Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН

1. 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
    
2. 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
    
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. D.V. Reshetnikov, I.D. Ivanov, D.S. Baev, T.V. Rybalova, E.S. Mozhaitsev, S.S. Patrushev, V.A. Vavilin, T.G. Tolstikova, E.E. Shults
   Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors
   Molecules 2022, 27(24), 8787 doi:10.3390/molecules27248787, IF=4.927
    
5. M.E. Mironov, S.A. Borisov, T.V. Rybalova, D.S. Baev, T.G. Tolstikova, E.E. Shults
   Synthesis of Anti-Inflammatory Spirostene-Pyrazole Conjugates by a Consecutive Multicomponent Reaction of Diosgenin with Oxalyl Chloride, Arylalkynes and Hydrazines or Hydrazones
   Molecules 2022, 27(1), 162 doi:10.3390/molecules27010162, IF=4.927
    
6. 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
    
7. 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
    
8. S.F. Vasilevsky, O.L. Krivenko, I.V. Sorokina, D.S. Baev, T.G. Tolstikova, I.V. Alabugin
   Cascade Transformations of 1-R-Ethynyl-9,10-anthraquinones with Amidines: Expanding Access to Isoaporphinoid Alkaloids
   Molecules 2021, 26(22), 6883 doi:10.3390/molecules26226883, IF=4.411
    
9. S. Kuranov, O. Luzina, M. Khvostov, D. Baev, D. Kuznetsova, N. Zhukova, P. Vassiliev, A. Kochetkov, T. Tolstikova, N. Salakhutdinov
   Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity
   Pharmaceuticals 2020, 13(11), 404 doi:10.3390/ph13110404, IF=4.285
    
10. T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
    Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
    Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929
     
11. S.F. Vasilevsky, A.I. Govdi, E.E. Shults, M.M. Shakirov, I.V. Sorokina, T.G. Tolstikova, D.S. Baev, G.A. Tolstikov, I.V. Alabugin
    Efficient synthesis of the first betulonic acid -acetylene hybrids and their hepatoprotective and anti-inflammatory activity
    Bioorg. Med. Chem. 2009, V. 17, N 14, 5164-5169. doi:0.1016/j.bmc.2009.05.059, IF=3.75
     
12. R. Kong, X. Zhu, E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, J. Yu, A.V. Dushkin, W. Su
    Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
    International Journal of Pharmaceutics, 2017, V. 534, N 1-2, Pp 108-118 doi:10.1016/j.ijpharm.2017.10.011, IF=3.648
     
13. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    11-Phenylundeca-5Z,9Z-dienoic Acid: Stereoselective Synthesis and Dual Topoisomerase I/IIα Inhibition
    CURRENT CANCER DRUG TARGETS, 2015, V. 15, N 6, Pp 504-510 doi:10.2174/1568009615666150506093155, IF=3.522
     
14. A.V. Lipeeva, M.A. Pokrovsky, D.S. Baev, M.M. Shakirov, I.Y. Bagryanskaya, T.G. Tolstikova, A.G. Pokrovsky, E.E. Shults
    Synthesis of 1H-1,2,3-triazole linked aryl(arylamidomethyl) - dihydrofurocoumarin hybrids and analysis of their cytotoxicity
    European Journal of Medicinal Chemistry, V.100, 2015, Pp 119-128 doi:10.1016/j.ejmech.2015.05.016, IF=3.447
     
15. R. Kong, X. Zhu, E.S. Meteleva, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, A.V. Dushkin, W. Su
    Atorvastatin calcium inclusion complexation with polysaccharide arabinogalactan and saponin disodium glycyrrhizate for increasing of solubility and bioavailability
    Drug Delivery and Translational Research, 2018, V 8, N 5, pp 1200-1213 doi:10.1007/s13346-018-0565-x, IF=3.394
     
16. N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
    1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
    Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267
     
17. K.P. Cheremnykh, V.A. Savelyev, S.A. Borisov, I.D. Ivanov, D.S. Baev, T.G. Tolstikova, V.A. Vavilin, E.E. Shults
    Hybrides of Alkaloid Lappaconitine with Pyrimidine Motif on the Anthranilic Acid Moiety: Design, Synthesis, and Investigation of Antinociceptive Potency
    Molecules 2020, 25(23), 5578 doi:10.3390/molecules25235578, IF=3.266
     
18. A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
    Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
    Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06
     
19. S.A. Kremis, D.S. Baev, A.V. Lipeeva, E.E. Shults, T.G. Tolstikova, O.I. Sinitsyna, A.V. Kochetov, T.S. Frolova
    Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
    Journal of biochemical and molecular toxicology, 2019, V. 33, N 11, e22396 doi:10.1002/jbt.22396, IF=2.965
     
20. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
    Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
    Natural Product Research (Formerly Natural Product ), 2021, V. 35, N 21, Pp 3850-3858 doi:10.1080/14786419.2020.1744139, IF=2.861