Abstract
The discovery of PPAR antagonists is emerging as an useful tool for elucidating the biological role of the receptor. Here we report the identification of N-(phenylsulfonyl)amides containing the benzothiazole scaffold, a novel class of potent PPARα antagonists obtained from chemical modification of carboxylic acid agonists. In this work, a group of phenylsulfonamides were synthesized and in vitro evaluated against the agonistic effect of GW7647; they showed an inhibitory effect on PPARα activation, with best compounds revealing a dose-dependent antagonistic profile. Some of these antagonists showed also an inhibitory effect on CPT1A pattern expression.
Copyright © 2011 Elsevier Ltd. All rights reserved.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Benzothiazoles / chemical synthesis
-
Benzothiazoles / chemistry
-
Benzothiazoles / pharmacology*
-
Butyrates / pharmacology
-
Carnitine O-Palmitoyltransferase / antagonists & inhibitors
-
Carnitine O-Palmitoyltransferase / metabolism
-
Dose-Response Relationship, Drug
-
HEK293 Cells
-
Humans
-
Molecular Structure
-
PPAR alpha / antagonists & inhibitors*
-
Phenylurea Compounds / pharmacology
-
Stereoisomerism
-
Structure-Activity Relationship
-
Sulfonamides / chemical synthesis
-
Sulfonamides / chemistry
-
Sulfonamides / pharmacology*
Substances
-
Benzothiazoles
-
Butyrates
-
GW 7647
-
PPAR alpha
-
Phenylurea Compounds
-
Sulfonamides
-
Carnitine O-Palmitoyltransferase
-
benzothiazole