The Current Landscape of 1,2,3-triazole Hybrids With Anticancer Therapeutic Potential: Part II

Zhi Xu1, Junna Liu2

  • 1Huanghuai University Industry Innovation & Research and Development Institute, Huanghuai University, Zhumadian, Henan, China.

Archiv Der Pharmazie
|April 2, 2025
PubMed

Insights

1,2,3-Triazole hybrids show promise as novel anticancer agents, effectively targeting multiple cancer pathways and overcoming drug resistance. This review explores their potential in cancer therapy, highlighting recent advancements.

Area of Science:

  • Medicinal Chemistry
  • Oncology
  • Drug Discovery

Background:

  • Chemotherapy is crucial for cancer treatment but faces challenges like multidrug resistance and severe side effects.
  • There is a critical need for novel therapeutic agents that can target multiple biological pathways in cancer.
  • 1,2,3-Triazole hybrids are emerging as promising scaffolds for developing new anticancer drugs.

Purpose of the Study:

  • To provide a comprehensive overview of 1,2,3-triazole hybrids as anticancer agents.
  • To discuss the in vitro and in vivo anticancer potential of these compounds.
  • To analyze structure-activity relationships and mechanisms of action for 1,2,3-triazole hybrids.

Main Methods:

  • Literature review of scientific articles published from 2021 onward.
  • Analysis of studies reporting the synthesis and biological evaluation of 1,2,3-triazole hybrids.
  • Examination of structure-activity relationships and proposed mechanisms of action.

Main Results:

  • 1,2,3-Triazole hybrids demonstrate significant potential for dual/multiple target engagement in cancer cells.
  • These compounds exhibit potent broad-spectrum anticancer activity, including efficacy against drug-resistant cancer types.
  • Recent research highlights diverse mechanisms through which these hybrids exert their cytotoxic effects.

Conclusions:

  • 1,2,3-Triazole hybrids represent a valuable scaffold for developing next-generation cancer therapeutics.
  • Their multitargeting capability offers a promising strategy to overcome current limitations in cancer treatment.
  • Further research into 1,2,3-triazole hybrids is warranted to fully exploit their therapeutic potential.

Related Concept Videos

Cancer Therapies02:49

Cancer Therapies

Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
7.5K
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
7.4K
Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
4.8K
Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
3.2K
Chemotherapy-Induced Nausea and Vomiting: 5-HT3 Receptor Antagonists01:27

Chemotherapy-Induced Nausea and Vomiting: 5-HT3 Receptor Antagonists

5-HT3 receptor antagonists, such as dolasetron, granisetron (Kytril), ondansetron (Zofran), and palonosetron (Axoli), are crucial in managing chemotherapy-induced nausea and vomiting (CINV) and postoperative nausea. These drugs selectively block 5-HT3 receptors in the visceral vagal and spinal afferent nerves, chemoreceptor trigger zone, and the vomiting center. They have a rapid onset of action and can be given as a single dose before chemotherapy. Ondansetron and granisetron, in particular,...
161
Aryldiazonium Salts to Azo Dyes: Diazo Coupling01:11

Aryldiazonium Salts to Azo Dyes: Diazo Coupling

The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the...
2.9K