Literature DB >> 19854048

Discovery of novel non-peptide inhibitors of BACE-1 using virtual high-throughput screening.

N Yi Mok1, James Chadwick, Katherine A B Kellett, Nigel M Hooper, A Peter Johnson, Colin W G Fishwick.   

Abstract

A novel series of isatin-based inhibitors of beta-secretase (BACE-1) have been identified using a virtual high-throughput screening approach. Structure-activity relationship studies revealed structural features important for inhibition. Docking studies suggest these inhibitors may bind within the BACE-1 active site through H-bonding interactions involving the catalytic aspartate residues.

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Year:  2009        PMID: 19854048     DOI: 10.1016/j.bmcl.2009.09.103

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  4 in total

1.  Creation of Novel Cores for β-Secretase (BACE-1) Inhibitors: A Multiparameter Lead Generation Strategy.

Authors:  Jenny Viklund; Karin Kolmodin; Gunnar Nordvall; Britt-Marie Swahn; Mats Svensson; Ylva Gravenfors; Fredrik Rahm
Journal:  ACS Med Chem Lett       Date:  2014-02-03       Impact factor: 4.345

Review 2.  The structural evolution of β-secretase inhibitors: a focus on the development of small-molecule inhibitors.

Authors:  Stefania Butini; Simone Brogi; Ettore Novellino; Giuseppe Campiani; Arun K Ghosh; Margherita Brindisi; Sandra Gemma
Journal:  Curr Top Med Chem       Date:  2013       Impact factor: 3.295

Review 3.  BACE1 (β-secretase) inhibitors for the treatment of Alzheimer's disease.

Authors:  Arun K Ghosh; Heather L Osswald
Journal:  Chem Soc Rev       Date:  2014-10-07       Impact factor: 54.564

4.  Changing Paradigm from one Target one Ligand Towards Multi-target Directed Ligand Design for Key Drug Targets of Alzheimer Disease: An Important Role of In Silico Methods in Multi-target Directed Ligands Design.

Authors:  Akhil Kumar; Ashish Tiwari; Ashok Sharma
Journal:  Curr Neuropharmacol       Date:  2018       Impact factor: 7.363

  4 in total

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