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Therapeutic modulators of peroxisome proliferator-activated receptors (PPAR): a patent review (2008–present)
- Source :
- Expert Opinion on Therapeutic Patents. 22:803-841
- Publication Year :
- 2012
- Publisher :
- Informa Healthcare, 2012.
-
Abstract
- Peroxisome proliferator-activated receptors (PPAR) are ligand-activated transcription factors belonging to the nuclear receptor superfamily. The three known subtypes PPARα, PPARγ and PPARδ have different tissue distribution and play a key role as regulators of glucose and lipid homeostasis as well as in cell proliferation, differentiation and inflammatory responses. They have gained a lot of interest as pharmaceutical targets over the last years and with the antidiabetic thiazolidindiones (TZDs) and the hypolipidemic fibrates, two classes of drugs had entered the market. Early observations of severe adverse events changed the situation in the recent past.Herein the authors summarize recent (2008-present) patent applications concerning PPAR ligands claimed for the use in metabolic disorders as well as patents indicating new applications for modulators of the PPAR subtypes.Looking at the recent patent activity regarding novel compounds, there have not been real innovations. As major applications for therapeutic PPAR ligands cancer therapy, skin-related disorders and systemic anti-inflammatory therapies might arise in the mid-term future. The known PPAR targeting drugs might see a repurposing for novel indications.
- Subjects :
- Pharmacology
chemistry.chemical_classification
Peroxisome proliferator
Peroxisome proliferator-activated receptor
General Medicine
Peroxisome
Biology
Ligands
PPAR agonist
PPAR gamma
Patents as Topic
Drug Delivery Systems
Metabolic Diseases
Nuclear receptor
chemistry
Drug Design
Drug Discovery
Animals
Humans
Patent activity
PPAR alpha
PPAR delta
Receptor
Transcription factor
Subjects
Details
- ISSN :
- 17447674 and 13543776
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Expert Opinion on Therapeutic Patents
- Accession number :
- edsair.doi.dedup.....f9d180d3e3d35d0e5f4dd6d7a3697a41
- Full Text :
- https://doi.org/10.1517/13543776.2012.699042