Design, synthesis, anticancer, and antibacterial evaluation of some quinazolinone‐based derivatives as DHFR inhibitors

• Published in: Drug development research 2023-08, Vol.84 (5), p.888-906
• Main Authors: Osman, Eman O., Emam, Soha H., Sonousi, Amr, Kandil, Mai M., Abdou, Amr M., Hassan, Rasha A.
• Format: Article
• Language: English
• Subjects: Antibacterial activity; Anticancer properties; antitumor activity; Apoptosis; Bacteria; Caspase; Cell cycle; cell cycle analysis; Cytotoxicity; DHFR inhibition; Dihydrofolate reductase; Doxorubicin; E coli; Gram-negative bacteria; Inhibitors; Leukemia; Methotrexate; molecular docking; Molecular modelling; Quinazolinone; Quinazolinones; quinazolin‐4(3H)‐one; Reductases; S phase; Trimethoprim
• ISSN: 0272-4391; 1098-2299
• DOI: 10.1002/ddr.22060

Two series of quinazolinone derivatives were designed and synthesized as dihydrofolate reductase (DHFR) inhibitors. All compounds were evaluated for their antibacterial and antitumor activities. Antibacterial activity was evaluated against three strains of Gram‐positive and Gram‐negative bacteria. Compound 3d exhibited the highest inhibitory activity against Staphylococcus aureus DHFR (SaDHFR) with IC50 of 0.769 ± 0.04 μM compared to 0.255 ± 0.014 μM for trimethoprim. Compound 3e was also more potent than trimethoprim against Escherichia coli DHFR (EcDHFR) with IC50 of 0.158 ± 0.01 μM and 0.226 ± 0.014 μM, respectively. Compound 3e exhibited a promising antiproliferative effect against most of the tested cancer cells. It also showed potent activity against leukemia (CCRF‐CEM, and RPMI‐8226); lung NCI‐H522, and CNS U251 with GI% of 65.2, 63.22, 73.28, and 97.22, respectively. The cytotoxic activity of compound 3e was almost half the activity of doxorubicin against CCRF‐CEM cell line with IC50 of 1.569 ± 0.06 μM and 0.822 ± 0.03 µM, respectively. In addition, compound 3e inhibited human DHFR with IC50 value of 0.527 ± 0.028 µM in comparison to methotrexate (IC50 = 0.118 ± 0.006 µM). Compound 3e caused an arrest of the cell cycle mainly at the S phase and caused a rise in the overall apoptotic percentage from 2.03% to 48.51%. (23.89‐fold). Treatment of CCRF‐CEM cells with compound 3e produced a significant increase in the active caspase‐3 level by 6.25‐fold compared to untreated cells. Molecular modeling studies were performed to evaluate the binding pattern of the most active compounds in the bacterial and human DHFR.