1. Ersan R.H., Kuzu B., Yetkin D., Alagoz M.A., Dogen A., Burmaoglu S. 2-Phenyl substituted Benzimidazole derivatives: Design, synthesis, and evaluation of their antiproliferative and antimicrobial activities. Med. Chem. Res, 2022, 16(31), 1192-1208. DOI:https://doi.org/10.1007/s00044-022-02900-3. EDN: https://elibrary.ru/HATCZA

2. Pham E.C., Le Thi T.V., Ly Hong H.H., Vo Thi B.N., Vong L.B., Vu T.T., Vo D.D., Tran Nguyen N.V., Bao Le K.N., Truong T.N. N,2,6-Trisubstituted 1H-benzimidazole derivatives as a new scaffold of antimicrobial and anticancer agents: design, synthesis, in vitro evaluation, and in silico studies. RSC Adv., 2022, 13(1), 399 420. DOIhttps://doi.org/10.1039/d2ra06667j. EDN: https://elibrary.ru/NXICQY

3. Bansal S., Gaur R., Bhardwaj H., Kumar N., Sharma G.K., Mishra S.S. Synthesis, biological evaluation, and molecular docking studies of benzimidazole derivatives substitutes as new antimicrobial agents. JDDMC, 2024, 10(2), 54-66. DOIhttps://doi.org/10.11648/j.jddmc.20241002.12. EDN: https://elibrary.ru/WSFDGG

4. Ahmed A.E.R., Hassan Y.A.-E. Benzimidazole derivatives as potential chemotherapeutic agents. Curr. Drug Ther. 2013, 8(1), 1-14. DOI:https://doi.org/10.2174/1574885511308010001 EDN: https://elibrary.ru/YDQRWH

5. Akhtar W., Khan M.F., Verma G., Shaquiquzzaman M., Rizvi M.A., Mehdi S.H., Akhter M., Alam M.M. Therapeutic evolution of benzimidazole derivatives in the last quinquennial period. Eur. J. Med. Chem., 2017, 126, 705-753. DOI:https://doi.org/10.1016/j.ejmech.2016.12.010 EDN: https://elibrary.ru/XZMBET

6. Begunov R.S., Egorov D.O., Chetvertakova A.V., Savina L.I., Zubishina A.A. Antibakterial'naya aktivnost' galogen- i nitroproizvodnyh benzimidazola v otnoshenii Bacillus subtilis. Antibiotiki i himioter., 2023, 68(3-4), 19-24. DOI:https://doi.org/10.37489/0235-2990-2023-68-3-4-19-24. EDN: https://elibrary.ru/BMKHKH

7. Begunov R.S., Zayceva Yu.V., Sokolov A.A., Egorov D.O., Filimonov S.I. Sintez i antibakterial'naya aktivnost' 1,2,3,4-tetragidro- i pirido[1,2-a]benzimidazolov. Him. farm. zhurnal, 2022, 56(1), 25-31. DOI:https://doi.org/10.30906/0023-1134-2022-56-1-25-31 EDN: https://elibrary.ru/FCHEAJ

8. Nandwana N.K., Singh R.P., Patel O.P.S., Dhiman S., Saini H.K., Jha P.N., Kumar A. Design and Synthesis of Imidazo/Benzimidazo[1,2-c]quinazoline Derivatives and Evaluation of Their Antimicrobial Activity. ACS Omega, 2018, 3(11), 16338-16346. DOI:https://doi.org/10.1021/acsomega.8b01592.

9. Mohamed B.G., Abdel-Alim A.M., Hussein M.A. Synthesis of 1-acyl-2-alkylthio-1,2,4-triazolobenzimidazoles with antifungal, anti-inflammatory and analgesic effects. Acta Pharm., 2006, 56(1), 31-48.

10. Huo X., Hou D., Wang H., He B., Fang J., Meng Y., Liu L., Wei Z., Wang Z., Liu F.W. Design, synthesis, in vitro and in vivo anti-respiratory syncytial virus (RSV) activity of novel oxizine fused benzimidazole derivatives. Eur. J. Med. Chem., 2021, 224, Article 113684. DOI:https://doi.org/10.1016/j.ejmech.2021.113684. EDN: https://elibrary.ru/OZOQKN

11. Wang H., Meng Y., Yang J., Huang H., Zhao Y., Zhu C., Wang C., Liu F.W. Design, synthesis and antitumour activity of novel 5(6)-amino-benzimidazolequinones containing a fused morpholine. Eur. J. Med. Chem., 2022, 238, Article 114420. DOI:https://doi.org/10.1016/j.ejmech.2022.114420. EDN: https://elibrary.ru/NLXEXR

12. Aleksandrova Y., Savina L., Shagina I., Lyubina A., Zubishina A., Makarova S., Bagylly A., Khokhlov A., Begunov R., Neganova M. New Dihalogenated Derivatives of Condensed Benzimidazole Diones Promotes Cancer Cell Death Through Regulating STAT3/HK2 Axis/Pathway. Molecules, 2025, 30(21), 4150. DOI:https://doi.org/10.3390/molecules30214150 EDN: https://elibrary.ru/EFUFIH

13. Begunov R.S., Aleksandrova Yu.R., Shagina I.A., Kucherenko M.V., Pelevin P.S., Hohlov A.L., Neganova M.E. Citotoksichnost' novogo kondensirovannogo proizvodnogo benzimidazoldiona v otnoshenii liniy kletok opuholevogo i normal'nogo proishozhdeniya. Acta Biomedica Scientifica, 2025, 10(6), 12-19. DOI:https://doi.org/10.29413/ABS.2025-10.6.2 EDN: https://elibrary.ru/OZXASW

14. Sondhi S.M., Rajvanshi S., Johar M., Bharti N., Azam A., Singh A.K. Anti-inflammatory, analgesic and antiamoebic activity evaluation of pyrimido[1,6-a]benzimidazole derivatives synthesized by the reaction of ketoisothiocyanates with mono and diamines. Eur. J. Med. Chem., 2002, 37(10), 835-843. DOI:https://doi.org/10.1016/s0223-5234(02)01403-4.

15. Sondhi S. M., Rani R., Singh J., Roy P., Agrawal S. K., Saxena A. K. Solvent free synthesis, anti-inflammatory and anticancer activity evaluation of tricyclic and tetracyclic benzimidazole derivatives. Bioorg. Med. Chem. Lett., 2010, 20(7), 2306-2310. DOI:https://doi.org/10.1016/j.bmcl.2010.01.147. EDN: https://elibrary.ru/NAKOUH

16. Begunov R.S., Savina L.I., Astaf'eva D.A. Vnutrimolekulyarnoe aminirovanie orto-nitro-tret-anilinov kak odin iz putey sinteza kondensirovannyh proizvodnyh benzimidazola s uzlovym atomom azota. Ot himii k tehnologii shag za shagom, 2025, 6(1), 22-33. DOI:https://doi.org/10.52957/2782-1900-2025-6-1-22-33 EDN: https://elibrary.ru/YUCJVL

17. Kucherenko M.V., Savina L.I., Begunov R.S., Zubishina A.A., Gracheva E.L. Regioselektivnost' reakcii SEAr 8-hlor-3,4-digdro-1H-[1,4]oksazino[4,3-a]benzimidazola. Ot himii k tehnologii shag za shagom, 2025, 6(4), 60-71. DOI:https://doi.org/10.52957/2782-1900-2025-6-4-60-71 EDN: https://elibrary.ru/OTRRTW

18. Balani S.K., Miwa G.T., Gan L.S., Wu J.T., Lee F.W. Strategy of utilizing in vitro and in vivo ADME tools for lead optimization and drug candidate selection. Curr Top Med Chem. 2005, 5(11), 1033-1038. DOIhttps://doi.org/10.2174/156802605774297038

19. Daina A., Michielin O., Zoete V. SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules. Sci. Rep., 2017, 7, Article 42717. DOI:https://doi.org/10.1038/srep42717 EDN: https://elibrary.ru/YZSVSD

20. Manikandan P., Nagini S. Cytochrome P450 Structure, Function and Clinical Significance: A Review. Curr Drug Targets. 2018, 19(1), 38-54. DOIhttps://doi.org/10.2174/1389450118666170125144557

21. Banerjee P., Kemmler E., Dunkel M., Preissner R. ProTox 3.0: a webserver for the prediction of toxicity of chemicals. Nucleic Acids Res., 2024, 52(W1), W513-W520. DOI:https://doi.org/10.1093/nar/gkae303 EDN: https://elibrary.ru/GXCWJQ