Synthesis and Characterization of a New RXR Agonist Based on the 6-tert-Butyl-1,1-dimethylindanyl Structure
摘要:
A new ligand for RXR is described, which is based on a 6-tert-butyl-1, 1-dimethylindanyl skeleton as bioisostere of the hydrophobic retinoid region. The Stille cross-coupling reaction allowed the attachment of the polyene side chain to the indanyl ring. Docking studies were carried out to explain the RXR binding profile of this analogue. (C) 2002 Elsevier Science Ltd. All rights reserved.
Synthesis and Characterization of a New RXR Agonist Based on the 6-tert-Butyl-1,1-dimethylindanyl Structure
摘要:
A new ligand for RXR is described, which is based on a 6-tert-butyl-1, 1-dimethylindanyl skeleton as bioisostere of the hydrophobic retinoid region. The Stille cross-coupling reaction allowed the attachment of the polyene side chain to the indanyl ring. Docking studies were carried out to explain the RXR binding profile of this analogue. (C) 2002 Elsevier Science Ltd. All rights reserved.