Literature DB >> 14572868

Synthesis and structure of novel 2,3, 5,6-tetrahydro-1H-imidazo[2,1-b][1,3,5]benzotriazepines with vasocontractile activity in rabbit aortic rings.

Franciszek Saczewski1, Ewa Kobierska, Jacek Petrusewicz, Anna Gendzwill, Maria Gdaniec.   

Abstract

A series of novel 2,3,5,6-tetrahydro-1H-imidazo[2,1-b][1,3,5]benzotriazepines (3a-n) and hydrochlorides (4a-b) were prepared and their structure was determined by IR and NMR spectroscopic data as well as by X-ray analysis of the hydrochloride 4a. The newly synthesized benzotriazepine 4b exhibited concentration-dependent vasocontractile activity in isolated rabbit aortic rings. Rimalkalim was found to induce a relaxation in rabbit aortic rings precontracted by 4b (3x10(-5) mol). Present results indicate that K(ATP)-dependant channels may contribute in the contractile activity of benzotriazepine 4b.

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Year:  2003        PMID: 14572868     DOI: 10.1016/S0014-827X(03)00200-3

Source DB:  PubMed          Journal:  Farmaco        ISSN: 0014-827X


  1 in total

1.  Synthesis, molecular structure and reactivity of 5-methylidene-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolines.

Authors:  Anita Kornicka; Franciszek Saczewski; Maria Gdaniec
Journal:  Molecules       Date:  2004-02-28       Impact factor: 4.411

  1 in total

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