Literature DB >> 15125959

Synthesis of 3a,4-dihydro-3H-[1]benzopyrano[4,3-c]isoxazoles, displaying combined 5-HT uptake inhibiting and alpha2-adrenoceptor antagonistic activities. Part 2: Further exploration on the cinnamyl moiety.

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.

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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


  1 in total

1.  Efficient Catalytic Synthesis of Condensed Isoxazole Derivatives via Intramolecular Oxidative Cycloaddition of Aldoximes.

Authors:  Irina A Mironova; Valentine G Nenajdenko; Pavel S Postnikov; Akio Saito; Mekhman S Yusubov; Akira Yoshimura
Journal:  Molecules       Date:  2022-06-16       Impact factor: 4.927

  1 in total

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