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
Ye Yuan, Muzi Li, Vasso Apostolopoulos, John Matsoukas, Wojciech M. Wolf, Mark A.T. Blaskovich, Joanna Bojarska, Zyta M. Ziora, European Journal of Medicinal Chemistry, 2024, 116870
H. S. Lalithamba, G. Nagendra, M. Ramya, G. K. Prashanth, Russ J Appl Chem, 97:8 (2024), 633
Chemistry — An Asian Journal, 18:10 (2023)
A. S. Samadov, Dzh. N. Khakimov, A. F. Stepnova, E. F. Faizullozoda, A. V. Kuzin, Russ. J. Phys. Chem., 97:4 (2023), 658
Ekaterina A. Ermakova, Julia A. Golubeva, Ksenia S. Smirnova, Lyubov S. Klyushova, Ilia V. Eltsov, Alexander A. Zubenko, Leonid N. Fetisov, Alexandra E. Svyatogorova, Elizaveta V. Lider, Polyhedron, 230 (2023), 116213
Rostislav E. Trifonov, Vladimir A. Ostrovskii, IJMS, 24:24 (2023), 17190
A. S. Samadov, J. N. Khakimov, A. F. Stepnova, E. F. Faizullozoda, A. V. Kuzin, Russian Journal of Physical Chemistry, 97:4 (2023), 512
O. V. Mikolaichuk, V. V. Sharoyko, E. A. Popova, A. V. Protas, A. V. Fonin, Yu. A. Anufrikov, A. M. Malkova, N. T. Shmaneva, V. A. Ostrovskii, O. E. Molchanov, D. N. Maistrenko, K. N. Semenov, Russ Chem Bull, 71:5 (2022), 1050
Vladimir V. Bakharev, Alexander A. Gidaspov, Vladimir A. Zalomlenkov, Victor E. Parfenov, Olga V. Golovina, Pavel A. Slepukhin, Chem Heterocycl Comp, 58:2-3 (2022), 153
Vladimir A. Ostrovskii, Elena A. Popova, Rostislav E. Trifonov, Comprehensive Heterocyclic Chemistry IV, 2022, 182
G. A. Smirnov, P. B. Gordeev, Russ Chem Bull, 71:2 (2022), 412
O. V. Mikolaichuk, A. V. Protas, E. A. Popova, O. E. Molchanov, D. N. Maistrenko, V. A. Ostrovskii, Yu. N. Pavlyukova, V. V. Sharoyko, K. N. Semenov, Russ J Gen Chem, 92:9 (2022), 1621
Madiha A. Siddiqui, Mubarak H. Shaikh, Amol A. Nagargoje, Tarannum T. Shaikh, Vijay M. Khedkar, Prathmesh P. Deshpande, Bapurao B. Shingate, Res Chem Intermed, 48:12 (2022), 5187