Antibacterial potential of selected 4-phenyl hydroxycoumarins: integrated in vitro and molecular docking studies

[1]  I. Damnjanovic,et al.  Monte Carlo Method Based QSAR Modeling of Coumarin Derivates as Potent HIV‐1 Integrase Inhibitors and Molecular Docking Studies of Selected 4‐phenyl Hydroxycoumarins , 2014 .

[2]  G. Nikolic,et al.  Antioxidant properties of selected 4-phenyl hydroxycoumarins: Integrated in vitro and computational studies. , 2014, Chemico-biological interactions.

[3]  Wei Zhou,et al.  4-Hydroxy-3-(naphthalen-1-ylmethyl)thiophen-2(5H)-one as inhibitors of tyrosyl-tRNA synthase: Synthesis, molecular docking and antibacterial evaluation , 2014 .

[4]  T. Tomašič,et al.  Prospects for developing new antibacterials targeting bacterial type IIA topoisomerases. , 2013, Current topics in medicinal chemistry.

[5]  C. Kaushik,et al.  Synthesis and biological evaluation of amino acid-linked 1,2,3-bistriazole conjugates as potential antimicrobial agents , 2013, Medicinal Chemistry Research.

[6]  S. Joshi,et al.  Synthesis, biological evaluation and docking studies of 4-aryloxymethyl coumarins derived from substructures and degradation products of vancomycin. , 2013, European journal of medicinal chemistry.

[7]  Cheng‐He Zhou,et al.  Current developments of coumarin compounds in medicinal chemistry. , 2013, Current pharmaceutical design.

[8]  Cheng‐He Zhou,et al.  Synthesis and biological activities of thio-triazole derivatives as novel potential antibacterial and antifungal agents , 2012, Science China Chemistry.

[9]  Cheng‐He Zhou,et al.  7-(6-Bromohexyloxy)-4-methyl-2H-chromen-2-one , 2012, Acta crystallographica. Section E, Structure reports online.

[10]  Y. Asiri,et al.  Design, synthesis and antibacterial activity of fluoroquinolones containing bulky arenesulfonyl fragment: 2D-QSAR and docking study. , 2011, European journal of medicinal chemistry.

[11]  Roman A. Laskowski,et al.  LigPlot+: Multiple Ligand-Protein Interaction Diagrams for Drug Discovery , 2011, J. Chem. Inf. Model..

[12]  X. Liang,et al.  Tyrosyl-tRNA synthetase inhibitors as antibacterial agents: synthesis, molecular docking and structure-activity relationship analysis of 3-aryl-4-arylaminofuran-2(5H)-ones. , 2011, European journal of medicinal chemistry.

[13]  Steven J. M. Jones,et al.  A Computational Approach to Finding Novel Targets for Existing Drugs , 2011, PLoS Comput. Biol..

[14]  F. Hsu,et al.  Synthesis and Evaluation of Antibacterial Activities of 5,7‐Dihydroxycoumarin Derivatives , 2011, Archiv der Pharmazie.

[15]  M. Saleem,et al.  Antimicrobial Natural Products: An Update on Future Antibiotic Drug Candidates , 2010 .

[16]  N. Farag,et al.  Design, synthesis and docking studies of new furobenzopyranones and pyranobenzopyranones as photoreagent towards DNA and as antimicrobial agents. , 2010, European journal of medicinal chemistry.

[17]  Abdul Jabbar,et al.  Antimicrobial natural products: an update on future antibiotic drug candidates. , 2010, Natural product reports.

[18]  Mark B Gerstein,et al.  Computational analysis of membrane proteins: the largest class of drug targets. , 2009, Drug discovery today.

[19]  Ruian Xu,et al.  The structure and pharmacological functions of coumarins and their derivatives. , 2009, Current medicinal chemistry.

[20]  Henry F. Chambers,et al.  Waves of resistance: Staphylococcus aureus in the antibiotic era , 2009, Nature Reviews Microbiology.

[21]  Christopher T. Walsh,et al.  Antibiotics for Emerging Pathogens , 2009, Science.

[22]  T. Smyth,et al.  A study of the antimicrobial activity of selected naturally occurring and synthetic coumarins. , 2009, International journal of antimicrobial agents.

[23]  R. Kroemer.  Structure-based drug design: docking and scoring. , 2007, Current protein & peptide science.

[24]  F. Ausubel,et al.  Prospects for plant-derived antibacterials , 2006, Nature Biotechnology.

[25]  René Thomsen,et al.  MolDock: a new technique for high-accuracy molecular docking. , 2006, Journal of medicinal chemistry.

[26]  F. Monache,et al.  Antibacterial Activity of Coumarins , 2005, Zeitschrift fur Naturforschung. C, Journal of biosciences.

[27]  E Uriarte,et al.  Simple coumarins and analogues in medicinal chemistry: occurrence, synthesis and biological activity. , 2005, Current medicinal chemistry.

[28]  A. Sartoratto,et al.  Composition and antimicrobial activity of essential oils from aromatic plants used in Brazil , 2004 .

[29]  S. Levy,et al.  Antibacterial resistance worldwide: causes, challenges and responses , 2004, Nature Medicine.

[30]  V. Khilya,et al.  Neoflavones. 1. Natural Distribution and Spectral and Biological Properties , 2004, Chemistry of Natural Compounds.

[31]  P. Geerlings,et al.  Conceptual density functional theory. , 2003, Chemical reviews.

[32]  Xiayang Qiu,et al.  Crystal structure of Staphylococcus aureus tyrosyl‐tRNA synthetase in complex with a class of potent and specific inhibitors , 2001, Protein science : a publication of the Protein Society.

[33]  O. Kayser,et al.  Antibacterial Activity of Simple Coumarins: Structural Requirements for Biological Activity , 1999, Zeitschrift fur Naturforschung. C, Journal of biosciences.

[34]  A. Becke.  Density-functional thermochemistry. , 1996 .

[35]  A. Becke.  Density-functional thermochemistry. III. The role of exact exchange , 1993 .

[36]  H. Neu,et al.  The Crisis in Antibiotic Resistance , 1992, Science.

[37]  T. Mabry,et al.  Two new neoflavonoids and C-glycosylflavones from Passiflora serratodigitata , 1982 .

[38]  H. Falk,et al.  Progress in the Chemistry of Organic Natural Products , 2017 .

[39]  M. Gellert,et al.  Novobiocin and coumermycin inhibit DNA supercoiling catalyzed by DNA gyrase. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[40]  G. Gribble,et al.  Progress in the Chemistry of Organic Natural Products , 2011 .