Synthesis Evaluation of Antibacterial Activity of New Derivatives of 1,3-Diaza-2-phenylamino-, 7-Amino-1,3,5-triaza-, 7-Carbamoylphenylamino-1,3,5-triazadamantanes

Capa

Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Acesso é pago ou somente para assinantes

Resumo

A number of new derivatives of diaza- and triazadamantanes were synthesized and their antibacterial activity was studied by the interaction of 2-(4-aminophenyl)-5,7-disubstituted-1,3-diazadamantanes, 1,3,5-triazadamantan-7-amine and 1,3,5-triazadamantan-7-yl-(aminophenyl)methanones with anhydrides of substituted succinic and glutaric acids. Among the synthesized compounds, some possess moderate activity, suppressing the growth of gram-positive and gram-negative microorganisms in a zone with a diameter of d = 14–16 mm.

Sobre autores

K. Gevorkyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry NAS RA

ORCID ID: 0000-0003-3604-6038
Yerevan, Armenia

M. Galstyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry NAS RA

ORCID ID: 0000-0002-9475-8810
Yerevan, Armenia

M. Aleksanyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry NAS RA

Email: amv196087@mail.ru
ORCID ID: 0009-0004-1722-9140
Yerevan, Armenia

J. Avakimyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry NAS RA

ORCID ID: 0000-0002-8470-5176
Yerevan, Armenia

H. Stepanyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry NAS RA

ORCID ID: 0000-0001-7236-5947
Yerevan, Armenia

R. Muradyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry NAS RA

ORCID ID: 0000-0002-4110-9454
Yerevan, Armenia

A. Harutyunyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry NAS RA

ORCID ID: 0000-0002-8320-0942
Yerevan, Armenia

Bibliografia

  1. Спасов А.А., Хамидова Т.В., Бугаева Л.И., Морозов И.С. Хим.-фарм. ж. 2000, 34, 3–9. doi: 10.1007/BF02524549
  2. Kuznetsov A.I., Zefirov N.S. Russ. Chem. Rev. 1989, 58, 1033–1047.
  3. Arutyunyan G.L., Chachoyan A.A., Agadzhanyan T.E., Garibdzhanyan B.T. Pharm. Chem. J. 1996, 30, 739–741. doi: 10.1007/BF02218824
  4. Zakharenko A.L., Ponomarev K.U., Suslov E.V., Korchagina D.V., Volcho K.P., Vasil'eva I.A., Salakhutdinov N.F., Lavrik O.I., Russ. J. Bioorg. Chem. 2015, 41, 657–662. doi: 10.1134/S1068162015060199
  5. Можайцев Е.Ц., Пономарев К.Ю., Патрушева О.С., Медведько А.В., Далингер А.И., Рогачев А.Д., Комарова Н.И. Корчагина Д.В., Суслов Е.В., Волчо К.П., Салахутдинов Н.Ф., Вацадзе С.З. ЖОрХ 2020, 56, 1768–1783. doi: 10.31857/SOS1474920110129
  6. Вацадзе С.З., Тюрин В.С., Зацман А.И., Манаенкова М.А., Семашко В.С., Крутько Д.П., Зык Н.В., Чураков А.В., Кузьмина Л.Г. ЖОрХ. 2006, 42, 1244–1249. doi: 10.1134/S1070428006080215
  7. Arutyunyan G.L., Arutyunyan A.D., Gevorkyan K.A., Gasparyan S.P., Paronikyan R.V., Stepanyan G.M., Minasyan N.S., Pharm. Chem. J., 2018, 52, 419–423. doi: 10.1007/S11094-018-1834-1
  8. Agadzhanyan Ts.E., Arutyunyan A.D., Saakyan G.S., Chem. Het. Compd., 1992, 28, 924–926. doi: 10.1007/BF00531328
  9. Arutyunyan G.L., Arutyunyan A.D., Gevorkyan K.A., Gasparyan S.P., Paronikyan R.V., Stepanyan G.M., Minasyan N.S., Pharm. Chem. J., 2018, 52, 419–423. doi: 10.1007/S11094-018-1834-1
  10. Arutyunyan A.D., Gevorkyan K.A., Galstyan M.V., Kocharov S.L. Chem. J. Arm., 2021, 74, 101–112.
  11. Harutyunyan G.L., Gevorkyan K.A., Harutyunyan A.D., Gasparyan S.P., Mamyan S.S. Chem. Het. Compd. 2012, 48, 1670–1675. doi: 10.1007/s10593-013-1191-7
  12. Kocharov S.L., Gevorkyan K.A., Arutyunyan A.D., Galstyan M.V., Panosyan H.A., Avakimyan J.A., Stepanyan H.M. Russ. J. Org. Chem. 2023, 59, 801–806. doi: 10.1134/S1070428023050093
  13. Пат. США 3301854; Chem. Abstr., 67, 2193h (1967).
  14. Shkulev V.A., Saakyan I.B., Agadzhanyan Ts.E. Chem. Het. Compd. 1992, 28, 1340–1345. doi: 10.1007/BF00532090
  15. Руководство по проведению доклинических исследований лекарственных средств. Ред. Миронов А.Н., М: Медицина, 2012, 509–525.
  16. Машковский М.Д. Лекарственные средства, М: Новая Волна, 2010, 85.

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML

Declaração de direitos autorais © Russian Academy of Sciences, 2025