Personal publications by the year

Personal publicalions (DB NIOCh)

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

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

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

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

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

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

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

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

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

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

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

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)

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

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

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

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