-
1
-
-
0011946740
-
Symbols and abbreviations are compliant with the recommendations made by the IUPAC-IUB Commission of Nomenclature
-
2,5]enkephalin, H-Tyr-[D-Pen-Gly-Phe-D-Pen]-OH; JOM-13, Tyr-c[D-Cys-Phe-D-Pen]OH; OtBu, tert-butyl ester; Fmoc, 9-fluoroenylmethyloxycarbonyl; GPI, guinea pig ileum; MVD, mouse vas deferens; HOBt, 1-hydroxybenzotriazole; Pen, β,β-dimethylcysteine; TIPP, H-Tyr-Tic-Phe-Phe-OH.
-
(1972)
J. Biol. Chem.
, pp. 247
-
-
-
2
-
-
0020696799
-
Distribution and physiological significance of opioid receptors in the brain
-
Atweh, S. F.; Kuhar, M. J. Distribution and physiological significance of opioid receptors in the brain. Br. Med. Bull. 1983, 39, 57-59.
-
(1983)
Br. Med. Bull.
, vol.39
, pp. 57-59
-
-
Atweh, S.F.1
Kuhar, M.J.2
-
3
-
-
0016701344
-
Identification of two related pentapeptides from the brain with potent opiate agonist activity
-
Hughes, J.; Smith, T. W.; Kosterlitz, H. W.; Fothergill, L. A.; Morgan, B. A.; Morris, H. R. Identification of two related pentapeptides from the brain with potent opiate agonist activity. Nature 1975, 258, 577-580.
-
(1975)
Nature
, vol.258
, pp. 577-580
-
-
Hughes, J.1
Smith, T.W.2
Kosterlitz, H.W.3
Fothergill, L.A.4
Morgan, B.A.5
Morris, H.R.6
-
4
-
-
0000979854
-
Isolation and structure of an untriakontapeptide with opiate activity from camel pituitary glands
-
Li, C. H.; Chung, D. Isolation and structure of an untriakontapeptide with opiate activity from camel pituitary glands. Proc. Natl. Acad. Sci. U.S.A. 1976, 73, 1145-1148.
-
(1976)
Proc. Natl. Acad. Sci. U.S.A.
, vol.73
, pp. 1145-1148
-
-
Li, C.H.1
Chung, D.2
-
5
-
-
0000881377
-
Dynorphin-(1-13), an extraordinary potent opioid peptide
-
Goldstein, A.; Tachibana, S.; Lowney, L. H.; Hunkapiller, M.; Hood, L. Dynorphin-(1-13), an extraordinary potent opioid peptide. Proc. Natl. Acad. Sci. U.S.A. 1979, 76, 6666-6670.
-
(1979)
Proc. Natl. Acad. Sci. U.S.A.
, vol.76
, pp. 6666-6670
-
-
Goldstein, A.1
Tachibana, S.2
Lowney, L.H.3
Hunkapiller, M.4
Hood, L.5
-
6
-
-
0030933655
-
A potent and selective endogenous agonist for the mu-opiate receptor
-
Zadina, J. E.; Hackler, L.; Gee, L. J., Kastin, A. J. A potent and selective endogenous agonist for the mu-opiate receptor. Nature 1997, 386, 499-502.
-
(1997)
Nature
, vol.386
, pp. 499-502
-
-
Zadina, J.E.1
Hackler, L.2
Gee, L.J.3
Kastin, A.J.4
-
7
-
-
0036645264
-
Rapid titration with intravenous morphine for severe cancer pain and immediate oral conversion
-
Mercadante, S.; Villari, P.; Ferrera, P.; Casuccio, A.; Fulfaro, F. Rapid titration with intravenous morphine for severe cancer pain and immediate oral conversion. Cancer 2002, 95, 203-208.
-
(2002)
Cancer
, vol.95
, pp. 203-208
-
-
Mercadante, S.1
Villari, P.2
Ferrera, P.3
Casuccio, A.4
Fulfaro, F.5
-
8
-
-
0036311555
-
Intranasal naloxone for life threatening opioid toxicity
-
Kelly, A. M.; Koutsogiannis, Z. Intranasal naloxone for life threatening opioid toxicity. Emerg. Med. J. 2002, 19, 375.
-
(2002)
Emerg. Med. J.
, vol.19
, pp. 375
-
-
Kelly, A.M.1
Koutsogiannis, Z.2
-
9
-
-
84921623020
-
Opioid antagonists with minimal sedation for opioid withdrawal
-
CD001333
-
Gowing, L.; Ali, R.; White, J. Opioid antagonists with minimal sedation for opioid withdrawal. Cochrane Database Syst. Rev. 2002, 2, CD001333.
-
(2002)
Cochrane Database Syst. Rev.
, vol.2
-
-
Gowing, L.1
Ali, R.2
White, J.3
-
10
-
-
0033681556
-
Opioid pseudopeptides containing heteroaromatic or heteroaliphatic nuclei
-
Balboni, G.; Salvadori, S.; Guerrini, R.; Bianchi, C.; Santagada, V.; Calliendo, G.; Bryant, S. D.; Lazarus, L. H. Opioid pseudopeptides containing heteroaromatic or heteroaliphatic nuclei. Peptides 2000, 21, 1663-1671.
-
(2000)
Peptides
, vol.21
, pp. 1663-1671
-
-
Balboni, G.1
Salvadori, S.2
Guerrini, R.3
Bianchi, C.4
Santagada, V.5
Calliendo, G.6
Bryant, S.D.7
Lazarus, L.H.8
-
11
-
-
0034684763
-
Assessment of substitution in the second pharmacophore of Dmt-Tic analogues
-
Santagada, V.; Balboni, G.; Caliendo, G.; Guerrini, R.; Salvadori, S.; Bianchi, C.; Bryant, S. D.; Lazarus, L. H. Assessment of substitution in the second pharmacophore of Dmt-Tic analogues. Bioorg. Med. Chem. Lett. 2000, 10, 2745-2748.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2745-2748
-
-
Santagada, V.1
Balboni, G.2
Caliendo, G.3
Guerrini, R.4
Salvadori, S.5
Bianchi, C.6
Bryant, S.D.7
Lazarus, L.H.8
-
12
-
-
0037204052
-
Evaluation of the Dmt-Tic pharmacophore: Conversion of a potent δ-opioid receptor antagonist into a potent δ-agonist and ligands with mixed properties
-
Balboni, G.; Guerrini, R.; Salvadori, S.; Bianchi, C.; Rizzi, D.; Bryant, S. D.; Lazarus, L. H. Evaluation of the Dmt-Tic pharmacophore: Conversion of a potent δ-opioid receptor antagonist into a potent δ-agonist and ligands with mixed properties. J. Med. Chem. 2002, 45, 713-720.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 713-720
-
-
Balboni, G.1
Guerrini, R.2
Salvadori, S.3
Bianchi, C.4
Rizzi, D.5
Bryant, S.D.6
Lazarus, L.H.7
-
13
-
-
0029366282
-
δ opioidmimetic antagonists: Prototypes for designing a new generation of ultraselective opioid peptides
-
Salvadori, S.; Attila, M.; Balboni, G.; Bianchi, C.; Bryant, S. D.; Crescenzi, O.; Guerrini, R.; Picone, D.; Tancredi, T.; Temussi, P. A.; Lazarus, L. H. δ opioidmimetic antagonists: Prototypes for designing a new generation of ultraselective opioid peptides. Mol. Med. 1995, 1, 678-689.
-
(1995)
Mol. Med.
, vol.1
, pp. 678-689
-
-
Salvadori, S.1
Attila, M.2
Balboni, G.3
Bianchi, C.4
Bryant, S.D.5
Crescenzi, O.6
Guerrini, R.7
Picone, D.8
Tancredi, T.9
Temussi, P.A.10
Lazarus, L.H.11
-
14
-
-
0031857993
-
Design of δ-opioid peptide antagonists for emerging drug applications
-
Lazarus, L. H.; Bryant, S. D.; Cooper, P. S.; Guerrini, R.; Balboni, G.; Salvadori, S. Design of δ-opioid peptide antagonists for emerging drug applications. Drug Discovery Today 1998, 3, 284-294.
-
(1998)
Drug Discovery Today
, vol.3
, pp. 284-294
-
-
Lazarus, L.H.1
Bryant, S.D.2
Cooper, P.S.3
Guerrini, R.4
Balboni, G.5
Salvadori, S.6
-
15
-
-
0026602250
-
Preparation and opioid activity of analogues of the analgesic dipeptide 2,6-dimethyl-L-tyrosyl-N-(3-phenylpropyl)-D-alaninamide
-
Chandrakumar, N. S.; Yonan, P. K.; Stapelfeld, A.; Savage, M.; Rorbacher, E.; Contreras, P. C.; Hammond, D. Preparation and opioid activity of analogues of the analgesic dipeptide 2,6-dimethyl-L-tyrosyl-N-(3-phenylpropyl)-D-alaninamide. J. Med. Chem. 1992, 35, 223-233.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 223-233
-
-
Chandrakumar, N.S.1
Yonan, P.K.2
Stapelfeld, A.3
Savage, M.4
Rorbacher, E.5
Contreras, P.C.6
Hammond, D.7
-
16
-
-
0026578014
-
5]enkephalin
-
5]enkephalin. J. Med. Chem. 1992, 35, 684-687.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 684-687
-
-
Hansen, J.D.W.1
Stapelfeld, A.2
Savage, M.A.3
Reichman, M.4
Hammond, D.L.5
Haaseth, R.C.6
Mosberg, H.I.7
-
17
-
-
0028201818
-
Enkephalin analogs as systematically active antinociceptive agents: O- and N-alkylated derivatives of the dipeptide amide L-2,6-dimethyltyrosyl-N-(3-phenylpropyl)-D-alaninamide
-
Pitzele, B. S.; Hamilton, R. W.; Kudla, K. D.; Tsymbalov, S.; Stapelfeld, A.; Savage, M. A.; Clare, M.; Hammond, D. L.; Hansen, J. D. W. Enkephalin analogs as systematically active antinociceptive agents: O- and N-alkylated derivatives of the dipeptide amide L-2,6-dimethyltyrosyl-N-(3-phenylpropyl)-D-alaninamide. J. Med. Chem. 1994, 37, 888-896.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 888-896
-
-
Pitzele, B.S.1
Hamilton, R.W.2
Kudla, K.D.3
Tsymbalov, S.4
Stapelfeld, A.5
Savage, M.A.6
Clare, M.7
Hammond, D.L.8
Hansen, J.D.W.9
-
18
-
-
0029975241
-
Opioid receptor selectivity alteration by single residue replacement: Synthesis and activity profile of [Dmtl]deltorphin B
-
Guerrini, R.; Capasso, A.; Sorrentino, L.; Anacardio, R.; Bryant, S. D.; Lazarus, L. H.; Attila, M.; Salvadori, S. Opioid receptor selectivity alteration by single residue replacement: synthesis and activity profile of [Dmtl]deltorphin B. Eur. J. Pharmacol. 1996, 302, 37-42.
-
(1996)
Eur. J. Pharmacol.
, vol.302
, pp. 37-42
-
-
Guerrini, R.1
Capasso, A.2
Sorrentino, L.3
Anacardio, R.4
Bryant, S.D.5
Lazarus, L.H.6
Attila, M.7
Salvadori, S.8
-
19
-
-
17944403436
-
Rational design of dynorphin A analogues with δ-receptor selectivity and antagonism for δ- and κ-receptors
-
Guerrini, R.; Capasso, A.; Marastoni, A.; Bryant, S. D.; Cooper, P. S.; Lazarus, L. H.; Temussi, P. A.; Salvadori, S. Rational design of dynorphin A analogues with δ-receptor selectivity and antagonism for δ- and κ-receptors. Bioorg. Med. Chem. 1998, 6, 57-62.
-
(1998)
Bioorg. Med. Chem.
, vol.6
, pp. 57-62
-
-
Guerrini, R.1
Capasso, A.2
Marastoni, A.3
Bryant, S.D.4
Cooper, P.S.5
Lazarus, L.H.6
Temussi, P.A.7
Salvadori, S.8
-
20
-
-
0032713301
-
Biological properties of opioid peptides replacing Tyr at position 1 by 2,6-dimethyl-Tyr
-
Sasaki, Y.; Suto, T.; Ambo, A.; Ouchi, H.; Yamamoto, Y. Biological properties of opioid peptides replacing Tyr at position 1 by 2,6-dimethyl-Tyr. Chem. Pharm. Bull. 1999, 47, 1506-1507.
-
(1999)
Chem. Pharm. Bull.
, vol.47
, pp. 1506-1507
-
-
Sasaki, Y.1
Suto, T.2
Ambo, A.3
Ouchi, H.4
Yamamoto, Y.5
-
21
-
-
0033748070
-
Synthesis and in vitro opioid activity profiles of DALDA analogues
-
Schiller, P. W.; Nguyen, T. M.-D.; Berezowska, I.; Dupuis, S.; Weltrowska, G.; Chung, N. N.; Lemieux, C. Synthesis and in vitro opioid activity profiles of DALDA analogues. Eur. J. Med. Chem. 2000, 35, 895-901.
-
(2000)
Eur. J. Med. Chem.
, vol.35
, pp. 895-901
-
-
Schiller, P.W.1
Nguyen, T.M.-D.2
Berezowska, I.3
Dupuis, S.4
Weltrowska, G.5
Chung, N.N.6
Lemieux, C.7
-
22
-
-
0033518261
-
Further studies on the Dmt-Tic pharmacophore: Hydrophobic substituents at the C-terminus endows δ antagonists to manifest μ agonism or μ antagonism
-
Salvadori, S.; Guerrini, R.; Balboni, G.; Bianchi, C.; Bryant, S. D.; Cooper, P. S.; Lazarus, L. H. Further studies on the Dmt-Tic pharmacophore: Hydrophobic substituents at the C-terminus endows δ antagonists to manifest μ agonism or μ antagonism. J. Med. Chem. 1999, 42, 5010-5019.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 5010-5019
-
-
Salvadori, S.1
Guerrini, R.2
Balboni, G.3
Bianchi, C.4
Bryant, S.D.5
Cooper, P.S.6
Lazarus, L.H.7
-
23
-
-
0034677117
-
Novel Dmt-Tic dipeptide analogues as selective delta-opioid receptor antagonists
-
Page, D.; McClory, A.; Mischki, T.; Schmidt, R.; Butterworth, J.; St-Onge, S.; Labarre, M.; Payza, K.; Brown, W. Novel Dmt-Tic dipeptide analogues as selective delta-opioid receptor antagonists. Bioorg. Med. Chem. Lett. 2000, 10, 167-170.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 167-170
-
-
Page, D.1
McClory, A.2
Mischki, T.3
Schmidt, R.4
Butterworth, J.5
St-Onge, S.6
Labarre, M.7
Payza, K.8
Brown, W.9
-
24
-
-
0035913055
-
Novel Cterminus modifications of the Dmt-Tic motif: A new class of dipeptide analogues showing altered pharmacological profiles toward the opioid receptors
-
Page, D.; Naismith, A.; Schmidt, R.; Coupal, M.; Labarre, M.; Gosselin, M.; Bellemare, D.; Payza, K.; Brown, W. Novel Cterminus modifications of the Dmt-Tic motif: A new class of dipeptide analogues showing altered pharmacological profiles toward the opioid receptors. J. Med. Chem. 2001, 44, 2387-2390.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2387-2390
-
-
Page, D.1
Naismith, A.2
Schmidt, R.3
Coupal, M.4
Labarre, M.5
Gosselin, M.6
Bellemare, D.7
Payza, K.8
Brown, W.9
-
25
-
-
0030880687
-
Evolution of the Dmt-Tic pharmacophore: N-terminal methylated derivatives with extraordinary δ opioid antagonist activity
-
Salvadori, S.; Balboni, G.; Guerrini, R.; Tomatis, R.; Bianchi, C.; Bryant, S. D.; Cooper, P. S.; Lazarus, L. H. Evolution of the Dmt-Tic pharmacophore: N-terminal methylated derivatives with extraordinary δ opioid antagonist activity. J. Med. Chem. 1997, 40, 3100-3108.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3100-3108
-
-
Salvadori, S.1
Balboni, G.2
Guerrini, R.3
Tomatis, R.4
Bianchi, C.5
Bryant, S.D.6
Cooper, P.S.7
Lazarus, L.H.8
-
26
-
-
0030755890
-
Design and solution structure of a partially rigid opioid antagonist lacking the basic center
-
Crescenzi, O.; Fraternali, F.; Picone, D.; Tancredi, T.; Balboni, G.; Guerrini, R.; Lazarus, L. H.; Salvadori, S.; Temussi, P. A. Design and solution structure of a partially rigid opioid antagonist lacking the basic center. Eur. J. Biochem. 1997, 247, 66-73.
-
(1997)
Eur. J. Biochem.
, vol.247
, pp. 66-73
-
-
Crescenzi, O.1
Fraternali, F.2
Picone, D.3
Tancredi, T.4
Balboni, G.5
Guerrini, R.6
Lazarus, L.H.7
Salvadori, S.8
Temussi, P.A.9
-
27
-
-
0030897933
-
Opioid diketopiperazines: Refinement of the δ opioid antagonist pharmacophore
-
Bryant, S. D.; Balboni, G.; Guerrini, R.; Salvadori, S.; Tomatis, R.; Lazarus, L. H. Opioid diketopiperazines: Refinement of the δ opioid antagonist pharmacophore. Biol. Chem. 1997, 378, 107-114.
-
(1997)
Biol. Chem.
, vol.378
, pp. 107-114
-
-
Bryant, S.D.1
Balboni, G.2
Guerrini, R.3
Salvadori, S.4
Tomatis, R.5
Lazarus, L.H.6
-
28
-
-
0031883575
-
New δ opioid antagonists as pharmacological probes
-
Bryant, S. D.; Salvadori, S.; Cooper, P. S.; Lazarus, L. H. New δ opioid antagonists as pharmacological probes. Trends Pharmacol. Sci. 1998, 19, 42-46.
-
(1998)
Trends Pharmacol. Sci.
, vol.19
, pp. 42-46
-
-
Bryant, S.D.1
Salvadori, S.2
Cooper, P.S.3
Lazarus, L.H.4
-
29
-
-
0034914627
-
Probing the shape of a hydrophobic pocket in the active site of δ-opioid antagonists
-
Santagada, V.; Caliendo, G.; Severino, B.; Perissutti, E.; Ceccarelli, F.; Giusti, L.; Mazzoni, R.; Salvadori, S.; Temussi, P. A. Probing the shape of a hydrophobic pocket in the active site of δ-opioid antagonists. J. Pept. Sci. 2001, 7, 374-385.
-
(2001)
J. Pept. Sci.
, vol.7
, pp. 374-385
-
-
Santagada, V.1
Caliendo, G.2
Severino, B.3
Perissutti, E.4
Ceccarelli, F.5
Giusti, L.6
Mazzoni, R.7
Salvadori, S.8
Temussi, P.A.9
-
30
-
-
0034776780
-
Natural peptide analgesics: The role of solution conformation
-
Spadaccini, R.; Temussi, P. A. Natural peptide analgesics: The role of solution conformation. Cell. Mol. Life Sci. 2001, 58, 1572-1582.
-
(2001)
Cell. Mol. Life Sci.
, vol.58
, pp. 1572-1582
-
-
Spadaccini, R.1
Temussi, P.A.2
-
31
-
-
0000566705
-
X-Ray structures of the δ opioid antagonist TIPP and a protected derivative of the δ antagonist ICI 174,864
-
Flippen-Anderson, J. L.; George, C.; Deschamps, J. R.; Reddy, P. A.; Lewin, A. H.; Brine, G. A. X-Ray structures of the δ opioid antagonist TIPP and a protected derivative of the δ antagonist ICI 174,864. Lett. Pept. Sci. 1994, 1, 107-115.
-
(1994)
Lett. Pept. Sci.
, vol.1
, pp. 107-115
-
-
Flippen-Anderson, J.L.1
George, C.2
Deschamps, J.R.3
Reddy, P.A.4
Lewin, A.H.5
Brine, G.A.6
-
32
-
-
0030919988
-
X-Ray structure of Tyr-D-Tic-Phe-Phe-NH2 (D-TIPP-NH2), a highly potent μ-receptor selective opioid agonist
-
Flippen-Anderson, J. L.; Deschamps, J. R.; George, C.; Reddy, P. A.; Lewin, A. H.; Brine, G. A.; Sheldrick, G.; Nikiforovich, G. X-Ray structure of Tyr-D-Tic-Phe-Phe-NH2 (D-TIPP-NH2), a highly potent μ-receptor selective opioid agonist. J. Pept. Res. 1997, 49, 384-393.
-
(1997)
J. Pept. Res.
, vol.49
, pp. 384-393
-
-
Flippen-Anderson, J.L.1
Deschamps, J.R.2
George, C.3
Reddy, P.A.4
Lewin, A.H.5
Brine, G.A.6
Sheldrick, G.7
Nikiforovich, G.8
-
33
-
-
0031248634
-
Tyrosinium-D-tetrahydroisoquinoline-3-carbox-ylate 1,5-hydrate and tyrosyl-D-tetrahydroisoquinoline-3-carboxamide hydrate
-
Deschamps, J. R.; Flippen-Anderson, J. L.; Moore, C.; Cudney, R.; George, C. Tyrosinium-D-tetrahydroisoquinoline-3-carbox-ylate 1,5-hydrate and tyrosyl-D-tetrahydroisoquinoline-3-carboxamide hydrate. Acta Crystallogr. C 1997, C53, 1478-1482.
-
(1997)
Acta Crystallogr. C
, vol.C53
, pp. 1478-1482
-
-
Deschamps, J.R.1
Flippen-Anderson, J.L.2
Moore, C.3
Cudney, R.4
George, C.5
-
34
-
-
0031425254
-
2]deltorphin I: Effects on opioid receptor affinities and activities in vitro and on antinociceptive potency
-
2]deltorphin I: Effects on opioid receptor affinities and activities in vitro and on antinociceptive potency. Peptides 1997, 18, 1615-1621.
-
(1997)
Peptides
, vol.18
, pp. 1615-1621
-
-
Schmidt, R.1
Menard, D.2
Mrestani-Klaus, C.3
Chung, N.N.4
Lemieux, C.5
Schiller, P.W.6
-
35
-
-
0032928689
-
What peptides these deltorphins be
-
Lazarus, L. H.; Bryant, S. D.; Cooper, P. S.; Salvadori, S. What peptides these deltorphins be. Prog. Neurobiol. 1999, 57, 377-420.
-
(1999)
Prog. Neurobiol.
, vol.57
, pp. 377-420
-
-
Lazarus, L.H.1
Bryant, S.D.2
Cooper, P.S.3
Salvadori, S.4
-
36
-
-
0032491267
-
A high affinity, muopioid receptor-selective enkephalin analogue lacking an N-terminal tyrosine
-
Mosberg, H. I.; Ho, J. C.; Sobczyk-Kojiro, K. A high affinity, muopioid receptor-selective enkephalin analogue lacking an N-terminal tyrosine. Bioorg. Med. Chem. Lett. 1998, 8, 2681-2684.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 2681-2684
-
-
Mosberg, H.I.1
Ho, J.C.2
Sobczyk-Kojiro, K.3
-
37
-
-
0027786962
-
The molecular basis of opioid potency and selectivity: Mophiceptins, dermorphins, deltorphins, and enkephalins
-
Goodman, M.; Ro, S.; Osapay, G.; Yamazaki, T.; Polinsky, A. The molecular basis of opioid potency and selectivity: Mophiceptins, dermorphins, deltorphins, and enkephalins. NIDA Res. Monogr. 1993, 143, 195-209.
-
(1993)
NIDA Res. Monogr.
, vol.143
, pp. 195-209
-
-
Goodman, M.1
Ro, S.2
Osapay, G.3
Yamazaki, T.4
Polinsky, A.5
-
38
-
-
0028476063
-
Molecular dynamics conformations of deltorphin analogues advocate δ opioid binding site models
-
Bryant, S. D.; Attila, M.; Salvadori, S.; Guerrini, R.; Lazarus, L. H. Molecular dynamics conformations of deltorphin analogues advocate δ opioid binding site models. Pept. Res. 1994, 7, 175-184.
-
(1994)
Pept. Res.
, vol.7
, pp. 175-184
-
-
Bryant, S.D.1
Attila, M.2
Salvadori, S.3
Guerrini, R.4
Lazarus, L.H.5
-
39
-
-
0030745579
-
Helix inducing α-aminoisobutyric acid in opioidmimetic deltorphin C analogues
-
Bryant, S. D.; Guerrini, R.; Salvadori, S.; Bianchi, C.; Tomatis, R.; Attila, M.; Lazarus, L. H. Helix inducing α-aminoisobutyric acid in opioidmimetic deltorphin C analogues. J. Med. Chem. 1997, 40, 2579-2587.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2579-2587
-
-
Bryant, S.D.1
Guerrini, R.2
Salvadori, S.3
Bianchi, C.4
Tomatis, R.5
Attila, M.6
Lazarus, L.H.7
-
40
-
-
0028142509
-
Crystal structure of deltakephalin: A δ-selective opioid peptide with a novel β-bend-like conformation
-
Flippen-Anderson, J. L.; Deschamps, J. R.; Ward, K. B.; George, C.; Houghten, R. Crystal structure of deltakephalin: A δ-selective opioid peptide with a novel β-bend-like conformation. Int. J. Pept. Protein Res. 1994, 44, 97-104.
-
(1994)
Int. J. Pept. Protein Res.
, vol.44
, pp. 97-104
-
-
Flippen-Anderson, J.L.1
Deschamps, J.R.2
Ward, K.B.3
George, C.4
Houghten, R.5
-
41
-
-
0024578743
-
A crystal molecular conformation of leucine-enkephalin related to the morphine molecule
-
Aubry, A.; Birlirakis, N.; Sakarellos-Daitsiotis, M.; Sakarellos, C.; Marraud, M. A crystal molecular conformation of leucine-enkephalin related to the morphine molecule. Biopolymers 1989, 28, 27-40.
-
(1989)
Biopolymers
, vol.28
, pp. 27-40
-
-
Aubry, A.1
Birlirakis, N.2
Sakarellos-Daitsiotis, M.3
Sakarellos, C.4
Marraud, M.5
-
44
-
-
0028100316
-
5] enkephalin, a highly potent, δ opioid receptor-selective compound: Comparison with proposed solution conformations
-
5] enkephalin, a highly potent, δ opioid receptor-selective compound: Comparison with proposed solution conformations. J. Am. Chem. Soc. 1994, 116, 7523-7531.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 7523-7531
-
-
Flippen-Anderson, J.1
Hruby, V.J.2
Collins, N.3
George, C.4
Cudney, B.5
-
46
-
-
0023024852
-
Molecular mechanism of opioid selection
-
Schwyzer, R. Molecular mechanism of opioid selection. Biochemistry 1986, 25, 6335-6342.
-
(1986)
Biochemistry
, vol.25
, pp. 6335-6342
-
-
Schwyzer, R.1
-
47
-
-
0029870521
-
3]DPDPE
-
3]DPDPE. J. Am. Chem. Soc. 1996, 118, 2143-2152.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 2143-2152
-
-
Collins, N.1
Flippen-Anderson, J.L.2
Haaseth, R.C.3
Deschamps, J.R.4
George, C.5
Kover, K.6
Hruby, V.J.7
-
48
-
-
0029925981
-
5): Novel conformationally constrained opioid peptides
-
5): Novel conformationally constrained opioid peptides. J. Am. Chem. Soc. 1996, 118, 959-969.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 959-969
-
-
Nikiforovich, G.V.1
Kover, K.E.2
Kolodziej, S.A.3
Nock, B.4
George, C.5
Deschamps, J.R.6
Flippen-Anderson, J.L.7
Marshall, G.R.8
-
49
-
-
0039413706
-
X-ray crystallographic and molecular modeling studies of 1-(2,6-diflourobenzoyl)-5-(4-chlorophenyl)biuret
-
Deschamps, J. R.; George, C.; Flippen-Anderson, J. L.; DeMilo, A. B.; Bordas, B. X-ray crystallographic and molecular modeling studies of 1-(2,6-diflourobenzoyl)-5-(4-chlorophenyl)biuret. J. Chem. Crystallogr. 1998, 28, 453-459.
-
(1998)
J. Chem. Crystallogr.
, vol.28
, pp. 453-459
-
-
Deschamps, J.R.1
George, C.2
Flippen-Anderson, J.L.3
DeMilo, A.B.4
Bordas, B.5
-
52
-
-
0004150157
-
-
Bruker Analytical X-ray Instruments: Madison, WI
-
Sheldrick, G. M. SHELXTL, Version 5.1; Bruker Analytical X-ray Instruments: Madison, WI, 1997.
-
(1997)
SHELXTL, Version 5.1
-
-
Sheldrick, G.M.1
|