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Synthesis and biological activity of [[(heterocycloamino)alkoxy] benzyl]-2,4-thiazolidinediones as PPAR gamma agonists

Authors
Jeon, RKim, YJCheon, YRyu, JH
Issue Date
May-2006
Publisher
PHARMACEUTICAL SOCIETY KOREA
Keywords
benzothiazole; thiazolidinediones; PPAR gamma; nitric oxide; diabetes
Citation
ARCHIVES OF PHARMACAL RESEARCH, v.29, no.5, pp 394 - 399
Pages
6
Journal Title
ARCHIVES OF PHARMACAL RESEARCH
Volume
29
Number
5
Start Page
394
End Page
399
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/15143
DOI
10.1007/BF02968589
ISSN
0253-6269
1976-3786
Abstract
Benzothiazole derivatives of thiazolidinediones (TZD) were synthesized using a modified Mitsunobu reaction of 2-(benzothiazol-2-ylmethylamino)ethanol (2) with 5-(4-hydroxybenzyl)-3triphenylmethylthiazolidine-2,4-dione and assayed for activity on peroxisome proliferator-activated receptor (PPAR) subtypes and inhibitory activity of NO production in lipopolysaccharide-activated macrophages. Most of the tested compounds were identified as potent PPAR7 agonists, indicating their potential as drug candidates for diabetes.
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