Computer modeling of ferrocene-substituted 3,7-diazabicyclo[3.3.1]nonanes as serine protease inhibitors
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[1] E. A. Khokhlova,et al. Organic and hybrid molecular systems , 2015 .
[2] S. N. Osipov,et al. Development of new methods in modern selective organic synthesis: preparation of functionalized molecules with atomic precision , 2014 .
[3] V. Chupakhin,et al. Synthesis of novel bridged dinitrogen heterocycles and their evaluation as potential fragments for the design of biologically active compounds , 2014 .
[4] A. Badshah,et al. Synthesis, chemical characterization, DNA binding and antioxidant studies of ferrocene incorporated selenoure , 2013 .
[5] Timothy Clark,et al. Halogen bonding and other σ-hole interactions: a perspective. , 2013, Physical chemistry chemical physics : PCCP.
[6] Marcus D. Hanwell,et al. Avogadro: an advanced semantic chemical editor, visualization, and analysis platform , 2012, Journal of Cheminformatics.
[7] Andreas Bender,et al. From in silico target prediction to multi-target drug design: current databases, methods and applications. , 2011, Journal of proteomics.
[8] Chris Morley,et al. Open Babel: An open chemical toolbox , 2011, J. Cheminformatics.
[9] Woody Sherman,et al. Contribution of Explicit Solvent Effects to the Binding Affinity of Small‐Molecule Inhibitors in Blood Coagulation Factor Serine Proteases , 2011, ChemMedChem.
[10] Alexander Hillisch,et al. Oral, direct thrombin and factor Xa inhibitors: the replacement for warfarin, leeches, and pig intestines? , 2011, Angewandte Chemie.
[11] C. Biot,et al. Ester prodrugs of ciprofloxacin as DNA-gyrase inhibitors: synthesis, antiparasitic evaluation and docking studies , 2011 .
[12] B. Kuhn,et al. A Medicinal Chemist’s Guide to Molecular Interactions , 2010, Journal of medicinal chemistry.
[13] David S. Goodsell,et al. AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility , 2009, J. Comput. Chem..
[14] G. Klebe,et al. Think twice: understanding the high potency of bis(phenyl)methane inhibitors of thrombin. , 2009, Journal of molecular biology.
[15] Arthur J. Olson,et al. AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading , 2009, J. Comput. Chem..
[16] I. Melnikova. The anticoagulants market , 2009, Nature Reviews Drug Discovery.
[17] Brett A Tounge,et al. Ligand efficiency and fragment-based drug discovery. , 2009, Drug discovery today.
[18] Thomas Lampe,et al. Discovery of the novel antithrombotic agent 5-chloro-N-({(5S)-2-oxo-3- [4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl}methyl)thiophene- 2-carboxamide (BAY 59-7939): an oral, direct factor Xa inhibitor. , 2005, Journal of medicinal chemistry.