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Russian Chemical Reviews, 2015, Volume 84, Issue 9, Pages 891–916
DOI: https://doi.org/10.1070/RCR4527
(Mi rcr4066)
 

This article is cited in 45 scientific papers (total in 45 papers)

Synthesis and biological properties of amino acids and peptides containing a tetrazolyl moiety

E. A. Popova, R. E. Trifonov

Saint Petersburg State University
Abstract: Literature data published mainly in the last 15 years on the synthesis and biological properties of amino acid analogues and derivatives containing tetrazolyl moieties are analyzed. Tetrazolyl analogues and derivatives of amino acids and peptides are shown to be promising for medicinal chemistry. Being polynitrogen heterocyclic systems comprising four endocyclic nitrogen atoms, tetrazoles can behave as acids and bases and form strong hydrogen bonds with proton donors (more rarely, with acceptors). They have high metabolic stability and are able to penetrate biological membranes. The review also considers the synthesis and properties of linear and cyclic peptides based on modified amino acids incorporating a tetrazolyl moiety. A special issue is the discussion of the biological properties of tetrazole-containing amino acids and peptides, which exhibit high biological activity and can be used to design new drugs.
The bibliography includes 200 references.
Received: 29.10.2014
Bibliographic databases:
Language: English
Original paper language: Russian
Citation: E. A. Popova, R. E. Trifonov, “Synthesis and biological properties of amino acids and peptides containing a tetrazolyl moiety”, Russian Chem. Reviews, 84:9 (2015), 891–916
Citation in format AMSBIB
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\by E.~A.~Popova, R.~E.~Trifonov
\paper Synthesis and biological properties of amino acids and peptides containing a tetrazolyl moiety
\jour Russian Chem. Reviews
\yr 2015
\vol 84
\issue 9
\pages 891--916
\mathnet{http://mi.mathnet.ru/eng/rcr4066}
\crossref{https://doi.org/10.1070/RCR4527}
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\elib{https://elibrary.ru/item.asp?id=23851040}
\scopus{https://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-84943240710}
Linking options:
  • https://www.mathnet.ru/eng/rcr4066
  • https://doi.org/10.1070/RCR4527
  • https://www.mathnet.ru/eng/rcr/v84/i9/p891
  • This publication is cited in the following 45 articles:
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    3. H. S. Lalithamba, G. Nagendra, M. Ramya, G. K. Prashanth, Russ J Appl Chem, 97:8 (2024), 633  crossref
    4. Chemistry — An Asian Journal, 18:10 (2023)  crossref
    5. A. S. Samadov, Dzh. N. Khakimov, A. F. Stepnova, E. F. Faizullozoda, A. V. Kuzin, Russ. J. Phys. Chem., 97:4 (2023), 658  crossref
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    7. Rostislav E. Trifonov, Vladimir A. Ostrovskii, IJMS, 24:24 (2023), 17190  crossref
    8. A. S. Samadov, J. N. Khakimov, A. F. Stepnova, E. F. Faizullozoda, A. V. Kuzin, Russian Journal of Physical Chemistry, 97:4 (2023), 512  crossref
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    12. Vladimir A. Ostrovskii, Elena A. Popova, Rostislav E. Trifonov, Comprehensive Heterocyclic Chemistry IV, 2022, 182  crossref
    13. G. A. Smirnov, P. B. Gordeev, Russ Chem Bull, 71:2 (2022), 412  crossref
    14. Pankuri Gupta, Abha Sharma, N-Heterocycles, 2022, 355  crossref
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    17. Batyrenko A.A., Mikolaichuk O.V., Ovsepyan G.K., Protas A.V., Kornyakov I.V., Lider E.V., Eremina Yu.A., Khlebnikova T.S., Lakhvich F.A., Trifonov R.E., Russ. J. Gen. Chem., 91:4 (2021), 666–671  crossref  isi
    18. Leyva-Ramos S., Cardoso-Ortiz J., Curr. Org. Chem., 25:3 (2021), 388–403  crossref  isi
    19. O. T. O'Sullivan, M. J. Zdilla, Chem. Rev., 120:12 (2020), 5682–5744  crossref  isi  scopus
    20. O. V. Salishcheva, A. Yu. Prosekov, Food Raw Mater., 8:2 (2020), 298–311  crossref  isi  scopus
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