Display Settings:

Format

Send to:

Choose Destination
    Bioorg Med Chem Lett. 2010 Sep 1;20(17):5329-33. Epub 2010 Jun 27.

    Fragment-based discovery and optimization of BACE1 inhibitors.

    Source

    Evotec UK Ltd, Abingdon, UK. james.madden@evotec.com

    Abstract

    A novel series of 2-aminobenzimidazole inhibitors of BACE1 has been discovered using fragment-based drug discovery (FBDD) techniques. The rapid optimization of these inhibitors using structure-guided medicinal chemistry is discussed.

    Copyright 2010 Elsevier Ltd. All rights reserved.

    PMID:
    20656487
    [PubMed - indexed for MEDLINE]

      Supplemental Content

      Icon for Elsevier Science

      Save items

      loading

      Structures reported by this article

      See all 4 structures...

      Recent activity

      Your browsing activity is empty.

      Activity recording is turned off.

      Turn recording back on

      See more...
      Write to the Help Desk