Expeditious synthesis and biological evaluation of new C-6 1,2,3-triazole adenosine derivatives A1 receptor antagonists or agonists. - Archive ouverte HAL
Article Dans Une Revue Organic & Biomolecular Chemistry Année : 2010

Expeditious synthesis and biological evaluation of new C-6 1,2,3-triazole adenosine derivatives A1 receptor antagonists or agonists.

Résumé

The synthesis of new C-6 1,2,3-triazole adenosine derivatives via microwave assisted 1,3-dipolar cycloaddition as key step is described. The binding on membranes of cells that over express A(1) adenosine receptors (A(1)AR) was also evaluated. Among them, four compounds increased cAMP production, in a dose-dependent manner acting as antagonists of the A(1)AR, while two compounds act as agonists.

Domaines

Chimie organique
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Dates et versions

hal-00682114 , version 1 (23-03-2012)

Identifiants

Citer

Smitha C Mathew, Youlet By, Aurélie Berthault, Marie-Alice Virolleaud, Louis Carrega, et al.. Expeditious synthesis and biological evaluation of new C-6 1,2,3-triazole adenosine derivatives A1 receptor antagonists or agonists.. Organic & Biomolecular Chemistry, 2010, 8 (17), pp.3874-81. ⟨10.1039/c0ob00017e⟩. ⟨hal-00682114⟩
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