420 Chemistry of Heterocyclic Compounds 2021, 57(4), 420–422 Antiviral activity of 1,2,4-triazole derivatives (microreview) Nataliia V. Simurova1*, Olena I. Maiboroda1 1 National University of Food Technologies, 68 Volodymyrska St., Kyiv 01601, Ukraine; e-mail: n.v.simurova@gmail.com Submitted November 29, 2020 Accepted after revision February 5, 2021 Olena I. Maiboroda is Associate Professor at the Department of Food Chemistry of the National University of Food Technologies (Kyiv, Ukraine). She completed her PhD thesis in Chemical Sciences carried out under the guidance of Professor A. I. Tolmachev and defended it in 2002 at the Institute of Organic Chemistry of the National Academy of Sciences of Ukraine. Her scientific interests include synthesis of biologically active oxygen- and nitrogen-containing heterocyclic compounds, chemistry of polymethine dyes. Nataliia V. Simurova is Associate Professor at the Department of Food Chemistry of the National University of Food Technologies (Kyiv, Ukraine). She completed her PhD thesis in Chemical Sciences carried out under the guidance of Professor A. D. Sinitsa and defended it in 1995 at the Institute of Organic Chemistry of the National Academy of Sciences of Ukraine. Her research interests include chemistry of heterocyclic compounds, chemistry of trivalent phosphorus derivatives, and medicinal chemistry. viral infections and the lack of effective chemotherapeutic agents for their treatment, the number of studies on the antiviral properties of 1,2,4-triazole derivatives has significantly increased. In the presented review, we focused on current publications devoted to the study of the antiviral properties of compounds containing the 1,2,4-triazole ring. Isosteric analogs of known drugs, as well as new molecules, are considered. Introduction Today, 1,2,4-triazole derivatives are the preferred structural moieties in the development of new drugs with a wide range of pharmacological activity, as evidenced by several reviews.1 This is due to the fact that the triazole ring can be considered a bioisostere of an amide, ester, or carboxyl groups.2 Relatively low toxicity, good pharmacokinetic and pharmacodynamic properties of triazole, its resistance to metabolic degradation are another advantages. In recent years, against the background of the emergence of new The microreview summarizes data published since 2015 on the antiviral properties and synthesis of compounds containing the 1,2,4-triazole ring. Analogs of ribavirin and doravirine Ribavirin has antiviral activity against RNA and DNA viruses (hepatitis C, influenza A and B, herpes type 1 and 2 viruses, etc.). The possibility of using this compound for the treatment of hantavirus, various hemorrhagic fevers, as well as coronavirus is currently being evaluated.3 Various mechanisms of action of ribavirin have been proposed. This molecule is thought to have different effects on different viruses. According to one hypothesis, ribavirin is an imitator of the purine guanosine cycle.4 Zhurilo et al.5 proposed two methods for the synthesis of ribavirin analogs 1 (chemical and chemoenzymatic methods starting from natural nucleoside substrates) by replacing the carboxamide fragment with the isostere 1,2,4- oxadiazole ring. The obtained compounds demonstrated high activity against viruses of hepatitis C, herpes simplex type 1, influenza A, comparable to the effect of ribavirin. Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2021, 57(4), 420–422 0009-3122/21/57(4)-0420©2021 Springer Science+Business Media, LLC DOI 10.1007/s10593-021-02919-1 Chemistry of Heterocyclic Compounds 2021, 57(4), 420–422 421 Analogs of ribavirin and doravirine (continued) A series of studies by Chudinov et al.,6 Tang et al.7 is devoted to the synthesis of ribavirin analogs 2 containing a vinylaryl substituent at position 5 of the triazole ring. The relationship between the structure and activity of the obtained compounds E/Z-2 in regards to hepatitis C, influenza, and herpes simplex viruses was studied. The obtained results6 indicate that all active compounds have common features: a rigid bond between the triazole and aryl rings, lipophilic substituents in the para position of the aryl ring. It was demonstrated that only the E-isomers possess high activity against herpes simplex virus comparable to the activity of ribavirin, while the Z-isomers are inactive. Wang et al.8 synthesized a series of acetamide-substituted analogs of doravirine, a potent non-nucleoside reverse transcriptase inhibitor (NNRTI). Most of the obtained compounds 3 had inhibitory properties against HIV-1. Compound 3 with the 1,2,4-triazole substituent in the amide fragment showed excellent efficacy, comparable to that of doravirine and significantly superior to that of lamivudine, with high selectivity. Acyclovir isosteres substituents R1 and R2 is also an important factor deter- mining the antiviral activity. As a result of physico- chemical studies using the ADMET principle,10 it was established that the closest analog of acyclovir, compound 8a, is a promising candidate for further development as an antiherpetic agent. It has also been shown9 that the replacement of the triazole ring with a thiadiazole one leads to the complete loss of antiviral activity. The introduction of the oxadiazole ring into compound 7 did not bring the desired result either. Acyclovir is the ancestor of antiherpetic drugs – blockers of viral DNA synthesis. A series of isosteric analogs of acyclovir 4–8 containing the 1,2,4-triazole ring was obtained.9 It was shown that derivatives substituted both at the endocyclic (compounds 4) and exocyclic (compound 5) nitrogen atoms are active against herpes simplex type 1 virus. Condensed triazolopyrimidines 8, which are structurally similar to purine bases, showed the highest activity with high selectivity and low toxicity. The authors of the study9 believe that the lipophilicity of the Chemistry of Heterocyclic Compounds 2021, 57(4), 420–422 422 References 1. (a) Aggarwal, R.; Sumran, G. Eur. J. Med. Chem. 2020, 205, 112652. (b) Vagish, C. B.; Sudeep, P.; Jayadevappa, H. P.; Ajay Kumar, K. Int. J. Curr. Res. 2020, 12, 12950. (c) Sathyanarayana, R.; Poojary, B. J. Chin. Chem. Soc. 2020, 67, 459. 2. Malik, M. S.; Ahmed, S. A.; Althagafi, I. I.; Ansari, M. A.; Kamal, A. RSC Med. Chem. 2020, 11, 327. 3. (a) Brocato, R. L.; Hooper, J. W. Viruses 2019, 11, 610. (b) De Clercq, E. Chem.–Asian J. 2019, 14, 3962. (c) Khalili, J. S.; Zhu, H.; Sze, N.; Mak, N. S. A; Yan, Y.; Zhu, Y. J. Med. Virol. 2020, 7, 740. 4. Zeidler, J.; Baraniak, D.; Ostrowski, T. Eur. J. Med. Chem. 2015, 97, 409. 5. Zhurilo, N. I.; Chudinov, M. V.; Matveev, A. V.; Smirnova, O. S.; Konstantinova, I. D.; Miroshnikov, A. I.; Prutkov, A. N.; Grebenkina, L. E.; Pulkova, N. V.; Shvets, V. I. Bioorg. Med. Chem. Lett. 2018, 28, 11. 6. (a) Chudinov, M. V.; Prutkov, A. N.; Matveev, A. V.; Grebenkina, L. E.; Konstantinova, I. D.; Berezovskaya, Y. V. Bioorg. Med. Chem. Lett. 2016, 26, 3223. (b) Chudinov, M. V.; Matveev, A. V.; Prutkov A. N.; Konstantinova, I. D.; Fateev, I. V.; Prasolov, V. S.; Smirnova, O. A.; Ivanov, A. V.; Galegov, G. A.; Deryabin, P. G. Mendeleev Commun. 2016, 26, 214. 7. Tang, J.; Cong, M.; Xia, Y.; Quéléver, G.; Fan, Y.; Qu, F.; Peng, L. Org. Biomol. Chem. 2015, 13, 110. 8. Wang, Z.; Yu, Z.; Kang, D.; Zhang, J.; Tian, Y.; Daelemans, D.; De Clercq, E.; Pannecouque, C.; Zhan, P.; Liu, X. Bioorg. Med. Chem. 2019, 27, 447. 9. Goma'a, H.-A. M.; Ghaly, M. A.; Abou-zeid, L. A.; Badria, F. A.; Shehata, I. A.; El-Kerdawy, M. M. ChemistrySelect 2019, 4, 6421. 10. Kauthale, S.; Tekale, S.; Damale, M.; Sangshetti, J.; Pawar, R. Bioorg. Med. Chem. Lett. 2017, 27, 3891. 11. Zaher, N. H.; Mostafa, M. I.; Altaher, A. Y. Acta Pharm. 2020, 70, 145. 12. Frączek, T.; Paneth, A.; Kamiński, R.; Krakowiak, A.; Paneth, P. J. Enzyme Inhib. Med. Chem. 2016, 31, 481. 13. Başaran, E.; Karaküçük-Iyidogan, A.; Schols, D.; Oruç-Emre, E. E. Chirality 2016, 28, 495. 14. Ulomskiy, E. N.; Ivanova, A. V.; Gorbunov, E. B.; Esaulkova, I. L.; Slita, A. V.; Sinegubova, E. O.; Voinkov, E. K.; Drokin, R. A.; Butorin, I. I.; Gazizullina, E. R.; Gerasimova, E. L.; Zarubaev, V. V.; Rusinov, V. L. Bioorg. Med. Chem. Lett. 2020, 30, 127216. Substituted triazolethiones and thiols Recently, Zaher et al.11 synthesized a number of 4-amino- 5-hydrazine-4H-1,2,4-triazole-3-thiol derivatives 9, 10 while searching for effective inhibitors of the Nsp13 helicase of the MERS coronavirus. It was shown that the most active compounds are those containing halogen atoms in the para position of the aryl substituent and the cyclo- pentene fragment. Frączek et al.12 synthesized a number of compounds 11, 12 based on 3,4-disubstituted triazole-5-thione. Compound 12 (R1 = Me, R2 = 4-carboxy-2-chlorophenyl, R3 = benzyl) showed high activity against HIV-1 and good pharmaco- kinetic properties. The authors believe that it may serve as the basis for the development of powerful new triazole NNRTIs for the treatment of HIV-1. A series of optically pure derivatives of 1,2,4-triazole- 3-thiones 13 with a benzenesulfonamide group was synthesized by Başaran et al.13 All compounds were tested for activity against a wide range of DNA and RNA viruses, including various strains of herpes simplex virus and HIV, as well as influenza A (H1N1, H3N2) and B viruses, varicella zoster virus, human cytomegalovirus, etc. It was demonstrated that enantiomers of 1,2,4-triazole-3-thiones of the R-configuration with electron-withdrawing substituents are potential candidates for the development of drugs against influenza A (H1N1) viruses, while the S-enantiomers do not exhibit antiviral activity. Condensed triazole derivatives Condensed 1,2,4-triazole derivatives possess a variety of biological activities, including antiviral activity, and therefore arouse considerable research interest. Stable σ-adducts of 1,2,4-triazolo[5,1-c]triazines and 1,2,4-triazolo- [1,5-a]-pyrimidines 14 with various polyphenols were obtained and their antiviral activity was investigated.14 Triazoloazines modified with fluoroglycine have the greatest activity against influenza A (H1N1) virus. Molecular modeling has shown that their action is directed Ph H NH2·HCl OMe O Ph H NH N H NH2 O PhO2S RNCS MeOH , 8–10 h Ph H H N HN NH OPhO2S H N S R Ph H NH PhO2S N NHN R S2 N NaOH 100°C, 4 h R = C6H11, PhCH2, PhCH2CH2, substituted Ar 13 1. Et3N, CH2Cl2, Py, 0°C, 30 min, then , 3 h 2. NH2NH2·H2O MeOH, , 6 h against viral hemagglutinin, a protein that ensures the ability of the virus to attach to the host cell. Introduction Analogs of ribavirin and doravirine Analogs of ribavirin and doravirine (continued) Acyclovir isosteres Substituted triazolethiones and thiols Condensed triazole derivatives References