Abstract
PPARγ and Nrf2 are important transcriptional factors involved in many signaling pathways, especially in the anti-infectious response of macrophages. Compounds bearing a Michael acceptor moiety are well known to activate such transcriptional factors, we thus evaluated the potency of α,β-unsaturated lactones synthesized using fluorous phase organic synthesis. Compounds were first screened for their cytotoxicity in order to select lactones for PPARγ and Nrf2 activation evaluation. Among them, two α-methylene-γ-lactones were identified as potent dual activators of PPARγ and Nrf2 in macrophages.
Keywords:
Michael acceptor; Nrf2; PPARγ; Protolichesterinic acid; α-Methylene-γ-lactones.
Copyright © 2014 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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4-Butyrolactone / analogs & derivatives*
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4-Butyrolactone / chemical synthesis
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4-Butyrolactone / chemistry
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4-Butyrolactone / pharmacology
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Animals
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Antineoplastic Agents / chemical synthesis
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Antineoplastic Agents / chemistry
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Antineoplastic Agents / pharmacology*
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Cell Line, Tumor
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Cell Proliferation / drug effects
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Dose-Response Relationship, Drug
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Drug Screening Assays, Antitumor
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Humans
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Lactones / chemical synthesis
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Lactones / chemistry
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Lactones / pharmacology*
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Macrophages / drug effects*
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Mice
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Molecular Structure
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NF-E2-Related Factor 2 / metabolism*
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PPAR gamma / metabolism*
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Structure-Activity Relationship
Substances
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Antineoplastic Agents
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Lactones
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NF-E2-Related Factor 2
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PPAR gamma
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protolichesterinic acid
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4-Butyrolactone