Personal publications by the year

Personal publicalions (DB NIOCh)

Reviews, articles

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

Reviews, articles

1. 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
2. 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
3. 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

Reviews, articles

1. 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
2. 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

Reviews, articles

1. 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
2. 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
3. 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
4. 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

Reviews, articles

1. A.V. Markov, A.E. Kel, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
   Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
   Oncotarget, 2019, V. 10, N 51, Pp 5267-5297 doi:10.18632/oncotarget.27085
2. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
   Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
   Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
3. 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
4. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
   Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
   Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636
5. 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

Reviews, articles

1. 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

Reviews, articles

1. 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
2. I.I. Popadyuk, A.V. Markov, E.A. Morozova, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, T.G. Tolstikova, N.F. Salakhutdinov
   Synthesis and evaluation of antitumor, anti-inflammatory and analgesic activity of novel deoxycholic acid derivatives bearing aryl- or hetarylsulfanyl moieties at the C-3 position
   Steroids, 2017, V. 127, Pp 1-12 doi:10.1016/j.steroids.2017.08.016, IF=2.282
3. 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
4. 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

Reviews, articles

1. 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

Reviews, articles

1. 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

Reviews, articles

1. A.L. Zakharenko, O.V. Salomatina, M.V. Sukhanova, M.M. Kutuzov, E.S. Ilina, S.N. Khodyreva, V. Schreiber, N.F. Salakhutdinov, O.I. Lavrik
   Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/apyrimidinic endonuclease 1 and DNA polymerase β
   Biopolym. Cell, 2012, V. 28, N 3, 223–228. doi:10.7124/bc.28.3

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. 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

Reviews, articles

1. О.В. Саломатина, Е.Б. Логашенко, Д.В. Корчагина, Н.Ф. Салахутдинов, М.А. Зенкова, В.В. Власов, Г.А. Толстиков
   Новые производные глицерретовой кислоты: синтез и биологическая активность
   Доклады Академии наук, 2010, Т. 430, N 4, C. 498–501. (Synthesis and biological activity of novel glycyrrhetic acid derivatives/ O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova, V.V. Vlasov, G.A. Tolstikov// Doklady Chemistry, 2010, V. 430, N 2, pp 35-38. doi:10.1134/S0012500810020011 Part: 2), IF=0.204

Reviews, articles

1. О.В. Саломатина, Д.В. Корчагина, Н.Ф. Салахутдинов, Г.А. Толстиков
   Получение метилового эфира 2-циано-3,12-диоксо-11-дезоксо-18βH-глициретт-1(2),11(9)-диеновой кислоты
   Химия в интересах устойчивого развития, 2009. Т. 17. N 3, С. 297-303.

Reviews, articles

1. 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

Reviews, articles

1. Т.М. Хоменко, О.В. Саломатина, С.Ю. Курбакова, И.В. Ильина, К.П. Волчо, Н.И. Комарова, Д.В. Корчагина, Н.Ф. Салахутдинов, A.Г. Толстиков
   Новые хиральные лиганды на основе миртеналя и кариофиллена для металлокомплексного асимметрического окисления сульфидов
   Журн. Орган. Химии, 2006, Т. 42, № 11, 1666-1673. (New chiral ligands from myrtenal and caryophyllene for asymmetric oxydation of sulfides catalyzed by metal complexes/ T. M. Khomenko, O. V. Salomatina, S. Yu. Kurbakova, I. V. Il’ina, K. P. Volcho, N. I. Komarova, D. V. Korchagina, N. F. Salakhutdinov, A. G. Tolstikov// Russian Journal of Organic Chemistry, 2006, V. 42, N 11, pp 1653-1661 doi:10.1134/S1070428006110091), IF=0.419
2. 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