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Identification of an Adamantyl Azaquinolone JNK Selective Inhibitor.

ABSTRACT: 3-[4-((1S,2S,3R,5S,7S)-5-Hydroxyadamantan-2-ylcarbamoyl)benzyl]-4-oxo-1-phenyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester (4) was identified as a novel, druglike and selective quinolone pan JNK inhibitor. In this communication, some of the structure-activity relationship of the azaquinolone analogues leading to 4 is discussed. The focus is on how changes at the amide functionality affected the biochemical potency, cellular potency, metabolic properties, and solubility of this class of JNK inhibitors. Optimization of these properties led to the identification of the adamantyl analogue, 4. 4 achieved proof of mechanism in both rat and mouse TNF-? challenge models.

SUBMITTER: Haynes NE

PROVIDER: S-EPMC4025727 | biostudies-literature | 2012 Sep

REPOSITORIES: biostudies-literature

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Identification of an Adamantyl Azaquinolone JNK Selective Inhibitor.

Haynes Nancy-Ellen NE Scott Nathan R NR Chen Li C LC Janson Cheryl A CA Li Jia Kui JK Lukacs Christine M CM Railkar Aruna A Tozzo Effie E Whittard Toni T Brown Nicholas F NF Cheung Adrian Wai-Hing AW

ACS medicinal chemistry letters 20120808 9

3-[4-((1S,2S,3R,5S,7S)-5-Hydroxyadamantan-2-ylcarbamoyl)benzyl]-4-oxo-1-phenyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester (4) was identified as a novel, druglike and selective quinolone pan JNK inhibitor. In this communication, some of the structure-activity relationship of the azaquinolone analogues leading to 4 is discussed. The focus is on how changes at the amide functionality affected the biochemical potency, cellular potency, metabolic properties, and solubility of this ...[more]

PMID: 24900545

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