In silico studies, synthesis and binding evaluation of substituted 2-pyrrolidinones as peptidomimetics of RGD tripeptide sequence - Université Sorbonne Paris Nord Accéder directement au contenu
Article Dans Une Revue European Journal of Medicinal Chemistry Année : 2015

In silico studies, synthesis and binding evaluation of substituted 2-pyrrolidinones as peptidomimetics of RGD tripeptide sequence

Julie Bolley
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Résumé

In silico optimisation, synthesis and binding evaluation of αvβ3 integrin's affinity for precursors of a new RGD peptidomimetics family are presented. The 2-pyrrolidinone building block was obtained by condensation of L-lysine with dimethoxydihydrofuran followed by reduction. The ring was functionalised functionalized with a carboxylic acid and a guanidinium appendage. On the pyrrolidinone heterocycle, the effects on affinity of position, length and relative .geometry of the two acid or basic functionalized side chains introduced on the pyrrolidinone ring have been previously evaluated by docking studies. Peptidomimetics have finally been evaluated by competition binding assays for αvβ3 integrin's affinity using radio-ligands.
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Dates et versions

hal-01904943 , version 1 (25-10-2018)

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Valérie Toum, Julie Bolley, Yoann Lalatonne, Carole Barbey, Laurence Motte, et al.. In silico studies, synthesis and binding evaluation of substituted 2-pyrrolidinones as peptidomimetics of RGD tripeptide sequence. European Journal of Medicinal Chemistry, 2015, 93, pp.360. ⟨10.1016/j.ejmech.2015.02.017⟩. ⟨hal-01904943⟩
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