| Oxidative metabolic stability in human liver microsomes assessed as compound remaining at 2 uM after 30 mins - BioAssay Summary In this Letter, we describe the discovery of selective JNK2 and JNK3 inhibitors, such as 10, that routinely exhibit >10-fold selectivity over JNK1 and >1000-fold selectivity over related MAPKs, p38## and ERK2. Substitution of the naphthalene ring affords an isoform selective JNK3 inhibitor, 30, with approximately 10-fold selectivity over both JNK1 and JNK2. A naphthalene ring penetrates deep into the selectivity pocket accounting for the differentiation amongst the kinases. Interestingly, the gatekeeper Met146 sulfide interacts with the naphthalene ring in a sulfur-# ..more |
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Tested Compounds: Description: Title: Highly selective c-Jun N-terminal kinase (JNK) 2 and 3 inhibitors with in vitro CNS-like pharmacokinetic properties prevent neurodegeneration. Abstract: In this Letter, we describe the discovery of selective JNK2 and JNK3 inhibitors, such as 10, that routinely exhibit >10-fold selectivity over JNK1 and >1000-fold selectivity over related MAPKs, p38## and ERK2. Substitution of the naphthalene ring affords an isoform selective JNK3 inhibitor, 30, with approximately 10-fold selectivity over both JNK1 and JNK2. A naphthalene ring penetrates deep into the selectivity pocket accounting for the differentiation amongst the kinases. Interestingly, the gatekeeper Met146 sulfide interacts with the naphthalene ring in a sulfur-# (PMID: 21112785) Comment Putative Target: ChEMBL Target ID: 102164 Target Type: SUBCELLULAR Pref Name: Liver microsomes Organism: Homo sapiens Tax ID: 9606 Confidence: Target assigned is subcellular fraction Relationship Type: Subcellular target assigned Categorized Comment ChEMBL Assay Type: ADMET ChEMBL Assay Data Source: Scientific Literature Result Definitions
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