AI Article Synopsis

  • The 5-(3'-Indolyl)oxazole moiety is a significant heterocyclic structure found in many natural products and has been linked to various biological activities, making it a focus for synthetic chemists.
  • This review covers the biological effects and synthetic methods of this scaffold from 1963 to 2024, emphasizing its potential as a lead compound in developing drugs for cancer, antimicrobial, antiviral, and other therapeutic uses.
  • It also discusses the mechanisms through which these compounds act in animal studies and suggests future directions for research on the 5-(3'-indolyl)oxazole scaffold.

Article Abstract

5-(3'-Indolyl)oxazole moiety is a privileged heterocyclic scaffold, embedded in many biologically interesting natural products and potential therapeutic agents. Compounds containing this scaffold, whether from natural sources or synthesized, have demonstrated a wide array of biological activities. This has piqued the interest of synthetic chemists, leading to a large number of reported synthetic approaches to 5-(3'-indolyl)oxazole scaffold in recent years. In this review, we comprehensively overviewed the different biological activities and chemical synthetic methods for the 5-(3'-indolyl)oxazole scaffold reported in the literatures from 1963 to 2024. The focus of this study is to highlight the significance of 5-(3'-indolyl)oxazole derivatives as the lead compounds for the lead discovery of anticancer, pesticidal, antimicrobial, antiviral, antioxidant and anti-inflammatory agents, to summarize the synthetic methods for the 5-(3'-indolyl)oxazole scaffold. In addition, the reported mechanism of action of 5-(3'-indolyl)oxazoles and advanced molecules studied in animal models are also reviewed. Furthermore, this review offers perspectives on how 5-(3'-indolyl)oxazole scaffold as a privileged structure might be exploited in the future.

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Source
http://dx.doi.org/10.1002/med.22078DOI Listing

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