-
1
-
-
27744431653
-
The endogenous opioid system and clinical pain management
-
Holden, J. E.; Jeong, Y.; Forrest, J. M. The endogenous opioid system and clinical pain management AACN Clin. Issues 2005, 16, 291-301
-
(2005)
AACN Clin. Issues
, vol.16
, pp. 291-301
-
-
Holden, J.E.1
Jeong, Y.2
Forrest, J.M.3
-
2
-
-
0017735536
-
Endogenous opioid peptides: multiple agonists and receptors
-
Lord, J. A.; Waterfield, A. A.; Hughes, J.; Kosterlitz, H. W. Endogenous opioid peptides: multiple agonists and receptors Nature 1977, 267, 495-499 (Pubitemid 8098466)
-
(1977)
Nature
, vol.267
, Issue.5611
, pp. 495-499
-
-
Lord, J.A.H.1
Waterfield, A.A.2
Hughes, J.3
Kosterlitz, H.W.4
-
3
-
-
82655187443
-
Endogenous opiates and behavior: 2010
-
Bodnar, R. J. Endogenous opiates and behavior: 2010 Peptides 2011, 32, 2522-2552
-
(2011)
Peptides
, vol.32
, pp. 2522-2552
-
-
Bodnar, R.J.1
-
4
-
-
0030933655
-
A potent and selective endogenous agonist for the μ-opiate receptor
-
DOI 10.1038/386499a0
-
Zadina, J. E.; Hackler, L.; Ge, L. J.; Kastin, A. J. A potent and selective endogenous agonist for the mu-opiate receptor Nature 1997, 386, 499-502 (Pubitemid 27164076)
-
(1997)
Nature
, vol.386
, Issue.6624
, pp. 499-502
-
-
Zadina, J.E.1
Hackler, L.2
Ge, L.-J.3
Kastin, A.J.4
-
5
-
-
0031426851
-
Isolation of relatively large amounts of endomorphin-1 and endomorphin- 2 from human brain cortex
-
DOI 10.1016/S0196-9781(97)00259-3, PII S0196978197002593
-
Hackler, L.; Zadina, J. E.; Ge, L. J.; Kastin, A. J. Isolation of relatively large amounts of endomorphin-1 and endomorphin-2 from human brain cortex Peptides 1997, 18, 1635-1639 (Pubitemid 28133009)
-
(1997)
Peptides
, vol.18
, Issue.10
, pp. 1635-1639
-
-
Hackler, L.1
Zadina, J.E.2
Ge, L.-J.3
Kastin, A.J.4
-
6
-
-
0034528235
-
Dissociation of analgesic and rewarding effects of endomorphin-1 in rats
-
DOI 10.1016/S0196-9781(00)00340-5, PII S0196978100003405
-
Wilson, A. M.; Soignier, R. D.; Zadina, J. E.; Kastin, A. J.; Nores, W. L.; Olson, R. D.; Olson, G. A. Dissociation of analgesic and rewarding effects of endomorphin-1 in rats Peptides 2000, 21, 1871-1874 (Pubitemid 32058862)
-
(2000)
Peptides
, vol.21
, Issue.12
, pp. 1871-1874
-
-
Wilson, A.M.1
Soignier, R.D.2
Zadina, J.E.3
Kastin, A.J.4
Nores, W.L.5
Olson, R.D.6
Olson, G.A.7
-
7
-
-
0033835786
-
Differential cardiorespiratory effects of endomorphin 1, endomorphin 2, DAMGO, and morphine
-
Czapla, M. A.; Gozal, D.; Alea, O. A.; Beckerman, R. C.; Zadina, J. E. Differential cardiorespiratory effects of endomorphin 1, endomorphin 2, DAMGO, and morphine Am. J. Respir. Crit. Care Med. 2000, 162, 994-999
-
(2000)
Am. J. Respir. Crit. Care Med.
, vol.162
, pp. 994-999
-
-
Czapla, M.A.1
Gozal, D.2
Alea, O.A.3
Beckerman, R.C.4
Zadina, J.E.5
-
8
-
-
2142826479
-
Opioid receptors and their ligands
-
Janecka, A.; Fichna, J.; Janecki, T. Opioid receptors and their ligands Curr. Top. Med. Chem. 2004, 4, 1-17 (Pubitemid 38842558)
-
(2004)
Current Topics in Medicinal Chemistry
, vol.4
, Issue.1
, pp. 1-17
-
-
Janecka, A.1
Fichna, J.2
Janecki, T.3
-
9
-
-
84860339691
-
Endomorphins: Potential roles and therapeutic indications in the development of opioid peptide analgesic drugs
-
Liu, W. X.; Wang, R. Endomorphins: potential roles and therapeutic indications in the development of opioid peptide analgesic drugs Med. Res. Rev. 2012, 32, 536-580
-
(2012)
Med. Res. Rev.
, vol.32
, pp. 536-580
-
-
Liu, W.X.1
Wang, R.2
-
10
-
-
0036711009
-
In vitro quantitative study of the degradation of endomorphins
-
DOI 10.1016/S0196-9781(02)00100-6, PII S0196978102001006
-
Tomboly, C.; Peter, A.; Toth, G. In vitro quantitative study of the degradation of endomorphins Peptides 2002, 23, 1573-1580 (Pubitemid 35246276)
-
(2002)
Peptides
, vol.23
, Issue.9
, pp. 1573-1580
-
-
Tomboly, C.1
Peter, A.2
Toth, G.3
-
11
-
-
33646051966
-
Unusual amino acids: Synthesis and introduction into naturally occurring peptides and biologically active analogues
-
Cardillo, G.; Gentilucci, L.; Tolomelli, A. Unusual amino acids: synthesis and introduction into naturally occurring peptides and biologically active analogues Mini-Rev. Med. Chem. 2006, 6, 293-304
-
(2006)
Mini-Rev. Med. Chem.
, vol.6
, pp. 293-304
-
-
Cardillo, G.1
Gentilucci, L.2
Tolomelli, A.3
-
13
-
-
0035181504
-
Conformational comparison of μ-selective endomorphin-2 with its C-terminal free acid in DMSO solution, by H NMR spectroscopy and molecular modeling calculation
-
DOI 10.1034/j.1399-3011.2001.00891.x
-
1H NMR spectroscopy and molecular modeling calculation J. Pept. Res. 2001, 58, 399-412 (Pubitemid 33095978)
-
(2001)
Journal of Peptide Research
, vol.58
, Issue.5
, pp. 399-412
-
-
In, Y.1
Minoura, K.2
Ohishi, H.3
Ishida, T.4
Minakata, H.5
Kamigauchi, M.6
Sugiura, M.7
-
14
-
-
71049116091
-
Agonist vs antagonist behavior of delta opioid peptides containing novel phenylalanine analogues in place of Tyr(1)
-
Berezowska, I.; Chung, N. N.; Lemieux, C.; Wilkes, B. C.; Schiller, P. W. Agonist vs antagonist behavior of delta opioid peptides containing novel phenylalanine analogues in place of Tyr(1) J. Med. Chem. 2009, 52, 6941-6945
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6941-6945
-
-
Berezowska, I.1
Chung, N.N.2
Lemieux, C.3
Wilkes, B.C.4
Schiller, P.W.5
-
15
-
-
14544294044
-
Conformationally restricted peptides as tools in opioid receptor studies
-
Janecka, A.; Kruszynski, R. Conformationally restricted peptides as tools in opioid receptor studies Curr. Med. Chem. 2005, 12, 471-481 (Pubitemid 40305633)
-
(2005)
Current Medicinal Chemistry
, vol.12
, Issue.4
, pp. 471-481
-
-
Janecka, A.1
Kruszynski, R.2
-
16
-
-
37549071395
-
Endomorphin analogs
-
Janecka, A.; Staniszewska, R.; Fichna, J. Endomorphin analogs Curr. Med. Chem. 2007, 14, 3201-3208
-
(2007)
Curr. Med. Chem.
, vol.14
, pp. 3201-3208
-
-
Janecka, A.1
Staniszewska, R.2
Fichna, J.3
-
17
-
-
37849005357
-
Endomorphin-2 with a beta-turn backbone constraint retains the potent micro-opioid receptor agonist properties
-
Tomboly, C.; Ballet, S.; Feytens, D.; Kover, K. E.; Borics, A.; Lovas, S.; Al-Khrasani, M.; Furst, Z.; Toth, G.; Benyhe, S.; Tourwe, D. Endomorphin-2 with a beta-turn backbone constraint retains the potent micro-opioid receptor agonist properties J. Med. Chem. 2008, 51, 173-177
-
(2008)
J. Med. Chem.
, vol.51
, pp. 173-177
-
-
Tomboly, C.1
Ballet, S.2
Feytens, D.3
Kover, K.E.4
Borics, A.5
Lovas, S.6
Al-Khrasani, M.7
Furst, Z.8
Toth, G.9
Benyhe, S.10
Tourwe, D.11
-
18
-
-
0033851469
-
Conformational and topographical considerations in designing agonist peptidomimetics from peptide leads
-
Hruby, V. J.; Balse, P. M. Conformational and topographical considerations in designing agonist peptidomimetics from peptide leads Curr. Med. Chem. 2000, 7, 945-970
-
(2000)
Curr. Med. Chem.
, vol.7
, pp. 945-970
-
-
Hruby, V.J.1
Balse, P.M.2
-
19
-
-
2142823653
-
Recent advances in the investigation of the bioactive conformation of peptides active at the μ-opioid receptor. Conformational analysis of endomorphins
-
DOI 10.2174/1568026043451627
-
Gentilucci, L.; Tolomelli, A. Recent advances in the investigation of the bioactive conformation of peptides active at the micro-opioid receptor. Conformational analysis of endomorphins Curr. Top. Med. Chem. 2004, 4, 105-121 (Pubitemid 38842562)
-
(2004)
Current Topics in Medicinal Chemistry
, vol.4
, Issue.1
, pp. 105-121
-
-
Gentilucci, L.1
Tolomelli, A.2
-
20
-
-
77950691301
-
Bi- or multifunctional opioid peptide drugs
-
Schiller, P. W. Bi- or multifunctional opioid peptide drugs Life Sci. 2010, 86, 598-603
-
(2010)
Life Sci.
, vol.86
, pp. 598-603
-
-
Schiller, P.W.1
-
21
-
-
0029953285
-
β-Peptides: Synthesis by Arndt-Eistert homologation with concomitant peptide coupling. Structure determination by NMR and CD spectroscopy and by X-ray crystallography. Helical secondary structure of a β-hexapeptide in solution and its stability towards pepsin
-
Seebach, D.; Overhand, M.; Kühnle, F.; Martinoni, B.; Oberer, L.; Hommel, U.; Widmer, H. β-Peptides: Synthesis by Arndt-Eistert homologation with concomitant peptide coupling. Structure determination by NMR and CD spectroscopy and by X-ray crystallography. Helical secondary structure of a β-hexapeptide in solution and its stability towards pepsin Helv. Chim. Acta 1996, 79, 913-941
-
(1996)
Helv. Chim. Acta
, vol.79
, pp. 913-941
-
-
Seebach, D.1
Overhand, M.2
Kühnle, F.3
Martinoni, B.4
Oberer, L.5
Hommel, U.6
Widmer, H.7
-
22
-
-
0030461803
-
β-Peptide foldamers: Robust helix formation in a new family of β-amino acid oligomers
-
DOI 10.1021/ja963290l, PII S0002786396032908
-
Appella, D. H.; Christianson, L. A.; Karle, I. L.; Powell, D. R.; Gellman, S. H. β-Peptide foldamers: robust helix formation in a new family of β-amino acid oligomers J. Am. Chem. Soc. 1996, 118, 13071-13072 (Pubitemid 27055313)
-
(1996)
Journal of the American Chemical Society
, vol.118
, Issue.51
, pp. 13071-13072
-
-
Appella, D.H.1
Christianson, L.A.2
Karle, I.L.3
Powell, D.R.4
Gellman, S.H.5
-
23
-
-
0036253489
-
Beta-amino acids: Versatile peptidomimetics
-
Steer, D. L.; Lew, R. A.; Perlmutter, P.; Smith, A. I.; Aguilar, M. I. Beta-amino acids: versatile peptidomimetics Curr. Med. Chem. 2002, 9, 811-822
-
(2002)
Curr. Med. Chem.
, vol.9
, pp. 811-822
-
-
Steer, D.L.1
Lew, R.A.2
Perlmutter, P.3
Smith, A.I.4
Aguilar, M.I.5
-
24
-
-
0035471135
-
Beta-Peptides: From structure to function
-
Cheng, R. P.; Gellman, S. H.; DeGrado, W. F. beta-Peptides: from structure to function Chem. Rev. 2001, 101, 3219-3232
-
(2001)
Chem. Rev.
, vol.101
, pp. 3219-3232
-
-
Cheng, R.P.1
Gellman, S.H.2
Degrado, W.F.3
-
25
-
-
0035382627
-
The outstanding biological stability of β- and γ-peptides toward proteolytic enzymes: An in vitro investigation with fifteen peptidases
-
Frackenpohl, J.; Arvidsson, P. I.; Schreiber, J. V.; Seebach, D. The outstanding biological stability of beta- and gamma-peptides toward proteolytic enzymes: an in vitro investigation with fifteen peptidases ChemBioChem 2001, 2, 445-455 (Pubitemid 33723576)
-
(2001)
ChemBioChem
, vol.2
, Issue.6
, pp. 445-455
-
-
Frackenpohl, J.1
Arvidsson, P.I.2
Schreiber, J.V.3
Seebach, D.4
-
26
-
-
0034684771
-
Synthesis and binding activity of endomorphin-1 analogues containing beta-amino acids
-
Cardillo, G.; Gentilucci, L.; Melchiorre, P.; Spampinato, S. Synthesis and binding activity of endomorphin-1 analogues containing beta-amino acids Bioorg. Med. Chem. Lett. 2000, 10, 2755-2758
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2755-2758
-
-
Cardillo, G.1
Gentilucci, L.2
Melchiorre, P.3
Spampinato, S.4
-
27
-
-
0037030643
-
Endomorphin-1 analogues containing β-proline are μ-opioid receptor agonists and display enhanced enzymatic hydrolysis resistance
-
DOI 10.1021/jm011059z
-
Cardillo, G.; Gentilucci, L.; Qasem, A. R.; Sgarzi, F.; Spampinato, S. Endomorphin-1 analogues containing beta-proline are mu-opioid receptor agonists and display enhanced enzymatic hydrolysis resistance J. Med. Chem. 2002, 45, 2571-2578 (Pubitemid 34595227)
-
(2002)
Journal of Medicinal Chemistry
, vol.45
, Issue.12
, pp. 2571-2578
-
-
Cardillo, G.1
Gentilucci, L.2
Qasem, A.R.3
Sgarzi, F.4
Spampinato, S.5
-
28
-
-
47749133409
-
New endomorphin analogues containing alicyclic β-amino acids: Influence on bioactive conformation and pharmacological profile
-
DOI 10.1021/jm800223t
-
Keresztes, A.; Szucs, M.; Borics, A.; Kover, K. E.; Forro, E.; Fulop, F.; Tomboly, C.; Peter, A.; Pahi, A.; Fabian, G.; Muranyi, M.; Toth, G. New endomorphin analogues containing alicyclic beta-amino acids: influence on bioactive conformation and pharmacological profile J. Med. Chem. 2008, 51, 4270-4279 (Pubitemid 352032451)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.14
, pp. 4270-4279
-
-
Keresztes, A.1
Szucs, M.2
Borics, A.3
Kover, K.E.4
Forro, E.5
Fulop, F.6
Tomboly, C.7
Peter, A.8
Pahi, A.9
Fabian, G.10
Muranyi, M.11
Toth, G.12
-
29
-
-
45449111798
-
Synthesis and biological activity of endomorphin-2 analogs incorporating piperidine-2-, 3- or 4-carboxylic acids instead of proline in position 2
-
DOI 10.1111/j.1747-0285.2008.00678.x
-
Staniszewska, R.; Fichna, J.; Gach, K.; Toth, G.; Poels, J.; Vanden Broeck, J.; Janecka, A. Synthesis and biological activity of endomorphin-2 analogs incorporating piperidine-2-, 3- or 4-carboxylic acids instead of proline in position 2 Chem. Biol. Drug Des. 2008, 72, 91-94 (Pubitemid 351852781)
-
(2008)
Chemical Biology and Drug Design
, vol.72
, Issue.1
, pp. 91-94
-
-
Staniszewska, R.1
Fichna, J.2
Gach, K.3
Toth, G.4
Poels, J.5
Vanden Broeck, J.6
Janecka, A.7
-
30
-
-
81355154682
-
Enantioselective Mannich reaction of a highly reactive Horner-Wadsworth-Emmons reagent with imines catalyzed by a bifunctional thiourea
-
Zhao, D. P.; Yang, D. X.; Wang, Y. J.; Wang, Y.; Mao, L. J.; Wang, R. Enantioselective Mannich reaction of a highly reactive Horner-Wadsworth-Emmons reagent with imines catalyzed by a bifunctional thiourea Chem. Sci. 2011, 2, 1918-1921
-
(2011)
Chem. Sci.
, vol.2
, pp. 1918-1921
-
-
Zhao, D.P.1
Yang, D.X.2
Wang, Y.J.3
Wang, Y.4
Mao, L.J.5
Wang, R.6
-
31
-
-
0000400242
-
Stimulant actions of volatile anaesthetics on smooth muscle
-
Rang, H. P. Stimulant actions of volatile anaesthetics on smooth muscle Br. J. Pharmacol. Chemother. 1964, 22, 356-365
-
(1964)
Br. J. Pharmacol. Chemother.
, vol.22
, pp. 356-365
-
-
Rang, H.P.1
-
32
-
-
0016632644
-
Effect of morphine on adrenergic transmission in the mouse vas deferens. Assessment of agonist and antogonist potencies of narcotic analgesics
-
Hughes, J.; Kosterlitz, H. W.; Leslie, F. M. Effect of morphine on adrenergic transmission in the mouse vas deferens. Assessment of agonist and antogonist potencies of narcotic analgesics Br. J. Pharmacol. 1975, 53, 371-381
-
(1975)
Br. J. Pharmacol.
, vol.53
, pp. 371-381
-
-
Hughes, J.1
Kosterlitz, H.W.2
Leslie, F.M.3
-
33
-
-
79952256084
-
Design, synthesis, pharmacological evaluation, and structure-activity study of novel endomorphin analogues with multiple structural modifications
-
Mallareddy, J. R.; Borics, A.; Keresztes, A.; Kover, K. E.; Tourwe, D.; Toth, G. Design, synthesis, pharmacological evaluation, and structure-activity study of novel endomorphin analogues with multiple structural modifications J. Med. Chem. 2011, 54, 1462-1472
-
(2011)
J. Med. Chem.
, vol.54
, pp. 1462-1472
-
-
Mallareddy, J.R.1
Borics, A.2
Keresztes, A.3
Kover, K.E.4
Tourwe, D.5
Toth, G.6
-
34
-
-
19944433385
-
Development of potent μ-opioid receptor ligands using unique tyrosine analogues of endomorphin-2
-
DOI 10.1021/jm049384k
-
Li, T.; Fujita, Y.; Tsuda, Y.; Miyazaki, A.; Ambo, A.; Sasaki, Y.; Jinsmaa, Y.; Bryant, S. D.; Lazarus, L. H.; Okada, Y. Development of potent mu-opioid receptor ligands using unique tyrosine analogues of endomorphin-2 J. Med. Chem. 2005, 48, 586-592 (Pubitemid 40139800)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.2
, pp. 586-592
-
-
Li, T.1
Fujita, Y.2
Tsuda, Y.3
Miyazaki, A.4
Ambo, A.5
Sasaki, Y.6
Jinsmaa, Y.7
Bryant, S.D.8
Lazarus, L.H.9
Okada, Y.10
-
35
-
-
33748996832
-
Utilization of combined chemical modifications to enhance the blood-brain barrier permeability and pharmacological activity of endomorphin-1
-
DOI 10.1124/jpet.106.106484
-
Liu, H. M.; Liu, X. F.; Yao, J. L.; Wang, C. L.; Yu, Y.; Wang, R. Utilization of combined chemical modifications to enhance the blood-brain barrier permeability and pharmacological activity of endomorphin-1 J. Pharmacol. Exp. Ther. 2006, 319, 308-316 (Pubitemid 44455137)
-
(2006)
Journal of Pharmacology and Experimental Therapeutics
, vol.319
, Issue.1
, pp. 308-316
-
-
Liu, H.-M.1
Liu, X.-F.2
Yao, J.-L.3
Wang, C.-L.4
Yu, Y.5
Wang, R.6
-
36
-
-
0037356635
-
Endomorphin 2 analogues containing Dmp residue as an aromatic amino acid surrogate with high μ-opioid receptor affinity and selectivity
-
DOI 10.1016/S0968-0896(02)00601-6, PII S0968089602006016
-
Sasaki, Y.; Sasaki, A.; Niizuma, H.; Goto, H.; Ambo, A. Endomorphin 2 analogues containing Dmp residue as an aromatic amino acid surrogate with high mu-opioid receptor affinity and selectivity Bioorg. Med. Chem. 2003, 11, 675-678 (Pubitemid 36132209)
-
(2003)
Bioorganic and Medicinal Chemistry
, vol.11
, Issue.5
, pp. 675-678
-
-
Sasaki, Y.1
Sasaki, A.2
Niizuma, H.3
Goto, H.4
Ambo, A.5
-
37
-
-
0030733077
-
Down-regulation of μ-opioid receptor by full but not partial agonists is independent of G protein coupling
-
Yabaluri, N.; Medzihradsky, F. Down-regulation of mu-opioid receptor by full but not partial agonists is independent of G protein coupling Mol. Pharmacol. 1997, 52, 896-902 (Pubitemid 27484183)
-
(1997)
Molecular Pharmacology
, vol.52
, Issue.5
, pp. 896-902
-
-
Yabaluri, N.1
Medzihradsky, F.2
-
38
-
-
44449179814
-
Synthesis and in vitro evaluation of a library of modified endomorphin 1 peptides
-
DOI 10.1016/j.bmc.2008.04.020, PII S0968089608003489
-
Koda, Y.; Del Borgo, M.; Wessling, S. T.; Lazarus, L. H.; Okada, Y.; Toth, I.; Blanchfield, J. T. Synthesis and in vitro evaluation of a library of modified endomorphin 1 peptides Bioorg. Med. Chem. 2008, 16, 6286-6296 (Pubitemid 351758816)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.11
, pp. 6286-6296
-
-
Koda, Y.1
Del Borgo, M.2
Wessling, S.T.3
Lazarus, L.H.4
Okada, Y.5
Toth, I.6
Blanchfield, J.T.7
-
39
-
-
0031594351
-
35S]GTPγs binding in rat brain: Evidence for partial agonist activity at μ-opioid receptors
-
35S]GTPgammaS binding in rat brain: evidence for partial agonist activity at mu-opioid receptors J. Neurochem. 1998, 70, 1567-1576 (Pubitemid 28136970)
-
(1998)
Journal of Neurochemistry
, vol.70
, Issue.4
, pp. 1567-1576
-
-
Sim, L.J.1
Liu, Q.2
Childers, S.R.3
Selley, D.E.4
-
40
-
-
0032478671
-
Endomorphin-1 and endomorphin-2 are partial agonists at the human μ- opioid receptor
-
DOI 10.1016/S0014-2999(98)00117-4, PII S0014299998001174
-
Hosohata, K.; Burkey, T. H.; Alfaro-Lopez, J.; Varga, E.; Hruby, V. J.; Roeske, W. R.; Yamamura, H. I. Endomorphin-1 and endomorphin-2 are partial agonists at the human mu-opioid receptor Eur. J. Pharmacol. 1998, 346, 111-114 (Pubitemid 28197096)
-
(1998)
European Journal of Pharmacology
, vol.346
, Issue.1
, pp. 111-114
-
-
Hosohata, K.1
Burkey, T.H.2
Alfaro-Lopez, J.3
Varga, E.4
Hruby, V.J.5
Roeske, W.R.6
Yamamura, H.I.7
-
41
-
-
0035823506
-
Mu-Opioid receptor-mediated ERK activation involves calmodulin-dependent epidermal growth factor receptor transactivation
-
Belcheva, M. M.; Szucs, M.; Wang, D.; Sadee, W.; Coscia, C. J. mu-Opioid receptor-mediated ERK activation involves calmodulin-dependent epidermal growth factor receptor transactivation J. Biol. Chem. 2001, 276, 33847-33853
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 33847-33853
-
-
Belcheva, M.M.1
Szucs, M.2
Wang, D.3
Sadee, W.4
Coscia, C.J.5
-
42
-
-
27744583096
-
Expression of the third intracellular loop of the δ-opioid receptor inhibits signaling by opioid receptors and other G protein-coupled receptors
-
DOI 10.1124/jpet.105.089946
-
Morou, E.; Georgoussi, Z. Expression of the third intracellular loop of the delta-opioid receptor inhibits signaling by opioid receptors and other G protein-coupled receptors J. Pharmacol. Exp. Ther. 2005, 315, 1368-1379 (Pubitemid 41635427)
-
(2005)
Journal of Pharmacology and Experimental Therapeutics
, vol.315
, Issue.3
, pp. 1368-1379
-
-
Morou, E.1
Georgoussi, Z.2
-
43
-
-
0344069680
-
Endomorphin-1 and endomorphin-2 show differences in their activation of μ opioid receptor-regulated G proteins in supraspinal antinociception in mice
-
Sanchez-Blazquez, P.; Rodriguez-Diaz, M.; DeAntonio, I.; Garzon, J. Endomorphin-1 and endomorphin-2 show differences in their activation of mu opioid receptor-regulated G proteins in supraspinal antinociception in mice J. Pharmacol. Exp. Ther. 1999, 291, 12-18 (Pubitemid 29451567)
-
(1999)
Journal of Pharmacology and Experimental Therapeutics
, vol.291
, Issue.1
, pp. 12-18
-
-
Sanchez-Blazquez, P.1
Rodriguez-Diaz, M.2
DeAntonio, I.3
Garzon, J.4
-
44
-
-
68949116093
-
Molecular modeling studies to predict the possible binding modes of endomorphin analogs in mu opioid receptor
-
Liu, X.; Kai, M.; Jin, L.; Wang, R. Molecular modeling studies to predict the possible binding modes of endomorphin analogs in mu opioid receptor Bioorg. Med. Chem. Lett. 2009, 19, 5387-5391
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 5387-5391
-
-
Liu, X.1
Kai, M.2
Jin, L.3
Wang, R.4
-
45
-
-
0030040907
-
The conserved aspartate residue in the third putative transmembrane domain of the delta-opioid receptor is not the anionic counterpart for cationic opiate binding but is a constituent of the receptor binding site
-
Befort, K.; Tabbara, L.; Bausch, S.; Chavkin, C.; Evans, C.; Kieffer, B. The conserved aspartate residue in the third putative transmembrane domain of the delta-opioid receptor is not the anionic counterpart for cationic opiate binding but is a constituent of the receptor binding site Mol. Pharmacol. 1996, 49, 216-223
-
(1996)
Mol. Pharmacol.
, vol.49
, pp. 216-223
-
-
Befort, K.1
Tabbara, L.2
Bausch, S.3
Chavkin, C.4
Evans, C.5
Kieffer, B.6
-
46
-
-
0029829892
-
3H] β- funaltrexamine covalent binding in the cloned rat μ opioid receptor
-
DOI 10.1074/jbc.271.35.21422
-
3H]beta-funaltrexamine covalent binding in the cloned rat mu-opioid receptor J. Biol. Chem. 1996, 271, 21422-21429 (Pubitemid 26293006)
-
(1996)
Journal of Biological Chemistry
, vol.271
, Issue.35
, pp. 21422-21429
-
-
Chen, C.1
Yin, J.2
Kim De Riel, J.3
DesJarlais, R.L.4
Raveglia, L.F.5
Zhu, J.6
Liu-Chen, L.-Y.7
-
47
-
-
0033523062
-
Asp147 in the third transmembrane helix of the rat μ opioid receptor forms ion-pairing with morphine and naltrexone
-
PII S0024320599002349
-
Li, J. G.; Chen, C.; Yin, J.; Rice, K.; Zhang, Y.; Matecka, D.; de Riel, J. K.; DesJarlais, R. L.; Liu-Chen, L. Y. ASP147 in the third transmembrane helix of the rat mu opioid receptor forms ion-pairing with morphine and naltrexone Life Sci. 1999, 65, 175-185 (Pubitemid 29292820)
-
(1999)
Life Sciences
, vol.65
, Issue.2
, pp. 175-185
-
-
Li, J.-G.1
Chen, C.2
Yin, J.3
Rice, K.4
Zhang, Y.5
Matecka, D.6
De Riel, J.K.7
DesJarlais, R.L.8
Liu-Chen, L.-Y.9
-
48
-
-
0031018775
-
Key residues defining the μ-opioid receptor binding pocket: A site- directed mutagenesis study
-
Mansour, A.; Taylor, L. P.; Fine, J. L.; Thompson, R. C.; Hoversten, M. T.; Mosberg, H. I.; Watson, S. J.; Akil, H. Key residues defining the mu-opioid receptor binding pocket: a site-directed mutagenesis study J. Neurochem. 1997, 68, 344-353 (Pubitemid 26427327)
-
(1997)
Journal of Neurochemistry
, vol.68
, Issue.1
, pp. 344-353
-
-
Mansour, A.1
Taylor, L.P.2
Fine, J.L.3
Thompson, R.C.4
Hoversten, M.T.5
Mosberg, H.I.6
Watson, S.J.7
Akil, H.8
-
49
-
-
0036945574
-
Development and validation of opioid ligand-receptor interaction models: The structural basis of mu vs. delta selectivity
-
DOI 10.1034/j.1399-3011.2002.21061.x
-
Mosberg, H. I.; Fowler, C. B. Development and validation of opioid ligand-receptor interaction models: the structural basis of mu vs delta selectivity J. Pept. Res. 2002, 60, 329-335 (Pubitemid 36071896)
-
(2002)
Journal of Peptide Research
, vol.60
, Issue.6
, pp. 329-335
-
-
Mosberg, H.I.1
Fowler, C.B.2
-
50
-
-
0028170438
-
μ opiate receptor. Charged transmembrane domain amino acids are critical for agonist recognition and intrinsic activity
-
Surratt, C. K.; Johnson, P. S.; Moriwaki, A.; Seidleck, B. K.; Blaschak, C. J.; Wang, J. B.; Uhl, G. R. -mu opiate receptor. Charged transmembrane domain amino acids are critical for agonist recognition and intrinsic activity J. Biol. Chem. 1994, 269, 20548-20553
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 20548-20553
-
-
Surratt, C.K.1
Johnson, P.S.2
Moriwaki, A.3
Seidleck, B.K.4
Blaschak, C.J.5
Wang, J.B.6
Uhl, G.R.7
-
51
-
-
0029863220
-
Studies on inhibition of mu and delta opioid receptor binding by dithiothreitol and N -ethylmaleimide. His223 is critical for mu opioid receptor binding and inactivation by N -ethylmaleimide
-
Shahrestanifar, M.; Wang, W. W.; Howells, R. D. Studies on inhibition of mu and delta opioid receptor binding by dithiothreitol and N -ethylmaleimide. His223 is critical for mu opioid receptor binding and inactivation by N -ethylmaleimide J. Biol. Chem. 1996, 271, 5505-5512
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 5505-5512
-
-
Shahrestanifar, M.1
Wang, W.W.2
Howells, R.D.3
-
52
-
-
84861096654
-
Crystal structure of the micro-opioid receptor bound to a morphinan antagonist
-
Manglik, A.; Kruse, A. C.; Kobilka, T. S.; Thian, F. S.; Mathiesen, J. M.; Sunahara, R. K.; Pardo, L.; Weis, W. I.; Kobilka, B. K.; Granier, S. Crystal structure of the micro-opioid receptor bound to a morphinan antagonist Nature 2012, 485, 321-326
-
(2012)
Nature
, vol.485
, pp. 321-326
-
-
Manglik, A.1
Kruse, A.C.2
Kobilka, T.S.3
Thian, F.S.4
Mathiesen, J.M.5
Sunahara, R.K.6
Pardo, L.7
Weis, W.I.8
Kobilka, B.K.9
Granier, S.10
-
53
-
-
44849121073
-
Structure-activity study of endomorphin-2 analogs with C-terminal modifications by NMR spectroscopy and molecular modeling
-
DOI 10.1016/j.bmc.2008.05.001, PII S0968089608004203
-
Wang, C. L.; Yao, J. L.; Yu, Y.; Shao, X.; Cui, Y.; Liu, H. M.; Lai, L. H.; Wang, R. Structure-activity study of endomorphin-2 analogs with C-terminal modifications by NMR spectroscopy and molecular modeling Bioorg. Med. Chem. 2008, 16, 6415-6422 (Pubitemid 351790763)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.12
, pp. 6415-6422
-
-
Wang, C.-l.1
Yao, J.-l.2
Yu, Y.3
Shao, X.4
Cui, Y.5
Liu, H.-m.6
Lai, L.-h.7
Wang, R.8
-
54
-
-
26244446907
-
1H-NMR spectroscopy, molecular calculation, and X-ray crystallography
-
DOI 10.1111/j.1742-4658.2005.04919.x
-
1H-NMR spectroscopy, molecular calculation, and X-ray crystallography FEBS J. 2005, 272, 5079-5097 (Pubitemid 41415128)
-
(2005)
FEBS Journal
, vol.272
, Issue.19
, pp. 5079-5097
-
-
In, Y.1
Minoura, K.2
Tomoo, K.3
Sasaki, Y.4
Lazarus, L.H.5
Okada, Y.6
Ishida, T.7
-
55
-
-
0025191899
-
5]enkephalin analogues with increased affinity and selectivity for δ opioid receptors
-
DOI 10.1021/jm00163a041
-
5] Enkephalin analogues with increased affinity and selectivity for delta opioid receptors J. Med. Chem. 1990, 33, 249-253 (Pubitemid 20038201)
-
(1990)
Journal of Medicinal Chemistry
, vol.33
, Issue.1
, pp. 249-253
-
-
Toth, G.1
Kramer, T.H.2
Knapp, R.3
Lui, G.4
Davis, P.5
Burks, T.F.6
Yamamura, H.I.7
Hruby, V.J.8
-
56
-
-
0030773558
-
Cyclic enkephalin analogues with exceptional potency and selectivity for δ-opioid receptors
-
DOI 10.1021/jm9704762
-
Hruby, V. J.; Bartosz-Bechowski, H.; Davis, P.; Slaninova, J.; Zalewska, T.; Stropova, D.; Porreca, F.; Yamamura, H. I. Cyclic enkephalin analogues with exceptional potency and selectivity for delta-opioid receptors J. Med. Chem. 1997, 40, 3957-3962 (Pubitemid 27512312)
-
(1997)
Journal of Medicinal Chemistry
, vol.40
, Issue.24
, pp. 3957-3962
-
-
Hruby, V.J.1
Bartosz-Bechowski, H.2
Davis, P.3
Slaninova, J.4
Zalewska, T.5
Stropova, D.6
Porreca, F.7
Yamamura, H.I.8
-
57
-
-
2942705905
-
Opioid receptor binding and in vivo antinociceptive activity of position 3-substituted morphiceptin analogs
-
DOI 10.1016/j.bbrc.2004.05.202, PII S0006291X04012501
-
Fichna, J.; do-Rego, J. C.; Costentin, J.; Chung, N. N.; Schiller, P. W.; Kosson, P.; Janecka, A. Opioid receptor binding and in vivo antinociceptive activity of position 3-substituted morphiceptin analogs Biochem. Biophys. Res. Commun. 2004, 320, 531-536 (Pubitemid 38798900)
-
(2004)
Biochemical and Biophysical Research Communications
, vol.320
, Issue.2
, pp. 531-536
-
-
Fichna, J.1
Do-Rego, J.-C.2
Costentin, J.3
Chung, N.N.4
Schiller, P.W.5
Kosson, P.6
Janecka, A.7
-
58
-
-
23844476819
-
Novel endomorphin-2 analogs with μ-opioid receptor antagonist activity
-
DOI 10.1111/j.1399-3011.2005.00282.x
-
Kruszynski, R.; Fichna, J.; do-Rego, J. C.; Chung, N. N.; Schiller, P. W.; Kosson, P.; Costentin, J.; Janecka, A. Novel endomorphin-2 analogs with mu-opioid receptor antagonist activity J. Pept. Res. 2005, 66, 125-131 (Pubitemid 41153085)
-
(2005)
Journal of Peptide Research
, vol.66
, Issue.3
, pp. 125-131
-
-
Kruszynski, R.1
Fichna, J.2
Do-Rego, J.-C.3
Chung, N.N.4
Schiller, P.W.5
Kosson, P.6
Costentin, J.7
Janecka, A.8
-
59
-
-
33846918825
-
4]endomorphin-2 (antanal-2)
-
4]endomorphin-2 (antanal-2) J. Med. Chem. 2007, 50, 512-520
-
(2007)
J. Med. Chem.
, vol.50
, pp. 512-520
-
-
Fichna, J.1
Do-Rego, J.C.2
Chung, N.N.3
Lemieux, C.4
Schiller, P.W.5
Poels, J.6
Broeck, J.V.7
Costentin, J.8
Janecka, A.9
-
60
-
-
0036758662
-
Phosphorylation of extracellular signal-regulated kinase in primary afferent neurons by noxious stimuli and its involvement in peripheral sensitization
-
Dai, Y.; Iwata, K.; Fukuoka, T.; Kondo, E.; Tokunaga, A.; Yamanaka, H.; Tachibana, T.; Liu, Y.; Noguchi, K. Phosphorylation of extracellular signal-regulated kinase in primary afferent neurons by noxious stimuli and its involvement in peripheral sensitization J. Neurosci. 2002, 22, 7737-7745 (Pubitemid 35386372)
-
(2002)
Journal of Neuroscience
, vol.22
, Issue.17
, pp. 7737-7745
-
-
Dai, Y.1
Iwata, K.2
Fukuoka, T.3
Kondo, E.4
Tokunaga, A.5
Yamanaka, H.6
Tachibana, T.7
Liu, Y.8
Noguchi, K.9
-
61
-
-
0034441889
-
Functional domains of δ- and μ-opioid receptors responsible for adenylyl cyclase inhibition
-
Megaritis, G.; Merkouris, M.; Georgoussi, Z. Functional domains of delta- and mu-opioid receptors responsible for adenylyl cyclase inhibition Recept. Channels 2000, 7, 199-212 (Pubitemid 32440339)
-
(2000)
Receptors and Channels
, vol.7
, Issue.3
, pp. 199-212
-
-
Megaritis, G.1
Merkouris, M.2
Georgoussi, Z.3
-
62
-
-
77049118216
-
On the use of cells or membranes for receptor binding: Growth hormone secretagogues
-
Pinyot, A.; Nikolovski, Z.; Bosch, J.; Segura, J.; Gutierrez-Gallego, R. On the use of cells or membranes for receptor binding: growth hormone secretagogues Anal. Biochem. 2010, 399, 174-181
-
(2010)
Anal. Biochem.
, vol.399
, pp. 174-181
-
-
Pinyot, A.1
Nikolovski, Z.2
Bosch, J.3
Segura, J.4
Gutierrez-Gallego, R.5
-
63
-
-
82555187413
-
Discovery of aminobenzyloxyarylamides as kappa opioid receptor selective antagonists: Application to preclinical development of a kappa opioid receptor antagonist receptor occupancy tracer
-
Mitch, C. H.; Quimby, S. J.; Diaz, N.; Pedregal, C.; de la Torre, M. G.; Jimenez, A.; Shi, Q.; Canada, E. J.; Kahl, S. D.; Statnick, M. A.; McKinzie, D. L.; Benesh, D. R.; Rash, K. S.; Barth, V. N. Discovery of aminobenzyloxyarylamides as kappa opioid receptor selective antagonists: application to preclinical development of a kappa opioid receptor antagonist receptor occupancy tracer J. Med. Chem. 2011, 54, 8000-8012
-
(2011)
J. Med. Chem.
, vol.54
, pp. 8000-8012
-
-
Mitch, C.H.1
Quimby, S.J.2
Diaz, N.3
Pedregal, C.4
De La Torre, M.G.5
Jimenez, A.6
Shi, Q.7
Canada, E.J.8
Kahl, S.D.9
Statnick, M.A.10
McKinzie, D.L.11
Benesh, D.R.12
Rash, K.S.13
Barth, V.N.14
-
64
-
-
0017249678
-
A simple ultrasensitive method for the assay of cyclic AMP and cyclic GMP in tissues
-
Frandsen, E. K.; Krishna, G. A simple ultrasensitive method for the assay of cyclic AMP and cyclic GMP in tissues Life Sci. 1976, 18, 529-541
-
(1976)
Life Sci.
, vol.18
, pp. 529-541
-
-
Frandsen, E.K.1
Krishna, G.2
-
65
-
-
0030604273
-
Expression of μ-, δ- and κ-opioid receptors in baculovirus-infected insect cells
-
DOI 10.1016/S0014-2999(96)00743-1, PII S0014299996007431
-
Obermeier, H.; Wehmeyer, A.; Schulz, R. Expression of mu-, delta- and kappa-opioid receptors in baculovirus-infected insect cells Eur. J. Pharmacol. 1996, 318, 161-166 (Pubitemid 27033219)
-
(1996)
European Journal of Pharmacology
, vol.318
, Issue.1
, pp. 161-166
-
-
Obermeier, H.1
Wehmeyer, A.2
Schulz, R.3
-
66
-
-
0034198716
-
Human mu-opioid receptor overexpressed in Sf9 insect cells functionally coupled to endogenous Gi/o proteins
-
Wei, Q.; Zhou, D. H.; Shen, Q. X.; Chen, J.; Chen, L. W.; Wang, T. L.; Pei, G.; Chi, Z. Q. Human mu-opioid receptor overexpressed in Sf9 insect cells functionally coupled to endogenous Gi/o proteins Cell Res. 2000, 10, 93-102
-
(2000)
Cell Res.
, vol.10
, pp. 93-102
-
-
Wei, Q.1
Zhou, D.H.2
Shen, Q.X.3
Chen, J.4
Chen, L.W.5
Wang, T.L.6
Pei, G.7
Chi, Z.Q.8
-
67
-
-
43649096451
-
Measurement of Second Messengers in Signal Transduction: CAMP and Inositol Phosphates
-
Wiley: New York, Chapter 7, Unit 7.12
-
Gusovsky, F. Measurement of Second Messengers in Signal Transduction: cAMP and Inositol Phosphates. In Current Protocols in Neuroscience; Wiley: New York, 2001; Chapter 7, Unit 7.12.
-
(2001)
Current Protocols in Neuroscience
-
-
Gusovsky, F.1
-
68
-
-
44449096273
-
Modulation of extracellular signal-regulated kinase (ERK) by opioid and cannabinoid receptors that are expressed in the same cell
-
Korzh, A.; Keren, O.; Gafni, M.; Bar-Josef, H.; Sarne, Y. Modulation of extracellular signal-regulated kinase (ERK) by opioid and cannabinoid receptors that are expressed in the same cell Brain Res. 2008, 1189, 23-32
-
(2008)
Brain Res.
, vol.1189
, pp. 23-32
-
-
Korzh, A.1
Keren, O.2
Gafni, M.3
Bar-Josef, H.4
Sarne, Y.5
-
69
-
-
23044509956
-
μ and κ opioid receptors activate ERK/MAPK via different protein kinase C isoforms and secondary messengers in astrocytes
-
DOI 10.1074/jbc.M502593200
-
Belcheva, M. M.; Clark, A. L.; Haas, P. D.; Serna, J. S.; Hahn, J. W.; Kiss, A.; Coscia, C. J. Mu and kappa opioid receptors activate ERK/MAPK via different protein kinase C isoforms and secondary messengers in astrocytes J. Biol. Chem. 2005, 280, 27662-27669 (Pubitemid 41076879)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.30
, pp. 27662-27669
-
-
Belcheva, M.M.1
Clark, A.L.2
Haas, P.D.3
Serna, J.S.4
Hahn, J.W.5
Kiss, A.6
Coscia, C.J.7
-
70
-
-
0033962013
-
Involvement of mitogen-activated protein kinase in agonist-induced phosphorylation of the μ-opioid receptor in HEK 293 cells
-
DOI 10.1046/j.1471-4159.2000.0740414.x
-
Schmidt, H.; Schulz, S.; Klutzny, M.; Koch, T.; Handel, M.; Hollt, V. Involvement of mitogen-activated protein kinase in agonist-induced phosphorylation of the mu-opioid receptor in HEK 293 cells J. Neurochem. 2000, 74, 414-22 (Pubitemid 30012796)
-
(2000)
Journal of Neurochemistry
, vol.74
, Issue.1
, pp. 414-422
-
-
Schmidt, H.1
Schulz, S.2
Klutzny, M.3
Koch, T.4
Handel, M.5
Hollt, V.6
-
71
-
-
0026564209
-
A specific enzyme assay for aminopeptidase M in rat brain
-
Gillespie, T. J.; Konings, P. N.; Merrill, B. J.; Davis, T. P. A specific enzyme assay for aminopeptidase M in rat brain Life Sci. 1992, 51, 2097-2106
-
(1992)
Life Sci.
, vol.51
, pp. 2097-2106
-
-
Gillespie, T.J.1
Konings, P.N.2
Merrill, B.J.3
Davis, T.P.4
-
72
-
-
67349220011
-
Computational study of the heterodimerization between mu and delta receptors
-
Liu, X.; Kai, M.; Jin, L.; Wang, R. Computational study of the heterodimerization between mu and delta receptors J. Comput.-Aided Mol. Des. 2009, 23, 321-332
-
(2009)
J. Comput.-Aided Mol. Des.
, vol.23
, pp. 321-332
-
-
Liu, X.1
Kai, M.2
Jin, L.3
Wang, R.4
-
73
-
-
0029633168
-
GROMACS: A message-passing parallel molecular dynamics implementation
-
Berendsen, H. J.; Vanderspoel, D.; Vandrunen, R. GROMACS: a message-passing parallel molecular dynamics implementation Comput. Phys. Commun. 1995, 91, 43-56
-
(1995)
Comput. Phys. Commun.
, vol.91
, pp. 43-56
-
-
Berendsen, H.J.1
Vanderspoel, D.2
Vandrunen, R.3
-
74
-
-
0011746241
-
A molecular dynamics study of the decane/water interface
-
Vanbuuren, A. R.; Marrink, S. J.; Berendsen, H. J. C. A molecular dynamics study of the decane/water interface J. Phys. Chem. 1993, 97, 9206-9212
-
(1993)
J. Phys. Chem.
, vol.97
, pp. 9206-9212
-
-
Vanbuuren, A.R.1
Marrink, S.J.2
Berendsen, H.J.C.3
-
75
-
-
33846823909
-
Particle mesh Ewald: An N -log(N) method for Ewald sums in large system
-
Darden, T.; York, D.; Pedersen, L. Particle mesh Ewald: an N -log(N) method for Ewald sums in large system J. Chem. Phys. 1993, 98, 10089-10092
-
(1993)
J. Chem. Phys.
, vol.98
, pp. 10089-10092
-
-
Darden, T.1
York, D.2
Pedersen, L.3
-
76
-
-
0000388705
-
LINCS: A Linear Constraint Solver for molecular simulations
-
Hess, B.; Bekker, H.; Berendsen, H. J. C.; Fraaije, J. LINCS: a linear constraint solver for molecular simulations J. Comput. Chem. 1997, 18, 1463-1472 (Pubitemid 127637344)
-
(1997)
Journal of Computational Chemistry
, vol.18
, Issue.12
, pp. 1463-1472
-
-
Hess, B.1
Bekker, H.2
Berendsen, H.J.C.3
Fraaije, J.G.E.M.4
-
77
-
-
33750587438
-
Molecular dynamics with coupling to an external bath
-
Berendsen, H. J. C.; Postma, J. P. M.; Vangunsteren, W. F.; Dinola, A.; Haak, J. R. Molecular dynamics with coupling to an external bath J. Chem. Phys. 1984, 81, 3684-3690
-
(1984)
J. Chem. Phys.
, vol.81
, pp. 3684-3690
-
-
Berendsen, H.J.C.1
Postma, J.P.M.2
Vangunsteren, W.F.3
Dinola, A.4
Haak, J.R.5
-
78
-
-
11644261806
-
Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function
-
Morris, G. M.; Goodsell, D. S.; Halliday, R. S.; Huey, R.; Hart, W. E.; Belew, R. K.; Olson, A. J. Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function J. Comput. Chem. 1998, 19, 1639-1662 (Pubitemid 128590223)
-
(1998)
Journal of Computational Chemistry
, vol.19
, Issue.14
, pp. 1639-1662
-
-
Morris, G.M.1
Goodsell, D.S.2
Halliday, R.S.3
Huey, R.4
Hart, W.E.5
Belew, R.K.6
Olson, A.J.7
-
79
-
-
38049054284
-
Structure-activity study on the spatial arrangement of the third aromatic ring of endomorphins 1 and 2 using an atypical constrained C terminus
-
Yu, Y.; Shao, X.; Cui, Y.; Liu, H. M.; Wang, C. L.; Fan, Y. Z.; Liu, J.; Dong, S. L.; Cui, Y. X.; Wang, R. Structure-activity study on the spatial arrangement of the third aromatic ring of endomorphins 1 and 2 using an atypical constrained C terminus ChemMedChem 2007, 2, 309-317
-
(2007)
ChemMedChem
, vol.2
, pp. 309-317
-
-
Yu, Y.1
Shao, X.2
Cui, Y.3
Liu, H.M.4
Wang, C.L.5
Fan, Y.Z.6
Liu, J.7
Dong, S.L.8
Cui, Y.X.9
Wang, R.10
-
80
-
-
0036084259
-
Efficient docking of peptides to proteins without prior knowledge of the binding site
-
DOI 10.1110/ps.0202302
-
Hetenyi, C.; van der Spoel, D. Efficient docking of peptides to proteins without prior knowledge of the binding site Protein Sci. 2002, 11, 1729-1737 (Pubitemid 34663553)
-
(2002)
Protein Science
, vol.11
, Issue.7
, pp. 1729-1737
-
-
Hetenyi, C.1
Van Der Spoel, D.2
-
81
-
-
32344440995
-
Blind docking of drug-sized compounds to proteins with up to a thousand residues
-
DOI 10.1016/j.febslet.2006.01.074, PII S001457930600144X
-
Hetenyi, C.; van der Spoel, D. Blind docking of drug-sized compounds to proteins with up to a thousand residues FEBS Lett. 2006, 580, 1447-1450 (Pubitemid 43222013)
-
(2006)
FEBS Letters
, vol.580
, Issue.5
, pp. 1447-1450
-
-
Hetenyi, C.1
Van Der Spoel, D.2
-
82
-
-
31944434856
-
Combination of a modified scoring function with two-dimensional descriptors for calculation of binding affinities of bulky, flexible ligands to proteins
-
DOI 10.1021/ja055804z
-
Hetenyi, C.; Paragi, G.; Maran, U.; Timar, Z.; Karelson, M.; Penke, B. Combination of a modified scoring function with two-dimensional descriptors for calculation of binding affinities of bulky, flexible ligands to proteins J. Am. Chem. Soc. 2006, 128, 1233-1239 (Pubitemid 43190635)
-
(2006)
Journal of the American Chemical Society
, vol.128
, Issue.4
, pp. 1233-1239
-
-
Hetenyi, C.1
Paragi, G.2
Maran, U.3
Timar, Z.4
Karelson, M.5
Penke, B.6
-
83
-
-
7544226311
-
PRODRG: A tool for high-throughput crystallography of protein-ligand complexes
-
DOI 10.1107/S0907444904011679
-
Schuttelkopf, A. W.; van Aalten, D. M. PRODRG: a tool for high-throughput crystallography of protein-ligand complexes Acta Crystallogr., Sect. D: Biol. Crystallogr. 2004, 60, 1355-1363 (Pubitemid 41079731)
-
(2004)
Acta Crystallographica Section D: Biological Crystallography
, vol.60
, Issue.8
, pp. 1355-1363
-
-
Schuttelkopf, A.W.1
Van Aalten, D.M.F.2
|