| Literature DB >> 27031215 |
Mohsine Driowya1, Julien Leclercq1, Valerie Verones1, Amélie Barczyk2, Marie Lecoeur3, Nicolas Renault2, Nathalie Flouquet1, Alina Ghinet4, Pascal Berthelot1, Nicolas Lebegue5.
Abstract
A series of 1-phenyl-[1,2,4]triazolo[4,3-a]quinazolin-5-ones designed as conformationally restricted CA-4 analogues, were tested for their tubulin polymerization and growth inhibitory activities. The 3-hydroxy-4-methoxy derivatives 11d and 12d are potent inhibitors of tubulin assembly but only the N-methylated amid counterpart 12d possesses potent anticancer activity in a large panel of cancer cell lines. Upon treatment with compound 12d, remarkable cell shape changes as cell migration and tube formation were elicited in HUVECs, consistent with vasculature damaging activity.Entities:
Keywords: Antivascular; Combretastatin; Cytotoxicity; Triazoloquinazolinone; Tubulin polymerization
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Year: 2016 PMID: 27031215 DOI: 10.1016/j.ejmech.2016.03.056
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514