4.5 Review

Therapeutic modulators of peroxisome proliferator-activated receptors (PPAR): a patent review (2008-present)

期刊

EXPERT OPINION ON THERAPEUTIC PATENTS
卷 22, 期 7, 页码 803-841

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1517/13543776.2012.699042

关键词

cancer; CS-7017; dyslipidemia; fibrates; GW-501516; GW-590735; hyperglycemia; inflammatory diseases; nuclear receptor modulators; nuclear receptors; PAM-1616; PAR-1622; PAR-5359; skin disorders; thiazolidindiones

资金

  1. LOEWE Schwerpunkt onkogene Signaltransduktion Frankfurt (OSF)

向作者/读者索取更多资源

Introduction: Peroxisome proliferator-activated receptors (PPAR) are ligand-activated transcription factors belonging to the nuclear receptor superfamily. The three known subtypes PPAR alpha, PPAR gamma and PPAR delta 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. Areas covered: 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. Expert opinion: 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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据