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Updated: Feb 16, 2026

Anticancer Efficacy of Photodynamic Therapy with Lung Cancer-Targeted Nanoparticles
Published on: December 1, 2016
Podophyllotoxin derivatives as an excellent anticancer aspirant for future chemotherapy: A key current imminent needs
Xu Zhang1, K P Rakesh1, C S Shantharam2
1Department of Pharmaceutical Engineering, School of Chemistry, Chemical Engineering and Life Science, Wuhan University of Technology, 205 Luoshi Road, Wuhan 430073, PR China.
Abstract:
Cancer is one of the leading groups of threatened caused by abnormal state cell growth and second leading diseases involved in the major global death. To treat this, research looking for promising anticancer drugs from natural resource, or synthesized novel molecules by diverse group of scientists worldwide. Currently, drugs get into clinical practices and showing side effects with target actions which in turn leading to multidrug resistance unknowingly. Podophyllotoxin, a naturally occurring lignan and with hybrids have become one of the most attractive subjects due to their broad spectrum of pharmacological activities. Podophyllotoxin derivatives have been the centre of attention of extensive chemical amendment and pharmacological investigation in modern decades. Mainly, the innovation of the semi-synthetic anticancer drugs etoposide and teniposide has stimulated prolonged research interest in this structural phenotype. The present review focuses mainly onnew anticancer drugs from podophyllotoxin analogs, mechanism of action and their structure-activity relationships (SAR) as potential anticancer candidates for future discovery of suitable drug candidates.
Insights
This review explores novel anticancer drugs derived from podophyllotoxin analogs. It examines their mechanisms of action and structure-activity relationships for future drug development against cancer.
Area of Science:
- Medicinal Chemistry
- Pharmacology
- Oncology
Background:
- Cancer remains a leading global cause of death, necessitating the development of new therapeutic agents.
- Existing cancer treatments can cause side effects and lead to multidrug resistance.
- Podophyllotoxin, a natural lignan, and its derivatives show significant pharmacological potential for cancer therapy.
Purpose of the Study:
- To review novel anticancer drugs based on podophyllotoxin analogs.
- To elucidate the mechanisms of action of these compounds.
- To analyze structure-activity relationships (SAR) for potential drug candidates.
Main Methods:
- Literature review of podophyllotoxin derivatives and their anticancer properties.
- Analysis of published data on mechanisms of action.
- Examination of SAR studies for efficacy and toxicity.
Main Results:
- Podophyllotoxin analogs, including semi-synthetic drugs like etoposide and teniposide, exhibit broad-spectrum anticancer activity.
- Various modifications of the podophyllotoxin scaffold have yielded compounds with improved efficacy and reduced toxicity.
- Understanding SAR is crucial for designing potent and selective anticancer agents.
Conclusions:
- Podophyllotoxin analogs represent a promising class of compounds for developing new anticancer drugs.
- Further research into their mechanisms and SAR can lead to effective cancer therapies.
- These natural product derivatives offer a valuable platform for future drug discovery in oncology.
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