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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
Siberian Branch of Russian Academy of Science

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Employee:  Salomatina Oksana Vladimirovna
Positions:  Senior Researcher (Cand. Chem.), LPhAC


 


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Personal publicalions (DB NIOCh)


2020

Reviews, articles

  1. 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
  2. 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

2019

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

2018

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

2017

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

2015

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

2014

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

2012

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

2011

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

2010

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

2009

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.

2007

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

2006

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



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