Flavonols Derived Platinum Group Metal Complexes as Potential Chemotherapeutic Agents

Authors

  • Khushboo Devi Department of Chemistry, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala, India Author
  • Nivedita Agnihotri Department of Chemistry, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala, India Author
  • Vikas Kumar Department of Microbiology, IMS, Kenzhegali Sagadiev University of International Business, Almaty, Kazakhstan Author
  • Tanu Arora Department of Chemistry, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala, India Author

DOI:

https://doi.org/10.70130/

Abstract

Platinum group metal (PGM) complexes have attracted a lot of interest in medicinal chemistry, especially in the treatment of cancer because of their strong cytotoxic qualities. Platinum-based complexes, such as cisplatin, carboplatin, and oxaliplatin, are essential chemotherapeutic medicines that have transformed the treatment of cancer. In the present work, the two chromogenic reagents derived from flavonol family viz. 3-hydroxy-2-(4-methoxyphenyl)-4H-chromen-4-one (HMPC) and 3-hydroxy-2-tolyl-4H-chromen-4-one complex (HToC) have been selected to prepare platinum and iridium complexes. The anti-proliferative potential of the three complexes related with PGMs, wasinvestigated against HaCat cancer cell line by applying MTT reduction assay. HaCaT cancer cell line is keratinocyte cell line derived from adult human skin. A comparison between the examined complexes indicated that the complexes of platinum metal in its divalent state have proven to be more potent anticancer agents as compared to those of iridium in the metal’s trivalent state. The results finally suggested that PGM complexes with a logical design may help create next-generation anticancer medications that are more effective than the existing ones.

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Published

2025-04-03

How to Cite

Devi, K., Agnihotri, N., Kumar, V., & Arora, T. (2025). Flavonols Derived Platinum Group Metal Complexes as Potential Chemotherapeutic Agents. RSYN Proceedings, 2(1), OP18. https://doi.org/10.70130/