3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      N-Acylhydrazones as inhibitors of PDE10A.

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Cyclic nucleotide phosphodiesterases (PDEs) are represented by a large superfamily of enzymes. A series of hydrazone-based inhibitors was synthesized and shown to be novel, potent, and selective against PDE10A. Optimized compounds of this class were efficacious in animal models of schizophrenia and may be useful for the treatment of this disease.

          Related collections

          Author and article information

          Journal
          Bioorg Med Chem Lett
          Bioorganic & medicinal chemistry letters
          Elsevier BV
          1464-3405
          0960-894X
          Jul 15 2011
          : 21
          : 14
          Affiliations
          [1 ] Omeros Corp., 1420 Fifth Ave., Suite 2600, Seattle, WA 98101, USA.
          Article
          S0960-894X(11)00741-4
          10.1016/j.bmcl.2011.05.100
          21696955
          06a3dad9-438e-4a57-bb42-2a08a36caebf
          Copyright © 2011 Elsevier Ltd. All rights reserved.
          History

          Comments

          Comment on this article