Bioorganic & Medicinal Chemistry 2012-08-15

Design and synthesis of marine fungal phthalide derivatives as PPAR-γ agonists.

Bin Xiao, Jun Yin, Minhi Park, Juan Liu, Jian Lin Li, Eun La Kim, Jongki Hong, Hae Young Chung, Jee H Jung

文献索引：Bioorg. Med. Chem. 20(16) , 4954-61, (2012)

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摘要

On the basis of a marine fungal phthalide (paecilocin A) skeleton, we synthesized 20 analogs and evaluated them for peroxisome proliferator-activated receptor gamma (PPAR-γ) binding and activation. Among these analogs, 6 and 7 had significant PPAR-γ binding activity, and 7 showed further PPAR-γ activation in rat liver Ac2F cells. In docking simulation, 7 formed H bonds with key amino acid residues of the PPAR-γ binding domain, and the overall positioning was similar to rosiglitazone. This new phthalide derivative is considered an interesting new molecular class of PPAR-γ ligands.Copyright © 2012 Elsevier Ltd. All rights reserved.