| Literature DB >> 27627626 |
Na Ye1, Haiying Chen1, Eric A Wold1, Pei-Yong Shi1, Jia Zhou1.
Abstract
Antiviral therapeutics with profiles of high potency, low resistance, panserotype, and low toxicity remain challenging, and obtaining such agents continues to be an active area of therapeutic development. Due to their unique three-dimensional structural features, spirooxindoles have been identified as privileged chemotypes for antiviral drug development. Among them, spiro-pyrazolopyridone oxindoles have been recently reported as potent inhibitors of dengue virus NS4B, leading to the discovery of an orally bioavailable preclinical candidate (R)-44 with excellent in vivo efficacy in a dengue viremia mouse model. This review highlights recent advances in the development of biologically active spirooxindoles for their antiviral potential, primarily focusing on the structure-activity relationships (SARs) and modes of action, as well as future directions to achieve more potent analogues toward a viable antiviral therapy.Entities:
Keywords: DENV; HIV; RSV; antiviral agents; influenza virus; spirooxindoles
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Year: 2016 PMID: 27627626 PMCID: PMC5417367 DOI: 10.1021/acsinfecdis.6b00041
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.084