Design and discovery of new antiproliferative 1,2,4-triazin-3(2H)-ones as tubulin polymerization inhibitors targeting colchicine binding site

• Published in: Bioorganic chemistry Vol. 112; pp. 104965 - 104982
• Main Authors: Eissa, Ibrahim H., Dahab, Mohammed A., Ibrahim, Mohamed K., Alsaif, Nawaf A., Alanazi, A.Z., Eissa, Sally I., Mehany, Ahmed B.M., Beauchemin, André M.
• Format: Journal Article
• Language: English
• Published: SAN DIEGO Elsevier Inc 01.07.2021; Elsevier
• Subjects: 1,2,4-Triazin-3(2H)-ones; Anti-cancer; Biochemistry & Molecular Biology; Chemistry; Chemistry, Organic; Colchicine analogues; Docking; Life Sciences & Biomedicine; Physical Sciences; Science & Technology; Tubulin polymerization; Colchicine analogues; Docking; Anti-cancer; 1,2,4-Triazin-3(2H)-ones; Tubulin polymerization; RAPID COLORIMETRIC ASSAY; APOPTOSIS; COMBRETASTATIN A-4 ANALOGS; POTENT; N-ISOCYANATES; ANTICANCER EVALUATION; BIOLOGICAL EVALUATION; PHARMACOPHORE; B-RING; DERIVATIVES
• ISSN: 0045-2068; 1090-2120
• DOI: 10.1016/j.bioorg.2021.104965

[Display omitted] •Thirty-five novel triazine-based compounds were designed and synthesized as colchicine binding site inhibitors.•Cytotoxicity was determined against MCF-7, HepG-2, and HCT-116 cell lines.•Tubulin polymerization inhibitory activities and apoptotic potential were evaluated.•In Silico studies and an evaluation of drug-likeness properties were carried out. Thirty-five new colchicine binding site inhibitors have been designed and synthesized based on the 1,2,4-triazin-3(2H)-one nucleus. Such molecules were synthesized through a cascade reaction between readily accessible α-amino ketones and phenyl carbazate as a masked N-isocyanate precursor. The synthesized derivatives are cisoid restricted combretastatin A4 analogues containing 1,2,4-triazin-3(2H)-one in place of the olefinic bond, and they have the same essential pharmacophoric features of colchicine binding site inhibitors. The synthesized compounds were evaluated in vitro for their antiproliferative activities against a panel of three human cancer cell lines (MCF-7, HepG-2, and HCT-116), using colchicine as a positive control. Among them, two compounds 5i and 6i demonstrated a significant antiproliferative effect against all cell lines with IC50 ranging from 8.2 − 18.2 µM. Further investigation was carried out for the most active cytotoxic agents as tubulin polymerization inhibitors. Compounds 5i and 6i effectively inhibited microtubule assembly with IC50 values ranging from 3.9 to 7.8 µM. Tubulin polymerization assay results were found to be comparable with the cytotoxicity results. The cell cycle analysis revealed significant G2/M cell cycle arrest of the analogue 5i in HepG-2 cells. The most active compounds 4i, 4j, 5 g, 5i and 6i did not induce significant cell death in normal human lung cells Wl-38, suggesting their selectivity against cancer cells. Also, These compounds upregulated the level of active caspase-3 and boosted the levels of the pro-apoptotic protein Bax by five to seven folds in comparison to the control. Moreover, apoptosis analyses were conducted for compound 5i to evaluate its apoptotic potential. Finally, in silico studies were conducted to reveal the probable interaction with the colchicine binding site. ADME prediction study of the designed compounds showed that they are not only with promising tubulin polymerization inhibitory activity but also with favorable pharmacokinetic and drug-likeness properties.