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Rhodanine derivatives: An insight into the synthetic and medicinal perspectives as antimicrobial and antiviral agents

期刊

CHEMICAL BIOLOGY & DRUG DESIGN
卷 101, 期 3, 页码 500-549

出版社

WILEY
DOI: 10.1111/cbdd.14163

关键词

2-thioxo-thiazolidin-4-one; antibacterial; antifungal; antimicrobial; antiviral; rhodanine

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Rhodanine and its derivatives are privileged heterocyclic compounds with wide opportunities for structural modification and lead development. They possess diverse biological activities due to their interaction with various protein targets. In recent years, significant progress has been made in developing rhodanine-based antimicrobial and antiviral agents.
Rhodanine or 2-Thioxothiazolidin-4-one is a privileged heterocyclic compound offering a wide opportunity for structural modification, lead development, and modification. It is one of the highly decorated scaffolds in the drug discovery process. Rhodanine derivatives possess a plethora of biological activities due to their ability to interact with a diverse range of protein targets, which provide tremendous opportunities to discover new drugs with different modes of action. The most common strategy for developing novel rhodanine derivatives is the introduction of structurally diverse substituents at the C-5 or N-3, or both positions. Since the inception of Epralestat into the market in 1992, the exploration of rhodanine-3-acetic acids has led to the development of novel leads against different biological targets such as MRSA, HHV-6, Mycobacterial tuberculosis, dengue, etc. In the current pandemic era, some rhodanine compounds have been explored against SARS-CoV-2. In recent years, rhodanine and its derivatives have witnessed significant progress in developing new drug leads as potential antimicrobial and antiviral agents. Different synthetic methodologies and recent developments in the medicinal chemistry of rhodanine derivatives, including biological activities, their mechanistic aspects, structure-activity relationships, and in silico findings, have been compiled in the present review. This article will benefit the scientific community and offer perspectives on how these scaffolds as privileged structures might be exploited in the future for rational design and discovery of rhodanine-based bio-active molecules.

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