The Sintesis and Antioxidant Activity of New bis-1,3,4-Oxadiazoles, bis-1,3,4-Thiadiazoles, and Their Derivatives

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Bis-1,3,4-oxadiazoles and bis-1,3,4-thiadiazoles with aryl and alkyl linkers were synthesized. In order to increase their hydrophilicity and potential biological activity, pharmacophore electron-deficient groups (carboxylic, nitrile) were introduced into the molecule. Functionalized compounds revealed a new type of biological activity such as inhibition of lipid oxidation in the form of a decrease in the amount of MDA.

作者简介

S. Dilanyan

The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA

编辑信件的主要联系方式.
Email: nana_dilanyan@mail.ru
ORCID iD: 0000-0003-1786-5548
亚美尼亚, prosp. Azatutyan, 26, Yerevan, 0014

Zh. Buniatyan

The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA

Email: nana_dilanyan@mail.ru
ORCID iD: 0000-0002-3152-3176
亚美尼亚, prosp. Azatutyan, 26, Yerevan, 0014

H. Panosyan

The Scientific Technological Centre of Organic and Pharmaceutical Chemistry NAS RA

Email: nana_dilanyan@mail.ru
ORCID iD: 0000-0001-8311-6276
亚美尼亚, prosp. Azatutyan, 26, Yerevan, 0014

参考

  1. Bala S., Kamboj S., Kajal A., Saini V., Prasad D.N. BioMed Res. Int. 2014, 2014, 1–18. doi: 10.1155/2014/172791
  2. Neelottama K., Swatantra K.S., Kushwaha, A.K., Int. J. Chem. Tech. Res. Coden (USA). 2012, 4, 517–531. IJCRGG ISSN: 0974-4290
  3. Clomb T., Swiatek P. Int. J. Molecular Sci. 2021, 22, 6979. doi: 10.3390/ijms 22136979
  4. Datoussaid Y., Othman A.A., Kirsch G. South African J. Chem. 2012, 65, 30–35.
  5. Dilanyan S.V., Hovsepyan T.R., Nersesyan L.E., Agaronyan A.S., Danielyan I.S., Minasyan N.S., Harutyunyan A.A. Russ. J. Gen. Chem. 2020, 90, 681–689. doi: 10.1134/S1070363220050047
  6. Holla B.S., Poojary K.N., Rao B.S., Shivavada M.K. Eur. J. Med Chem., 2002, 37, 511. doi: 10.1016/S02235234(02)01358-2
  7. Wang Q.P., Zhang J.Q., Damu G.L.Y., Wan Kun, Zhang Huizen, Zhou Cheng He, Sci. China Chem. 2012, 55, 2134. doi: 10.1007/S11426-012-4602-1
  8. Parameshwara C.J., Allam V., Perugu S., Rajeswar R.V. J. Heterocycl. Chem., 2019, 56, 1012. doi: 10.1002/jhot.3484
  9. Liu, P., Zhu, S. L., Li. P., Xie, W.J., Jin, Y.S., Sen, Q.Y., Sun, P., Zhani, Y.J., Yang, X.H., Jiang, Y.Y., and Zhang, D.Z., Bioorg. Med. Chem. Lett., 2008, 18, 3261. doi 10.16/j.bmci.2008.04.056
  10. Владимиров Ю.А., Азизова О.А., Доев А.И., Козлов А.В.//Свободные радикалы в живых системах. ВИНИТИ, 1991, 29, 126–130.
  11. Арутюнян Д.В., Дубинина Е., Зыбина Н.Н.//Методы оценки свободнорадикального окисления и антиоксидантной системы организма.СПБ, 2000, 91–94.
  12. Гринеева О.В. Определение АОА соединений растительного и синтетического происхождения. М.Акад.мед.наук, 2017, 4, 180–197.

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