| Literature DB >> 8676348 |
J L Mokrosz1, A Dereń-Wesołek, E Tatarczyńska, B Duszyńska, A J Bojarski, M J Mokrosz, E Chojnacka-Wójcik.
Abstract
A new analog of buspirone (1), i.e., 8-[4-[2-(1,2,3,4-tetrahydroisoquinolinyl)]butyl]-8-azaspiro- [4.5]decane-7,9-dione (6a), was synthesized. In was demonstrated that buspirone and its analog 6a were equipotent 5-HT(1A) ligands. Several behavioral models showed that 6a had essentially the same functional profile at 5-HT(1A) receptors as buspirone. The obtained results permit a conclusion that the basic nitrogen atom and terminal, bulky cycloimide moiety, but not the 2-pyrimidinyl group, of buspirone are directly involved in the formation of the bioactive complex with 5-Ht1A receptors.Entities:
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Year: 1996 PMID: 8676348 DOI: 10.1021/jm950662c
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446