메뉴 건너뛰기




Volumn 50, Issue 8, 2010, Pages 1510-1520

Pharmacophore modeling of substituted 1,2,4-trioxanes for quantitative prediction of their antimalarial activity

Author keywords

[No Author keywords available]

Indexed keywords

HYDROGEN BONDS; HYDROPHOBICITY; MOLECULES;

EID: 77956053752     PISSN: 15499596     EISSN: 1549960X     Source Type: Journal    
DOI: 10.1021/ci100180e     Document Type: Article
Times cited : (24)

References (47)
  • 2
    • 64349121305 scopus 로고    scopus 로고
    • Malaria-Infected Mice are Cured by a Single Oral Dose of New Dimeric Trioxane Sulfones Which are also Selectively and Powerfully Cytotoxic to Cancer Cells
    • Rosenthal, A. S.; Chen, X.; Liu, J. O.; West, D. C.; Hergenrother, P. J.; Shapiro, T. A.; Posner, G. H. Malaria-Infected Mice are Cured by a Single Oral Dose of New Dimeric Trioxane Sulfones Which are also Selectively and Powerfully Cytotoxic to Cancer Cells J. Med. Chem. 2009, 52, 1198-1203
    • (2009) J. Med. Chem. , vol.52 , pp. 1198-1203
    • Rosenthal, A.S.1    Chen, X.2    Liu, J.O.3    West, D.C.4    Hergenrother, P.J.5    Shapiro, T.A.6    Posner, G.H.7
  • 3
    • 15044338866 scopus 로고    scopus 로고
    • The Global Distribution of Clinical Episodes of Plasmodium falciparum Malaria
    • Snow, R. W.; Guerra, C. A.; Noor, A. M.; Myint, H. Y.; Hay, S. I. The Global Distribution of Clinical Episodes of Plasmodium falciparum Malaria Nature 2005, 434, 214-217
    • (2005) Nature , vol.434 , pp. 214-217
    • Snow, R.W.1    Guerra, C.A.2    Noor, A.M.3    Myint, H.Y.4    Hay, S.I.5
  • 5
    • 23044507928 scopus 로고    scopus 로고
    • Traditional Antimalarials and the Development of Novel Antimalarial Drugs
    • Wright, C. W. Traditional Antimalarials and the Development of Novel Antimalarial Drugs J. Ethnopharmacol. 2005, 100, 67-71
    • (2005) J. Ethnopharmacol. , vol.100 , pp. 67-71
    • Wright, C.W.1
  • 6
    • 0021948029 scopus 로고
    • Qinghaosu (Artemisinin) An Antimalarial Drug from China
    • Klayman, D. L. Qinghaosu (Artemisinin) An Antimalarial Drug from China Science 1985, 228, 1049-1055
    • (1985) Science , vol.228 , pp. 1049-1055
    • Klayman, D.L.1
  • 7
    • 1642442453 scopus 로고    scopus 로고
    • Development of Artemisinin and its Structurally Simplified Trioxane Derivatives as Antimalarial Drugs
    • Ploypradith, P. Development of Artemisinin and its Structurally Simplified Trioxane Derivatives as Antimalarial Drugs Acta Trop. 2004, 89, 329-342
    • (2004) Acta Trop. , vol.89 , pp. 329-342
    • Ploypradith, P.1
  • 8
    • 42349104331 scopus 로고    scopus 로고
    • Qinghaosu (Artemisinin): The Price of Success
    • White, N. J. Qinghaosu (Artemisinin): The Price of Success Science 2008, 320, 330-334
    • (2008) Science , vol.320 , pp. 330-334
    • White, N.J.1
  • 9
    • 31944444061 scopus 로고    scopus 로고
    • Malaria Parasites can Develop Stable Resistance to Artemisinin but Lack Mutations in Candidate Genes atp6 (Encoding the Sarcoplasmic and Endoplasmic Reticulam Ca2+ ATPase), tctp, mdr1 and cg10
    • Afonso, A.; Hunt, P.; Cheeseman, S.; Alves, A. C.; Cunha, C. V.; Rosario, V. do; Carvo, P. Malaria Parasites can Develop Stable Resistance to Artemisinin but Lack Mutations in Candidate Genes atp6 (Encoding the Sarcoplasmic and Endoplasmic Reticulam Ca2+ ATPase), tctp, mdr1 and cg10 Antimicrob. Agents Chemother. 2006, 50, 480-489
    • (2006) Antimicrob. Agents Chemother. , vol.50 , pp. 480-489
    • Afonso, A.1    Hunt, P.2    Cheeseman, S.3    Alves, A.C.4    Cunha, C.V.5    Rosario, V.D.6    Carvo, P.7
  • 12
    • 2542640961 scopus 로고    scopus 로고
    • A Medicinal Chemistry Perspective on Artemisinin and Related Endoperoxides
    • ONeill, P. M.; Posner, G. H. A Medicinal Chemistry Perspective on Artemisinin and Related Endoperoxides J. Med. Chem. 2004, 47, 2945-2964
    • (2004) J. Med. Chem. , vol.47 , pp. 2945-2964
    • Oneill, P.M.1    Posner, G.H.2
  • 13
    • 2942654745 scopus 로고    scopus 로고
    • Knowledge of the Proposed Chemical Mechanism of Action and Cytochrome P450 Metabolism of Antimalarial Trioxanes Like Artemisinin Allows Rational Design of New Antimalarial Peroxides
    • Posner, G. H.; ONeill, P. M. Knowledge of the Proposed Chemical Mechanism of Action and Cytochrome P450 Metabolism of Antimalarial Trioxanes Like Artemisinin Allows Rational Design of New Antimalarial Peroxides Acc. Chem. Res. 2004, 37, 97-404
    • (2004) Acc. Chem. Res. , vol.37 , pp. 97-404
    • Posner, G.H.1    Oneill, P.M.2
  • 16
    • 4544268106 scopus 로고    scopus 로고
    • Application of Thiol-Olefin Cooxygenation Methodology to a New Synthesis of the 1,2,4-Trioxane Pharmacopoeia
    • ONeill, P. M.; Mukhtar, A.; Ward, S. A.; Bickley, J. F.; Davies, J.; Bachi, M. D.; Stocks, P. A. Application of Thiol-Olefin Cooxygenation Methodology to a New Synthesis of the 1,2,4-Trioxane Pharmacopoeia Org. Lett. 2004, 18, 3035-3038
    • (2004) Org. Lett. , vol.18 , pp. 3035-3038
    • Oneill, P.M.1    Mukhtar, A.2    Ward, S.A.3    Bickley, J.F.4    Davies, J.5    Bachi, M.D.6    Stocks, P.A.7
  • 19
    • 57349129495 scopus 로고    scopus 로고
    • Novel Bis- and Tris-1, 2, 4-trioxanes: Synthesis and Antimalarial Activity Against Multidrug-Resistant Plasmodium yoelii in Swiss Mice
    • Singh, C.; Verma, V. P.; Naikade, N. K.; Singh, A. S.; Hassam, M.; Puri, S. K. Novel Bis- and Tris-1, 2, 4-trioxanes: Synthesis and Antimalarial Activity Against Multidrug-Resistant Plasmodium yoelii in Swiss Mice J. Med. Chem. 2008, 51, 7581-7592
    • (2008) J. Med. Chem. , vol.51 , pp. 7581-7592
    • Singh, C.1    Verma, V.P.2    Naikade, N.K.3    Singh, A.S.4    Hassam, M.5    Puri, S.K.6
  • 22
    • 0035817267 scopus 로고    scopus 로고
    • CoMFA of Artemisinin Derivatives: Effect of Location and Size of Lattice
    • Jung, M.; Kim, H. CoMFA of Artemisinin Derivatives: Effect of Location and Size of Lattice Bioorg. Med. Chem. Lett. 2001, 11, 2041-2044
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 2041-2044
    • Jung, M.1    Kim, H.2
  • 23
    • 0037122747 scopus 로고    scopus 로고
    • Structure-Activity Relationships of the Antimalarial Agent Artemisinin: The Development of Predictive in vitro Potency Models Using CoMFA and HQSAR Methodologies
    • Avery, M. A.; Gaston, M. A.; Rodrigues, C. R.; Barreiro, E. J.; Cohen, F. E.; Sabnis, Y. A.; Woolfrey, J. R. Structure-Activity Relationships of the Antimalarial Agent Artemisinin: The Development of Predictive in vitro Potency Models Using CoMFA and HQSAR Methodologies J. Med. Chem. 2002, 45, 292-303
    • (2002) J. Med. Chem. , vol.45 , pp. 292-303
    • Avery, M.A.1    Gaston, M.A.2    Rodrigues, C.R.3    Barreiro, E.J.4    Cohen, F.E.5    Sabnis, Y.A.6    Woolfrey, J.R.7
  • 25
    • 69849099807 scopus 로고    scopus 로고
    • Artemisinin-Resistant Plasmodium falciparum: Can the Genie be Put Back in the Bottle
    • Egan, T. J. Artemisinin-Resistant Plasmodium falciparum: Can the Genie be Put Back in the Bottle Future Microbiol. 2009, 4, 637-639
    • (2009) Future Microbiol. , vol.4 , pp. 637-639
    • Egan, T.J.1
  • 26
    • 0029995163 scopus 로고    scopus 로고
    • Evidence for the Importance of High-Valent Fe=O and of a di Ketone in the Molecular Mechanism of Action of Antimalarial Trioxane Analogs of Artemisinin
    • Posner, G. H.; Park, S. B.; Gonzalez, L.; Wang, D.; Cumming, J. N.; Klinedinst, D.; Shapiro, T. A.; Bachi, M. D. Evidence for the Importance of High-Valent Fe=O and of a di Ketone in the Molecular Mechanism of Action of Antimalarial Trioxane Analogs of Artemisinin J. Am. Chem. Soc. 1996, 118, 3537-3538
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 3537-3538
    • Posner, G.H.1    Park, S.B.2    Gonzalez, L.3    Wang, D.4    Cumming, J.N.5    Klinedinst, D.6    Shapiro, T.A.7    Bachi, M.D.8
  • 27
    • 0032510451 scopus 로고    scopus 로고
    • Orally Active Antimalarial 3-Substituted Trioxanes: New Synthetic Methodology and Biological Evaluation
    • Posner, G. H.; Cumming, J. N.; Woo, S. H.; Ploypradith, P.; Xie, S.; Shapiro, T. A. Orally Active Antimalarial 3-Substituted Trioxanes: New Synthetic Methodology and Biological Evaluation J. Med. Chem. 1998, 41, 940-951
    • (1998) J. Med. Chem. , vol.41 , pp. 940-951
    • Posner, G.H.1    Cumming, J.N.2    Woo, S.H.3    Ploypradith, P.4    Xie, S.5    Shapiro, T.A.6
  • 28
    • 0032510380 scopus 로고    scopus 로고
    • Design, Synthesis, Derivatization, and Structure-Activity Relationships of Simplified, Tricyclic, 1,2,4-Trioxane Alcohol Analogues of the Antimalarial Artemisinin
    • Cumming, J. N.; Wang, D.; Park, S. B.; Shapiro, T. A.; Posner, G. H. Design, Synthesis, Derivatization, and Structure-Activity Relationships of Simplified, Tricyclic, 1,2,4-Trioxane Alcohol Analogues of the Antimalarial Artemisinin J. Med. Chem. 1998, 41, 952-964
    • (1998) J. Med. Chem. , vol.41 , pp. 952-964
    • Cumming, J.N.1    Wang, D.2    Park, S.B.3    Shapiro, T.A.4    Posner, G.H.5
  • 30
    • 0032962098 scopus 로고    scopus 로고
    • Orally Active, Hydrolytically Stable, Semisynthetic, Antimalarial Trioxanes in the Artemisinin Family
    • Posner, G. H.; Parker, M. H.; Northrop, J.; Elias, J. S.; Ploypradith, P.; Xie, S.; Shapiro, T. A. Orally Active, Hydrolytically Stable, Semisynthetic, Antimalarial Trioxanes in the Artemisinin Family J. Med. Chem. 1999, 42, 300-304
    • (1999) J. Med. Chem. , vol.42 , pp. 300-304
    • Posner, G.H.1    Parker, M.H.2    Northrop, J.3    Elias, J.S.4    Ploypradith, P.5    Xie, S.6    Shapiro, T.A.7
  • 31
    • 0033583161 scopus 로고    scopus 로고
    • Antimalarial Artemisinin Analogs. Synthesis via Chemoselective C-C Bond Formation and Preliminary Biological Evaluation
    • ODowd, H.; Ploypradith, P.; Xie, S.; Shapiro, T. A.; Posner, G. H. Antimalarial Artemisinin Analogs. Synthesis via Chemoselective C-C Bond Formation and Preliminary Biological Evaluation Tetrahedron. 1999, 55, 3625-3636
    • (1999) Tetrahedron. , vol.55 , pp. 3625-3636
    • Odowd, H.1    Ploypradith, P.2    Xie, S.3    Shapiro, T.A.4    Posner, G.H.5
  • 33
    • 0034100290 scopus 로고    scopus 로고
    • Building a Common Feature Hypothesis for Thymidylate Synthase Inhibition
    • Kim, S. G.; Yoon, C.; Kim, S.; Cho, Y.; Kang, D. Building a Common Feature Hypothesis for Thymidylate Synthase Inhibition Bioorg. Med. Chem. 2000, 8, 11-17
    • (2000) Bioorg. Med. Chem. , vol.8 , pp. 11-17
    • Kim, S.G.1    Yoon, C.2    Kim, S.3    Cho, Y.4    Kang, D.5
  • 34
    • 0027990218 scopus 로고
    • Enhancement of Hemin-Induced Membrane Damage by Artemisinin
    • Wei, N.; Sadrzadeh, S. M. Enhancement of Hemin-Induced Membrane Damage by Artemisinin Biochem. Pharmacol. 1994, 48, 737-41
    • (1994) Biochem. Pharmacol. , vol.48 , pp. 737-741
    • Wei, N.1    Sadrzadeh, S.M.2
  • 36
    • 36749000794 scopus 로고    scopus 로고
    • Malaria Chemotherapeutics Part I: History of Antimalarial Drug Development, Currently Used Therapeutics and Drugs in Clinical Development
    • Schlitzer, M. Malaria Chemotherapeutics Part I: History of Antimalarial Drug Development, Currently Used Therapeutics and Drugs in Clinical Development ChemMedChem. 2007, 2, 944-986
    • (2007) ChemMedChem. , vol.2 , pp. 944-986
    • Schlitzer, M.1
  • 37
    • 37549066714 scopus 로고    scopus 로고
    • In vitro and in vivo Interaction of Synthetic Peroxide RBx11160 (OZ277) with Piperaquine in Plasmodium Models
    • Snydera, C.; Cholleta, J.; Santo-Tomasa, J.; Scheurera, C.; Wittlin, S. In vitro and in vivo Interaction of Synthetic Peroxide RBx11160 (OZ277) with Piperaquine in Plasmodium Models Exp. Parasitol. 2007, 115, 296-300
    • (2007) Exp. Parasitol. , vol.115 , pp. 296-300
    • Snydera, C.1    Cholleta, J.2    Santo-Tomasa, J.3    Scheurera, C.4    Wittlin, S.5
  • 39
    • 0038458856 scopus 로고    scopus 로고
    • Chemical Feature-Based Pharmacophores and Virtual Library Screening for Discovery of New Leads
    • Langer, T.; Krovat, E. M. Chemical Feature-Based Pharmacophores and Virtual Library Screening for ?iscovery of New Leads Curr. Opin. Drug Discovery Dev. 2003, 6, 370-376
    • (2003) Curr. Opin. Drug Discovery Dev. , vol.6 , pp. 370-376
    • Langer, T.1    Krovat, E.M.2
  • 40
    • 77956036697 scopus 로고    scopus 로고
    • version 2.5; Schrödinger, LLC: New York.
    • CombiGlide, version 2.5; Schrödinger, LLC: New York, 2009.
    • (2009) CombiGlide
  • 41
    • 29544437054 scopus 로고    scopus 로고
    • 8-(1-Naphthalen-2-yl-vinyl)-6, 7, 10-Trioxaspiro (4,5)Decane, a New 1,2,4-Trioxane Effective Against Rodent and Simian Malaria
    • Singh, C.; Kanchan, R.; Srivastava, D.; Puri, S. K. 8-(1-Naphthalen-2-yl- vinyl)-6, 7, 10-Trioxaspiro (4,5)Decane, a New 1,2,4-Trioxane Effective Against Rodent and Simian Malaria Bioorg. Med. Chem. Lett. 2006, 16, 584-586
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 584-586
    • Singh, C.1    Kanchan, R.2    Srivastava, D.3    Puri, S.K.4
  • 43
    • 37249062877 scopus 로고    scopus 로고
    • version 2.0; Accelrys Software Inc.: San Diego, CA.
    • Discovery Studio, version 2.0; Accelrys Software Inc.: San Diego, CA 2001.
    • (2001) Discovery Studio
  • 45
    • 18344383893 scopus 로고    scopus 로고
    • Comparision of Conformational Analysis Techniques to Generate Pharmacophore Hypotheses Using Catalyst
    • Kristam, R.; Gillet, V. J.; Lewis, R. A.; Thorner, D. Comparision of Conformational Analysis Techniques to Generate Pharmacophore Hypotheses Using Catalyst J. Chem. Inf. Model. 2005, 45, 461-476
    • (2005) J. Chem. Inf. Model. , vol.45 , pp. 461-476
    • Kristam, R.1    Gillet, V.J.2    Lewis, R.A.3    Thorner, D.4
  • 46
    • 0035352430 scopus 로고    scopus 로고
    • A Comparison of Methods for Pharmacophore Generation with the Catalyst Software and Their Use for 3D-QSAR: Application to a Set of 4-Aminopyridine Thrombin Inhibitors
    • Greenidge, P. A.; Weiser, J. A Comparison of Methods for Pharmacophore Generation with the Catalyst Software and Their Use for 3D-QSAR: Application to a Set of 4-Aminopyridine Thrombin Inhibitors Mini-Rev. Med. Chem. 2001, 1, 79-87
    • (2001) Mini-Rev. Med. Chem. , vol.1 , pp. 79-87
    • Greenidge, P.A.1    Weiser, J.2
  • 47
    • 1342279612 scopus 로고    scopus 로고
    • Structure-Activity Relationship Study of Antimalarial Indolo [2,1-B]Quinazoline-6,12-Diones (Tryptanthrins).Three-Dimensional Pharmacophore Modeling and Identification of New Antimalarial Candidates
    • Bhattacharjee, A. K.; Hartell, M. G.; Nichols, D. A.; Hicks, R. P.; Stanton, B. Structure-Activity Relationship Study of Antimalarial Indolo [2,1-B]Quinazoline-6,12-Diones (Tryptanthrins).Three-Dimensional Pharmacophore Modeling and Identification of New Antimalarial Candidates Eur. J. Med. Chem. 2004, 39, 59-67
    • (2004) Eur. J. Med. Chem. , vol.39 , pp. 59-67
    • Bhattacharjee, A.K.1    Hartell, M.G.2    Nichols, D.A.3    Hicks, R.P.4    Stanton, B.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.