Synthesis and biological activities of 4-substituted pyrrolo[2,3-a]carbazole Pim kinase inhibitors. - Archive ouverte HAL
Article Dans Une Revue European Journal of Medicinal Chemistry Année : 2012

Synthesis and biological activities of 4-substituted pyrrolo[2,3-a]carbazole Pim kinase inhibitors.

Résumé

Pyrrolo[2,3-a]carbazole-3-carbaldehydes are potent Pim kinase inhibitors with in vitro antiproliferative activities. In the present study, we report the synthesis and biological activities (Pim kinase inhibition and in vitro antiproliferative potency) of new 4-substituted pyrrolo[2,3-a]carbazoles. The results demonstrated that the Pim kinase inhibitory potency (especially Pim-3) can be conserved for pyrrolo [2,3-a]carbazoles bearing a methoxycarbonyl group at the 4-position without a formyl at the 3-position. Moreover, compound 27 that was found to be active against Pim-1 and Pim-3 kinases showed antiproliferative activities in the micromolar range.
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Dates et versions

hal-00786353 , version 1 (08-02-2013)

Identifiants

  • HAL Id : hal-00786353 , version 1

Citer

Francis Giraud, Rufine Akué-Gédu, Lionel Nauton, Nicolas Candelon, Eric Debiton, et al.. Synthesis and biological activities of 4-substituted pyrrolo[2,3-a]carbazole Pim kinase inhibitors.. European Journal of Medicinal Chemistry, 2012, 56, pp.225-236. ⟨hal-00786353⟩
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