Synthesis and pharmacology of 6-substituted benztropines: discovery of novel dopamine uptake inhibitors possessing low binding affinity to the dopamine transporter.

نویسندگان

  • Daniele Simoni
  • Marcello Rossi
  • Valerio Bertolasi
  • Marinella Roberti
  • Daniela Pizzirani
  • Riccardo Rondanin
  • Riccardo Baruchello
  • Francesco Paolo Invidiata
  • Manlio Tolomeo
  • Stefania Grimaudo
  • Stefania Merighi
  • Katia Varani
  • Stefania Gessi
  • Pier Andrea Borea
  • Silvia Marino
  • Sabrina Cavallini
  • Clementina Bianchi
  • Anna Siniscalchi
چکیده

A series of 6alpha- and 6beta-substituted benztropines were synthesized. A marked enantioselectivity was observed for the 6beta-methoxylated benztropines, the (1R)-isomers being more potent than the corresponding (1S) compounds. The racemic 6alpha-methoxy-3-(4',4' '-difluorodiphenylmethoxy)tropane (5 g) was the most potent compound. It has been found that modifications at the 6-position of benztropine might reduce the DAT binding affinity, maintaining otherwise a significant dopamine uptake inhibitory activity. A reinvestigation of the absolute configuration of 6beta-methoxytropinone proved the 6R configuration for the (+)-enantiomer.

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عنوان ژورنال:
  • Journal of medicinal chemistry

دوره 48 9  شماره 

صفحات  -

تاریخ انتشار 2005