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Synthesis of triazoloquinazolinone based compounds as tubulin polymerization inhibitors and vascular disrupting agents.
Driowya, Mohsine; Leclercq, Julien; Verones, Valerie; Barczyk, Amélie; Lecoeur, Marie; Renault, Nicolas; Flouquet, Nathalie; Ghinet, Alina; Berthelot, Pascal; Lebegue, Nicolas.
Afiliação
  • Driowya M; Université de Lille, F-59000 Lille, France; Inserm UMR-S1172, Onco and NeuroChemistry, Jean-Pierre Aubert Research Center, F-59000 Lille, France.
  • Leclercq J; Université de Lille, F-59000 Lille, France; Inserm UMR-S1172, Onco and NeuroChemistry, Jean-Pierre Aubert Research Center, F-59000 Lille, France.
  • Verones V; Université de Lille, F-59000 Lille, France; Inserm UMR-S1172, Onco and NeuroChemistry, Jean-Pierre Aubert Research Center, F-59000 Lille, France.
  • Barczyk A; Université de Lille, F-59000 Lille, France; Inserm UMR-995, Institut de Chimie Pharmaceutique Albert Lespagnol, F-59000 Lille, France.
  • Lecoeur M; Université de Lille, F-59000 Lille, France; UDSL, EA 7365 GRITA, 59000 Lille Cedex, France.
  • Renault N; Université de Lille, F-59000 Lille, France; Inserm UMR-995, Institut de Chimie Pharmaceutique Albert Lespagnol, F-59000 Lille, France.
  • Flouquet N; Université de Lille, F-59000 Lille, France; Inserm UMR-S1172, Onco and NeuroChemistry, Jean-Pierre Aubert Research Center, F-59000 Lille, France.
  • Ghinet A; Université de Lille, F-59000 Lille, France; Inserm UMR-995, Hautes Etudes Ingénieur, F-59000 Lille, France.
  • Berthelot P; Université de Lille, F-59000 Lille, France; Inserm UMR-S1172, Onco and NeuroChemistry, Jean-Pierre Aubert Research Center, F-59000 Lille, France.
  • Lebegue N; Université de Lille, F-59000 Lille, France; Inserm UMR-S1172, Onco and NeuroChemistry, Jean-Pierre Aubert Research Center, F-59000 Lille, France. Electronic address: nicolas.lebegue@univ-lille2.fr.
Eur J Med Chem ; 115: 393-405, 2016 Jun 10.
Article em En | MEDLINE | ID: mdl-27031215
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.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Tubulina (Proteína) / Vasos Sanguíneos / Moduladores de Tubulina / Quinazolinonas Idioma: En Revista: Eur J Med Chem Ano de publicação: 2016 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Tubulina (Proteína) / Vasos Sanguíneos / Moduladores de Tubulina / Quinazolinonas Idioma: En Revista: Eur J Med Chem Ano de publicação: 2016 Tipo de documento: Article País de afiliação: França