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

   Вернуться в список сотрудников      

Employee:  Luzina Olga Anatolievna
Positions:  Leading Researcher (Doct. Chem), LPhAC


 


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Personal publicalions (DB NIOCh)


2023

Reviews, articles

  1. D. Pon'kina, S. Kuranov, M. Khvostov, N. Zhukova, Yu. Meshkova, M. Marenina, O. Luzina, T. Tolstikova, N. Salakhutdinov
    Hepatoprotective Effect of a New FFAR1 Agonist-N-Alkylated Isobornylamine
    Molecules 2023, 28(1), 396; doi:10.3390/molecules28010396, IF=4.927
  2. 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
  3. M.V. Khvostov, E.D. Gladkova, S.A. Borisov, M.S. Fedotova, N.A. Zhukova, M.K. Marenina, Yu.V. Meshkova, N. Valutsa, O.A. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
    9-N-n-alkyl Berberine Derivatives: Hypoglycemic Activity Evaluation
    Pharmaceutics 2023, 15(1), 44; doi:10.3390/pharmaceutics15010044, IF=6.525

2022

Reviews, articles

  1. S. Kuranov, M. Marenina, D. Ivankin, M. Blokhin, S. Borisov, T. Khomenko, O. Luzina, M. Khvostov, K. Volcho, T. Tolstikova, N. Salakhutdinov
    The Study of Hypoglycemic Activity of 7-Terpenylcoumarins
    Molecules 2022, 27(24), 8663 doi:10.3390/molecules27248663, IF=4.927
  2. С.А. Борисов, О.А. Лузина, М.В. Хвостов, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Синтез новых производных усниновой кислоты и изучение их гипогликемических свойств
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 599-604. doi:10.15372/KhUR2022420 (SYNTHESIS OF THE NEW DERIVATIVES OF USNIC ACID AND INVESTIGATION OF THEIR HYPOGLYCEMIC PROPERTIES/ Borisov S.A., Luzina O.A., Khvostov M.V., Tolstikova T.G., Salakhutdinov N.F.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 579-584. doi:10.15372/CSD2022420)
  3. M.V. Khvostov, E.D. Gladkova, S.A. Borisov, M.S. Fedotova, N.A. Zhukova, M.K. Marenina, Yu.V. Meshkova, O.A. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
    Study of Hypoglycemic Activity of Novel 9-N-alkyltetrahydroberberine Derivatives
    Int. J. Mol. Sci. 2022, 23(22), 14186 doi:10.3390/ijms232214186, IF=6.208
  4. S.A. Borisov, O.A. Luzina, M.V. Khvostov, T.G. Tolstikova, N.F. Salakhutdinov
    Synthesis and Pharmacological Evaluation of (+)-Usnic Acid Derivatives as Hypoglycemic Agents
    Molbank 2022, 2022(4), M1459; doi:10.3390/M1459
  5. D.I. Ivankin, N.S. Dyrkheeva, A.a L. Zakharenko, E.S. Ilina, T.O. Zarkov, J. Reynisson, O.A. Luzina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Monoterpene substituted thiazolidin-4-ones as novel TDP1 inhibitors: synthesis, biological evaluation and docking
    Bioorganic & Medicinal Chemistry Letters, V. 73, 1 October 2022, 128909 doi:10.1016/j.bmcl.2022.128909, IF=2.94
  6. 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
  7. S. Wang, Ya.V. Zonov, V.M. Karpov, O.A. Luzina, T.V. Mezhenkova
    Carbonylation of Polyfluorinated 1-Arylalkan-1-ols and Diols in Superacids
    Molecules 2022, 27(24), 8757 doi:10.3390/molecules27248757, IF=4.927

2021

Reviews, articles

  1. M.V. Khvostov, E.D. Gladkova, S.A. Borisov, N.A. Zhukova, M.K. Marenina, Yu.V. Meshkova, O.A. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
    Discovery of the First in Class 9-N-Berberine Derivative as Hypoglycemic Agent with Extra-Strong Action
    Pharmaceutics 2021, 13(12), 2138 doi:10.3390/pharmaceutics13122138, IF=6.321
  2. Д.И. Иванкин, М.С. Борисова, Д.Н. Соколов, О.А. Лузина, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Дизайн, синтез и противоязвенная активность новых производных 1-тиа-4,8-диазаспиро[4.5]декан-3-она
    Химико-фармацевтический журнал. 2021. Т. 55. № 12. С. 22-26. doi:10.30906/0023-1134-2021-55-12-22-26 (Ddesign, synthesis, and anti-ulcer activity of new 1-thia-4,8-diazaspiro[4.5]decan-3-one derivatives/ Ivankin D. I., Borisova M. S., Sokolov D. N., Luzina O. A., Tolstikova T. G., Salakhutdinov N. F.// Pharmaceutical Chemistry Journal, 2021, V.55, N 9, Pp doi:30906/0023-1134-2021-55-12-22-26), IF=0.837
  3. E.D. Gladkova, O.A. Luzina, N.F. Salakhutdinov
    Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine
    Chemistry of Natural Compounds, 2021, V. 57, N 6, Pp 1062-1065 doi:10.1007/s10600-021-03550-4, IF=0.809
  4. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  5. V.P. Nikolin, N.A. Popova, V.I. Kaledin, O.A. Luzina, A.L. Zakharenko, N.F. Salakhutdinov, O.I. Lavrik
    The influence of an enamine usnic acid derivative (a tyrosyl-DNA phosphodiesterase 1 inhibitor) on the therapeutic effect of topotecan against transplanted tumors in vivo
    Clinical & Experimental Metastasis, 2021, 38, Pp 431-440 doi:10.1007/s10585-021-10113-y, IF=5.15
  6. M.S. Borisova, D.I. Ivankin, D.N. Sokolov, O.A. Luzina, T.V. Rybalova, T.G. Tolstikova, N.F. Salakhutdinov
    Synthesis, antiulcerative, and anti-inflammatory activities of new campholenic derivatives-1,3-thiazolidin-4-ones, 1,3-thiazolidine-2,4-diones, and 1,3-thiazinan-4-ones
    Chemical Papers, 2021, V. 75, Pp 5503–5514 doi:10.1007/s11696-021-01741-5, IF=2.097
  7. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, A.L. Zakharenko, E.S. Ilina, A.A. Malakhova, S.P. Medvedev, J. Reynisson, K.P. Volcho, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Monoterpenoids for Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibition
    Biomolecules, 2021, 11(7), 973 doi:10.3390/biom11070973, IF=4.81
  8. E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
    Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
    Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=4.411
  9. A. Filimonov, O. Luzina, N. Salakhutdinov
    New Dibenzofuran Compounds Obtained by Dihydrousnic Acid Hydrogenation
    Chemistry Proceedings. 2021, 3(1), 21 doi:10.3390/ecsoc-24-08460
  10. A. Filimonov, O. Luzina, N. Salakhutdinov
    New Heterocyclic Derivatives of Usnic Acid Chemistry
    Chemistry Proceedings. 2021, 3(1), 66 doi:10.3390/ecsoc-24-08459
  11. Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
    Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
    Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi: 10.31857/S0026898421020051 (Antitumor Activity of the Combination of Topotecan and Tyrosyl-DNA-Phosphodiesterase 1 Inhibitor on Model Krebs-2 Mouse Ascite Carcinoma/ N. S. Dyrkheeva, A. L. Zakharenko, E. S. Novoselova, A. A. Chepanova, N. A. Popova, V. P. Nikolin, O. A. Luzina, N. F. Salakhutdinov, E. I. Ryabchikova, O. I. Lavrik// Molecular Biology, 2021, V 55, N 2, Pp 273-277 doi:10.1134/S0026893321020060), IF=1.374
  12. V. Fomenko, M. Blokhin, S. Kuranov, M. Khvostov, D. Baev, M.S. Borisova, O. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
    Triterpenic Acid Amides as a Promising Agent for Treatment of Metabolic Syndrome
    Sci. Pharm. 2021, 89(1), 4 doi:10.3390/scipharm89010004

2020

Reviews, articles

  1. 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
  2. S.O. Kuranov, O.A. Luzina, N.F. Salakhutdinov
    FFA1 (GPR40) Receptor Agonists Based on Phenylpropanoic Acid as Hypoglycemic Agents: Structure–Activity Relationship
    Russian Journal of Bioorganic Chemistry, 2020, V. 46, N 6, Pp 972-988 doi:10.1134/S1068162020060151, IF=0.682
  3. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
    Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
  4. O. Luzina, A. Filimonov, A. Zakharenko, A. Chepanova, O. Zakharova, E. Ilina, N. Dyrkheeva, G. Likhatskaya, N. Salakhutdinov, O. Lavrik
    Usnic Acid Conjugates with Monoterpenoids as Potent Tyrosyl-DNA Phosphodiesterase 1 Inhibitors
    Journal of Natural Products, 2020, 83, 8, 2320–2329 doi:10.1021/acs.jnatprod.9b01089, IF=3.779
  5. S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
    Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
    Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567

2019

Reviews, articles

  1. П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
    Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
    Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541
  2. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  3. Куранов С.О., Блохин М.Е., Борисов С.А., Хвостов М.В., Лузина О.А., Салахутдинов Н.Ф.
    Синтез и гипогликемическая активность цианопирролидинамидов арил(гетарил)пропеновых кислот
    Биоорганическая химия. 2019. Т. 45. № 5. С. 534-541 (Synthesis and Hypoglycemic Activity of Aryl(Hetaryl)Propenoic Cyanopyrrolidine Amides/ S. O. Kuranov, M. E. Blokhin, S. A. Borisov, M. V. Khvostov, O. A. Luzina, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 5, pp 374-380 doi:10.1134/S1068162019050078), IF=0.794
  4. 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
  5. И.В. Нечепуренко, Е.Д. Широкова, М.В. Хвостов, Т.С. Фролова, О.И. Синицина, А.М. Максимов, Р.А. Бредихин, Н.И. Комарова, Д.С. Фадеев, О.А. Лузина, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Синтез, гиполипидемическая и противогрибковая активность сульфонатов тетрагидроберберрубина
    Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1052-1060 (Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y), IF=1.014
  6. Yu.N. Antonenko, L.S. Khailova, T.I. Rokitskaya, E.S. Nosikova, P.A. Nazarov, O.A. Luzina, N.F. Salakhutdinov, E.A. Kotova
    Mechanism of action of an old antibiotic revisited: Role of calcium ions in protonophoric activity of usnic acid
    Biochimica et Biophysica Acta (BBA) - Bioenergetics, V. 1860, N 4, 1 April 2019, Pp 310-316 doi:10.1016/j.bbabio.2019.01.005, IF=4.441
  7. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  8. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833

2018

Reviews, articles

  1. Е.В. Колдышева, А.П. Меньщикова, Е.Л. Лушникова, Н.А. Попова, В.И. Каледин, В.П. Николин, А.Л. Захаренко, О.А. Лузина, Н.Ф. Салахутдинов, О.И. Лаврик
    Антиметастатическая активность комбинации топотекана и ингибитора тирозил-ДНК-фосфодиэстеразы 1 на модели карциномы легкого Льюис
    Бюллетень экспериментальной биологии и медицины 2018 г., том 166, № 11 ноябрь, р.609-615 (Antimetastatic Activity of Combined Topotecan and Tyrosyl-DNA Phosphodiesterase-1 Inhibitor on Modeled Lewis Lung Carcinoma/ E. V. Koldysheva, A. P. Men'shchikova, E. L. Lushnikova, N. A. Popova, V. I. Kaledin, V. P. Nikolin, A. L. Zakharenko, O. A. Luzina, N. F. Salakhutdinov, O. I. Lavrik// Bulletin of Experimental Biology and Medicine, March 2019, V. 166, N 5, pp 661-666 doi:10.1007/s10517-019-04413-3), IF=0.546
  2. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  3. S.O. Kuranov, I.P. Tsypysheva, M.V. Khvostov, L.F. Zainullina, S.S. Borisevich, Yu.V. Vakhitova, O.A. Luzina, N.F. Salakhutdinov
    Synthesis and evaluation of camphor and cytisine-based cyanopyrrolidines as DPP-IV inhibitors for the treatment of type 2 diabetes mellitus
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4402-4409 doi:10.1016/j.bmc.2018.07.018, IF=2.881
  4. O.A. Luzina, N.F. Salakhutdinov
    Usnic acid and its derivatives for pharmaceutical use: a patent review (2000–2017)
    Expert Opinion on Therapeutic Patents, 2018, V.28, N 6, Pp 477-491 doi:10.1080/13543776.2018.1472239, IF=2.867
  5. V.Yu. Krukov, O.G. Tomilova, O.A. Luzina, O.N. Yaroslavtseva, Yu.B. Akhanaev, M.V. Tyurin, B.A. Duisembekov, N.F. Salakhutdinov, V.V. Glupov
    Effects of fluorine-containing usnic acid and fungus Beauveria bassiana on the survival and immune-physiological reactions of Colorado potato beetle larvae
    Pest Management Science, 2018, V. 74, N 3, Pp 598-606 doi:10.1002/ps.4741, IF=3.249
  6. D.N. Sokolov, O.A. Luzina, N.F. Salakhutdinov
    Synthesis of Sulfones and Sulfoxides Based on (+)-usnic Acid
    Chemistry of Natural Compounds, 2018, V. 54, N 1, pp 46-49 doi:10.1007/s10600-018-2256-8, IF=0.45

2017

Reviews, articles

  1. А.Л. Захаренко, О.А. Лузина, Д.Н. Соколов, О.Д. Захарова, М.Е. Рахманова, А.А. Чепанова, Н.С. Дырхеева, О.И. Лаврик, Н.Ф. Салахутдинов
    Производные усниновой кислоты как эффективные ингибиторы тирозил-ДНК-фосфодиэстеразы 1
    Биоорганическая химия. 2017. Т. 43. № 1. С. 97-104. (Usnic acid derivatives are effective inhibitors of tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, O.D. Zakharova, M.E. Rakhmanova, A.A. Chepanova, N.S. Dyrkheeva, O.I. Lavrik, N.F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, January 2017, Volume 43, Issue 1, pp 84-90 doi:10.1134/S1068162017010125), IF=0.689

2016

Reviews, articles

  1. A.A. Shtro, V.V. Zarubaev, O.A. Luzina, D.N. Sokolov, N.F. Salakhutdinov
    Derivatives of usnic acid inhibit broad range of influenza viruses and protect mice from lethal influenza infection
    Antivir Chem Chemotherapy, V.24, N 3-4, August 2015, pp. 92-98, Published March 27, 2016 doi:10.1177/2040206616636992
  2. A.Zakharenko, O. Luzina, O.Koval, D. Nilov, I. Gushchina, N. Dyrkheeva, V. Svedas, N. Salakhutdinov, O. Lavrik
    Tyrosyl-DNA phosphodiesterase 1 inhibitors: usnic acid enamines enhance the cytotoxic effect of camptothecin
    J. Nat. Prod., 2016, 79 (11), pp 2961-2967 doi:10.1021/acs.jnatprod.6b00979, IF=3.661
  3. О.А. Лузина, Н.Ф. Салахутдинов
    Биологическая активность усниновой кислоты и ее производных. Часть 2. Действие усниновой кислоты и ее производных на высшие организмы, молекулярные и физико-химические аспекты биологической активности
    Биоорганическая химия. 2016. Т. 42. № 3. С. 276-300. (Biological activity of usnic acid and its derivatives: Part 2. effects on higher organisms. Molecular and physicochemical aspects/ O. A. Luzina , N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2016, V. 42, N 3, pp 249-268 doi:10.1134/S1068162016030109), IF=0.66
  4. О.А. Лузина, Н.Ф. Салахутдинов
    Биологическая активность усниновой кислоты и ее производных. Часть 1. активность в отношении одноклеточных организмов
    Биоорганическая химия. 2016. Т. 42. № 2. С. 129-149. (Biological activity of usnic acid and its derivatives: Part 1. Activity against unicellular organisms/ O. A. Luzina , N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, March 2016, V. 42, N 2, pp 115-132 doi:10.1134/S1068162016020084), IF=0.66
  5. М.Е. Рахманова, О.А. Лузина, М.А. Покровский, А.Г. Покровский, Н.Ф. Салахутдинов
    Синтез цианэтильных производных усниновой кислоты и их цитотоксическая активность
    Известия Академии наук. Серия химическая. 2016. № 2. С. 566-569 (Synthesis and cytotoxic activity of usnic acid cyanoethyl derivatives/ M. E. RakhmanovaO. A. LuzinaEmail authorM. A. PokrovskiiA. G. PokrovskiiN. F. Salakhutdinov// Russian Chemical Bulletin, February 2016, V. 65, N 2, pp 566-569 doi:10.1007/s11172-016-1338-7), IF=0.578

2015

Reviews, articles

  1. O.B. Bekker, D.N. Sokolov, O.A. Luzina, N.I. Komarova, Yu.V. Gatilov, S.N. Andreevskaya, T.G. Smirnova, D.A. Maslov, L.N. Chernousova, N.F. Salakhutdinov, V.N. Danilenko
    Synthesis and activity of (+)-usnic acid and (-)-usnic acid derivatives containing 1,3-thiazole cycle against Mycobacterium tuberculosis
    Medicinal Chemistry Research, 2015, V. 24, N 7, pp 2926-2938 doi:10.1007/s00044-015-1348-2, IF=1.401
  2. O.A. Luzina, D.N. Sokolov, M.A. Pokrovskii, A.G. Pokrovskii, O.B. Bekker, V.N. Danilenko, N.F. Salakhutdinov
    Synthesis and Biological Activity of Usnic Acid Enamine Derivatives
    Chemistry of Natural Compounds, July 2015, V. 51, N 4, pp 646-651 doi:10.1007/s10600-015-1376-7, IF=0.509

2014

Reviews, articles

  1. A.A. Shtro, V.V. Zarubaev, O.A. Luzina, D.N. Sokolov, O.I. Kiselev, N.F. Salakhutdinov
    Novel derivatives of usnic acid effectively inhibiting reproduction of influenza A virus
    Bioorganic & Medicinal Chemistry, V. 22, N 24, 15 December 2014, Pp 6826-6836. doi:10.1016/j.bmc.2014.10.033, IF=2.95
  2. O. A. Luzina, D. N. Sokolov, N. I. Komarova, N. F. Salakhutdinov
    Synthesis of Sulfides Based on (+)-Usninic Acid
    Chemistry of Natural Compounds, 2014, V. 50, N 2, pp 266-271. doi:10.1007/s10600-014-0928-6, IF=0.5

2013

Reviews, articles

  1. Д.Н. Соколов, М.Е. Рахманова, О.А. Лузина, А.В. Шернюков, Н.Ф. Салахутдинов
    Синтез новых производных (+)-усниновой кислоты с флавоновым остовом
    Известия АН. Серия химическая, 2013, N 1, С. 211–215. (Synthesis of new (+)-usnic acid derivatives with the flavone structure/ D. N. Sokolov, M. E. Rakhmanova, O. A. Luzina, A. V. Shernyukov, N. F. Salakhutdinov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 212-216 doi:10.1007/s11172-013-0031-3), IF=0.423

2012

Reviews, articles

  1. D.N. Sokolov, V.V. Zarubaev, A.A. Shtro, O.A. Luzina, N.I. Komarova, N.F. Salakhutdinov, O.I. Kiselev
    Anti-viral activity of (-)- and (+)-usnic acids and their derivatives against influenza virus A(H1N1)2009
    Bioorg. Med. Chem. Lett., V. 22, N. 23, 7060-7064. doi:10.1016/j.bmcl.2012.09.084, IF=2.553
  2. A. Zakharenko, D. Sokolov, O. Luzina, M. Sukhanova, S. Khodyreva, O. Zakharova, N. Salakhutdinov, O. Lavrik
    Influence of Usnic Acid and its Derivatives on the Activity of Mammalian Poly(ADP-ribose)polymerase 1 and DNA Polymerase β
    Med. Chem., 2012, V. 8, № 5, 883-893. doi:10.2174/1573406411309050013, IF=1.496
  3. Д.Н. Соколов, О.А. Лузина, Н.Ф. Салахутдинов
    Усниновая кислота: получение, строение, свойства и химические превращения
    Успехи химии, 2012, №8, 747-768. (Usnic acid: preparation, structure, properties and chemical transformations/ D.N. Sokolov, O.A. Luzina, N.F. Salakhutdinov// RUSS CHEM REV+, 2012, V. 81, N 8, pp. 747-768. doi:10.1070/RC2012v081n08ABEH004245), IF=2.644
  4. M.P. Polovinka, N.I. Komarova, D.V. Korchagina, D.N. Sokolov, O.A. Luzina, N.G. Vlasenko, A.A. Malyuga, E.V. Romanova, N.F. Salakhutdinov
    Secondary metabolites of the lichen Cladonia stellaris
    Chem. Nat. Compd., 2012, V. 48, N 3, pp. 392-395. doi:10.1007/s10600-012-0259-4, IF=1.29
  5. O.A. Luzina, D.N. Sokolov, A.V. Shernyukov, N.F. Salakhutdinov
    Synthesis of aurones based on usninic acid
    Chem. Nat. Compd., 2012, V. 48, N 3, pp. 385-391. doi:10.1007/s10600-012-0258-5, IF=1.29
  6. D.N. Sokolov, O.A. Luzina, N.F. Salakhutdinov
    Synthesis of ethers of (+)-usninic acid pyrazole derivatives
    Chem. Nat. Compd., 2012, V. 48, N 3, pp. 379-384. doi:10.1007/s10600-012-0257-6, IF=1.29
  7. В.Ю. Крюков, О.А. Лузина, М.П. Половинка, О.Н. Ярославцева, Н.Ф. Салахутдинов, В.В. Глупов
    Скрининг модификантов усниновой кислоты – потенциальных синергистов энтомопатогенного гриба Beauveria Bassiana для регуляции численности колорадского жука
    Агрохимия, 2012, № 2, 59-66. (Screening of Usnic Acid Derivatives as Potential Synergists of the Entomopathogenic Fungus Beauveria bassiana for the Control of Colorado Potato Beetle/ Kryukov V.Yu.1, Luzina O.A.2, Yaroslavtseva O.N.1, Polovinka M.P.2, Salakhutdinov N.F.2, Glupov V.V.// Agricultural Chemistry)

2011

Reviews, articles

  1. D.N. Sokolov, O.A. Luzina, D.V. Korchagina, M.P. Polovinka, N.F. Salakhutdinov
    Reaction of (+)-usninic acid and several of its derivatives with diazomethane
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 708-712. doi:10.1007/s10600-011-0041-z, IF=0.693
  2. Д.Н. Соколов, О.А. Лузина, М.П. Половинка, Н.Ф. Салахутдинов, Г.А. Толстиков
    Синтез халконов на основе (+)- и (-)-усниновой кислоты
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, № 11, 2359-2364. (Synthesis of chalcones derived from (+)- and (-)-usnic acids/ D.N. Sokolov, O.A. Luzina, M.P. Polovinka, N.F. Salakhutdinov, G.A. Tolstikov// RUSS CHEM B+, 2011, V. 60, N 11, pp 2406-2411. doi:10.1007/s11172-011-0370-x), IF=0.629
  3. D.N. Sokolov, O.A. Luzina, M.P. Polovinka, N.F. Salakhutdinov
    Reduction of (+)-usninic acid and its pyrazole derivative by sodium borohydride
    Chem. Nat. Compd., 2011, V. 47, N 2, pp 203-205. doi:10.1007/s10600-011-9882-8, IF=0.693

2010

Reviews, articles

  1. D.N. Sokolov, O.A. Luzina, M.P. Polovinka, D.V. Korchagina, u.V. Gatilov, N.F. Salakhutdinov
    Oxidation of usninic acid
    Chemistry of Natural Compounds, 2010, V. 46, N 5, pp 730-733. doi:10.1007/s10600-010-9727-x, IF=0.572

2009

Reviews, articles

  1. О.А. Лузина, М.П. Половинка, Н.Ф. Салахутдинов, Г.А. Толстиков
    Химическая модификация усниновой кислоты. III. Реакции (+)-усниновой кислоты с замещенными фенилгидразинами
    Журнал органической химии, 2009, Т. 45, N 12, 1790–1795. (Chemical modification of usnic acid: III. Reaction of (+)-usnic acid with substituted phenylhydrazines/ O.A. Luzina, M.P. Polovinka, N.F. Salakhutdinov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 12, pp 1783-1789 doi:10.1134/S1070428009120069), IF=0.556
  2. A.A. Tazetdinova, O.A. Luzina, M.P. Polovinka, N.F. Salakhutdinov, G.A. Tolstikov
    Amino-derivatives of usninic acid
    Chemistry of Natural Compounds, 2009, V. 45, N 6, pp 800-804. doi:10.1007/s10600-010-9502-z, IF=0.467
  3. O.A. Luzina, M.P. Polovinka, N.F. Salakhutdinov, G.A. Tolstikov
    Schmidt reaction of usnic acid
    Chemistry of Natural Compounds, 2009, V. 45, N 2, pp 251-252. doi:10.1007/s10600-009-9267-4, IF=0.467

2007

Reviews, articles

  1. О.А. Лузина, М.П. Половинка, Н.Ф. Салахутдинов, Г.А. Толстиков
    Химическая модификация усниновой кислоты. Сообщение 2. Взаимодействие (+)-усниновой кислоты с аминокислотами
    Изв. АН, Сер. Хим., 2007, Т. 56, № 6, 1203-1205. (Chemical modification of usnic acid - 2. Reactions of (+)-usnic acid with amino acids/ O. A. Luzina, M. P. Polovinka, N. F. Salakhutdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2007, V. 56, N 6, pp 1249-1251 doi:10.1007/s11172-007-0189-7), IF=0.504
  2. Г.Г. Фурин, О.А. Лузина, Р.И. Сокуев, М.П. Половинка, Н.Ф. Салахутдинов, Г.А. Толстиков
    Химическая модификация усниновой кислоты. Сообщение 1. Взаимодействие (+)-усниновой кислоты с перфторолефинами
    Изв. АН, Сер. Хим., 2007, Т. 56, № 6, 1198-1202. (Chemical modification of usnic acid 1. Reaction of (+)-usnic acid with perfluoroolefins/ G. G. Furin, O. A. Luzina, R. I. Sokuev, M. P. Polovinka, N. F. Salakhutdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2007, V. 56, N 6, pp 1244-1248 doi:10.1007/s11172-007-0188-8), IF=0.504



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