Inhibitors of c-jun-N-Terminal Kinase (JNK)
Authors: LoGrasso, Philip; Kamenecka, Theodore
Source: Mini Reviews in Medicinal Chemistry, Volume 8, Number 8, July 2008 , pp. 755-766(12)
Publisher: Bentham Science Publishers
Abstract:
Inhibitors of c-jun-N-Terminal Kinase (JNK) have many potential therapeutic indications ranging from neurodegenerative disease, to metabolic disorders, inflammation, cardiovascular disease, and cancer. This overview will highlight biological inhibitors such as JNK-interacting protein (JIP) as well as small molecule inhibitors from various structural classes including, aminopyrimidines and indazoles.Keywords: c-jun-N-Terminal Kinase (JNK); mitogen activated protein (MAP); benzothiazole pyrimidines; benzothien-2-yl amides; indazoles; aminopyrimidines; aminopyridines; quinolines
Document Type: Research article
DOI: http://dx.doi.org/10.2174/138955708784912120
Publication date: 2008-07-01
- The aim of Mini-Reviews in Medicinal Chemistry is to publish short reviews on the important recent developments in medicinal chemistry and allied disciplines.
The scope of Mini-Reviews in Medicinal Chemistry will cover all areas of medicinal chemistry including developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, drug targets, and natural product research and structure-activity relationship studies.
Mini-Reviews in Medicinal Chemistry is an essential journal for every medicinal and pharmaceutical chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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- In this Subject: Chemistry (General) , Pharmacology
- By this author: LoGrasso, Philip ; Kamenecka, Theodore

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