RAR-RXR selectivity and biological activity of new retinoic acid analogues with heterocyclic or polycyclic aromatic systems

Archive ouverte

Ivanova, Diana I. | Gaudon, Claudine | Rossin, Aurélie | Bourguet, William | Gronemeyer, Hinrich

Edité par CCSD ; Elsevier -

The cell biological activity of novel retinoids and rexinoids is described. The stereochemistry of the new compounds was analyzed and ligand docking experiments revealed the structural basis of their RAR binding characteristics. The new ligands activate nuclear retinoic acid receptors (RAR, RXR) with distinct selectivity patterns, as determined in genetically engineered 'reporter' cells. The biological activity of the novel retinoids was assessed by differentiation of NB4 acute promyelocytic leukemia cells.

Consulter en ligne

Suggestions

Du même auteur

Differential action on coregulator interaction defines inverse retinoid agonists and neutral antagonists.

Archive ouverte | Germain, Pierre | CCSD

International audience. Retinoic acid receptors (RARs) are ligand-dependent transcription factors that control a plethora of physiological processes. RARs exert their functions by regulating gene networks controllin...

Differential Action on Coregulator Interaction Defines Inverse Retinoid Agonists and Neutral Antagonists

Archive ouverte | Germain, Pierre | CCSD

International audience

Synthesis of the PPARbeta/delta-selective agonist GW501516 and C4-thiazole-substituted analogs.

Archive ouverte | Pereira, Raquel | CCSD

Sequential, position-selective, Pd-catalyzed cross-coupling reactions of 2,4-dibromo-5-hydroxymethylthiazole provided the scaffold for the synthesis of GW501516, the most potent PPARbeta/delta agonist yet described, and equally se...

Chargement des enrichissements...