Literature DB >> 21806375

The benefits of constructing leads from fragment hits.

N Foloppe1.   

Abstract

'Fragments' refer to particularly small molecular starting points in medicinal chemistry. The small size of fragments requires adapted techniques for their screening and subsequent elaboration. The detection of the weak binding affinity of fragments for their target, and associated screening issues, have been debated at length. Since it is now clear that fragments can be developed into clinical candidates, the discussion is shifting to the design of good-quality lead compounds from fragment hits. The increasing ability to control and tailor this construction process highlights the potential benefits of fragment-based drug discovery.

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Year:  2011        PMID: 21806375     DOI: 10.4155/fmc.11.46

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  9 in total

1.  Hot spot analysis for driving the development of hits into leads in fragment-based drug discovery.

Authors:  David R Hall; Chi Ho Ngan; Brandon S Zerbe; Dima Kozakov; Sandor Vajda
Journal:  J Chem Inf Model       Date:  2011-12-15       Impact factor: 4.956

Review 2.  Exploring chemical space for drug discovery using the chemical universe database.

Authors:  Jean-Louis Reymond; Mahendra Awale
Journal:  ACS Chem Neurosci       Date:  2012-04-25       Impact factor: 4.418

3.  Sustainable synthesis and automated deposition: an accessible discovery screening library of fragment-like purines.

Authors:  Christoph Kamper; Katharina Korpis; Edgar Specker; Lennart Anger; Martin Neuenschwander; Patrick J Bednarski; Andreas Link
Journal:  Mol Divers       Date:  2012-08-14       Impact factor: 2.943

4.  Identification of Cys255 in HIF-1α as a novel site for development of covalent inhibitors of HIF-1α/ARNT PasB domain protein-protein interaction.

Authors:  Rosa Cardoso; Robert Love; Carol L Nilsson; Simon Bergqvist; Dawn Nowlin; Jiangli Yan; Kevin K-C Liu; Jing Zhu; Ping Chen; Ya-Li Deng; H Jane Dyson; Michael J Greig; Alexei Brooun
Journal:  Protein Sci       Date:  2012-11-09       Impact factor: 6.725

Review 5.  Lessons from Hot Spot Analysis for Fragment-Based Drug Discovery.

Authors:  David R Hall; Dima Kozakov; Adrian Whitty; Sandor Vajda
Journal:  Trends Pharmacol Sci       Date:  2015-11-01       Impact factor: 14.819

6.  Antibody Peptide based antifungal immunotherapy.

Authors:  Walter Magliani; Stefania Conti; Laura Giovati; Pier Paolo Zanello; Martina Sperindè; Tecla Ciociola; Luciano Polonelli
Journal:  Front Microbiol       Date:  2012-06-01       Impact factor: 5.640

Review 7.  Current progress in Structure-Based Rational Drug Design marks a new mindset in drug discovery.

Authors:  Valère Lounnas; Tina Ritschel; Jan Kelder; Ross McGuire; Robert P Bywater; Nicolas Foloppe
Journal:  Comput Struct Biotechnol J       Date:  2013-04-02       Impact factor: 7.271

8.  Identification of novel, in vivo active Chk1 inhibitors utilizing structure guided drug design.

Authors:  Andrew J Massey; Stephen Stokes; Helen Browne; Nicolas Foloppe; Andreá Fiumana; Simon Scrace; Mandy Fallowfield; Simon Bedford; Paul Webb; Lisa Baker; Mark Christie; Martin J Drysdale; Mike Wood
Journal:  Oncotarget       Date:  2015-11-03

9.  Toward rational fragment-based lead design without 3D structures.

Authors:  Morkos A Henen; Nicolas Coudevylle; Leonhard Geist; Robert Konrat
Journal:  J Med Chem       Date:  2012-08-30       Impact factor: 7.446

  9 in total

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