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Updated: Aug 16, 2025

Facile Preparation of 4-Substituted Quinazoline Derivatives
Published on: February 15, 2016
Molecular Target Interactions of Quinoline Derivatives as Anticancer Agents: A Review
Vikas Pradhan1, Salahuddin1, Rajnish Kumar1
1Department of Pharmaceutical Chemistry, Noida Institute of Engineering and Technology (Pharmacy Institute), Greater Noida.
Abstract:
One of the leading causes of death worldwide is cancer, which poses substantial risks to both society and an individual's life. Cancer therapy is still challenging, despite developments in the field and continued research into cancer prevention. The search for novel anticancer active agents with a broader cytotoxicity range is therefore continuously ongoing. The benzene ring gets fused to a pyridine ring at two carbon atoms close to one another to form the double ring structure of the heterocyclic aromatic nitrogen molecule known as quinoline (1-azanaphthalene). Quinoline derivatives contain a wide range of pharmacological activities, including antitubercular, antifungal, antibacterial, and antimalarial properties. Quinoline derivatives have also been shown to have anticancer properties. There are many quinoline derivatives widely available as anticancer drugs that act via a variety of mechanisms on various molecular targets, such as inhibition of topoisomerase, inhibition of tyrosine kinases, inhibition of heat shock protein 90 (Hsp90), inhibition of histone deacetylases (HDACs), inhibition of cell cycle arrest and apoptosis, and inhibition of tubulin polymerization.
Insights
Quinoline derivatives show promise as anticancer agents. Their diverse mechanisms target key cancer pathways, offering potential for new cancer therapies.
Area of Science:
- Medicinal Chemistry
- Pharmacology
- Oncology
Background:
- Cancer remains a leading global cause of death, necessitating novel therapeutic strategies.
- Despite advancements, cancer treatment presents ongoing challenges, driving the search for new anticancer agents.
- Quinoline, a heterocyclic aromatic molecule, and its derivatives are explored for diverse pharmacological activities.
Purpose of the Study:
- To review the anticancer properties of quinoline derivatives.
- To highlight the various molecular targets and mechanisms of action of quinoline-based anticancer drugs.
Main Methods:
- Literature review of quinoline derivatives in cancer research.
- Analysis of documented pharmacological activities and mechanisms of action.
Main Results:
- Quinoline derivatives exhibit a broad spectrum of anticancer activities.
- These compounds act through diverse mechanisms, including inhibition of topoisomerase, tyrosine kinases, Hsp90, and HDACs.
- Other mechanisms include induction of cell cycle arrest, apoptosis, and inhibition of tubulin polymerization.
Conclusions:
- Quinoline derivatives represent a significant class of compounds with demonstrated anticancer potential.
- Their versatile mechanisms of action make them valuable candidates for developing novel cancer therapies.
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