Molecules (Jul 2022)

Synthesis and Biological Activity Screening of Newly Synthesized Trimethoxyphenyl-Based Analogues as Potential Anticancer Agents

  • Tarfah Al-Warhi,
  • Matokah Abualnaja,
  • Ola A. Abu Ali,
  • Fayez Althobaiti,
  • Fahad Alharthi,
  • Fahmy G. Elsaid,
  • Ali A. Shati,
  • Eman Fayad,
  • Doaa Elghareeb,
  • Ali H. Abu Almaaty,
  • Islam Zaki

DOI
https://doi.org/10.3390/molecules27144621
Journal volume & issue
Vol. 27, no. 14
p. 4621

Abstract

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A group of novel trimethoxyphenyl (TMP)-based analogues were synthesized by varying the azalactone ring of 2-(3,4-dimethoxyphenyl)-4-(3,4,5-trimethoxybenzylidene)oxazolone 1 and characterized using NMR spectral data as well as elemental microanalyses. All synthesized compounds were screened for their cytotoxic activity utilizing the hepatocellular carcinoma (HepG2) cell line. Compounds 9, 10 and 11 exhibited good cytotoxic potency with IC50 values ranging from 1.38 to 3.21 μM compared to podophyllotoxin (podo) as a reference compound. In addition, compounds 9, 10 and 11 exhibited potent inhibition of β-tubulin polymerization. DNA flow cytometry analysis of compound 9 shows cell cycle disturbance at the G2/M phase and a significant increase in Annexin-V-positive cells compared with the untreated control. Compound 9 was further studied regarding its apoptotic potential in HepG2 cells; it decreased the level of MMP and Bcl-2 as well as boosted the level of p53 and Bax compared with the control HepG2 cells.

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