| Literature DB >> 32038782 |
Abstract
Targeting protein kinases has been active area in drug discovery. The c-Jun N-terminal kinases (JNKs) have also been target for development of novel therapy in various diseases, since the roles of JNK signaling in pathological conditions were revealed in studies using jnk-deficient mice. Small molecule inhibitors and peptide inhibitors are identified for therapeutic intervention of JNK signaling pathway. SP-600125, an anthrapyrazole small molecule inhibitor for JNK with high potency and selectivity has been widely used for dissecting JNK signaling pathway. CC-401 is the first JNK inhibitor that went into clinical trial for inflammation and leukemia. Inhibitor for mixed lineage kinase (MLK), CEP-1347 also negatively regulates JNK signaling, and tried for potential use in Parkinson's disease. Cell-permeable peptide inhibitor D-JNKI-1 is being developed for the treatment of hearing loss. The current status of these JNK inhibitors and safety issue is discussed in the minireview. © Korean Society of Toxicology 2008.Entities:
Keywords: AS-602801; CC-401; CEP-1347; D-JNKI-1; Inhibitors; JNK; SP-600125
Year: 2008 PMID: 32038782 PMCID: PMC7006258 DOI: 10.5487/TR.2008.24.2.093
Source DB: PubMed Journal: Toxicol Res ISSN: 1976-8257