Personal publications by the year

Personal publicalions (DB NIOCh)

Reviews, articles

1. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
   Синтез конъюгатов (aR,7S)-колхицина с монотерпеноидами и изучение их биологиче ской активности
   Известия Академии наук. Серия химическая. 2023, № 1, стр. 248, IF=1.703
2. А.И. Далингер, Д.С. Баев, О.И. Яровая, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков, Н.Ф. Салахутдинов, С.З. Вацадзе
   Синтез несимметричных амидов N-бензилбиспидинола и изучение их ингибирующей активности по отношению к основной вирусной протеазе SARS-CoV-2
   Известия Академии наук. Серия химическая. 2023, № 1, стр. 239, IF=1.703
3. D.S. Baev, M.E. Blokhin, V.Yu. Chirkova, S.V. Belenkaya, O.A. Luzina, O.I. Yarovaya, N.F. Salakhutdinov, D.N. Shcherbakov
   Triterpenic Acid Amides as Potential Inhibitors of the SARS-CoV-2 Main Protease
   Molecules 2023, 28(1), 303 doi:10.3390/molecules28010303, IF=4.927
4. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
   Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
   Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817

Reviews, articles

1. A.S. Sokolova, O.I. Yarovaya, L.V. Kuzminykh, A.A. Shtro, A.M. Klabukov, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.S. Borisevich, E.M. Khamitov, N.F. Salakhutdinov
   Discovery of N-Containing (-)-Borneol Esters as Respiratory Syncytial Virus Fusion Inhibitors
   Pharmaceuticals 2022, 15(11), 1390 doi:10.3390/ph15111390, IF=5.215
2. O.I. Yarovaya, K.S. Kovaleva, S.S. Borisevich, T.V. Rybalova, Yu.V. Gatilov, E.O. Sinegubova, A.S. Volobueva, V.V. Zarubaev
   Synthesis and antiviral properties of tricyclic amides derived from α-humulene and β-caryophyllene
   Mendeleev Communications, 2022, 32(5), pp. 609-611 doi:10.1016/j.mencom.2022.09.013, IF=1.837
3. A.S. Filimonov, O.I. Yarovaya, A.V. Zaykovskaya, N.B. Rudometova, D.N. Shcherbakov, V.Yu. Chirkova, D.S. Baev, S.S. Borisevich, O.A. Luzina, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
   (+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
   Viruses 2022, 14(10), 2154 doi:10.3390/v14102154, IF=5.817
4. A. G. Nemolochnova, A. D. Rogachev, O. P. Salnikova, T. M. Khomenko, K. P. Volcho, O. I. Yarovaya, A. V. Fatianova, A. G. Pokrovsky, N. F. Salakhutdinov
   Stability Study, Quantification Method and Pharmacokinetics Investigation of a Coumarin–Monoterpene Conjugate Possessing Antiviral Properties against Respiratory Syncytial Virus
   Pharmaceuticals 2022, 15(9), 1158 doi:10.3390/ph15091158, IF=5.215
5. V.V. Chernyshov, I.I. Popadyuk, O.I. Yarovaya, N.F. Salakhutdinov
   Nitrogen-Containing Heterocyclic Compounds Obtained from Monoterpenes or Their Derivatives: Synthesis and Properties
   Topics in Current Chemistry, 2022, V. 380, Art. number: 42 doi:10.1007/s41061-022-00399-1, IF=8.904
6. V.V. Oreshko, K.S. Kovaleva, E.D. Mordvinova, O.I. Yarovaya, Yu.V. Gatilov, D.N. Shcherbakov, N.I. Bormotov, O.A. Serova, L.N. Shishkina, N.F. Salakhutdinov
   Synthesis and Antiviral Properties of Camphor-Derived Iminothiazolidine-4-Ones and 2,3-Dihydrothiazoles
   Molecules 2022, 27(15), 4761 doi:10.3390/molecules27154761, IF=4.927
7. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
   Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
   Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
8. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
   Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
   ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
9. V.V. Zarubaev, A.V. Garshinina, A.S. Volobueva, A.V. Slita, O.I. Yarovaya, V.V. Bykov, K.A. Leonov, V.S. Motov, V.A. Khazanov, N.F. Salakhutdinov
   Optimization of application schedule of camphecene, a novel anti-influenza compound, based on its pharmacokinetic characteristics
   Fundamental & Clinical Pharmacology, 2022, V.36, N 3, 2022, Pp 518-525 doi:10.1111/fcp.12750, IF=2.747
10. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
    Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
    Journal of Biomolecular Structure and Dynamics, 2022, V.40, N 12, Pp 5481-5492 doi:10.1080/07391102.2020.1871414, IF=5.235
11. K. Kovaleva, O. Oleshko, O. Yarovaya, S. Cheresiz, A. Zakharenko, K. Ponomarev, O. Lavrik, A. Pokrovsky, N. Salakhutdinov
    Inhibition of the DNA repair enzyme TDP1 by the resin acid derivatives as a new way to increase the efficiency of glioblastoma chemotherapy
    AIP Conference Proceedings 2390, 020036 (2022) doi:10.1063/5.0069407
12. S.S. Borisevich, E.M. Khamitov, M.A. Gureev, O.I. Yarovaya, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, D.N. Shcherbakov, R.A. Maksyutov, N.F. Salakhutdinov
    Simulation of Molecular Dynamics of SARS-CoV-2 S-Protein in the Presence of Multiple Arbidol Molecules: Interactions and Binding Mode Insights
    Viruses 2022, 14(1), 119 doi:10.3390/v14010119, IF=5.818
13. V.V. Fomenko, N.B. Rudometova, O.I. Yarovaya, A.D. Rogachev, A.A. Fando, A.V. Zaykovskaya, N.I. Komarova, D.N. Shcherbakov, O.V. Pyankov, A.G. Pokrovsky, L.I. Karpenko, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
    Molecules 2022, 27(1), 295 doi:10.3390/molecules27010295, IF=4.927
14. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
15. V.V. Chernyshov, O.I. Yarovaya, Ia.L. Esaulkova, E. Sinegubova, S.S. Borisevich, I.I. Popadyuk, V.V. Zarubaev, N.F. Salakhutdinov
    Novel O-acylated amidoximes and substituted 1,2,4-oxadiazoles synthesised from (+)-ketopinic acid possessing potent virus-inhibiting activity against phylogenetically distinct influenza A viruses
    Bioorganic & Medicinal Chemistry Letters, V. 55, 1 January 2022, 128465 doi:10.1016/j.bmcl.2021.128465, IF=2.94

Reviews, articles

1. K.S. Kovaleva, O.I. Yarovaya, Yu.V. Gatilov, A.V. Slita, Ya.L. Esaulkova, V.V. Zarubaev, N.B. Rudometova, N.S. Shcherbakova, D.N. Shcherbakov, N.F. Salakhutdinov
   Synthesis and Antiviral Activity of N-Heterocyclic Hydrazine Derivatives of Camphor and Fenchone
   Chemistry of Heterocyclic Compounds (2021), 57, N. 4, Pp 455-461 doi:10.1007/s10593-021-02923-5, IF=1.277
2. O. Yarovaya, A. Zaykovskaya, K. Kovaleva, O. Pyankov, N. Salakhutdinov
   Development and application of the cytopathic model of Hantaan viruses
   AIP Conference Proceedings 2388, 040021 (2021) doi:10.1063/5.0069403
3. A.S. Volobueva, O.I. Yarovaya, M.V. Kireeva, S.S. Borisevich, K.S. Kovaleva, I.Ya. Mainagashev, Yu.V. Gatilov, M.G. Ilyina, V.V. Zarubaev, N.F. Salakhutdinov
   Discovery of New Ginsenol-like Compounds with High Antiviral Activity
   Molecules, 2021, 26(22), 6794 doi:10.3390/molecules26226794, IF=4.41
4. K. Kovaleva, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, O. Lavrik, N. Salakhutdinov
   Dehydroabietylamine-based thiazolidin-4-ones and 2-thioxoimidazolidin-4-ones as novel tyrosyl-DNA phosphodiesterase 1 inhibitors
   Molecular Diversity, 2021, V. 25, N 4, Pp 2389-2397 doi:10.1007/s11030-020-10132-z, IF=2.229
5. A.A. Okhina, A.D. Rogachev, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
   Stability study of the antiviral agent camphecene in dried blood spots at different temperatures
   Drug Testing and Analysis, V.13, N 10, October 2021, Pp 1797-1802 doi:10.1002/dta.3148, IF=3.345
6. A.S. Sokolova, O.I. Yarovaya, D.V. Baranova, A.V. Galochkina, A.A. Shtro, M.V. Kireeva, S.S. Borisevich, Y.V. Gatilov, V.V. Zarubaev, N.F. Salakhutdinov
   Quaternary ammonium salts based on (-)-borneol as effective inhibitors of influenza virus
   Archives of Virology, 2021, V. 166, N. 7, Pp 1965-1976 doi:10.1007/s00705-021-05102-1, IF=2.574
7. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
   (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
   ArchPharm, 2021, V.354, N 6, Art. Num. 2100038 doi:10.1002/ardp.202100038, IF=3.751
8. A.D. Rogachev, V.P. Putilova, A.V. Zaykovskaya, O.I. Yarovaya, A.S. Sokolova, V.V. Fomenko, O.V. Pyankov, R.A. Maksyutov, A.G. Pokrovsky, N.F. Salakhutdinov
   Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
   Journal of Pharmaceutical and Biomedical Analysis, 2021, V. 199, 114062 doi:10.1016/j.jpba.2021.114062, IF=3.935
9. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
   New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
   Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
10. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
11. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
12. N.O. Vorozhtsov, O.I. Yarovaya, V.A. Roznyatovskii, B.N. Tarasevich, Yu.A. Kozlovskaya, A.I. Petkova, A.V. Slita, E.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov, E.K. Beloglazkina
    Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N 4, Pp 432-441 doi:10.1007/s10593-021-02921-7, IF=1.277
13. О.И. Яровая, Н.Ф. Салахутдинов
    Моно- и сесквитерпены в качестве стартовой платформы для создания противовирусных средств
    Успехи химии, 2021, Т. 90, N 4, Сc 488-510 (Mono- and sesquiterpenes as a starting platform for the development of antiviral drugs/ O I Yarovaya, N F Salakhutdinov// RUSS CHEM REV, 2021, 90 (4), 488-510 doi:10.1070/RCR4969), IF=6.926
14. V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
    Unexpected ring opening during the imination of camphor-type bicyclic ketones
    European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=3.021

Reviews, articles

1. A.S. Sokolova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, N.S. Shcherbakova, A.V. Zaykovskaya, D.S. Baev, T.G. Tolstikova, D.N. Shcherbakov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
   Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process
   European Journal of Medicinal Chemistry, 2020, V. 207, 112726 doi:10.1016/j.ejmech.2020.112726, IF=5.572
2. E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
   New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
   RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
3. М.В. Киреева, О.И. Яровая, В.В. Зарубаев
   Ингибирующая активность каркасных соединений на основе кариофиллена в отношении гемагглютинина вируса гриппа А
   Проблемы медицинской микологии. 2020. Т. 22. № 3. С. 86.
4. V.V. Chernyshov, O.I. Yarovaya, R.Yu. Peshkov, N.F. Salakhutdinov
   Synthesis of cyclic D-(+)-camphoric acid imides and study of their antiviral activity
   Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 763-768 doi:10.1007/s10593-020-02728-y, IF=1.491
5. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
   Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
   Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
6. A.A. Okhina, A.D. Rogachev, O.I. Yarovaya, M.V. Khvostov, T.G. Tolstikova, A.G. Pokrovsky, V.A. Khazanov, N.F. Salakhutdinov
   Development and validation of an LC-MS/MS method for the quantitative analysis of the anti-influenza agent camphecene in rat plasma and its application to study the blood-to-plasma distribution of the agent
   Journal of Pharmaceutical and Biomedical Analysis, 2020, V. 180, 113039 doi:10.1016/j.jpba.2019.113039, IF=3.209

Reviews, articles

1. V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
   The first example of the stereoselective synthesis and crystal structure of a spirobi­cyclo­quinazolinone based on (–)-fenchone and anthranilamide
   Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93
2. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
   Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
   Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
3. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
   Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
   Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
4. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
   Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
   Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
5. А.С. Соколова, Д.В. Баранова, О.И. Яровая, Д.С. Баев, О.А. Полежаева, А.В. Зыбкина, Д.Н. Щербаков, Т.Г. Толстикова, Н.Ф. Салахутдинов
   Синтез производных (1S)-(+)-камфора-10-сульфокислоты и изучение их противовирусной активности в качестве ингибиторов филовирусных инфекций in vitro и in silico
   Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1041-1046 (Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections/ A. S. Sokolova, D. V. Baranova, O. I. Yarovaya, D. S. Baev, O. A. Polezhaeva, A. V. Zybkina, D. N. Shcherbakov, T. G. Tolstikova, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V 68, N 5, pp 1041-1046 doi:10.1007/s11172-019-2517-0), IF=1.014

Reviews, articles

1. K.S. Kovaleva, F.I. Zubkov, N.I. Bormotov, R.A. Novikov, P.V. Dorovatovskii, V.N. Khrustalev, Yu.V. Gatilov, V.V. Zarubaev, O.I. Yarovaya, L.N. Shishkina, N.F. Salakhutdinov
   Synthesis of D-(+)-camphor-based N-acylhydrazones and their antiviral activity
   Med. Chem. Commun., 2018, V. 9, N 12, Pp 2072-2082 doi:10.1039/C8MD00442K, IF=2.342
2. A.D. Rogachev, O.I. Yarovaya, A.V. Fatianova, V.A. Lavrinenko, E.V. Amosov, V.V. Zarubaev, A.G. Pokrovsky, N.F. Salakhutdinov
   Untargeted search and identification of metabolites of antiviral agent camphecene in rat urine by liquid chromatography and mass spectrometry and studying their distribution in organs following peroral administration of the compound
   Journal of Pharmaceutical and Biomedical Analysis, 2018, V. 161, Pp 383-392 doi:10.1016/j.jpba.2018.09.003, IF=2.831
3. V.V. Zarubaev, E.A. Pushkina, S.S. Borisevich, A.V. Galochkina, A.V. Garshinina, A.A. Shtro, A.A. Egorova, A.S. Sokolova, S.L. Khursan, O.I. Yarovaya, N.F. Salakhutdinov
   Selection of influenza virus resistant to the novel camphor-based antiviral camphecene results in loss of pathogenicity
   Virology, V. 524, November 2018, Pp 69-77 doi:10.1016/j.virol.2018.08.011, IF=3.374
4. A.S. Sokolova, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, N.F. Salakhutdinov
   Synthesis and antiviral activity of camphor-based 1,3-thiazolidin-4-one and thiazole derivatives as Orthopoxvirus-reproduction inhibitors
   Med. Chem. Commun,, 2018, V. 9, N 10, Pp 1746-1753 doi:10.1039/C8MD00347E, IF=2.342
5. A.S. Sokolova, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, N.F. Salakhutdinov
   Discovery of a new class of inhibitors of Vaccinia virus based on (-)-borneol from Abies sibirica and (+)-camphor
   Chemistry & Biodiversity, 2018, V. 15, N 9, e1800153 doi:10.1002/cbdv.201800153, IF=1.617
6. М.С. Борисова, О.И. Яровая, М.Д. Семенова, Т.Г. Толстикова, Н.Ф. Салахутдинов
   Противоязвенная активность производных борнеола
   Известия Академии наук. Серия химическая. 2018. № 3. С. 558-561. (Antiulcerogenic activity of borneol derivatives/ M. S. Borisova, O. I. Yarovaya, M. D. Semenova, T. G. Tolstikova, N. F. Salakhutdinov// Russian Chemical Bulletin, 2018, V. 67, N 3, Pp 558-561 doi:10.1007/s11172-018-2110-y), IF=0.781

Reviews, articles

1. A. Kononova, A. Sokolova, S. Cheresiz, O. Yarovaya, R. Nikitina, A. Chepurnov, A.G. Pokrovsky, N. Salakhutdonov
   N-Heterocyclic borneol derivatives as the inhibitors of Marburg virus glycoprotein-mediated VSIV pseudotype entry
   Med. Chem. Commun., 2017, V. 8, N 12, Pp 2233-2237 doi:10.1039/C7MD00424A, IF=2.608
2. А.С. Соколова, О.И. Яровая, А.А. Нефедов, Н.Ф. Салахутдинов
   Разработка и валидация методики определения нового эффективного ингибитора вируса гриппа H1N1 в плазме крови
   Химико-фармацевтический журнал, 2017, том 51, №12, 30-33 (Development and Validation of a Method for Determination of a New Effective Inhibitor of Influenza Virus H1N1 in Blood Plasma/ A. S. Sokolova, O. I. Yarovaya, A. A. Nefedov, N. F. Salakhutdinov// Pharmaceutical Chemistry Journal, 2018, V. 51, N 12, pp 1102-1105 doi:10.1007/s11094-018-1748-y), IF=0.444
3. N.F. Salakhutdinov, K.P. Volcho, O.I. Yarovaya
   Monoterpenes as a renewable source of biologically active compounds
   Pure and Applied Chemistry, 2017, V.89, N 8, pp 1105-1118 doi:10.1515/pac-2017-0109, IF=2.625
4. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
   Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
   Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
5. A.S. Sokolova, O.I. Yarovaya, M.D. Semenova, A.A. Shtro, I.R. Orshanskaya, V.V. Zarubaev, N.F. Salakhutdinov
   Synthesis and in vitro study of novel borneol derivatives as potent inhibitors of the influenza A virus
   Med. Chem. Commun., 2017, 8(5), 960-963 doi:10.1039/C6MD00657D, IF=2.608
6. K.S. Kovaleva, O.I. Yarovaya, D.S. Fadeev, N.F. Salakhutdinov
   One-pot synthesis of 1,5,3-oxathiazepanes via the three-component condensation of primary amines, formaldehyde and 2-mercaptoethanol
   Tetrahedron Letters, 2017, V. 58, N 19, Pp 1868-1870 doi:10.1016/j.tetlet.2017.03.090, IF=2.193
7. A.S. Sokolova, O.I. Yarovaya, A.A. Shtro, M.S. Borisova, E.A. Morozova, T.G. Tolstikova, V.V. Zarubaev, N.F. Salakhutdinov
   Synthesis and biological activity of heterocyclic borneol derivatives
   Chemistry of Heterocyclic Compounds, 2017, V. 53, N 3, pp 371-377 doi:10.1007/s10593-017-2063-3, IF=0.893
8. K.S. Kovaleva, O.I. Yarovaya, A.V. Shernyukov, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, N.F. Salakhutdinov
   Synthesis of new heterocyclic dehydroabietylamine derivatives and their biological activity
   Chemistry of Heterocyclic Compounds, 2017, V. 53, N 3, pp 364-370 doi:10.1007/s10593-017-2058-0, IF=0.893
9. A.S. Sokolova, О.I. Yarovaya, D.S. Baev, А.V. Shernyukov, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
   Aliphatic and alicyclic camphor imines as effective inhibitors of influenza virus H1N1
   European Journal of Medicinal Chemistry, 2017, V. 127, Pp 661-670 doi:10.1016/j.ejmech.2016.10.035, IF=4.519

Reviews, articles

1. A.D. Rogachev, O.I. Yarovaya, S.V. Ankov, M.V. Khvostov, T.G. Tolstikova, A.G. Pokrovsky, N.F. Salakhutdinov
   Development and validation of ultrafast LC–MS/MS method for quantification of anti-influenza agent camphecene in whole rat blood using dried blood spots and its application to pharmacokinetic studies
   Journal of Chromatography B, Volumes 1036-1037, 15 November 2016, Pages 136-141 doi:10.1016/j.jchromb.2016.10.009, IF=2.687
2. А.В. Бабина, В.А. Лавриненко, О.И. Яровая, Н.Ф. Салахутдинов
   Действие нового противовирусного агента камфецина на поведение мышей
   Бюллетень экспериментальной биологии и медицины. 2016. Т. 162. № 9. С. 329-332. (Effect of New Antiviral Agent Camphecin on Behavior of Mice/ A. V. Babina, V. A. Lavrinenko, O. I. Yarovaya, N. F. Salakhutdinov// Bulletin of Experimental Biology and Medicine, January 2017, V. 162, N 3, pp 346-348 doi:10.1007/s10517-017-3612-6), IF=0.448
3. A. Sokolova, A. Pavlova, N. Komarova, O. Ardashov, A. Shernyukov, Yu. Gatilov, O. Yarovaya, T. Tolstikova, N. Salakhutdinov
   Synthesis and analgesic activity of new α-truxillic acid derivatives with monoterpenoid fragments
   Medicinal Chemistry Research, 2016, V. 25, N 8, pp 1608-1615 doi:10.1007/s00044-016-1593-z, IF=1.435
4. E.V. Sharova, G.K. Genkina, N.M. Vinogradova, O.I. Artyushin, O.I. Yarovaya, V.K. Brel
   Phosphorylation of natural productsCytisine, anabasine, and camphor using click chemistry methodology
   Phosphorus, Sulfur, and Silicon and the Related Elements, 2016, V. 191, N 11-12, Pp 1556-1557 (21st International Conference on Phosphorus Chemistry (ICPC-2016),Kazan, RUSSIA, JUN 05-10, 2016 doi:10.1080/10426507.2016.1213257, IF=0.722
5. K.S. Kovaleva, A.A. Kononova, V.A. Korobeynikov, S.V. Cheresiz, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
   Cytotoxic and Antiviral Properties of Novel Dehydroabietylamine Salts
   Med Chem (Los Angeles) 6:10, 642-646 doi:10.4172/2161-0444.1000408

Reviews, articles

1. A.S. Sokolova, О.I. Yarovaya, А.V. Shernyukov, Yu.V. Gatilov, Yu.V. Razumova, V.V. Zarubaev, T.S. Tretiak, А.G. Pokrovsky, O.I. Kiselev, N.F. Salakhutdinov
   Discovery of a new class of antiviral compounds: Camphor imine derivatives
   European Journal of Medicinal Chemistry, V. 105, 13 November 2015, Pp 263-273 doi:10.1016/j.ejmech.2015.10.010, IF=3.447
2. V.V. Zarubaev, A.V. Garshinina, T.S. Tretiak, V.A. Fedorova, A.A. Shtro, A.S. Sokolova, O.I. Yarovaya, N.F. Salakhutdinov
   Broad range of inhibiting action of novel camphor-based compound with anti-hemagglutinin activity against influenza viruses in vitro and in vivo
   Antiviral Research, V. 120, 2015, Pp 126-133 doi:10.1016/j.antiviral.2015.06.004, IF=3.938
3. А.С. Соколова, E.А. Морозова, В.Г. Васильев, О.И. Яровая, Т.Г. Толстикова, Н.Ф. Салахутдинов
   Курареподобные производные камфоры и их биологическая активность
   Биоорганическая химия. 2015. Т. 41. № 2. С. 203-211. (Curare-like camphor derivatives and their biological activity/ A. S. Sokolova, E. A. Morozova, V. G. Vasilev, O. I. Yarovaya, T. G. Tolstikova, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, March 2015, Volume 41, Issue 2, pp 178-185 doi:10.1134/S1068162015020156), IF=0.535

Reviews, articles

1. A.S. Sokolova, О.I. Yarovaya, D.V. Korchagina, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, N.F. Salakhutdinov
   Camphor-based symmetric diimines as inhibitors of influenza virus reproduction
   Bioorganic & Medicinal Chemistry, 2014, V. 22, N 7, Pp 2141-2148. doi:10.1016/j.bmc.2014.02.038, IF=2.95
2. S. Kurbakova, I. Il'ina, A. Pavlova, D. Korchagina, O. Yarovaya, T. Tolstikova, K. Volcho, N. Salakhutdinov
   Synthesis and analgesic activity of monoterpenoid-derived 2-aryl-4,4,7-trimethyl-4a,5,8,8a-tetrahydro-4H-benzo[d][1,3]dioxin-8-ols
   Medicinal Chemistry Research, 2014, V. 23, N 4, pp 1709-1717. doi:10.1007/s00044-013-0772-4

Reviews, articles

1. A.S. Sokolova, О. I. Yarovaya, А.V. Shernyukov, М.A. Pokrovsky, А.G. Pokrovsky, V.A. Lavrinenko, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, A.B. Beklemishev, N.F. Salakhutdinov
   New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity
   Bioorganic & Medicinal Chemistry, 2013, V. 21, N 21, P: 6690-6698. doi:10.1016/j.bmc.2013.08.014, IF=2.903

Reviews, articles

1. O.I. Yarovaya, D.V. Korchagina, N.F. Salakhutdinov, G.A. Tolstikov
   Reaction of isocembrol and alcohols on clay
   Chem. Nat. Compd., 2012, V. 48, N 1, pp. 56-59. doi:10.1007/s10600-012-0158-8, IF=1.29

Reviews, articles

1. О.В. Саломатина, О.И. Яровая, Д.В. Корчагина, Ю.В. Гатилов, В.А. Бархаш
   Превращения диэпоксипроизводных терпинолена в условиях кислотного катализа
   Журнал органической химии, 2011, Т. 47, N 10, 1455-1461. (Acid-catalyzed transformations of diepoxy derivatives of terpinolene/ O. V. Salomatina, O. I. Yarovaya, D. V. Korchagina, Yu. V. Gatilov, V. A. Barkhash// RUSS J ORG CHEM+, 2011, V. 47, N 10, pp 1479-1486. doi:10.1134/S1070428011100046), IF=0.634
2. С.А. Кондратьев, В.И. Ростовцев, О.И. Яровая, Н.Ф. Салахутдинов
   Флотореагенты на основе скипидара и их использование при флотации медно-никелевой руды
   Физ.-техн. Пробл. Разр. Полезн. Ископ. (J. Min. Sci), 2011, № 4, 117-124. (Turpentine-based flotation agents in copper-nickel ore flotation/ S.A. Kondrat'ev, V.I. Rostovtsev, O.I. Yarovaya, N.F. Salakhutdinov// J MIN SCI+, -2011, V. 47, N 4, pp 514-521. doi:10.1134/S1062739147040149), IF=0.389

Reviews, articles

1. К.П. Волчо, О.И. Яровая, С.Ю. Курбакова, Д.В. Корчагина, В.А. Бархаш, Н.Ф. Салахутдинов
   Получение из цитраля эпоксидинитрилов и их кислотно-катализируемые превращения
   Журн. Орган. Химии, 2007, Т. 43, N 4, 514-520. (Synthesis of epoxy dinitriles from citral and their acid-catalyzed transformations/ K. P. Volcho, O. I. Yarovaya, S. Yu. Kurbakova, D. V. Korchagina, V. A. Barkhash, N. F. Salakhutdinov// Russian Journal of Organic Chemistry, 2007, V. 43, N 4, pp 511-517 doi:10.1134/S1070428007040045), IF=0.492

Reviews, articles

1. О.В. Саломатина, О.И. Яровая, Д.В. Корчагина, Ю.В. Гатилов, М.П.Половинка, В.А. Бархаш
   Превращения диэпоксипроизводных лимонена в условиях гомогенного кислотного катализа
   Журн. Орган. Химии, 2006, Т. 42, № 9, 1333-1340. (Transformations of diepoxy derivatives of limonene in homogeneous acidic media/ O. V. Salomatina, O. I. Yarovaya, D. V. Korchagina, Yu. V. Gatilov, M. P. Polovinka, V. A. Barkhash// Russian Journal of Organic Chemistry, 2006, V. 42, N 9, pp 1313-1320 doi:10.1134/S1070428006090107), IF=0.419