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Homology Modeling Inspired Synthesis of 5-HT2A Receptor Inhibitors: A Diazepine Analogue of the Atypical Antipsychotic JL13.
Mongeau, Enrico; Yuan, Gengyang; Minden, Zachary; Waldron, Scott; Booth, Raymond; Felsing, Daniel; Ondrechen, Mary J; Jones, Graham B.
Afiliação
  • Mongeau E; Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, MA, 02115. United States.
  • Yuan G; Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, MA, 02115. United States.
  • Minden Z; Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, MA, 02115. United States.
  • Waldron S; Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, MA, 02115. United States.
  • Booth R; Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, MA, 02115. United States.
  • Felsing D; Department of Pharmaceutical Science, Northeastern University, 360 Huntington Avenue, Boston, MA, 02115. United States.
  • Ondrechen MJ; Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, MA, 02115. United States.
  • Jones GB; Clinical and Translational Science Institute, Tufts University Medical Center, 800 Washington Street, Boston, MA 02111. United States.
Cent Nerv Syst Agents Med Chem ; 17(3): 239-244, 2017.
Article em En | MEDLINE | ID: mdl-28462720
ABSTRACT

BACKGROUND:

The benzoxazepine JL13 is an analogue of the clozapine family of antipsychotic agents which target the 5-HT2A receptor, and has showed promise as an atypical antipsychotic agent. Based on the dearth of clinically effective anti-psychotic agents available, we sought to design and chemically synthesize additional analogues.

METHODS:

Structure function analysis was conducted using state of art computational methods, which were designed to highlight new candidates for chemical synthesis. Efficient syntheses were then conducted and the products screened for affinity to the receptor.

RESULTS:

Among many new analogues prepared, an aza analogue demonstrated seventeen times greater affinity for the receptor than JL13.

CONCLUSION:

An efficient synthetic route to an aza-analogue of JL13 was developed and will allow rapid modifications of the core and synthesis of related libraries.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxazepinas / Piperazinas / Piridinas / Antipsicóticos / Desenho de Fármacos / Antagonistas do Receptor 5-HT2 de Serotonina Limite: Humans Idioma: En Revista: Cent Nerv Syst Agents Med Chem Assunto da revista: FARMACOLOGIA / NEUROLOGIA / QUIMICA CLINICA Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxazepinas / Piperazinas / Piridinas / Antipsicóticos / Desenho de Fármacos / Antagonistas do Receptor 5-HT2 de Serotonina Limite: Humans Idioma: En Revista: Cent Nerv Syst Agents Med Chem Assunto da revista: FARMACOLOGIA / NEUROLOGIA / QUIMICA CLINICA Ano de publicação: 2017 Tipo de documento: Article