Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Green Synthesis and Anticancer Evaluation of Novel Chrysin Hydrazone Derivatives Publisher



Pouramiri B1 ; Seyedhosseini SR1 ; Nematollahi MH2, 3 ; Faramarz S2, 4 ; Seyedi F5 ; Ayati A6
Authors
Show Affiliations
Authors Affiliations
  1. 1. Student Research Committee, Jiroft University of Medical Sciences, Jiroft, Iran
  2. 2. Department of Biochemistry, School of Medicine, Kerman University of Medical Sciences, Kerman, Iran
  3. 3. Physiology Research Center, Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences, Kerman, Iran
  4. 4. Student Research Committee, Kerman University of Medical Sciences, Kerman, Iran
  5. 5. Department of Anatomy, School of Medicine, Jiroft University of Medical Sciences, Jiroft, Iran
  6. 6. Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran

Source: Polycyclic Aromatic Compounds Published:2023


Abstract

Chrysin, a natural flavonoid, has been investigated for its anticancer biological properties. Antifungal and anticancer properties of hydrazone derivatives have been proven. In this study, eight compounds of substituted Chrysin hydrazine derivatives have been designed, synthesized, and screened against cancerous cell lines, including MCF-7 and HepG-2. All products are reported for the first time. Most compounds exhibited significant cytotoxic activity against selected cell lines. The chemical structures of all compounds were confirmed by spectroscopic methods and elemental analyzes. In vitro evaluation of these synthesized compounds showed most of them have potential antiproliferative activity. Compounds 3e and 3f have shown significant anti-proliferative activity against MCF-7 and HepG-2 cell lines, respectively, compared to Chrysin (P < 0.05). The IC50 values of compounds 3e and 3f were 101.44 and 166.19 µM after 48 h, respectively. Moreover, the compounds 3e and 3f induced significant apoptosis more than Chrysin (P < 0.05). The Results of this research might help the design and synthesis of novel drugs toward developing new antitumor agents for cancer treatment. © 2021 Taylor & Francis Group, LLC.