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Sybyl, Version 6.4
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49
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0344200720
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Delta opioid selectivity of N-substituted noroxymorphindoles
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Abstracts
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McLamore, S. M.; Coop, A.; Dersch, C. M.; McCullough, K.; Horel, R.; Rothman, R. B.; Rice, K. C. Delta Opioid Selectivity of N-Substituted Noroxymorphindoles. Abstracts of the 60th Meeting of the College on Drug Dependence, 1998.
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(1998)
60th Meeting of the College on Drug Dependence
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McLamore, S.M.1
Coop, A.2
Dersch, C.M.3
McCullough, K.4
Horel, R.5
Rothman, R.B.6
Rice, K.C.7
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50
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9844261704
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Discovery of a novel class of substituted pyrrolooctahydroisoquinolines as potent and selective δ opioid agonists, based on an extension of the message-address concept
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Dondio, G.; Ronzoni, S.; Eggleston, D. S.; Artico, M.; Petrillo, P.; Petrone, G.; Visentin, L.; Farina, C.; Vecchietti, V.; Clarke, G. D. Discovery of a Novel Class of Substituted Pyrrolooctahydroisoquinolines as Potent and Selective δ Opioid Agonists, Based on an Extension of the Message-Address Concept. J. Med. Chem. 1997, 40, 3192-3198.
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J. Med. Chem.
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Dondio, G.1
Ronzoni, S.2
Eggleston, D.S.3
Artico, M.4
Petrillo, P.5
Petrone, G.6
Visentin, L.7
Farina, C.8
Vecchietti, V.9
Clarke, G.D.10
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51
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0031045077
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Opioid diketopiperazines: Synthesis and activity of a prototypic class of opioid antagonists
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Balboni, G.; Guerrini, R.; Salvadori, S.; Tomatis, R.; Bryant, S. D.; Bianchi, C.; Attila, M.; Lazarus, L. H. Opioid Diketopiperazines: Synthesis and Activity of a Prototypic Class of Opioid Antagonists. Biol. Chem. 1997, 378, 19-29.
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Biol. Chem.
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, pp. 19-29
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Balboni, G.1
Guerrini, R.2
Salvadori, S.3
Tomatis, R.4
Bryant, S.D.5
Bianchi, C.6
Attila, M.7
Lazarus, L.H.8
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52
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7844239326
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De Novo design, synthesis, and biological activities of high-affinity and selective non-peptide agonists of the δ-opioid receptor
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Liao, S.; Alfaro-Lopez, J.; Shenderovich, M. D.; Hosohata, K.; Lin, J.; Li, X.; Stropova, D.; Davis, P.; Jernigan, K. A.; Porreca, P.; Yamamura, H. I.; Hruby, V. J. De Novo Design, Synthesis, and Biological Activities of High-Affinity and Selective Non-Peptide Agonists of the δ-Opioid Receptor. J. Med. Chem. 1998, 41, 4767-4776.
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, vol.41
, pp. 4767-4776
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Liao, S.1
Alfaro-Lopez, J.2
Shenderovich, M.D.3
Hosohata, K.4
Lin, J.5
Li, X.6
Stropova, D.7
Davis, P.8
Jernigan, K.A.9
Porreca, P.10
Yamamura, H.I.11
Hruby, V.J.12
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53
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0345494466
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note
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It was shown that significant decomposition occurred if an aqueous solution of 13 was allowed to stand for 24 h open to the atmosphere.
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54
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0031808576
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Signal transduction correlates of Mu opioid agonist intrinsic efficacy: Receptor-stimulated [S-35]GTP gamma S binding in mMOR-CHO cells and rat thalamus
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Selley, D. E.; Liu, Q. X.; Childers, S. R. Signal Transduction Correlates of Mu Opioid Agonist Intrinsic Efficacy: Receptor-stimulated [S-35]GTP Gamma S Binding in mMOR-CHO Cells and Rat Thalamus. J. Pharmacol. Exp. Ther. 1998, 285, 496-505.
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J. Pharmacol. Exp. Ther.
, vol.285
, pp. 496-505
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Selley, D.E.1
Liu, Q.X.2
Childers, S.R.3
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55
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0018100610
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Formamidesulfinic acid reduction of dihydrocodeinone derivatives
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Brine, G. A.; Boldt, K G.; Coleman, M. L.; Bradley, D. J.; Carroll, F. I. Formamidesulfinic Acid Reduction of Dihydrocodeinone Derivatives. J. Org. Chem. 1978, 43, 1555-1557.
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(1978)
J. Org. Chem.
, vol.43
, pp. 1555-1557
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Brine, G.A.1
Boldt, K.G.2
Coleman, M.L.3
Bradley, D.J.4
Carroll, F.I.5
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56
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0344632425
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note
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Detailed spectral analysis of 8 can be found in ref 39.
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