Literature DB >> 19939189

Patented PDE10A inhibitors: novel compounds since 2007.

Jan Kehler1, John Paul Kilburn.   

Abstract

IMPORTANCE OF THE FIELD: PDE10A inhibition has generated much excitement as a potential novel mechanism for the treatment of the positive symptoms of schizophrenia. PDE10A is only '10 years old' as a drug discovery target since it was first discovered in 1999, and thus PDE10A is an example of the modern drug discovery paradigm demonstrating the highly increased speed by which novel targets can be validated, hits identified, lead-optimization performed and compounds progressed into clinical trials. At least one PDE10A inhibitor compound has been progressed to clinical Phase II for the treatment of schizophrenia. And preclinical evidence suggests that a PDE10A inhibitor could provide antipsychotic, pro-cognitive and negative symptom efficacy in the same dose range. AREAS COVERED IN THIS REVIEW: The review surveys advances in the medicinal chemistry of PDE10A through the patent literature since 2007. The article is supplemented with selected publications from the scientific literature. WHAT THE READER WILL GAIN: Readers will gain an up to date overview of all patents published in the PDE10A field within the last 2 years and be able to judge about the structure-activity relationship and drugability of most progressed PDE10A compounds. TAKE HOME MESSAGE: PDE10A inhibitors will possibly be involved in the treatment of schizophrenia. The field is rapidly approaching a clinical validation of PDE10A inhibitors.

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Year:  2009        PMID: 19939189     DOI: 10.1517/13543770903431050

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  7 in total

1.  Radiosynthesis and in vivo evaluation of [11C]MP-10 as a PET probe for imaging PDE10A in rodent and non-human primate brain.

Authors:  Zhude Tu; Jinda Fan; Shihong Li; Lynne A Jones; Jinquan Cui; Prashanth K Padakanti; Jinbin Xu; Dexing Zeng; Kooresh I Shoghi; Joel S Perlmutter; Robert H Mach
Journal:  Bioorg Med Chem       Date:  2011-01-22       Impact factor: 3.641

2.  Synthesis and in vitro evaluation of new analogues as inhibitors for phosphodiesterase 10A.

Authors:  Zhanbin Zhang; Xiaoxia Lu; Jinbin Xu; Justin Rothfuss; Robert H Mach; Zhude Tu
Journal:  Eur J Med Chem       Date:  2011-06-12       Impact factor: 6.514

3.  Synthesis and in vitro biological evaluation of pyrazole group-containing analogues for PDE10A.

Authors:  Junfeng Li; Hongjun Jin; Haiying Zhou; Justin Rothfuss; Zhude Tu
Journal:  Medchemcomm       Date:  2013-02-01       Impact factor: 3.597

4.  Inhibition of the striatal specific phosphodiesterase PDE10A ameliorates striatal and cortical pathology in R6/2 mouse model of Huntington's disease.

Authors:  Carmela Giampà; Daunia Laurenti; Serenella Anzilotti; Giorgio Bernardi; Frank S Menniti; Francesca Romana Fusco
Journal:  PLoS One       Date:  2010-10-15       Impact factor: 3.240

5.  PDE10A inhibitors stimulate or suppress motor behavior dependent on the relative activation state of the direct and indirect striatal output pathways.

Authors:  Anton A H P Megens; Herman M R Hendrickx; Michel M A Mahieu; Annemie L Y Wellens; Peter de Boer; Greet Vanhoof
Journal:  Pharmacol Res Perspect       Date:  2014-06-12

6.  Radiosynthesis and Radiotracer Properties of a 7-(2-[18F]Fluoroethoxy)-6-methoxypyrrolidinylquinazoline for Imaging of Phosphodiesterase 10A with PET.

Authors:  Uta Funke; Winnie Deuther-Conrad; Gregor Schwan; Aurélie Maisonial; Matthias Scheunemann; Steffen Fischer; Achim Hiller; Detlef Briel; Peter Brust
Journal:  Pharmaceuticals (Basel)       Date:  2012-02-06

7.  Effect of chronic antipsychotic treatment on striatal phosphodiesterase 10A levels: a [¹¹C]MP-10 PET rodent imaging study with ex vivo confirmation.

Authors:  S Natesan; S Ashworth; J Nielsen; S-P Tang; C Salinas; S Kealey; J B Lauridsen; T B Stensbøl; R N Gunn; E A Rabiner; S Kapur
Journal:  Transl Psychiatry       Date:  2014-04-01       Impact factor: 6.222

  7 in total

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