp. Ther. 291 1999 1093 1099
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.291
, pp. 1093-1099
-
-
Traynor, J.R.1
Guo, L.2
Coop, A.3
Lewis, J.L.4
Woods, J.H.5
-
38
-
-
0018822636
-
A classification of opiate receptors that mediate antinociception in animals
-
M.B. Tyers A classification of opiate receptors that mediate antinociception in animals Br. J. Pharmacol. 69 1980 503 512
-
(1980)
Br. J. Pharmacol.
, vol.69
, pp. 503-512
-
-
Tyers, M.B.1
-
39
-
-
0028991723
-
Methoclocinnamox: A μ partial agonist with pharmacotherapeutic potential for heroin abuse
-
J.H. Woods, J.W. Lewis, G. Winger, E. Butelman, J. Broadbear, and G. Zernig Methoclocinnamox: a μ partial agonist with pharmacotherapeutic potential for heroin abuse NIDA Res. Monogr. 147 1995 195 219
-
(1995)
NIDA Res. Monogr.
, vol.147
, pp. 195-219
-
-
Woods, J.H.1
Lewis, J.W.2
Winger, G.3
Butelman, E.4
Broadbear, J.5
Zernig, G.6
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