Novel thiazolidinedione derivatives with anti-obesity effects: dual action as PTP1B inhibitors and PPAR-γ activators.

Abstract

Benzylidene-2,4-thiazolidinedione derivatives with substitutions at both the ortho and para-positions of the phenyl group were synthesized as PTP1B inhibitors with IC(50) values in a low micromolar range. Compound 18l, the lowest, bore an IC(50) of 1.3 μM. In a peroxisome proliferator-activated receptor-γ (PPAR-γ) promoter reporter gene assay, 18l was found to activate the transcription of the reporter gene with potencies comparable to those of troglitazone, rosiglitazone, and pioglitazone. In vivo efficacy of 18l as an anti-obesity and hypoglycemic agent was evaluated in a mouse model system. Compound 18l significantly suppressed weight gain and significantly improved blood parameters such as TG, total cholesterol and NEFA without overt toxic effects.

• Authors: Bharat Raj Bhattarai, Bhooshan Kafle, Ji-Sun Hwang, Seung Wook Ham, Keun-Hyeung Lee, Hwangseo Park, Inn-Oc Han, Hyeongjin Cho
• Journal: Bioorganic & medicinal chemistry letters (Bioorg Med Chem Lett) Vol. 20 Issue 22 Pg. 6758-63 (Nov 15 2010) ISSN: 1464-3405 [Electronic] England
• PMID: 20850970 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2010 Elsevier Ltd. All rights reserved.

Chemical References

• Anti-Obesity Agents
• Blood Glucose
• Fatty Acids, Nonesterified
• Hypoglycemic Agents
• PPAR gamma
• Thiazolidinediones
• Triglycerides
• Cholesterol
• Protein Tyrosine Phosphatase, Non-Receptor Type 1

Topics

• Animals
• Anti-Obesity Agents (pharmacology)
• Blood Glucose (metabolism)
• Cholesterol (blood)
• Fatty Acids, Nonesterified (blood)
• Hypoglycemic Agents (pharmacology)
• Mice
• PPAR gamma (agonists)
• Protein Tyrosine Phosphatase, Non-Receptor Type 1 (antagonists & inhibitors)
• Thiazolidinediones (pharmacology)
• Triglycerides (blood)