| Literature DB >> 30122040 |
Benjamin G Richardson1, Atul D Jain1, Haranatha R Potteti, Phillip R Lazzara1, Brian P David1, Chandra R Tamatam, Ewelina Choma1, Kornelia Skowron1, Katherine Dye, Zamia Siddiqui1, Yue-Ting Wang, Aleksej Krunic1, Sekhar P Reddy, Terry W Moore1.
Abstract
Activators of nuclear factor-erythroid 2-related factor 2 (NRF2) could lead to promising therapeutics for prevention and treatment of oxidative stress and inflammatory disorders. Ubiquitination and subsequent degradation of the transcription factor NRF2 is mediated by Kelch-like ECH-associated protein-1 (KEAP1). Inhibition of the KEAP1/NRF2 interaction with small molecules leads to NRF2 activation. Previously, we and others described naphthalene-based NRF2 activators, but the 1,4-diaminonaphthalene scaffold may not represent a drug-like scaffold. Paying particular attention to aqueous solubility, metabolic stability, potency, and mutagenicity, we modified a previously known, naphthalene-based nonelectrophilic NRF2 activator to give a series of non-naphthalene and heterocyclic scaffolds. We found that, compared to previously reported naphthalene-based compounds, a 1,4-isoquinoline scaffold provides a better mutagenic profile without sacrificing potency, stability, or solubility.Entities:
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Year: 2018 PMID: 30122040 PMCID: PMC6190829 DOI: 10.1021/acs.jmedchem.8b01133
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446