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Volumn 4, Issue 8, 2013, Pages 795-799

Structural and biological exploration of Phe3-Phe 4-modified endomorphin-2 peptidomimetics

Author keywords

conformational analysis; docking studies; opioid receptors; Peptidomimetics; amino acids

Indexed keywords

ENDOMORPHIN 2; LIGAND; MU OPIATE RECEPTOR; PEPTIDOMIMETIC AGENT;

EID: 84881435753     PISSN: None     EISSN: 19485875     Source Type: Journal    
DOI: 10.1021/ml400189r     Document Type: Article
Times cited : (13)

References (28)
  • 1
    • 0017735536 scopus 로고
    • 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
    • (1977) Nature , vol.267 , pp. 495-499
    • Lord, J.A.1    Waterfield, A.A.2    Hughes, J.3    Kosterlitz, H.W.4
  • 2
    • 33847366597 scopus 로고    scopus 로고
    • The Endomorphin System and Its Evolving Neurophysiological Role
    • Fichna, J.; Janecka, A.; Costentin, J.; Do Rego, J.-C. The Endomorphin System and Its Evolving Neurophysiological Role Pharmacol. Rev. 2007, 59, 88-123
    • (2007) Pharmacol. Rev. , vol.59 , pp. 88-123
    • Fichna, J.1    Janecka, A.2    Costentin, J.3    Do Rego, J.-C.4
  • 4
    • 38049066463 scopus 로고    scopus 로고
    • Structural Investigation of Endomorphins by Experimental and Theoretical Methods: Hunting for the Bioactive Conformation
    • Leitgeb, B. Structural Investigation of Endomorphins by Experimental and Theoretical Methods: Hunting for the Bioactive Conformation Chem. Biodiversity 2007, 4, 2703-2724
    • (2007) Chem. Biodiversity , vol.4 , pp. 2703-2724
    • Leitgeb, B.1
  • 5
    • 84876248490 scopus 로고    scopus 로고
    • Design, Synthesis, and Pharmacological Characterization of Novel Endomorphin-1 Analogues As Extremely Potent μ-Opioid Agonists
    • Liu, X.; Wang, Y.; Xing, Y.; Yu, J.; Ji, H.; Kai, M.; Wang, Z.; Wang, D.; Zhang, Y.; Zhao, D.; Wang, R. Design, Synthesis, and Pharmacological Characterization of Novel Endomorphin-1 Analogues As Extremely Potent μ-Opioid Agonists J. Med. Chem. 2013, 56, 3102-3114
    • (2013) J. Med. Chem. , vol.56 , pp. 3102-3114
    • Liu, X.1    Wang, Y.2    Xing, Y.3    Yu, J.4    Ji, H.5    Kai, M.6    Wang, Z.7    Wang, D.8    Zhang, Y.9    Zhao, D.10    Wang, R.11
  • 6
    • 20444365510 scopus 로고    scopus 로고
    • Aromatic-Aromatic and Proline-Aromatic Interactions in Endomorphin-1 and Endomorphin-2
    • Leitgeb, B.; Tóth, G. Aromatic-Aromatic and Proline-Aromatic Interactions in Endomorphin-1 and Endomorphin-2 Eur. J. Med. Chem. 2005, 40, 674-686
    • (2005) Eur. J. Med. Chem. , vol.40 , pp. 674-686
    • Leitgeb, B.1    Tóth, G.2
  • 7
    • 30344433455 scopus 로고    scopus 로고
    • C-Terminal Amide to Alcohol Conversion Changes the Cardiovascular Effects of Endomorphins in Anesthetized Rats
    • Yu, Y.; Wang, C. L.; Cui, Y.; Fan, Y. Z.; Liu, J.; Shao, X.; Liu, H. M.; Wang, R. C-Terminal Amide to Alcohol Conversion Changes the Cardiovascular Effects of Endomorphins in Anesthetized Rats Peptides 2006, 27, 136-143
    • (2006) Peptides , vol.27 , pp. 136-143
    • Yu, Y.1    Wang, C.L.2    Cui, Y.3    Fan, Y.Z.4    Liu, J.5    Shao, X.6    Liu, H.M.7    Wang, R.8
  • 11
    • 79952256084 scopus 로고    scopus 로고
    • Design, Synthesis, Pharmacological Evaluation, and Structure-Activity Study of Novel Endomorphin Analogues with Multiple Structural Modifications
    • Mallareddy, J. R.; Borics, A.; Keresztes, A.; Kövér, K.; Tourwé, D.; Tóth, 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    Kövér, K.4    Tourwé, D.5    Tóth, G.6
  • 16
    • 79951650747 scopus 로고    scopus 로고
    • Structural Chemistry of Peptides Containing Backbone Expanded Amino Acid Residues: Conformational Features of β, γ, and Hybrid Peptides
    • Vasudev, P. G.; Chatterjee, S.; Shamala, N.; Balaram, P. Structural Chemistry of Peptides Containing Backbone Expanded Amino Acid Residues: Conformational Features of β, γ, and Hybrid Peptides Chem. Rev. 2011, 111, 657-687
    • (2011) Chem. Rev. , vol.111 , pp. 657-687
    • Vasudev, P.G.1    Chatterjee, S.2    Shamala, N.3    Balaram, P.4
  • 17
    • 57349134690 scopus 로고    scopus 로고
    • Foldamers with Heterogeneous Backbones
    • Horne, W. S.; Gellman, S. H. Foldamers with Heterogeneous Backbones Acc. Chem. Res. 2008, 41, 1399-1408
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1399-1408
    • Horne, W.S.1    Gellman, S.H.2
  • 18
    • 57149097169 scopus 로고    scopus 로고
    • β-Peptidic Peptidomimetics
    • Seebach, D.; Gardiner, J. β-Peptidic Peptidomimetics Acc. Chem. Res. 2008, 41, 1366-1375
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1366-1375
    • Seebach, D.1    Gardiner, J.2
  • 19
    • 0028826307 scopus 로고
    • Synthesis of Enantiopure N- and C-Protected Homo-β-Amino Acids by Direct Homologation of α-Amino Acids
    • Caputo, R.; Cassano, E.; Longobardo, L.; Palumbo, G. Synthesis of Enantiopure N- and C-Protected Homo-β-Amino Acids by Direct Homologation of α-Amino Acids Tetrahedron 1995, 51, 12337-12350
    • (1995) Tetrahedron , vol.51 , pp. 12337-12350
    • Caputo, R.1    Cassano, E.2    Longobardo, L.3    Palumbo, G.4
  • 20
    • 0242515860 scopus 로고    scopus 로고
    • Efficient Synthesis of Enantiomerically Pure β2-Amino Acids via Chiral Isoxazolidinones
    • Lee, H.-S.; Park, J.-S.; Kim, B. M.; Gellman, S. H. Efficient Synthesis of Enantiomerically Pure β2-Amino Acids via Chiral Isoxazolidinones J. Org. Chem. 2003, 68, 1575-1578
    • (2003) J. Org. Chem. , vol.68 , pp. 1575-1578
    • Lee, H.-S.1    Park, J.-S.2    Kim, B.M.3    Gellman, S.H.4
  • 22
    • 34047174129 scopus 로고    scopus 로고
    • Conformational Analysis of Endomorphin-2 Analogs with Phenylalanine Mimics by NMR and Molecular Modeling
    • Shao, X.; Gao, Y.; Zhu, C.; Liu, X.; Yao, J.; Cui, Y.; Wang, R. Conformational Analysis of Endomorphin-2 Analogs with Phenylalanine Mimics by NMR and Molecular Modeling Bioorg. Med. Chem. 2007, 15, 3539-3547
    • (2007) Bioorg. Med. Chem. , vol.15 , pp. 3539-3547
    • Shao, X.1    Gao, Y.2    Zhu, C.3    Liu, X.4    Yao, J.5    Cui, Y.6    Wang, R.7
  • 24
    • 74649085205 scopus 로고    scopus 로고
    • Structural Comparison of μ-Opioid Receptor Selective Peptides Confirmed Four Parameters of Bioactivity
    • Borics, A.; Toth, G. Structural Comparison of μ-Opioid Receptor Selective Peptides Confirmed Four Parameters of Bioactivity J. Mol. Graphics Modell. 2010, 28, 495-505
    • (2010) J. Mol. Graphics Modell. , vol.28 , pp. 495-505
    • Borics, A.1    Toth, G.2
  • 25
  • 26
    • 84867098319 scopus 로고    scopus 로고
    • Spatial Relationships between the Pharmacophores of Endomorphin-2: A Comparative Study of Stereoisomers
    • Leitgeb, B. Spatial Relationships between the Pharmacophores of Endomorphin-2: A Comparative Study of Stereoisomers Cent. Eur. J. Chem. 2012, 10, 1791-1798
    • (2012) Cent. Eur. J. Chem. , vol.10 , pp. 1791-1798
    • Leitgeb, B.1
  • 28
    • 0036945574 scopus 로고    scopus 로고
    • Development and Validation of Opioid Ligand-Receptor Interaction Models: The Structural Basis of mu vs. delta Selectivity
    • 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
    • (2002) J. Pept. Res. , vol.60 , pp. 329-335
    • Mosberg, H.I.1    Fowler, C.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.