ПРОГНОЗИРОВАНИЕ БИОЛОГИЧЕСКОЙ АКТИВНОСТИ 2-(ФЕНИЛМЕТИЛ)-1H-БЕНЗИМИДАЗОЛА
A comprehensive in silico study of 2-(phenylmethyl)-1H-benzimidazole (FAB), an organic compound with potential biological activity, was conducted in this work. Using the PASS Online web platform, the pharmacological properties and predicted mechanisms of action of the compound were assessed. The GUSAR program was employed to evaluate acute and environmental toxicity, including LD50 prediction models for rats and mice, as well as ecological parameters such as LD50 for Daphnia magna, Fathead minnow, Tetrahymena pyriformis, and the logarithmic bioconcentration factor (BCF). The results of PASS Online indicated that FAB may exhibit antibacterial, anti-inflammatory, and antioxidant activities, as well as inhibitory effects on various enzymes. These findings suggest the advisability of further investigation of FAB as a pharmacologically active compound, alongside parallel evaluation of its environmental safety.
1. Alka, A. et al. Benzimidazole: A bioactive scaffold for drug development. Eur. J. Med. Chem. 2020, 207, 112739.
2. Zarrin, G. et al. Design and synthesis of novel benzimidazole derivatives with antimicrobial activity. Bioorg. Med. Chem. Lett. 2019, 29(17), 2547-2551.
3. Park, S. J. et al. Benzimidazole-based inhibitors targeting cancer pathways. Med. Chem. Res. 2021, 30, 541–550.
4. Holla, B. S. et al. Synthesis and antimicrobial activity of some benzimidazole derivatives. Eur. J. Med. Chem. 2005, 40, 1173–1178.
5. Vora, J. et al. In silico screening of benzimidazole derivatives for anticancer activity. J. Mol. Graph. Model. 2022, 115, 108215.
6. Pratibha, K. et al. Benzimidazole as potent antiviral scaffold. Curr. Top. Med. Chem. 2020, 20(3), 208–223.
7. Shingalapur, R. V. et al. Anti-inflammatory activity of benzimidazole derivatives. Bioorg. Med. Chem. Lett. 2009, 19(9), 2633–2636.
8. Pandey, A. et al. Antiparasitic activity of benzimidazole hybrids. Bioorg. Chem. 2021, 107, 104638.
9. Raj, R. et al. Molecular docking studies of benzimidazole-based kinase inhibitors. Comput. Biol. Chem. 2020, 89, 107388.
10. Aroua L. M., et al. Benzimidazole (s): synthons, bioactive lead structures, total synthesis, and the profiling of major bioactive categories // RSC advances. (2025). 15(10), 7571-7608.
11. Al-Soud, Y. A. et al. Synthesis and antimicrobial evaluation of new benzimidazole derivatives. J. Enzyme Inhib. Med. Chem. 2017, 32(1), 728-737.
12. Lagunin, A. A. et al. PASS: prediction of activity spectra for biologically active substances. Bioinformatics 2000, 16(8), 747–748.
13. Molinspiration Cheminformatics. [https://www.molinspiration.com]
14. Trott, O., Olson, A. J. AutoDock Vina: improving the speed and accuracy of docking. J. Comput. Chem. 2010, 31(2), 455–461.
15. Santos-Martins, D. et al. DockThor-VS: a web server for virtual screening. J. Chem. Inf. Model. 2020, 60(11), 5608–5612
Copyright (c) 2025 «ACTA NUUz»

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.






.jpg)

1.png)





