1. Academic Validation
  2. N-Methylanilide and N-methylbenzamide derivatives as phosphodiesterase 10A (PDE10A) inhibitors

N-Methylanilide and N-methylbenzamide derivatives as phosphodiesterase 10A (PDE10A) inhibitors

  • Bioorg Med Chem. 2013 Oct 1;21(19):6053-62. doi: 10.1016/j.bmc.2013.07.030.
John Paul Kilburn 1 Jan Kehler Morten Langgård Mette N Erichsen Sebastian Leth-Petersen Mogens Larsen Claus Tornby Christoffersen Jacob Nielsen
Affiliations

Affiliation

  • 1 H. Lundbeck A/S, Department of Medicinal Chemistry, DK-2500 Valby, Denmark. [email protected]
Abstract

PDE10A is a recently identified phosphodiesterase with a quite remarkable localization since the protein is abundant only in brain tissue. Based on this unique localization, research has focused extensively on using PDE10A modulators as a novel therapeutic approach for dysfunction in the basal ganglia circuit including Parkinson's disease, Huntington's disease, schizophrenia, addiction and obsessive compulsive disorder. Medicinal chemistry efforts identified the N-methyl-N-[4-(quinolin-2-ylmethoxy)-phenyl]-isonicotinamide (8) as a nanomolar PDE10A inhibitor. A subsequent Lead-optimization program identified analogous N-methylanilides and their corresponding N-methylbenzamides (29) as potent PDE10A inhibitors, concurrently some interesting and unexpected binding modes were identified.

Keywords

Antipsychotics; MPO; Molecular modeling; Phosphodieasterase 10A inhibitors; Schizophrenia.

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