In vitro cytotoxicity screening of some 3-substituted-4-oxo-imidazolidin-2-(1H)-thione derivatives as anticancer drug.
Ibrahim Mohey El-DeenElsayed H EltamanyNourhan M AliPublished in: Future medicinal chemistry (2024)
Aim: This study aimed to investigate the in vitro antitumor activity of new series of 2-thiohydanotin derivatives ( 7 and 9 ) against two cancer cell lines. Materials & methods: A new series of 2-thioxoimidazolidine derivatives ( 3-9 ) were synthesized and investigated for its structure through spectral analysis and also tested against (HepG-2) and (HCT-116) cell line. Results: Among the synthesized compounds, compound 7 halted liver cancer cells at the G0/G1 phase and triggered apoptosis of liver cancer. Contrarily, compound 9 caused colon cancer cells to be arrested at the S phase and trigger apoptosis. Also, they had a good inhibitory effect on (Nrf2). Conclusion: Both compounds had attractive lead molecules for the creation of colon and liver cancer medications.
Keyphrases
- cell cycle arrest
- oxidative stress
- endoplasmic reticulum stress
- cell death
- papillary thyroid
- pi k akt
- optical coherence tomography
- molecular docking
- structure activity relationship
- squamous cell
- atomic force microscopy
- magnetic resonance
- mass spectrometry
- lymph node metastasis
- adverse drug
- drug induced
- high speed
- dual energy