- PII
- S30345596S0044460X25030013-1
- DOI
- 10.7868/S3034559625030013
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 95 / Issue number 3-4
- Pages
- 80-91
- Abstract
- A series of 19 derivatives of sulfanilamide was synthesized by the reaction of chloroacetamide, trichloroacetamide and chloropropionamide with N-nucleophiles. It was shown that N-trichloroacetylsulfanilamide in reactions with amines forms products of substitution of the trichloromethyl group, while N-chloroacetylsulfanilamide and N-chloropropionylsulfanilamide react with substitution of the halogen atom. An assessment of the antibacterial properties of the synthesized structures was carried out, showing the absence of activity with respect to E. coli and St. aureus strains. Two aminoalkyl-containing sulfonamides - 2-(4-benzylpiperidin-1-yl)-N-(4-sulfamoylphenyl)acetamide and 2-(4-nitropyrazol-1-yl)-N-(4-sulfamoylphenyl)acetamide - showed inhibitory properties against the human monoamine oxidase enzyme, comparable in IC50 value to the drug zonisamide.
- Keywords
- сульфонамид N-алкилирование моноаминооксидаза ингибитор антимикробная активность
- Date of publication
- 06.02.2026
- Year of publication
- 2026
- Number of purchasers
- 0
- Views
- 4
References
- 1. Scholar E. // xPharm: The Comprehensive Pharmacology Reference. 2007. P. 1. doi 10.1016/b978-008055232-3.62694-7
- 2. Курышева Н.И. // Офтальмология. 2020. Т. 17. № 4. С. 676. doi 10.18008/1816-5095-2020-4-676-682
- 3. Abdel-Aziz A., El-Azab A.S., Abou-Zeid L.A., Eltahir K.E., Abdel-Aziz N.I., Ayyad R.R., Al-Obaid A.M. // Eur. J. Med. Chem. 2016. Vol. 115. P. 121. doi 10.1016/j.ejmech.2016.03.011.
- 4. Bua S., Osman M., Al-Othman Z., Supuran C., Nocentini A. // Bioorg. Chem. 2019. Vol. 86. P. 39. doi 10.1016/j.bioorg.2019.01.030
- 5. El-Azab A., Abdel-Aziz A., Bua S., Nocentini A., El-Gendy M., Mohamed M., Shawer T., Al-Saif N., Supuran C. // Bioorg. Chem. 2019. Vol. 87. P. 78. doi 10.1016/j.bioorg.2019.03.007
- 6. Tanini D., Capperucci A., Scopelliti M., Milaneschi A., Angeli A., Supuran C. // Bioorg. Chem. 2019. Vol. 89. P. 102984. doi 10.1016/j.bioorg.2019.102984
- 7. Krymov S.K., Salnikova D.I., Dezhenkova L.G., Bogdanov F.B., Scherbakov A.M., Shchekotikhin A.E. // Chem. Heterocycl. Compd. 2024. Vol. 60. P. 473. doi 10.1007/s10593-024-03365-5
- 8. Kandile N.G., Elzamly R.A., Mohamed M.I., Zaky H.T., Harding D.R.K., Mohamed H.M. // Int. J. Biol. Macromol. 2023. Vol. 239. P. 1. doi 10.1016/j.ijbiomac.2023.124280
- 9. Ibrahim H., Eldehna W., Abdel-Aziz H., Elaasser M., Abdel-Aziz M. // Eur. J. Med. Chem. 2014. Vol. 85. P. 480. doi 10.1016/j.ejmech.2014.08.016
- 10. Singh P., Purnachander Yadav P., Swain B., Thacker P., Angeli A., Supuran C., Arifuddin M. // Bioorg. Chem. 2021. Vol. 108. Art. 104647. doi 0.1016/j.bioorg.2021.104647
- 11. Krasavin M., Shetnev A., Baykov S., Kalinin S., Nocentini A., Sharoyko V., Poli G., Tuccinardi T., Korsakov M., Tennikova T., Supuran Claudiu T. // Eur. J. Med. Chem. 2019. Vol. 168. P. 301. doi 10.1016/j.ejmech.2019.02.044
- 12. Turkmen H., Durgun M., Yilmaztekin S., Emul M., Innocenti A., Vullo D., Supuran C. // Bioorg. Med. Chem. Lett. 2005. Vol. 15. N 2. P. 367. doi 10.1016/j.bmcl.2004.10.070
- 13. Georgey H., Manhi F., Mahmoud W., Mohamed N., Berrino E., Supuran C. // Bioorg. Chem. 2019. Vol. 82. P. 109. doi 10.1016/j.bioorg.2018.09.037
- 14. Mishra C.B., Kumari S., Angeli A., Monti S.M., Buonanno M., Ti-wari M., Supuran C. // J. Med. Chem. 2017. Vol. 60. N 6. P. 2456. doi 10.1021/acs.jmedchem.6b01804
- 15. Hanan H., Georgey F., Manhi W., Mahmoud N., Mohamed E.B., Supuran C. // Bioorg. Chem. 2019. Vol. 82. P. 109. doi 10.1016/j.bioorg.2018.09.037
- 16. Khokhlov A.L., Yaichkov I.I., Korsakov M.K., Shetnev A.A., Ivanovskiy S.A., Alexeev M.A., Gasilina O.A., Volkhin N.N., Petukhov S.S. // Res. Results Pharmacol. 2024. Vol. 10. N 1. P. 53. doi 10.18413/rrpharmacology.10.431
- 17. Shetnev A., Efimova J., Gasilina O., Shabalina E., Baykov B., Lifanov D., Petersen E., Korsakov M., Petzer A., Petzer J.P. // Med. Chem. Res. 2025. Vol. 34. P. 357. doi 10.1007/s00044-024-03346-5
- 18. Sağlık B.N., Osmaniye D., Acar Çevik U., Levent S., Kaya Çavuşoğlu B., Atlı Eklioğlu Ö., Kaplancıklı Z.A. // J. Enzyme Inhib. Med. Chem. 2020. Vol. 35. N 1. P. 1422. doi 10.1080/14756366.2020.1784892
- 19. Alafeefy A.M., Ceruso M., Al-Tamimi A.M.S., Del Prete S., Capasso C., Supuran C. // Bioorg. Med. Chem. 2014. Vol. 22. N 19. P. 5133. doi 10.1016/j.bmc.2014.08.015
- 20. Turkmen H., Durgun M., Yilmaztekin S., Emul M., Innocenti A., Vull D., Scozzafava A., Supuran C.T. // Bioorg. Med. Chem. Lett. 2005. Vol. 15. N 2. Р. 367. doi 10.1016/j.bmcl.2004.10.070
- 21. Mahdy H.A., Ibrahim M.K., Metwaly A.M., Belal A., Mehany A.B.M., El-Gamal K.M.A., El-Sharkawy A., Elhendawy M.A., Radwan M.M., Elsohly M.A., Eissa I.H. // Bioorg. Chem. 2019. Vol. 94. P. 103422. doi 10.1016/j.bioorg.2019.103422
- 22. Eissa I.H., Ibrahim M.K., Metwaly A.M., Belal A., Mehany A.B.M., Abdel-hady A.A., Elhendawy M.A., Radwan M.M., El-Sohly M.A., Mahdy H.A. // Bioorg. Chem. 2021. Vol. 107. P. 104532. doi 10.1016/j.bioorg.2020.104532
- 23. Monforte A.M., Ferro S., De Luca L., Lo Surdo G., Morreale F., Panne-couque C., Balzarini J., Chimirri A. // Bioorg. Med. Chem. 2014. Vol. 22. N. 4. P. 1459. doi 10.1016/j.bmc.2013.12.045
- 24. Kulabaş N., Tatar E., Bingöl Ö., Özsavcı D., Panne-couque C., De Clercq E., Küçükgüzel İ. // Eur. J. Med. Chem. 2016. Vol. 121. P. 58. doi 10.1016/j.ejmech.2016.05.017
- 25. Lu X., Li X., Yang J., Huang B., Kang D., Zhao F., Zhou Z., De Clercq E., Daelemans D., Pannecouque C., Zhan P., Liu X. // Bioorg. Med. Chem. 2016. Vol. 24. N 18. P. 4424. doi 10.1016 /j.bmc.2016.07.041
- 26. Mohamed M.M., Khalil A.K., Abbass E.M., El-Naggar A.M. // Synth. Commun. 2017. Vol. 47. N 16. P. 1441. doi 10.1080/00397911.2017.1332223
- 27. Abutayeh R.F., Almaliti J., Taha M.O. // Med. Chem. 2020. Vol. 16. N 3. P. 403. doi 10.2174/1573406415666190401144053
- 28. Определение чувствительности микроорганизмов к антибактериальным препаратам (МУК 4.2.1890-04) // Клин. микробиол. антимикроб. химиотер. 2004. Т. 6. Вып. 4. C. 306.
- 29. Mostert S., Petzer A., Petzer J.P. // Chem. Med. Chem. 2015. Vol. 10. P. 862. doi 10.1002/cmdc.201500059
- 30. Sonsalla P.K., Wong L.Y., Winnik B., Buckley B. // Exp. Neurol. 2010. Vol. 221. P. 329. doi 10.1016/j.expneurol.2009.11.018
- 31. Petzer A., Pienaar A., Petzer J.P. // Drug Res. 2013. Vol. 63. P. 462. doi 10.1055/s-0033-1345163
- 32. Al-Sha’er M.A., Taha M.O. // Med. Chem. Res. 2011. Vol. 21. N 4. P. 487. doi 10.1007/s00044-011-9557-9
- 33. Hu H., Bajorath J. // Mol. Pharm. 2020. Vol. 17. N 3. P. 979. doi 10.1021/acs.molpharmaceut