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Novel thiazolidinedione derivatives with anti-obesity effects: Dual action as PTP1B inhibitors and PPAR-gamma activators

Authors
Bhattarai, Bharat RajKafle, BhooshanHwang, Ji-SunHam, Seung WookLee, Keun-HyeungPark, HwangseoHan, Inn-OcCho, Hyeongjin
Issue Date
Nov-2010
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Protein tyrosine phosphatase; Thiazolidinedione; PTP1B inhibitor; PPAR-gamma activator; Anti-obesity
Citation
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.20, no.22, pp 6758 - 6763
Pages
6
Journal Title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume
20
Number
22
Start Page
6758
End Page
6763
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/22081
DOI
10.1016/j.bmcl.2010.08.130
ISSN
0960-894X
1464-3405
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 IC50 values in a low micromolar range. Compound 18l, the lowest, bore an IC50 of 1.3 mu M. In a peroxisome proliferator-activated receptor-gamma (PPAR-gamma) 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. (C) 2010 Elsevier Ltd. All rights reserved.
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자연과학대학 (화학과)
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