Synthesis and Biological Evaluation of N-Aminoalkil Derivatives of Sulfanilamide Reaction
- 作者: Vasilyeva E.A.1,2, Proskurina I.K.1, Shetnev A.А.1,3, Romanycheva A.A.1, Korovina A.V.1, Belchenko M.V.1, Grunina E.O.1, Petzer A.4, Kotov A.D.1, Petzer J.4
-
隶属关系:
- Ushinsky Yaroslavl State Pedagogical University
- Kosygin Russian State University
- Moscow Institute of Physics and Technology
- North-West University
- 期: 卷 95, 编号 3-4 (2025)
- 页面: 80-91
- 栏目: Articles
- URL: https://archivog.com/0044-460X/article/view/686598
- DOI: https://doi.org/10.31857/S0044460X25030013
- EDN: https://elibrary.ru/DCOCLA
- ID: 686598
如何引用文章
详细
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.
全文:

作者简介
Elena Vasilyeva
Ushinsky Yaroslavl State Pedagogical University; Kosygin Russian State University
Email: a.shetnev@yspu.org
ORCID iD: 0000-0001-6855-0883
俄罗斯联邦, Yaroslavl; Moscow
Irina Proskurina
Ushinsky Yaroslavl State Pedagogical University
Email: a.shetnev@yspu.org
ORCID iD: 0000-0001-6086-1978
俄罗斯联邦, Yaroslavl
Anton Shetnev
Ushinsky Yaroslavl State Pedagogical University; Moscow Institute of Physics and Technology
编辑信件的主要联系方式.
Email: a.shetnev@yspu.org
ORCID iD: 0000-0002-4389-461X
俄罗斯联邦, Yaroslavl; Dolgoprudny
Anna Romanycheva
Ushinsky Yaroslavl State Pedagogical University
Email: a.shetnev@yspu.org
ORCID iD: 0000-0002-7931-1711
俄罗斯联邦, Yaroslavl
Alyona Korovina
Ushinsky Yaroslavl State Pedagogical University
Email: a.shetnev@yspu.org
ORCID iD: 0009-0003-5743-6948
俄罗斯联邦, Yaroslavl
Maria Belchenko
Ushinsky Yaroslavl State Pedagogical University
Email: a.shetnev@yspu.org
ORCID iD: 0009-0006-9589-0756
俄罗斯联邦, Yaroslavl
Ekaterina Grunina
Ushinsky Yaroslavl State Pedagogical University
Email: a.shetnev@yspu.org
ORCID iD: 0009-0007-4551-1866
俄罗斯联邦, Yaroslavl
Anelle Petzer
North-West University
Email: a.shetnev@yspu.org
ORCID iD: 0000-0001-8114-8223
南非, Potchefstroom
Alexander Kotov
Ushinsky Yaroslavl State Pedagogical University
Email: a.shetnev@yspu.org
ORCID iD: 0000-0002-0567-2880
俄罗斯联邦, Yaroslavl
Jacob Petzer
North-West University
Email: a.shetnev@yspu.org
ORCID iD: 0000-0002-7114-8120
南非, Potchefstroom
参考
- Scholar E. // xPharm: The Comprehensive Pharmacology Reference. 2007. P. 1. doi: 10.1016/b978-008055232-3.62694-7
- Курышева Н.И. // Офтальмология. 2020. Т. 17. № 4. С. 676. doi: 10.18008/1816-5095-2020-4-676-682
- 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.
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- Kulabaş N., Tatar E., Bingöl Ö., Özsavcı D., Pannecouque C., De Clercq E., Küçükgüzel İ. // Eur. J. Med. Chem. 2016. Vol. 121. P. 58. doi 10.1016/ j.ejmech.2016.05.017
- 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
- 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
- Abutayeh R.F., Almaliti J., Taha M.O. // Med. Chem. 2020. Vol. 16. N 3. P. 403. doi 10.2174/ 1573406415666190401144053
- Определение чувствительности микроорганизмов к антибактериальным препаратам (МУК 4.2.1890-04) // Клин. микробиол. антимикроб. химиотер. 2004. Т. 6. Вып. 4. C. 306.
- Mostert S., Petzer A., Petzer J.P. // Chem. Med. Chem. 2015. Vol. 10. P. 862. doi: 10.1002/cmdc.201500059
- 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
- Petzer A., Pienaar A., Petzer J.P. // Drug Res. 2013. Vol. 63. P. 462. doi: 10.1055/s-0033-1345163
- 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
- Hu H., Bajorath J. // Mol. Pharm. 2020. Vol. 17. N 3. P. 979. doi: 10.1021/acs.molpharmaceut
补充文件
