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Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Updates on Receptors Targeted by Heterocyclic Scaffolds: New Horizon in Anticancer Drug Development
1Centre for Pharmaceutical Chemistry & Pharmaceutical Analysis, Amity Institute of Pharmacy, Amity University Uttar Pradesh, Noida-201313, Uttar Pradesh, India.
Abstract:
Anticancer is a high priority research area for scientists as cancer is one of the leading causes of death globally. It is pertinent to mention here that conventional anticancer drugs such as methotrexate, vincristine, cyclophosphamide, etoposide, doxorubicin, cisplatin, etc. are not much efficient for the treatment of different types of cancer; also these suffer from serious side effects leading to therapy failure. A large variety of cancerrelated receptors such as carbonic anhydrase, tyrosine kinase, topoisomerase, protein kinase, histone deacetylase, etc. have been identified which can be targeted by anticancer drugs. Heterocycles like oxadiazole, thiazole, thiadiazole, indole, pyridine, pyrimidine, benzimidazole, etc. play a pivotal role in modern medicinal chemistry because they have a broad spectrum of pharmacological activities including prominent anticancer activity. Therefore, it was considered significant to explore heterocyclic compounds reported in recent most literature which can bind effectively with the cancer-related receptors. This will not only provide a targeted approach to deal with cancer but also the safety profile of the drugs can be further improved. The information provided in this manuscript may be found useful for the design and development of anticancer drugs.
Insights
Conventional anticancer drugs show limited efficacy and severe side effects. This study explores novel heterocyclic compounds as targeted anticancer agents, aiming for improved efficacy and safety in cancer treatment.
Area of Science:
- Oncology
- Medicinal Chemistry
- Drug Discovery
Background:
- Cancer remains a leading global cause of death, with conventional treatments often proving inefficient and causing significant side effects.
- Existing anticancer drugs like methotrexate and cisplatin have limitations in efficacy and tolerability, necessitating the development of improved therapeutic strategies.
- Numerous cancer-related receptors (e.g., tyrosine kinase, histone deacetylase) have been identified as potential therapeutic targets for novel anticancer agents.
Purpose of the Study:
- To review and identify heterocyclic compounds with potential anticancer activity from recent scientific literature.
- To explore the ability of these heterocyclic compounds to effectively bind with cancer-related receptors.
- To provide insights for the design and development of safer and more effective targeted anticancer drugs.
Main Methods:
- Literature review of recent scientific publications focusing on heterocyclic compounds and their anticancer properties.
- Analysis of identified heterocyclic compounds for their potential to interact with specific cancer-related molecular targets.
- Evaluation of pharmacological activities and safety profiles of promising heterocyclic drug candidates.
Main Results:
- Heterocyclic compounds, including oxadiazole, thiazole, and benzimidazole derivatives, exhibit significant anticancer potential.
- These heterocycles demonstrate broad-spectrum pharmacological activities, including potent anticancer effects.
- The review highlights specific heterocyclic structures capable of effective binding to key cancer-related receptors.
Conclusions:
- Heterocyclic compounds represent a promising class of molecules for developing novel anticancer therapeutics.
- Targeting cancer-related receptors with specifically designed heterocyclic compounds can enhance treatment efficacy and improve safety profiles.
- This research provides a foundation for future drug design and development in the field of oncology, aiming for more effective cancer therapies.
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