Literature DB >> 16513345

Vasorelaxant activity of phthalazinones and related compounds.

Esther del Olmo1, Bianca Barboza, Maria Inés Ybarra, José Luis López-Pérez, Rosalía Carrón, Maria Angeles Sevilla, Cinthia Boselli, Arturo San Feliciano.   

Abstract

Several series of dihydrostilbenamide, imidazo[2,1-a]isoindole, pyrimido[2,1-a]isoindole and phthalazinone derivatives were obtained and their vasorelaxant activity was measured on isolated rat aorta rings pre-contracted with phenylephrine (10(-5)M). Some phthalazinones attained, practically, the total relaxation of the organ at micromolar concentrations. For the most potent compound 9h (EC(50)=0.43microM) the affinities for alpha(1A), alpha(1B) and alpha(1D) adrenergic sub-receptors were determined.

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Year:  2006        PMID: 16513345     DOI: 10.1016/j.bmcl.2006.02.003

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  2-[(2,4,6-Tri-methyl-benzene)-sulfon-yl]phthalazin-1(2H)-one: crystal structure, Hirshfeld surface analysis and computational study.

Authors:  David Chukwuma Izuogu; Jonnie Niyi Asegbeloyin; Mukesh M Jotani; Edward R T Tiekink
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2020-04-21

2.  The facile construction of the phthalazin-1(2H)-one scaffold via copper-mediated C-H(sp(2))/C-H(sp) coupling under mild conditions.

Authors:  Wei Zhu; Bao Wang; Shengbin Zhou; Hong Liu
Journal:  Beilstein J Org Chem       Date:  2015-09-14       Impact factor: 2.883

  2 in total

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