Personal publications by the year

Personal publicalions (DB NIOCh)

Reviews, articles

1. Е.С. Можайцев, А.А. Охина, К.Ю. Пономарев, А.Д. Рогачев, Е.В. Суслов, К.П. Волчо, Н.Ф. Салахутдинов, С.З. Вацадзе
   N,N-замещенные биспидины как лиганды металлокомплексных катализаторов реакции этинилирования
   Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 615-619. doi:10.15372/KhUR2022422 (N,N-SUBSTITUTED BISPIDINES AS LIGANDS OF METAL COMPLEX CATALYSTS FOR THE ETHYNYLATION REACTION/ Mozhaitsev E.S., Okhina A.A., Ponomarev K.Yu., Rogachev A.D., Suslov E.V., Volcho K.P., Salakhutdinov N.F., Vatsadze S.Z.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 595-599. doi:10.15372/CSD2022422)
2. Н.В. Басов, А.Д. Рогачев, Ю.С. Сотникова, Ю.В. Патрушев, А.Г. Покровский
   Исследование хроматографического поведения метаболитов из плазмы крови методом ВЭЖХ-МС/МС с использованием монолитной колонки с сорбентом на основе 1-винил-1,2,4-триазола
   Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 591-598. doi:10.15372/KhUR2022419 (INVESTIGATION OF THE CHROMATOGRAPHIC BEHAVIOUR OF METABOLITES FROM BLOOD PLASMA BY HPLC-MS/MS USING A MONOLITHIC COLUMN WITH A SORBENT BASED ON 1-VINYL-1,2,4-TRIAZOLE/ Basov N.V., Rogachev A.D., Sotnikova Yu.S., Patrushev Yu.V., Pokrovsky A.G.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 571-578. doi:10.15372/CSD2022419)
3. A. Kotlyarova, A.V. Podturkina, A.V. Pavlova, D.S. Gorina, A.V. Lastovka, O.V. Ardashov, A.D. Rogachev, A.E. Izyurov, A.B. Arefieva, A.V. Kulikov, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov, Yu. Sidorova
   A Newly Identified Monoterpenoid-Based Small Molecule Able to Support the Survival of Primary Cultured Dopamine Neurons and Alleviate MPTP-Induced Toxicity In Vivo
   Molecules 2022, 27(23), 8286; doi:10.3390/molecules27238286, IF=4.927
4. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
   Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
   Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
5. A. G. Nemolochnova, A. D. Rogachev, O. P. Salnikova, T. M. Khomenko, K. P. Volcho, O. I. Yarovaya, A. V. Fatianova, A. G. Pokrovsky, N. F. Salakhutdinov
   Stability Study, Quantification Method and Pharmacokinetics Investigation of a Coumarin–Monoterpene Conjugate Possessing Antiviral Properties against Respiratory Syncytial Virus
   Pharmaceuticals 2022, 15(9), 1158 doi:10.3390/ph15091158, IF=5.215
6. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
   Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
   Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
7. 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
8. V.V. Fomenko, N.B. Rudometova, O.I. Yarovaya, A.D. Rogachev, A.A. Fando, A.V. Zaykovskaya, N.I. Komarova, D.N. Shcherbakov, O.V. Pyankov, A.G. Pokrovsky, L.I. Karpenko, R.A. Maksyutov, N.F. Salakhutdinov
   Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
   Molecules 2022, 27(1), 295 doi:10.3390/molecules27010295, IF=4.927

Reviews, articles

1. E.V. Suslov, K.Yu. Ponomarev, O.S. Patrusheva, S.O. Kuranov, A.A. Okhina, A.D. Rogachev, A.A. Munkuev, R.V. Ottenbacher, A.I. Dalinger, M.A. Kalinin, S.Z. Vatsadze, K.P. Volcho, N.F. Salakhutdinov
   Novel Bispidine-Monoterpene Conjugates—Synthesis and Application as Ligands for the Catalytic Ethylation of Chalcones
   Molecules, 2021, 26(24), 7539 doi:10.3390/molecules26247539, IF=4.411
2. M. Neganova, Yu. Aleksandrova, E. Suslov, E. Mozhaitsev, A. Munkuev, D. Tsypyshev, M. Chicheva, A. Rogachev, O. Sukocheva, K. Volcho, S. Klochkov
   Novel Multitarget Hydroxamic Acids with a Natural Origin CAP Group against Alzheimer’s Disease: Synthesis, Docking and Biological Evaluation
   Pharmaceutics, 2021, 13(11), 1893 doi:10.3390/pharmaceutics13111893, IF=6.321
3. A.A. Okhina, A.D. Rogachev, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
   Stability study of the antiviral agent camphecene in dried blood spots at different temperatures
   Drug Testing and Analysis, V.13, N 10, October 2021, Pp 1797-1802 doi:10.1002/dta.3148, IF=3.345
4. A.D. Rogachev, V.P. Putilova, A.V. Zaykovskaya, O.I. Yarovaya, A.S. Sokolova, V.V. Fomenko, O.V. Pyankov, R.A. Maksyutov, A.G. Pokrovsky, N.F. Salakhutdinov
   Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
   Journal of Pharmaceutical and Biomedical Analysis, 2021, V. 199, 114062 doi:10.1016/j.jpba.2021.114062, IF=3.935
5. A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
   Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
   Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.932

Reviews, articles

1. Е.С. Можайцев, К.Ю. Пономарев, О.С. Патрушева, А.В. Медведько, А.И. Далингер, А.Д. Рогачев, Н.И. Комарова, Д.В. Корчагина, Е.В. Суслов, К.П. Волчо, Н.Ф. Салахутдинов, С.З. Вацадзе
   Конъюгаты биспидина и монотерпеноидов как лиганды металлокомплексных катализаторов реакции Анри
   Журнал органической химии. 2020. Т. 56. № 11. С. 1768-1783 doi:10.31857/S0514749220110129. (Conjugates of Bispidine and Monoterpenoids as Ligands of Metal Complex Catalysts for the Henry Reaction/ E. S. Mozhaitsev, K. Y. Ponomarev, O. S. Patrusheva, A. V. Medvedko, A. I. Dalinger, A. D. Rogachev, N. I. Komarova, D. V. Korchagina, E. V. Suslov, K. P. Volcho, N. F. Salakhutdinov, S. Z. Vatsadze// Russian Journal of Organic Chemistry, 2020, V.56, N 11, Pp 1969-1981 doi:10.1134/S1070428020110123), IF=0.624
2. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
   Changes in Amino Acid and Acylcarnitine Plasma Profiles for Distinguishing Patients with Multiple Sclerosis from Healthy Controls
   Multiple Sclerosis International, 2020, V. 2020, Art. Number 9010937 doi:10.1155/2020/9010937
3. A.D. Rogachev, D.V. Trebushat, A.N. Kudryashov, A.G. Pokrovsky
   Study of Sirolimus Adsorption and Preparation of Its Samples in Methanol, Acetonitrile and Their Mixtures with Water for HPLC-MS/MS Analysis
   Chromatographia, 2020, V. 83, N 2, pp 299-304 doi:10.1007/s10337-019-03835-5, IF=1.596
4. A.A. Okhina, A.D. Rogachev, O.I. Yarovaya, M.V. Khvostov, T.G. Tolstikova, A.G. Pokrovsky, V.A. Khazanov, N.F. Salakhutdinov
   Development and validation of an LC-MS/MS method for the quantitative analysis of the anti-influenza agent camphecene in rat plasma and its application to study the blood-to-plasma distribution of the agent
   Journal of Pharmaceutical and Biomedical Analysis, 2020, V. 180, 113039 doi:10.1016/j.jpba.2019.113039, IF=3.209

Reviews, articles

1. A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
   Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
   Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789
2. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
   Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
   Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394

Reviews, articles

1. A.D. Rogachev, O.I. Yarovaya, A.V. Fatianova, V.A. Lavrinenko, E.V. Amosov, V.V. Zarubaev, A.G. Pokrovsky, N.F. Salakhutdinov
   Untargeted search and identification of metabolites of antiviral agent camphecene in rat urine by liquid chromatography and mass spectrometry and studying their distribution in organs following peroral administration of the compound
   Journal of Pharmaceutical and Biomedical Analysis, 2018, V. 161, Pp 383-392 doi:10.1016/j.jpba.2018.09.003, IF=2.831
2. Т.В. Рыбалова, А.Д. Рогачев, Т.М. Хоменко, К.П. Волчо, Н.Ф. Салахутдинов
   Молекулярная и супрамолекулярная структура 8-(трифторметил)бензо[F[1,2,3,4,5]пентатиепин-6-амина - представителя конденсированных аренпентатиепинов
   Журнал структурной химии. 2018. Т. 59. № 7. С. 1811-1815. DOI:10.26902/JSC20180732 (Molecular and Supramolecular Structure of 8-(Trifluoromethyl)Benzo[f][1,2,3,4,5] Pentathiepin-6-Amine - A Representative of Condensed Arene Pentathiepines/ T. V. Rybalova, A. D. Rogachev, T. M. Khomenko, K. P. Volcho, N. F. Salakhutdinov// Journal of Structural Chemistry, 2018, V. 59, N 7, pp 1753-1758 doi:10.1134/S0022476618070326), IF=0.521
3. K.Yu. Ponomarev, E.V. Suslov, A.L. Zakharenko, O.D. Zakharova, A.D. Rogachev, D.V. Korchagina, A. Zafar, J. Reynisson, A.A. Nefedov, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
   Aminoadamantanes Containing Monoterpene-derived Fragments as Potent Tyrosyl-DNA phosphodiesterase 1 Inhibitors
   Bioorganic Chemistry, V.76, February 2018, Pp. 392-399 doi:10.1016/j.bioorg.2017.12.005, IF=3.929

Reviews, articles

1. А.Д. Рогачев, С.О. Куранов, Н.Ф. Салахутдинов
   Противодиабетические соединения: эффективный подход к разработке препаратов
   Успехи химии, 2016, Т.85, N 12, Сс 1313-1337 (Chemical approach to the design of effective antidiabetic agents/ A D Rogachev, ab S O Kuranov, a N F Salakhutdinov// RUSS CHEM REV, 2016, V. 85, N 12, Pp 1313-1337 doi:10.1070/RCR4624), IF=3.687
2. A.D. Rogachev, O.I. Yarovaya, S.V. Ankov, M.V. Khvostov, T.G. Tolstikova, A.G. Pokrovsky, N.F. Salakhutdinov
   Development and validation of ultrafast LC–MS/MS method for quantification of anti-influenza agent camphecene in whole rat blood using dried blood spots and its application to pharmacokinetic studies
   Journal of Chromatography B, Volumes 1036-1037, 15 November 2016, Pages 136-141 doi:10.1016/j.jchromb.2016.10.009, IF=2.687

Reviews, articles

1. A. Pavlova, O. Mikhalchenko, A. Rogachev, I. Il'ina, D. Korchagina, Yu. Gatilov, T. Tolstikova, K. Volcho, N. Salakhutdinov
   Synthesis and analgesic activity of stereoisomers of 2-(3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols
   Medicinal Chemistry Research, 2015, V 24, N 11, pp 3821-3830 doi:10.1007/s00044-015-1426-5, IF=1.401
2. E.V. Suslov, K.Yu. Ponomarev, A.D. Rogachev, M.A. Pokrovsky, A.G. Pokrovsky, M.B. Pykhtina, A.B. Beklemishev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
   Compounds Combining Aminoadamantane and Monoterpene Moieties: Cytotoxicity and Mutagenic Effects
   Medicinal Chemistry, V. 11, N 7, Pp 629 - 635 doi:10.2174/1573406411666150518110053, IF=1.363
3. A.D. Rogachev, N.F. Salakhutdinov
   Chemical Composition of Pinus sibirica (Pinaceae)
   Chemistry & Biodiversity, 2015, V. 12, N 1, pp 1-53 doi:10.1002/cbdv.201300195, IF=1.515

Reviews, articles

1. M.A. Gilinsky, A.D. Rogachev, N.I. Komarova, N.F. Salakhutdinov, G.A. Tolstikov, S.E. Naumenko, T.V. Latysheva
   Cardioprotective Effect of Resveratrol and Resveratroloside
   Cardiovascular & Hematological Agents in Medicinal Chemistry., 2013, V. 11 N 3, P. 207 - 210. doi:10.2174/187152571103140120103302
2. G.V. Teplov, E.V. Suslov, V.V. Zarubaev, A.A. Shtro, L.A. Karpinskaya, A.D. Rogachev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
   Synthesis of New Compounds Combining Adamantanamine and Monoterpene Fragments and their Antiviral Activity Against Influenza Virus A(H1N1)pdm09
   Letters in Drug Design & Discovery, 2013, V. 10, N 6, P. 477-485. doi:10.2174/1570180811310060002, IF=0.845
3. A.V. Pozdeeva, N.I. Komarova, V.G. Vasiliev, A.D. Rogachev, N.F. Salakhutdinov, G.A. Tolstikov
   Aryloxyacetamides derived from resveratroloside and pinostilbenoside
   Mendeleev Communications, 2013, V. 23, N 1, P. 37-38. doi:10.1016/j.mencom.2013.01.013, IF=1.52

Reviews, articles

1. A.D. Rogachev, N.I. Komarova, D.V. Korchagina, V.G. Vasil'Ev, N.F. Salakhutdinov, G.A. Tolstikov, A.V. Pozdeeva
   REACTION OF SEVERAL RESVERATROL GLYCOSIDE DERIVATIVES WITH HYPOCHLORITES IN VARIOUS MEDIA
   Chem. Nat. Compd., 2012, V. 48, N 1, pp. 1-7. doi:10.1007/s10600-012-0146-z, IF=1.29

Reviews, articles

1. А.Д. Рогачев, Н.И. Комарова, Д.В. Корчагина, М.П. Долгих, И.В. Сорокина, Д.С. Баев, Т.Г. Толстикова, В.В. Фоменко, Н.Ф. Салахутдинов
   Некоторые пренилированные фенолы рододендрона Адамса Rhododendron adamsii: выделение, модификация и фармакологические испытания
   Химия в интересах устойчивого развития, 2009. Т.17. N 2, C. 191-198.
2. N.I. Komarova, A.D. Rogachev, E.I. Chernyak, S.V. Morozov, V.V. Fomenko, N.F. Salakhutdinov
   Quantitative HPLC determination of main flavonoid content of Rhododendron adamsii leaves and stems
   Chemistry of Natural Compounds, 2009, V. 45, N 1, pp 27-31. doi:10.1007/s10600-009-9215-3, IF=0.467

Reviews, articles

1. А.Д. Рогачев, С.В. Морозов, А.И. Вялков, В.В. Фоменко, Н.Ф. Салахутдинов
   Фитохимическое исследование рододендрона Адамса Rhododendron adamsii Rehder. Количественное содержание жирных кислот в листьях и стеблях
   Хим. Инт. Уст. Разв., 2007, Т. 15, № 5, 575-579.

Reviews, articles

1. A. D. Rogachev, V. V. Fomenko, O. I. Sal’nikova, L. M. Pokrovskii, N. F. Salakhutdinov
   Comparative analysis of essential oil compositions from leaves and stems of Rhododendron adamsii, R. aureum, and R. dauricum
   Chemistry of Natural Compounds, 2006, V. 42, N 4, pp 426-430 doi:10.1007/s10600-006-0172-9, IF=0.31