Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН

1. A.V. Sen'kova, I.A. Savin, K.V. Odarenko, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
   Protective effect of soloxolone derivatives in carrageenan- and LPS-driven acute inflammation: Pharmacological profiling and their effects on key inflammation-related processes
   Biomedicine & Pharmacotherapy, V. 159, March 2023, 114231 doi:10.1016/j.biopha.2023.114231, IF=7.419
    
2. O.V. Salomatina, A.V. Sen'kova, A.D. Moralev, I.A. Savin, N.I. Komarova, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
   Novel Epoxides of Soloxolone Methyl: An Effect of the Formation of Oxirane Ring and Stereoisomerism on Cytotoxic Profile, Anti-Metastatic and Anti-Inflammatory Activities In Vitro and In Vivo
   Int. J. Mol. Sci. 2022, 23(11), 6214; doi:10.3390/ijms23116214, IF=6.208
    
3. A.V. Markov, A.A. Ilyina, O.V. Salomatina, A.V. Sen'kova, A.A. Okhina, A.D. Rogachev, N.F. Salakhutdinov, M.A. Zenkova
   Novel Soloxolone Amides as Potent Anti-Glioblastoma Candidates: Design, Synthesis, In Silico Analysis and Biological Activities In Vitro and In Vivo
   Pharmaceuticals 2022, 15(5), 603; doi:10.3390/ph15050603, IF=5.215
    
4. O.V. Salomatina, N.S. Dyrkheeva, I.I. Popadyuk, A.L. Zakharenko, E.S. Ilina, N.I. Komarova, J. Reynisson, N.F. Salakhutdinov, O.I. Lavrik, K.P. Volcho
   New Deoxycholic Acid Derived Tyrosyl-DNA Phosphodiesterase 1 Inhibitors Also Inhibit Tyrosyl-DNA Phosphodiesterase 2
   Molecules 2022, 27(1), 72 doi:10.3390/molecules27010072, IF=4.927
    
5. И.И. Попадюк, О.В. Саломатина, Н.Ф. Салахутдинов
   Современные подходы к модификации желчных кислот с целью синтеза соединений, обладающих ценными физико-химическими и биологическими свойствами
   Успехи химии. 2017. Т. 86. № 5. С. 388-443 (Modern approaches to modification of bile acids for the synthesis of compounds possessing valuable physicochemical and biological properties/ I.I. Popadyuk, O.V. Salomatina, N. F. Salakhutdinov// Russian Chemical Reviews, 2017, V. 86, N 5, Pp 388-443 doi:10.1070/RCR4683), IF=4.58
    
6. A.V. Markov, A.V. Sen'kova, V.O. Babich, K.V. Odarenko, V.A. Talyshev, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
   Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
   Int. J. Mol. Sci. 2020, 21(21), 7876 doi:10.3390/ijms21217876, IF=4.556
    
7. A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
   Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
   Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556
    
8. A.V. Markov, A.V. Sen'kova, D. Warszycki, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
   Soloxolone methyl inhibits influenza virus replication and reduces virus-induced lung inflammation
   Scientific Reports, 2017, V. 7, Номер статьи 13968 doi:10.1038/s41598-017-14029-0, IF=4.258
    
9. E.B. Logashenko, O.V. Salomatina, A.V. Markov, D.V. Korchagina, N.F. Salakhutdinov, G.A. Tolstikov, V.V. Vlasov, M.A. Zenkova
   Synthesis of Pro-Apoptopic Activity of Novel Glycyrrhetinic Acid Derivatives
   ChemBioChem, 2011, V. 12, N 5, 784-794. doi:10.1002/cbic.201000618, IF=3.944
    
10. P. Alper, O.V. Salomatina, N.F. Salakhutdinov, E. Ulukaya, F. Ari
    Soloxolone methyl, as a 18&bi;H-glycyrrhetinic acid derivate, may result in endoplasmic reticulum stress to induce apoptosis in breast cancer cells
    Bioorganic & Medicinal Chemistry, 2021, V.30, 115963 doi:10.1016/j.bmc.2020.115963, IF=3.641
     
11. A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
    Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
    Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59
     
12. A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
    Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
    Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267
     
13. A.V. Markov, K.V. Odarenko, A.V. Sen’kova, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova
    Cyano Enone-Bearing Triterpenoid Soloxolone Methyl Inhibits Epithelial-Mesenchymal Transition of Human Lung Adenocarcinoma Cells in Vitro and Metastasis of Murine Melanoma in Vivo
    Molecules 2020, 25(24), 5925 doi:10.3390/molecules25245925, IF=3.266
     
14. O.V. Salomatina, I.I. Popadyuk, A.L. Zakharenko, O.D. Zakharova, D.S. Fadeev, N.I. Komarova, J. Reynisson, H.J. Arabshahi, R. Chand, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel semisynthetic derivatives of bile acids as effective tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecules, 2018, V. 23, N 3, art. number 679 doi:10.3390/molecules23030679, IF=3.098
     
15. O.V. Salomatina, A.V. Markov, E.B. Logashenko, D.V. Korchagina, M.A. Zenkova, N.F. Salakhutdinov, V.V. Vlassov, G.A. Tolstikov
    Synthesis of novel 2-cyano substituted glycyrrhetinic acid derivatives as inhibitors of cancer cells growth and NO production in LPS-activated J-774 cells
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 1, Pp 585-593. doi:10.1016/j.bmc.2013.10.049, IF=2.95
     
16. I.I. Popadyuk, A.V. Markov, O.V. Salomatina, E.B. Logashenko, A.V. Shernyukov, M.A. Zenkova, N.F. Salakhutdinov
    Synthesis and biological activity of novel deoxycholic acid derivatives
    Bioorganic & Medicinal Chemistry, V. 23, N 15, 2015, Pp 5022-5034 doi:10.1016/j.bmc.2015.05.012, IF=2.792
     
17. O. V.Salomatina, I. I.Popadyuk, A. L.Zakharenko, O. D.Zakharova, A. A.Chepanova, N..S.Dyrkheeva, N.I.Komarova, J.Reynisson, R. O.Anarbaev, N. F.Salakhutdinov, O. I.Lavrik, K. P.Volcho
    Deoxycholic acid as a molecular scaffold for tyrosyl-DNA phosphodiesterase 1 inhibition: a synthesis, structure-activity relationship and molecular modeling study
    Steroids, V. 165, January 2021, 108771 doi:10.1016/j.steroids.2020.108771, IF=2.668
     
18. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
     
19. O.V. Salomatina, T.G. Kuznetsova, D.V. Korchagina, E.A. Paukshtis, E.M. Moroz, K.P. Volcho, V.A. Barkhash, N.F. Salakhutdinov
    Effects of the Properties of SO₄/ZrO₂ Solid Catalysts on the Products of Transformation and Reaction Mechanism of R-(+)-limonene Diepoxides
    J. Mol. Catal. A: Chemical, V. 269, N 1-2, 72-80. doi:10.1016/j.molcata.2007.01.005, IF=2.51
     
20. I.I. Popadyuk, A.V. Markov, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, N.F. Salakhutdinov
    Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: synthesis and evaluation of anti-proliferative activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 16, Pp 3755-3759 doi:10.1016/j.bmcl.2017.06.072, IF=2.453