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N,N-disubstituted aminomethyl benzofuran derivatives: synthesis and preliminary binding evaluation.
Boyé, S; Pfeiffer, B; Renard, P; Rettori, M C; Guillaumet, G; Viaud, M C.
Affiliation
  • Boyé S; Institut de Chimie Organique et Analytique, associé au CNRS, Université d'Orléans, France.
Bioorg Med Chem ; 7(2): 335-41, 1999 Feb.
Article in En | MEDLINE | ID: mdl-10218826
ABSTRACT
A series of new N-substituted 2,3-dihydro-2-aminomethyl-2H-1-benzofuran derivatives was prepared and evaluated for affinity at 5-HT1A, 5-HT2A, 5-HT2C, 5-HT3, D2, and D3 receptors. Compound 9, 8-[4-[N-propyl-N-(7-hydroxy-2,3-dihydro -2H-1-benzofuran-2-yl)methyl]aminobutyl]-8-azaspiro[4,5]decane-7,9 -dione, bound at 5-HT1A sites with nanomolar affinity (IC50= 1.5 nM) and high selectivity over 5-HT2A, 5-HT2C, 5-HT3, D2, and D3 receptors.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Benzofurans Limits: Animals Language: En Journal: Bioorg Med Chem Journal subject: BIOQUIMICA / QUIMICA Year: 1999 Document type: Article Affiliation country: Francia
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Benzofurans Limits: Animals Language: En Journal: Bioorg Med Chem Journal subject: BIOQUIMICA / QUIMICA Year: 1999 Document type: Article Affiliation country: Francia
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