Literature DB >> 21696955

N-Acylhydrazones as inhibitors of PDE10A.

Jennifer L Gage1, Rene Onrust, Derek Johnston, Andrew Osnowski, Wendy Macdonald, Lee Mitchell, László Urögdi, Alex Rohde, Kevin Harbol, Sasha Gragerov, György Dormán, Tom Wheeler, Vince Florio, Neil S Cutshall.   

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.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21696955     DOI: 10.1016/j.bmcl.2011.05.100

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


  2 in total

1.  Novel orally active analgesic and anti-inflammatory cyclohexyl-N-acylhydrazone derivatives.

Authors:  Tiago Fernandes da Silva; Walfrido Bispo Júnior; Magna Suzana Alexandre-Moreira; Fanny Nascimento Costa; Carlos Eduardo da Silva Monteiro; Fabio Furlan Ferreira; Regina Cely Rodrigues Barroso; François Noël; Roberto Takashi Sudo; Gisele Zapata-Sudo; Lídia Moreira Lima; Eliezer J Barreiro
Journal:  Molecules       Date:  2015-02-12       Impact factor: 4.411

2.  Design, synthesis, antinociceptive and anti-inflammatory activities of novel piroxicam analogues.

Authors:  Amanda Silva de Miranda; Walfrido Bispo Júnior; Yolanda Karla Cupertino da Silva; Magna Suzana Alexandre-Moreira; Rosane de Paula Castro; José Ricardo Sabino; Luciano Morais Lião; Lídia Moreira Lima; Eliezer J Barreiro
Journal:  Molecules       Date:  2012-11-28       Impact factor: 4.411

  2 in total

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