| Literature DB >> 15125959 |
Joaquín Pastor1, Jesús Alcázar, Rosa M Alvarez, J Ignacio Andrés, José M Cid, Ana I De Lucas, Adolfo Díaz, Javier Fernández, Luis M Font, Laura Iturrino, Celia Lafuente, Sonia Martínez, Margot H Bakker, Ilse Biesmans, Lieve I Heylen, Anton A Megens.
Abstract
In our previous paper we have described the synthesis of a series of 3-piperazinylmethyl-3a,4-dihydro-3H-[1]benzopyrano[4,3-c]isoxazoles, as novel dual 5-HT reuptake inhibitors and alpha2-adrenoceptor antagonists. That investigation led to the identification of the cinnamyl fragment as the most suitable moiety for combined activity. This paper outlines a further optimisation programme, focused on the exploration of the aromatic ring present on the cinnamyl moiety of compounds 1, 2 and 3.Entities:
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Year: 2004 PMID: 15125959 DOI: 10.1016/j.bmcl.2004.03.031
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823