Imidazoles as potential anticancer agents.

Medchemcomm

Pharmaceutical and Medicinal Chemistry Department , Pharmaceutical and Drug Industries Research Division , National Research Centre, Dokki , Giza 12622 , Egypt.

Published: September 2017

AI Article Synopsis

  • Cancer remains a significant challenge in modern medicine, with existing treatments often facing issues of toxicity and low effectiveness.
  • Imidazole compounds show promise as potential anticancer agents, with scientists exploring their chemical and biological properties for safer therapeutic options.
  • The article reviews various imidazole classes, their mechanisms, therapeutic benefits compared to established drugs, and outlines the current challenges and future directions in developing these compounds for cancer treatment.

Article Abstract

Cancer is a black spot on the face of humanity in this era of science and technology. Presently, several classes of anticancer drugs are available in the market, but issues such as toxicity, low efficacy and solubility have decreased the overall therapeutic indices. Thus, the search for new promising anticancer agents continues, and the battle against cancer is far from over. Imidazole is an aromatic diazole and alkaloid with anticancer properties. There is considerable interest among scientists in developing imidazoles as safe alternatives to anticancer chemotherapy. The present article describes the structural, chemical, and biological features of imidazoles. Several classes of imidazoles as anticancer agents based on their mode of action have been critically discussed. A careful observation has been made into pharmacologically active imidazoles with better or equal therapeutic effects compared to well-known imidazole-based anticancer drugs, which are available on the market. A brief discussion of the toxicities of imidazoles has been made. Finally, the current challenges and future perspectives of imidazole based anticancer drug development are conferred.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6084102PMC
http://dx.doi.org/10.1039/c7md00067gDOI Listing

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