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Total synthesis and dual PPARα/γ agonist effects of amorphastilbol and its synthetic derivatives.
Kim, Taejung; Lee, Woojung; Jeong, Kyu Hyuk; Song, Jung Ho; Park, Soon-Hye; Choi, Pilju; Kim, Su-Nam; Lee, Seokjoon; Ham, Jungyeob.
Affiliation
  • Kim T; Natural Medicine Center, Korea Institute of Science and Technology, Gangneung 210-340, Republic of Korea.
Bioorg Med Chem Lett ; 22(12): 4122-6, 2012 Jun 15.
Article in En | MEDLINE | ID: mdl-22579420
Amorphastilbol (APH-1), isolated from a Robinia pseudoacacia var. umbraculifer [corrected] seed extract, is a biologically interesting natural trans-stilbene compound with dual peroxisome proliferator-activated receptor (PPAR) α/γ agonist activity. After total synthesis of APH-1 and its derivatives by Pd-catalyzed Suzuki-Miyaura cross-coupling of a common (E)-styryl bromide intermediate and various aromatic trifluoroborate compounds, we biologically evaluated APH-2-APH-12 for PPAR agonist activity. APH-4 and APH-11 were effective PPARα/γ transcriptional activators, compared with APH-1. Therefore, we suggest that APH-4 and APH-11 are novel dual PPARα/γ agonists and are potentially useful for treating type 2 diabetes by enhancing glucose and lipid metabolism.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stilbenes / Cannabinoids / Robinia / PPAR alpha / PPAR gamma / Hypoglycemic Agents Limits: Animals / Humans Language: En Journal: Bioorg Med Chem Lett Journal subject: BIOQUIMICA / QUIMICA Year: 2012 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stilbenes / Cannabinoids / Robinia / PPAR alpha / PPAR gamma / Hypoglycemic Agents Limits: Animals / Humans Language: En Journal: Bioorg Med Chem Lett Journal subject: BIOQUIMICA / QUIMICA Year: 2012 Document type: Article Country of publication: